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Record Information

Version

5.0

Status

Expected but not Quantified

Creation Date

2007-05-25 09:44:33 UTC

Update Date

2021-09-14 15:46:06 UTC

HMDB ID

HMDB0006607

Secondary Accession Numbers

HMDB06607

Metabolite Identification

Common Name

3'-Sialyllactosamine

Description

3'-Sialyllactosamine is an oligosaccharide found in human milk. Oligosaccharides in human milk inhibit enteric pathogens in vitro and in vivo. (PMID:10683228 )

Helicobacter pylori-induced activation of neutrophils occurs by lectinophagocytosis, the recognition of sialylated glycoconjugates (3'-sialyllactosamine was the most efficient inhibitor) on the neutrophil cell surface by a bacterial adhesin leads to phagocytosis and an oxidative burst with the production of reactive oxygen metabolites. (PMID: 11087709 )

Structure

MOL 3D MOL SDF 3D SDF PDB 3D PDB SMILES InChI


  Mrv0541 02231220452D          

 43 44  0  0  1  0            999 V2000
   11.3918   -8.6123    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.5189   -7.4853    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   14.6622   -6.2478    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   13.5353   -9.8498    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   13.9478   -5.0103    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   13.9478   -8.3103    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.5189   -5.8353    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.6775  -10.6747    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.9629   -8.6123    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.8689   -7.4853    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.1064   -6.7708    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   16.0912   -7.0729    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.5340   -9.4373    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   15.3767   -3.3603    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   15.3767   -5.8353    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   13.5353  -10.6747    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   16.8057   -5.0103    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   14.6622   -2.1228    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.1064  -10.6747    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   13.2334   -3.7728    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   12.1064   -8.1998    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   12.1064   -9.8498    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   11.3918   -9.4373    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.8208   -9.4373    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   13.2334   -7.0729    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   12.8208   -8.6123    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.9478   -7.4853    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   13.2334   -6.2478    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   10.6775   -9.8498    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   14.6622   -7.0729    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   13.9478   -5.8353    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    9.9629   -9.4373    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   11.6939   -7.4853    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.3767   -7.4853    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.6622   -4.5978    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    9.2485   -9.8498    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.6622   -3.7728    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   12.8208  -11.0872    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.3767   -5.0103    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   13.9478   -3.3603    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   16.0912   -4.5978    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.8208  -11.9122    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.9478   -2.5353    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1 21  1  0  0  0  0
  1 23  1  0  0  0  0
 21  2  1  6  0  0  0
 25  2  1  6  0  0  0
  3 30  1  0  0  0  0
  3 31  1  0  0  0  0
 24  4  1  6  0  0  0
 31  5  1  6  0  0  0
 35  5  1  1  0  0  0
 27  6  1  6  0  0  0
 28  7  1  1  0  0  0
 29  8  1  6  0  0  0
 32  9  1  1  0  0  0
 10 33  1  0  0  0  0
 11 33  2  0  0  0  0
 12 34  1  0  0  0  0
 13 36  1  0  0  0  0
 37 14  1  1  0  0  0
 39 15  1  1  0  0  0
 16 38  2  0  0  0  0
 17 41  1  0  0  0  0
 18 43  2  0  0  0  0
 22 19  1  1  0  0  0
 19 38  1  0  0  0  0
 40 20  1  1  0  0  0
 21 26  1  0  0  0  0
 21 33  1  0  0  0  0
 22 23  1  0  0  0  0
 22 24  1  0  0  0  0
 23 29  1  0  0  0  0
 24 26  1  0  0  0  0
 25 27  1  0  0  0  0
 25 28  1  0  0  0  0
 27 30  1  0  0  0  0
 28 31  1  0  0  0  0
 29 32  1  0  0  0  0
 30 34  1  6  0  0  0
 32 36  1  0  0  0  0
 35 37  1  0  0  0  0
 35 39  1  0  0  0  0
 37 40  1  0  0  0  0
 38 42  1  0  0  0  0
 39 41  1  0  0  0  0
 40 43  1  0  0  0  0
M  END

HMDB0006607
     RDKit          3D
3'-Sialyllactosamine
 83 84  0  0  0  0  0  0  0  0999 V2000
   -7.4894    0.4948    0.2504 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2549    0.1447   -0.4944 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2770    0.1212   -1.7457 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0654   -0.1598    0.1783 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8039   -0.5154   -0.4935 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.6984    0.3979   -0.1234 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9776    1.0218   -1.2963 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.2285    2.0849   -0.7387 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8430    1.6153   -2.3452 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.9583    2.2140   -3.2789 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7445    2.7188   -1.8750 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0189    3.7557   -1.2630 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7701   -0.0267    0.7675 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6137   -1.3698    0.9903 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.2324   -1.6015    1.1332 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3055   -0.9079    2.1609 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.0995   -1.6661    3.1811 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.3868   -2.7799    3.6677 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3479   -2.1521    2.5408 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.2422   -3.6491    2.2749 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3727   -3.9369    1.2265 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7866   -1.5434    1.4164 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5207   -0.2140    1.2675 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.6954    0.0869   -0.0814 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7909    0.9899   -0.2692 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.1728    2.2380   -0.9079 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.2408    2.8114   -0.0833 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4196    1.8385   -2.1794 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4052    0.9345   -1.8839 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7919    0.3736   -1.1847 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.0126   -0.9684   -0.6893 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.1938    0.9854   -1.1213 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.0597    0.2508   -2.0502 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.3255    2.4134   -1.1577 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1803    3.1281   -0.1413 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2015    0.2467    1.7221 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.3125    1.1830    2.7686 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3953   -1.7112    2.1987 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9927   -0.8103    2.8887 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5654   -2.9937    2.7001 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1143   -2.2390   -0.1307 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5981   -1.9699   -0.2379 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.2238   -2.7690   -1.1818 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.3810    0.0241   -0.2089 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3972    0.2906    1.3322 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5934    1.6162    0.1759 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0631   -0.1355    1.2297 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0708   -0.4473   -1.5945 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1919    1.2946    0.3775 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2545    0.3472   -1.7652 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7806    2.5976   -1.4396 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4396    0.9134   -2.9454 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1844    2.0197   -4.2005 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5921    2.4112   -1.2702 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1812    3.1994   -2.8011 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5802    4.3478   -0.7400 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5571   -0.3616    2.6728 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3689   -1.0029    4.0517 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0534   -3.3741    2.9874 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1605   -2.0553    3.3248 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8895   -4.1343    3.1941 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2888   -3.9754    2.0275 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7391   -4.6211    0.6123 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3116    0.3538    1.8204 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2386    1.2525    0.6705 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9318    2.9281   -1.2256 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2910    3.8087   -0.1186 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9298    2.7675   -2.5467 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0891    1.4876   -2.9759 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1116    0.5417   -2.7499 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4945    0.2252   -2.2162 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2558   -0.9425    0.2526 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5770    0.6429   -0.1024 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.4456   -0.6086   -1.6516 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6040    0.1757   -2.9649 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5597    3.0156   -2.0497 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6692    0.7658    0.9010 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1354    1.7273    2.6682 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4272   -3.8386    2.1467 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0041   -3.2953    0.1942 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5692   -2.1235   -1.0647 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0155   -2.2102    0.7753 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8604   -3.6935   -1.1630 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  2  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  7  9  1  0
  9 10  1  0
  9 11  1  0
 11 12  1  0
  6 13  1  0
 13 14  1  0
 14 15  1  1
 15 16  1  0
 16 17  1  0
 17 18  1  0
 17 19  1  0
 19 20  1  0
 20 21  1  0
 19 22  1  0
 22 23  1  0
 23 24  1  0
 24 25  1  0
 25 26  1  0
 26 27  1  0
 26 28  1  0
 28 29  1  0
 25 30  1  0
 30 31  1  0
 30 32  1  0
 32 33  1  0
 32 34  1  0
 34 35  2  0
 23 36  1  0
 36 37  1  0
 14 38  1  0
 38 39  2  0
 38 40  1  0
 14 41  1  0
 41 42  1  0
 42 43  1  0
 42  5  1  0
 36 16  1  0
  1 44  1  0
  1 45  1  0
  1 46  1  0
  4 47  1  0
  5 48  1  6
  6 49  1  0
  7 50  1  6
  8 51  1  0
  9 52  1  6
 10 53  1  0
 11 54  1  0
 11 55  1  0
 12 56  1  0
 16 57  1  1
 17 58  1  1
 18 59  1  0
 19 60  1  1
 20 61  1  0
 20 62  1  0
 21 63  1  0
 23 64  1  1
 25 65  1  1
 26 66  1  6
 27 67  1  0
 28 68  1  0
 28 69  1  0
 29 70  1  0
 30 71  1  6
 31 72  1  0
 32 73  1  1
 33 74  1  0
 33 75  1  0
 34 76  1  0
 36 77  1  6
 37 78  1  0
 40 79  1  0
 41 80  1  0
 41 81  1  0
 42 82  1  1
 43 83  1  0
M  END


  Mrv0541 02231220452D          

 43 44  0  0  1  0            999 V2000
   11.3918   -8.6123    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.5189   -7.4853    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   14.6622   -6.2478    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   13.5353   -9.8498    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   13.9478   -5.0103    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   13.9478   -8.3103    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.5189   -5.8353    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.6775  -10.6747    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.9629   -8.6123    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.8689   -7.4853    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.1064   -6.7708    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   16.0912   -7.0729    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.5340   -9.4373    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   15.3767   -3.3603    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   15.3767   -5.8353    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   13.5353  -10.6747    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   16.8057   -5.0103    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   14.6622   -2.1228    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.1064  -10.6747    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   13.2334   -3.7728    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   12.1064   -8.1998    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   12.1064   -9.8498    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   11.3918   -9.4373    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.8208   -9.4373    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   13.2334   -7.0729    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   12.8208   -8.6123    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.9478   -7.4853    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   13.2334   -6.2478    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   10.6775   -9.8498    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   14.6622   -7.0729    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   13.9478   -5.8353    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    9.9629   -9.4373    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   11.6939   -7.4853    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.3767   -7.4853    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.6622   -4.5978    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    9.2485   -9.8498    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.6622   -3.7728    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   12.8208  -11.0872    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.3767   -5.0103    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   13.9478   -3.3603    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   16.0912   -4.5978    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.8208  -11.9122    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.9478   -2.5353    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1 21  1  0  0  0  0
  1 23  1  0  0  0  0
 21  2  1  6  0  0  0
 25  2  1  6  0  0  0
  3 30  1  0  0  0  0
  3 31  1  0  0  0  0
 24  4  1  6  0  0  0
 31  5  1  6  0  0  0
 35  5  1  1  0  0  0
 27  6  1  6  0  0  0
 28  7  1  1  0  0  0
 29  8  1  6  0  0  0
 32  9  1  1  0  0  0
 10 33  1  0  0  0  0
 11 33  2  0  0  0  0
 12 34  1  0  0  0  0
 13 36  1  0  0  0  0
 37 14  1  1  0  0  0
 39 15  1  1  0  0  0
 16 38  2  0  0  0  0
 17 41  1  0  0  0  0
 18 43  2  0  0  0  0
 22 19  1  1  0  0  0
 19 38  1  0  0  0  0
 40 20  1  1  0  0  0
 21 26  1  0  0  0  0
 21 33  1  0  0  0  0
 22 23  1  0  0  0  0
 22 24  1  0  0  0  0
 23 29  1  0  0  0  0
 24 26  1  0  0  0  0
 25 27  1  0  0  0  0
 25 28  1  0  0  0  0
 27 30  1  0  0  0  0
 28 31  1  0  0  0  0
 29 32  1  0  0  0  0
 30 34  1  6  0  0  0
 32 36  1  0  0  0  0
 35 37  1  0  0  0  0
 35 39  1  0  0  0  0
 37 40  1  0  0  0  0
 38 42  1  0  0  0  0
 39 41  1  0  0  0  0
 40 43  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0006607

> <DATABASE_NAME>
hmdb

> <SMILES>
CC(=O)N[C@@H]1[C@@H](O)C[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(OC1[C@H](O)[C@H](O)CO)C(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C23H40N2O18/c1-7(30)25-13-9(31)2-23(22(38)39,42-19(13)15(35)10(32)4-27)43-20-16(36)12(6-29)40-21(17(20)37)41-18(11(33)5-28)14(34)8(24)3-26/h3,8-21,27-29,31-37H,2,4-6,24H2,1H3,(H,25,30)(H,38,39)/t8-,9-,10+,11+,12+,13+,14+,15+,16-,17+,18+,19?,20-,21-,23-/m0/s1

> <INCHI_KEY>
MKNNYTWMAUAKMA-FRLIKFETSA-N

> <FORMULA>
C23H40N2O18

> <MOLECULAR_WEIGHT>
632.5663

> <EXACT_MASS>
632.227612486

> <JCHEM_ACCEPTOR_COUNT>
19

> <JCHEM_AVERAGE_POLARIZABILITY>
58.97566619414229

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
13

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2S,4S,5R)-2-{[(2S,3R,4S,5S,6R)-2-{[(2R,3S,4R,5R)-5-amino-1,2,4-trihydroxy-6-oxohexan-3-yl]oxy}-3,5-dihydroxy-6-(hydroxymethyl)oxan-4-yl]oxy}-5-acetamido-4-hydroxy-6-[(1R,2R)-1,2,3-trihydroxypropyl]oxane-2-carboxylic acid

> <ALOGPS_LOGP>
-2.95

> <JCHEM_LOGP>
-10.113091384356675

> <ALOGPS_LOGS>
-0.90

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.05855639007434

> <JCHEM_PKA_STRONGEST_ACIDIC>
2.537854356784232

> <JCHEM_PKA_STRONGEST_BASIC>
7.157525326494104

> <JCHEM_POLAR_SURFACE_AREA>
348.7099999999999

> <JCHEM_REFRACTIVITY>
131.68769999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
15

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
7.96e+01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2S,4S,5R)-2-{[(2S,3R,4S,5S,6R)-2-{[(2R,3S,4R,5R)-5-amino-1,2,4-trihydroxy-6-oxohexan-3-yl]oxy}-3,5-dihydroxy-6-(hydroxymethyl)oxan-4-yl]oxy}-5-acetamido-4-hydroxy-6-[(1R,2R)-1,2,3-trihydroxypropyl]oxane-2-carboxylic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0006607
     RDKit          3D
3'-Sialyllactosamine
 83 84  0  0  0  0  0  0  0  0999 V2000
   -7.4894    0.4948    0.2504 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2549    0.1447   -0.4944 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2770    0.1212   -1.7457 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0654   -0.1598    0.1783 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8039   -0.5154   -0.4935 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.6984    0.3979   -0.1234 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9776    1.0218   -1.2963 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.2285    2.0849   -0.7387 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8430    1.6153   -2.3452 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.9583    2.2140   -3.2789 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7445    2.7188   -1.8750 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0189    3.7557   -1.2630 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7701   -0.0267    0.7675 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6137   -1.3698    0.9903 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.2324   -1.6015    1.1332 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3055   -0.9079    2.1609 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.0995   -1.6661    3.1811 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.3868   -2.7799    3.6677 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3479   -2.1521    2.5408 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.2422   -3.6491    2.2749 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3727   -3.9369    1.2265 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7866   -1.5434    1.4164 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5207   -0.2140    1.2675 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.6954    0.0869   -0.0814 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7909    0.9899   -0.2692 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.1728    2.2380   -0.9079 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.2408    2.8114   -0.0833 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4196    1.8385   -2.1794 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4052    0.9345   -1.8839 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7919    0.3736   -1.1847 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.0126   -0.9684   -0.6893 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.1938    0.9854   -1.1213 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.0597    0.2508   -2.0502 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.3255    2.4134   -1.1577 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1803    3.1281   -0.1413 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2015    0.2467    1.7221 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.3125    1.1830    2.7686 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3953   -1.7112    2.1987 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9927   -0.8103    2.8887 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5654   -2.9937    2.7001 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1143   -2.2390   -0.1307 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5981   -1.9699   -0.2379 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.2238   -2.7690   -1.1818 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.3810    0.0241   -0.2089 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3972    0.2906    1.3322 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5934    1.6162    0.1759 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0631   -0.1355    1.2297 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0708   -0.4473   -1.5945 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1919    1.2946    0.3775 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2545    0.3472   -1.7652 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7806    2.5976   -1.4396 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4396    0.9134   -2.9454 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1844    2.0197   -4.2005 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5921    2.4112   -1.2702 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1812    3.1994   -2.8011 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5802    4.3478   -0.7400 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5571   -0.3616    2.6728 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3689   -1.0029    4.0517 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0534   -3.3741    2.9874 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1605   -2.0553    3.3248 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8895   -4.1343    3.1941 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2888   -3.9754    2.0275 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7391   -4.6211    0.6123 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3116    0.3538    1.8204 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2386    1.2525    0.6705 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9318    2.9281   -1.2256 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2910    3.8087   -0.1186 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9298    2.7675   -2.5467 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0891    1.4876   -2.9759 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1116    0.5417   -2.7499 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4945    0.2252   -2.2162 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2558   -0.9425    0.2526 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5770    0.6429   -0.1024 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.4456   -0.6086   -1.6516 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6040    0.1757   -2.9649 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5597    3.0156   -2.0497 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6692    0.7658    0.9010 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1354    1.7273    2.6682 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4272   -3.8386    2.1467 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0041   -3.2953    0.1942 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5692   -2.1235   -1.0647 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0155   -2.2102    0.7753 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8604   -3.6935   -1.1630 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  2  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  7  9  1  0
  9 10  1  0
  9 11  1  0
 11 12  1  0
  6 13  1  0
 13 14  1  0
 14 15  1  1
 15 16  1  0
 16 17  1  0
 17 18  1  0
 17 19  1  0
 19 20  1  0
 20 21  1  0
 19 22  1  0
 22 23  1  0
 23 24  1  0
 24 25  1  0
 25 26  1  0
 26 27  1  0
 26 28  1  0
 28 29  1  0
 25 30  1  0
 30 31  1  0
 30 32  1  0
 32 33  1  0
 32 34  1  0
 34 35  2  0
 23 36  1  0
 36 37  1  0
 14 38  1  0
 38 39  2  0
 38 40  1  0
 14 41  1  0
 41 42  1  0
 42 43  1  0
 42  5  1  0
 36 16  1  0
  1 44  1  0
  1 45  1  0
  1 46  1  0
  4 47  1  0
  5 48  1  6
  6 49  1  0
  7 50  1  6
  8 51  1  0
  9 52  1  6
 10 53  1  0
 11 54  1  0
 11 55  1  0
 12 56  1  0
 16 57  1  1
 17 58  1  1
 18 59  1  0
 19 60  1  1
 20 61  1  0
 20 62  1  0
 21 63  1  0
 23 64  1  1
 25 65  1  1
 26 66  1  6
 27 67  1  0
 28 68  1  0
 28 69  1  0
 29 70  1  0
 30 71  1  6
 31 72  1  0
 32 73  1  1
 33 74  1  0
 33 75  1  0
 34 76  1  0
 36 77  1  6
 37 78  1  0
 40 79  1  0
 41 80  1  0
 41 81  1  0
 42 82  1  1
 43 83  1  0
M  END

HEADER    PROTEIN                                 23-FEB-12   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   23-FEB-12         0                                  
HETATM    1  O   UNK     0      21.265 -16.076   0.000  0.00  0.00           O+0
HETATM    2  O   UNK     0      23.369 -13.973   0.000  0.00  0.00           O+0
HETATM    3  O   UNK     0      27.369 -11.663   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0      25.266 -18.386   0.000  0.00  0.00           O+0
HETATM    5  O   UNK     0      26.036  -9.353   0.000  0.00  0.00           O+0
HETATM    6  O   UNK     0      26.036 -15.513   0.000  0.00  0.00           O+0
HETATM    7  O   UNK     0      23.369 -10.893   0.000  0.00  0.00           O+0
HETATM    8  O   UNK     0      19.931 -19.926   0.000  0.00  0.00           O+0
HETATM    9  O   UNK     0      18.597 -16.076   0.000  0.00  0.00           O+0
HETATM   10  O   UNK     0      20.289 -13.973   0.000  0.00  0.00           O+0
HETATM   11  O   UNK     0      22.599 -12.639   0.000  0.00  0.00           O+0
HETATM   12  O   UNK     0      30.037 -13.203   0.000  0.00  0.00           O+0
HETATM   13  O   UNK     0      15.930 -17.616   0.000  0.00  0.00           O+0
HETATM   14  O   UNK     0      28.703  -6.273   0.000  0.00  0.00           O+0
HETATM   15  O   UNK     0      28.703 -10.893   0.000  0.00  0.00           O+0
HETATM   16  O   UNK     0      25.266 -19.926   0.000  0.00  0.00           O+0
HETATM   17  O   UNK     0      31.371  -9.353   0.000  0.00  0.00           O+0
HETATM   18  O   UNK     0      27.369  -3.963   0.000  0.00  0.00           O+0
HETATM   19  N   UNK     0      22.599 -19.926   0.000  0.00  0.00           N+0
HETATM   20  N   UNK     0      24.702  -7.043   0.000  0.00  0.00           N+0
HETATM   21  C   UNK     0      22.599 -15.306   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      22.599 -18.386   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      21.265 -17.616   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      23.932 -17.616   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      24.702 -13.203   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      23.932 -16.076   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      26.036 -13.973   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      24.702 -11.663   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      19.931 -18.386   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      27.369 -13.203   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      26.036 -10.893   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      18.597 -17.616   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      21.829 -13.973   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      28.703 -13.973   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      27.369  -8.583   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      17.264 -18.386   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0      27.369  -7.043   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0      23.932 -20.696   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0      28.703  -9.353   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0      26.036  -6.273   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0      30.037  -8.583   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0      23.932 -22.236   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0      26.036  -4.733   0.000  0.00  0.00           C+0
CONECT    1   21   23                                                       
CONECT    2   21   25                                                       
CONECT    3   30   31                                                       
CONECT    4   24                                                            
CONECT    5   31   35                                                       
CONECT    6   27                                                            
CONECT    7   28                                                            
CONECT    8   29                                                            
CONECT    9   32                                                            
CONECT   10   33                                                            
CONECT   11   33                                                            
CONECT   12   34                                                            
CONECT   13   36                                                            
CONECT   14   37                                                            
CONECT   15   39                                                            
CONECT   16   38                                                            
CONECT   17   41                                                            
CONECT   18   43                                                            
CONECT   19   22   38                                                       
CONECT   20   40                                                            
CONECT   21    1    2   26   33                                             
CONECT   22   19   23   24                                                  
CONECT   23    1   22   29                                                  
CONECT   24    4   22   26                                                  
CONECT   25    2   27   28                                                  
CONECT   26   21   24                                                       
CONECT   27    6   25   30                                                  
CONECT   28    7   25   31                                                  
CONECT   29    8   23   32                                                  
CONECT   30    3   27   34                                                  
CONECT   31    3    5   28                                                  
CONECT   32    9   29   36                                                  
CONECT   33   10   11   21                                                  
CONECT   34   12   30                                                       
CONECT   35    5   37   39                                                  
CONECT   36   13   32                                                       
CONECT   37   14   35   40                                                  
CONECT   38   16   19   42                                                  
CONECT   39   15   35   41                                                  
CONECT   40   20   37   43                                                  
CONECT   41   17   39                                                       
CONECT   42   38                                                            
CONECT   43   18   40                                                       
MASTER        0    0    0    0    0    0    0    0   43    0   88    0
END

COMPND    HMDB0006607
HETATM    1  C1  UNL     1      -7.489   0.495   0.250  1.00  0.00           C  
HETATM    2  C2  UNL     1      -6.255   0.145  -0.494  1.00  0.00           C  
HETATM    3  O1  UNL     1      -6.277   0.121  -1.746  1.00  0.00           O  
HETATM    4  N1  UNL     1      -5.065  -0.160   0.178  1.00  0.00           N  
HETATM    5  C3  UNL     1      -3.804  -0.515  -0.494  1.00  0.00           C  
HETATM    6  C4  UNL     1      -2.698   0.398  -0.123  1.00  0.00           C  
HETATM    7  C5  UNL     1      -1.978   1.022  -1.296  1.00  0.00           C  
HETATM    8  O2  UNL     1      -1.229   2.085  -0.739  1.00  0.00           O  
HETATM    9  C6  UNL     1      -2.843   1.615  -2.345  1.00  0.00           C  
HETATM   10  O3  UNL     1      -1.958   2.214  -3.279  1.00  0.00           O  
HETATM   11  C7  UNL     1      -3.744   2.719  -1.875  1.00  0.00           C  
HETATM   12  O4  UNL     1      -3.019   3.756  -1.263  1.00  0.00           O  
HETATM   13  O5  UNL     1      -1.770  -0.027   0.768  1.00  0.00           O  
HETATM   14  C8  UNL     1      -1.614  -1.370   0.990  1.00  0.00           C  
HETATM   15  O6  UNL     1      -0.232  -1.601   1.133  1.00  0.00           O  
HETATM   16  C9  UNL     1       0.305  -0.908   2.161  1.00  0.00           C  
HETATM   17  C10 UNL     1       1.100  -1.666   3.181  1.00  0.00           C  
HETATM   18  O7  UNL     1       0.387  -2.780   3.668  1.00  0.00           O  
HETATM   19  C11 UNL     1       2.348  -2.152   2.541  1.00  0.00           C  
HETATM   20  C12 UNL     1       2.242  -3.649   2.275  1.00  0.00           C  
HETATM   21  O8  UNL     1       1.373  -3.937   1.227  1.00  0.00           O  
HETATM   22  O9  UNL     1       2.787  -1.543   1.416  1.00  0.00           O  
HETATM   23  C13 UNL     1       2.521  -0.214   1.267  1.00  0.00           C  
HETATM   24  O10 UNL     1       2.695   0.087  -0.081  1.00  0.00           O  
HETATM   25  C14 UNL     1       3.791   0.990  -0.269  1.00  0.00           C  
HETATM   26  C15 UNL     1       3.173   2.238  -0.908  1.00  0.00           C  
HETATM   27  O11 UNL     1       2.241   2.811  -0.083  1.00  0.00           O  
HETATM   28  C16 UNL     1       2.420   1.839  -2.179  1.00  0.00           C  
HETATM   29  O12 UNL     1       1.405   0.934  -1.884  1.00  0.00           O  
HETATM   30  C17 UNL     1       4.792   0.374  -1.185  1.00  0.00           C  
HETATM   31  O13 UNL     1       5.013  -0.968  -0.689  1.00  0.00           O  
HETATM   32  C18 UNL     1       6.194   0.985  -1.121  1.00  0.00           C  
HETATM   33  N2  UNL     1       7.060   0.251  -2.050  1.00  0.00           N  
HETATM   34  C19 UNL     1       6.326   2.413  -1.158  1.00  0.00           C  
HETATM   35  O14 UNL     1       6.180   3.128  -0.141  1.00  0.00           O  
HETATM   36  C20 UNL     1       1.201   0.247   1.722  1.00  0.00           C  
HETATM   37  O15 UNL     1       1.313   1.183   2.769  1.00  0.00           O  
HETATM   38  C21 UNL     1      -2.395  -1.711   2.199  1.00  0.00           C  
HETATM   39  O16 UNL     1      -2.993  -0.810   2.889  1.00  0.00           O  
HETATM   40  O17 UNL     1      -2.565  -2.994   2.700  1.00  0.00           O  
HETATM   41  C22 UNL     1      -2.114  -2.239  -0.131  1.00  0.00           C  
HETATM   42  C23 UNL     1      -3.598  -1.970  -0.238  1.00  0.00           C  
HETATM   43  O18 UNL     1      -4.224  -2.769  -1.182  1.00  0.00           O  
HETATM   44  H1  UNL     1      -8.381   0.024  -0.209  1.00  0.00           H  
HETATM   45  H2  UNL     1      -7.397   0.291   1.332  1.00  0.00           H  
HETATM   46  H3  UNL     1      -7.593   1.616   0.176  1.00  0.00           H  
HETATM   47  H4  UNL     1      -5.063  -0.136   1.230  1.00  0.00           H  
HETATM   48  H5  UNL     1      -4.071  -0.447  -1.594  1.00  0.00           H  
HETATM   49  H6  UNL     1      -3.192   1.295   0.378  1.00  0.00           H  
HETATM   50  H7  UNL     1      -1.255   0.347  -1.765  1.00  0.00           H  
HETATM   51  H8  UNL     1      -0.781   2.598  -1.440  1.00  0.00           H  
HETATM   52  H9  UNL     1      -3.440   0.913  -2.945  1.00  0.00           H  
HETATM   53  H10 UNL     1      -2.184   2.020  -4.200  1.00  0.00           H  
HETATM   54  H11 UNL     1      -4.592   2.411  -1.270  1.00  0.00           H  
HETATM   55  H12 UNL     1      -4.181   3.199  -2.801  1.00  0.00           H  
HETATM   56  H13 UNL     1      -3.580   4.348  -0.740  1.00  0.00           H  
HETATM   57  H14 UNL     1      -0.557  -0.362   2.673  1.00  0.00           H  
HETATM   58  H15 UNL     1       1.369  -1.003   4.052  1.00  0.00           H  
HETATM   59  H16 UNL     1       0.053  -3.374   2.987  1.00  0.00           H  
HETATM   60  H17 UNL     1       3.160  -2.055   3.325  1.00  0.00           H  
HETATM   61  H18 UNL     1       1.889  -4.134   3.194  1.00  0.00           H  
HETATM   62  H19 UNL     1       3.289  -3.975   2.027  1.00  0.00           H  
HETATM   63  H20 UNL     1       1.739  -4.621   0.612  1.00  0.00           H  
HETATM   64  H21 UNL     1       3.312   0.354   1.820  1.00  0.00           H  
HETATM   65  H22 UNL     1       4.239   1.252   0.670  1.00  0.00           H  
HETATM   66  H23 UNL     1       3.932   2.928  -1.226  1.00  0.00           H  
HETATM   67  H24 UNL     1       2.291   3.809  -0.119  1.00  0.00           H  
HETATM   68  H25 UNL     1       1.930   2.768  -2.547  1.00  0.00           H  
HETATM   69  H26 UNL     1       3.089   1.488  -2.976  1.00  0.00           H  
HETATM   70  H27 UNL     1       1.112   0.542  -2.750  1.00  0.00           H  
HETATM   71  H28 UNL     1       4.494   0.225  -2.216  1.00  0.00           H  
HETATM   72  H29 UNL     1       5.256  -0.942   0.253  1.00  0.00           H  
HETATM   73  H30 UNL     1       6.577   0.643  -0.102  1.00  0.00           H  
HETATM   74  H31 UNL     1       7.446  -0.609  -1.652  1.00  0.00           H  
HETATM   75  H32 UNL     1       6.604   0.176  -2.965  1.00  0.00           H  
HETATM   76  H33 UNL     1       6.560   3.016  -2.050  1.00  0.00           H  
HETATM   77  H34 UNL     1       0.669   0.766   0.901  1.00  0.00           H  
HETATM   78  H35 UNL     1       2.135   1.727   2.668  1.00  0.00           H  
HETATM   79  H36 UNL     1      -2.427  -3.839   2.147  1.00  0.00           H  
HETATM   80  H37 UNL     1      -2.004  -3.295   0.194  1.00  0.00           H  
HETATM   81  H38 UNL     1      -1.569  -2.123  -1.065  1.00  0.00           H  
HETATM   82  H39 UNL     1      -4.016  -2.210   0.775  1.00  0.00           H  
HETATM   83  H40 UNL     1      -3.860  -3.693  -1.163  1.00  0.00           H  
CONECT    1    2   44   45   46
CONECT    2    3    3    4
CONECT    4    5   47
CONECT    5    6   42   48
CONECT    6    7   13   49
CONECT    7    8    9   50
CONECT    8   51
CONECT    9   10   11   52
CONECT   10   53
CONECT   11   12   54   55
CONECT   12   56
CONECT   13   14
CONECT   14   15   38   41
CONECT   15   16
CONECT   16   17   36   57
CONECT   17   18   19   58
CONECT   18   59
CONECT   19   20   22   60
CONECT   20   21   61   62
CONECT   21   63
CONECT   22   23
CONECT   23   24   36   64
CONECT   24   25
CONECT   25   26   30   65
CONECT   26   27   28   66
CONECT   27   67
CONECT   28   29   68   69
CONECT   29   70
CONECT   30   31   32   71
CONECT   31   72
CONECT   32   33   34   73
CONECT   33   74   75
CONECT   34   35   35   76
CONECT   36   37   77
CONECT   37   78
CONECT   38   39   39   40
CONECT   40   79
CONECT   41   42   80   81
CONECT   42   43   82
CONECT   43   83
END

HMDB0006607
     RDKit          3D
3'-Sialyllactosamine
 83 84  0  0  0  0  0  0  0  0999 V2000
   -7.4894    0.4948    0.2504 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2549    0.1447   -0.4944 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2770    0.1212   -1.7457 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0654   -0.1598    0.1783 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8039   -0.5154   -0.4935 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.6984    0.3979   -0.1234 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9776    1.0218   -1.2963 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.2285    2.0849   -0.7387 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8430    1.6153   -2.3452 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.9583    2.2140   -3.2789 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7445    2.7188   -1.8750 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0189    3.7557   -1.2630 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7701   -0.0267    0.7675 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6137   -1.3698    0.9903 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.2324   -1.6015    1.1332 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3055   -0.9079    2.1609 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.0995   -1.6661    3.1811 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.3868   -2.7799    3.6677 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3479   -2.1521    2.5408 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.2422   -3.6491    2.2749 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3727   -3.9369    1.2265 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7866   -1.5434    1.4164 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5207   -0.2140    1.2675 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.6954    0.0869   -0.0814 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7909    0.9899   -0.2692 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.1728    2.2380   -0.9079 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.2408    2.8114   -0.0833 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4196    1.8385   -2.1794 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4052    0.9345   -1.8839 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7919    0.3736   -1.1847 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.0126   -0.9684   -0.6893 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.1938    0.9854   -1.1213 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.0597    0.2508   -2.0502 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.3255    2.4134   -1.1577 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1803    3.1281   -0.1413 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2015    0.2467    1.7221 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.3125    1.1830    2.7686 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3953   -1.7112    2.1987 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9927   -0.8103    2.8887 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5654   -2.9937    2.7001 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1143   -2.2390   -0.1307 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5981   -1.9699   -0.2379 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.2238   -2.7690   -1.1818 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.3810    0.0241   -0.2089 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3972    0.2906    1.3322 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5934    1.6162    0.1759 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0631   -0.1355    1.2297 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0708   -0.4473   -1.5945 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1919    1.2946    0.3775 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2545    0.3472   -1.7652 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7806    2.5976   -1.4396 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4396    0.9134   -2.9454 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1844    2.0197   -4.2005 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5921    2.4112   -1.2702 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1812    3.1994   -2.8011 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5802    4.3478   -0.7400 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5571   -0.3616    2.6728 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3689   -1.0029    4.0517 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0534   -3.3741    2.9874 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1605   -2.0553    3.3248 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8895   -4.1343    3.1941 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2888   -3.9754    2.0275 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7391   -4.6211    0.6123 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3116    0.3538    1.8204 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2386    1.2525    0.6705 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9318    2.9281   -1.2256 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2910    3.8087   -0.1186 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9298    2.7675   -2.5467 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0891    1.4876   -2.9759 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1116    0.5417   -2.7499 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4945    0.2252   -2.2162 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2558   -0.9425    0.2526 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5770    0.6429   -0.1024 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.4456   -0.6086   -1.6516 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6040    0.1757   -2.9649 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5597    3.0156   -2.0497 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6692    0.7658    0.9010 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1354    1.7273    2.6682 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4272   -3.8386    2.1467 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0041   -3.2953    0.1942 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5692   -2.1235   -1.0647 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0155   -2.2102    0.7753 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8604   -3.6935   -1.1630 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  2  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  7  9  1  0
  9 10  1  0
  9 11  1  0
 11 12  1  0
  6 13  1  0
 13 14  1  0
 14 15  1  1
 15 16  1  0
 16 17  1  0
 17 18  1  0
 17 19  1  0
 19 20  1  0
 20 21  1  0
 19 22  1  0
 22 23  1  0
 23 24  1  0
 24 25  1  0
 25 26  1  0
 26 27  1  0
 26 28  1  0
 28 29  1  0
 25 30  1  0
 30 31  1  0
 30 32  1  0
 32 33  1  0
 32 34  1  0
 34 35  2  0
 23 36  1  0
 36 37  1  0
 14 38  1  0
 38 39  2  0
 38 40  1  0
 14 41  1  0
 41 42  1  0
 42 43  1  0
 42  5  1  0
 36 16  1  0
  1 44  1  0
  1 45  1  0
  1 46  1  0
  4 47  1  0
  5 48  1  6
  6 49  1  0
  7 50  1  6
  8 51  1  0
  9 52  1  6
 10 53  1  0
 11 54  1  0
 11 55  1  0
 12 56  1  0
 16 57  1  1
 17 58  1  1
 18 59  1  0
 19 60  1  1
 20 61  1  0
 20 62  1  0
 21 63  1  0
 23 64  1  1
 25 65  1  1
 26 66  1  6
 27 67  1  0
 28 68  1  0
 28 69  1  0
 29 70  1  0
 30 71  1  6
 31 72  1  0
 32 73  1  1
 33 74  1  0
 33 75  1  0
 34 76  1  0
 36 77  1  6
 37 78  1  0
 40 79  1  0
 41 80  1  0
 41 81  1  0
 42 82  1  1
 43 83  1  0
M  END

View in JSmol View NMR Assignments View Stereo Labels

Synonyms

Value	Source
3'-SLN	HMDB
3-Sialyllactosamine	HMDB
O-(N-Acetyl-alpha-neuraminosyl)-(2->3)-O-beta-D-galactopyranosyl-(1->4)-2-amino-2-deoxy- D-glucose	HMDB
O-(N-Acetyl-alpha-neuraminosyl)-(2->3)-O-beta-delta-galactopyranosyl-(1->4)-2-amino-2-deoxy- D-glucose	HMDB
(2S,4S,5R)-2-{[(2S,3R,4S,5S,6R)-2-{[(2R,3S,4R,5R)-5-amino-1,2,4-trihydroxy-6-oxohexan-3-yl]oxy}-3,5-dihydroxy-6-(hydroxymethyl)oxan-4-yl]oxy}-4-hydroxy-5-[(1-hydroxyethylidene)amino]-6-[(1R,2R)-1,2,3-trihydroxypropyl]oxane-2-carboxylate	Generator, HMDB

Chemical Formula

C₂₃H₄₀N₂O₁₈

Average Molecular Weight

632.5663

Monoisotopic Molecular Weight

632.227612486

IUPAC Name

(2S,4S,5R)-2-{[(2S,3R,4S,5S,6R)-2-{[(2R,3S,4R,5R)-5-amino-1,2,4-trihydroxy-6-oxohexan-3-yl]oxy}-3,5-dihydroxy-6-(hydroxymethyl)oxan-4-yl]oxy}-5-acetamido-4-hydroxy-6-[(1R,2R)-1,2,3-trihydroxypropyl]oxane-2-carboxylic acid

Traditional Name

CAS Registry Number

126151-66-4

SMILES

CC(=O)N[C@@H]1[C@@H](O)C[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(OC1[C@H](O)[C@H](O)CO)C(O)=O

InChI Identifier

InChI=1S/C23H40N2O18/c1-7(30)25-13-9(31)2-23(22(38)39,42-19(13)15(35)10(32)4-27)43-20-16(36)12(6-29)40-21(17(20)37)41-18(11(33)5-28)14(34)8(24)3-26/h3,8-21,27-29,31-37H,2,4-6,24H2,1H3,(H,25,30)(H,38,39)/t8-,9-,10+,11+,12+,13+,14+,15+,16-,17+,18+,19?,20-,21-,23-/m0/s1

InChI Key

MKNNYTWMAUAKMA-FRLIKFETSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as n-acylneuraminic acids. These are neuraminic acids carrying an N-acyl substituent.

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Carbohydrates and carbohydrate conjugates

Direct Parent

N-acylneuraminic acids

Alternative Parents

Substituents

N-acylneuraminic acid
Neuraminic acid
Fatty acyl glycoside
Fatty acyl glycoside of mono- or disaccharide
C-glucuronide
Alkyl glycoside
C-glycosyl compound
Glycosyl compound
O-glycosyl compound
Ketal
Amino saccharide
Fatty acyl
Beta-hydroxy aldehyde
Monosaccharide
Pyran
Oxane
Acetamide
Amino acid or derivatives
Secondary carboxylic acid amide
Carboxamide group
Amino acid
Secondary alcohol
Polyol
Monocarboxylic acid or derivatives
Oxacycle
Organoheterocyclic compound
Acetal
Carboxylic acid derivative
Carboxylic acid
Organic nitrogen compound
Organic oxide
Aldehyde
Carbonyl group
Organopnictogen compound
Alcohol
Hydrocarbon derivative
Amine
Primary aliphatic amine
Primary amine
Organonitrogen compound
Primary alcohol
Aliphatic heteromonocyclic compound

Molecular Framework

Aliphatic heteromonocyclic compounds

External Descriptors

Not Available

Ontology

Not Available

Physical Properties

State

Solid

Experimental Molecular Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Experimental Chromatographic Properties

Not Available

Predicted Molecular Properties

Property	Value	Source
Water Solubility	79.6 g/L	ALOGPS
logP	-3	ALOGPS
logP	-10	ChemAxon
logS	-0.9	ALOGPS
pKa (Strongest Acidic)	2.54	ChemAxon
pKa (Strongest Basic)	7.16	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	19	ChemAxon
Hydrogen Donor Count	13	ChemAxon
Polar Surface Area	348.71 Å²	ChemAxon
Rotatable Bond Count	15	ChemAxon
Refractivity	131.69 m³·mol⁻¹	ChemAxon
Polarizability	58.98 Å³	ChemAxon
Number of Rings	2	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

Predicted Chromatographic Properties

Predicted Collision Cross Sections

Predictor	Adduct Type	CCS Value (Å²)	Reference
DeepCCS	[M+H]+	235.165	30932474
DeepCCS	[M-H]-	233.36	30932474
DeepCCS	[M-2H]-	267.394	30932474
DeepCCS	[M+Na]+	241.413	30932474
AllCCS	[M+H]+	233.2	32859911
AllCCS	[M+H-H2O]+	232.4	32859911
AllCCS	[M+NH4]+	234.0	32859911
AllCCS	[M+Na]+	234.2	32859911
AllCCS	[M-H]-	230.3	32859911
AllCCS	[M+Na-2H]-	231.5	32859911
AllCCS	[M+HCOO]-	233.0	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
3'-Sialyllactosamine	CC(=O)N[C@@H]1[C@@H](O)C[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(OC1[C@H](O)[C@H](O)CO)C(O)=O	3712.6	Standard polar	33892256
3'-Sialyllactosamine	CC(=O)N[C@@H]1[C@@H](O)C[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(OC1[C@H](O)[C@H](O)CO)C(O)=O	4592.5	Standard non polar	33892256
3'-Sialyllactosamine	CC(=O)N[C@@H]1[C@@H](O)C[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(OC1[C@H](O)[C@H](O)CO)C(O)=O	5042.7	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
3'-Sialyllactosamine,1TMS,isomer #1	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O[Si](C)(C)C	4645.6	Semi standard non polar	33892256
3'-Sialyllactosamine,1TMS,isomer #10	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O	4641.4	Semi standard non polar	33892256
3'-Sialyllactosamine,1TMS,isomer #11	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O[Si](C)(C)C)C[C@@H]1O	4588.7	Semi standard non polar	33892256
3'-Sialyllactosamine,1TMS,isomer #12	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)C(N)=CO[Si](C)(C)C)[C@@H]2O)(C(=O)O)C[C@@H]1O	4804.8	Semi standard non polar	33892256
3'-Sialyllactosamine,1TMS,isomer #13	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@H](C=O)N[Si](C)(C)C)[C@@H]2O)(C(=O)O)C[C@@H]1O	4872.6	Semi standard non polar	33892256
3'-Sialyllactosamine,1TMS,isomer #14	CC(=O)N([C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O)[Si](C)(C)C	4666.0	Semi standard non polar	33892256
3'-Sialyllactosamine,1TMS,isomer #2	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O[Si](C)(C)C)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O	4637.2	Semi standard non polar	33892256
3'-Sialyllactosamine,1TMS,isomer #3	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO[Si](C)(C)C)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O	4638.8	Semi standard non polar	33892256
3'-Sialyllactosamine,1TMS,isomer #4	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O	4658.3	Semi standard non polar	33892256
3'-Sialyllactosamine,1TMS,isomer #5	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O	4650.1	Semi standard non polar	33892256
3'-Sialyllactosamine,1TMS,isomer #6	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O[Si](C)(C)C)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O	4674.3	Semi standard non polar	33892256
3'-Sialyllactosamine,1TMS,isomer #7	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O[Si](C)(C)C)(C(=O)O)C[C@@H]1O	4658.4	Semi standard non polar	33892256
3'-Sialyllactosamine,1TMS,isomer #8	CC(=O)N[C@H]1C([C@H](O[Si](C)(C)C)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O	4676.5	Semi standard non polar	33892256
3'-Sialyllactosamine,1TMS,isomer #9	CC(=O)N[C@H]1C([C@H](O)[C@@H](CO)O[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O	4648.8	Semi standard non polar	33892256
3'-Sialyllactosamine,2TMS,isomer #1	CC(=O)N[C@H]1C([C@H](O[Si](C)(C)C)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O[Si](C)(C)C	4528.6	Semi standard non polar	33892256
3'-Sialyllactosamine,2TMS,isomer #10	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O[Si](C)(C)C)C[C@@H]1O[Si](C)(C)C	4475.1	Semi standard non polar	33892256
3'-Sialyllactosamine,2TMS,isomer #11	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)C(N)=CO[Si](C)(C)C)[C@@H]2O)(C(=O)O)C[C@@H]1O[Si](C)(C)C	4676.0	Semi standard non polar	33892256
3'-Sialyllactosamine,2TMS,isomer #12	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@H](C=O)N[Si](C)(C)C)[C@@H]2O)(C(=O)O)C[C@@H]1O[Si](C)(C)C	4741.6	Semi standard non polar	33892256
3'-Sialyllactosamine,2TMS,isomer #13	CC(=O)N([C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O[Si](C)(C)C)[Si](C)(C)C	4550.2	Semi standard non polar	33892256
3'-Sialyllactosamine,2TMS,isomer #14	CC(=O)N[C@H]1C([C@H](O[Si](C)(C)C)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O[Si](C)(C)C)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O	4514.4	Semi standard non polar	33892256
3'-Sialyllactosamine,2TMS,isomer #15	CC(=O)N[C@H]1C([C@H](O)[C@@H](CO)O[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O[Si](C)(C)C)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O	4495.0	Semi standard non polar	33892256
3'-Sialyllactosamine,2TMS,isomer #16	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O[Si](C)(C)C)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O	4473.8	Semi standard non polar	33892256
3'-Sialyllactosamine,2TMS,isomer #17	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O[Si](C)(C)C)[C@@H](CO[Si](C)(C)C)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O	4501.1	Semi standard non polar	33892256
3'-Sialyllactosamine,2TMS,isomer #18	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O[Si](C)(C)C)[C@@H](CO)O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O	4507.5	Semi standard non polar	33892256
3'-Sialyllactosamine,2TMS,isomer #19	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O[Si](C)(C)C)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O	4500.4	Semi standard non polar	33892256
3'-Sialyllactosamine,2TMS,isomer #2	CC(=O)N[C@H]1C([C@H](O)[C@@H](CO)O[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O[Si](C)(C)C	4507.1	Semi standard non polar	33892256
3'-Sialyllactosamine,2TMS,isomer #20	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O[Si](C)(C)C)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O[Si](C)(C)C)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O	4518.1	Semi standard non polar	33892256
3'-Sialyllactosamine,2TMS,isomer #21	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O[Si](C)(C)C)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O[Si](C)(C)C)(C(=O)O)C[C@@H]1O	4510.7	Semi standard non polar	33892256
3'-Sialyllactosamine,2TMS,isomer #22	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O[Si](C)(C)C)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O[Si](C)(C)C)C[C@@H]1O	4438.2	Semi standard non polar	33892256
3'-Sialyllactosamine,2TMS,isomer #23	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O[Si](C)(C)C)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)C(N)=CO[Si](C)(C)C)[C@@H]2O)(C(=O)O)C[C@@H]1O	4654.3	Semi standard non polar	33892256
3'-Sialyllactosamine,2TMS,isomer #24	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O[Si](C)(C)C)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@H](C=O)N[Si](C)(C)C)[C@@H]2O)(C(=O)O)C[C@@H]1O	4730.9	Semi standard non polar	33892256
3'-Sialyllactosamine,2TMS,isomer #25	CC(=O)N([C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O[Si](C)(C)C)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O)[Si](C)(C)C	4506.9	Semi standard non polar	33892256
3'-Sialyllactosamine,2TMS,isomer #26	CC(=O)N[C@H]1C([C@H](O[Si](C)(C)C)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO[Si](C)(C)C)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O	4511.0	Semi standard non polar	33892256
3'-Sialyllactosamine,2TMS,isomer #27	CC(=O)N[C@H]1C([C@H](O)[C@@H](CO)O[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO[Si](C)(C)C)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O	4492.2	Semi standard non polar	33892256
3'-Sialyllactosamine,2TMS,isomer #28	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO[Si](C)(C)C)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O	4474.4	Semi standard non polar	33892256
3'-Sialyllactosamine,2TMS,isomer #29	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO[Si](C)(C)C)O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O	4506.5	Semi standard non polar	33892256
3'-Sialyllactosamine,2TMS,isomer #3	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O[Si](C)(C)C	4486.3	Semi standard non polar	33892256
3'-Sialyllactosamine,2TMS,isomer #30	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO[Si](C)(C)C)O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O	4499.2	Semi standard non polar	33892256
3'-Sialyllactosamine,2TMS,isomer #31	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO[Si](C)(C)C)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O[Si](C)(C)C)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O	4511.7	Semi standard non polar	33892256
3'-Sialyllactosamine,2TMS,isomer #32	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO[Si](C)(C)C)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O[Si](C)(C)C)(C(=O)O)C[C@@H]1O	4504.2	Semi standard non polar	33892256
3'-Sialyllactosamine,2TMS,isomer #33	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO[Si](C)(C)C)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O[Si](C)(C)C)C[C@@H]1O	4435.6	Semi standard non polar	33892256
3'-Sialyllactosamine,2TMS,isomer #34	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO[Si](C)(C)C)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)C(N)=CO[Si](C)(C)C)[C@@H]2O)(C(=O)O)C[C@@H]1O	4666.7	Semi standard non polar	33892256
3'-Sialyllactosamine,2TMS,isomer #35	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO[Si](C)(C)C)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@H](C=O)N[Si](C)(C)C)[C@@H]2O)(C(=O)O)C[C@@H]1O	4739.6	Semi standard non polar	33892256
3'-Sialyllactosamine,2TMS,isomer #36	CC(=O)N([C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO[Si](C)(C)C)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O)[Si](C)(C)C	4518.8	Semi standard non polar	33892256
3'-Sialyllactosamine,2TMS,isomer #37	CC(=O)N[C@H]1C([C@H](O[Si](C)(C)C)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O	4533.4	Semi standard non polar	33892256
3'-Sialyllactosamine,2TMS,isomer #38	CC(=O)N[C@H]1C([C@H](O)[C@@H](CO)O[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O	4510.8	Semi standard non polar	33892256
3'-Sialyllactosamine,2TMS,isomer #39	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O	4492.5	Semi standard non polar	33892256
3'-Sialyllactosamine,2TMS,isomer #4	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O[Si](C)(C)C)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O[Si](C)(C)C	4493.3	Semi standard non polar	33892256
3'-Sialyllactosamine,2TMS,isomer #40	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@@H](CO[Si](C)(C)C)O[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O	4525.6	Semi standard non polar	33892256
3'-Sialyllactosamine,2TMS,isomer #41	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O	4539.3	Semi standard non polar	33892256
3'-Sialyllactosamine,2TMS,isomer #42	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@@H]2O[Si](C)(C)C)(C(=O)O)C[C@@H]1O	4529.1	Semi standard non polar	33892256
3'-Sialyllactosamine,2TMS,isomer #43	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O[Si](C)(C)C)C[C@@H]1O	4473.5	Semi standard non polar	33892256
3'-Sialyllactosamine,2TMS,isomer #44	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C)[C@H](O)C(N)=CO[Si](C)(C)C)[C@@H]2O)(C(=O)O)C[C@@H]1O	4685.0	Semi standard non polar	33892256
3'-Sialyllactosamine,2TMS,isomer #45	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C)[C@H](O)[C@H](C=O)N[Si](C)(C)C)[C@@H]2O)(C(=O)O)C[C@@H]1O	4748.0	Semi standard non polar	33892256
3'-Sialyllactosamine,2TMS,isomer #46	CC(=O)N([C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O)[Si](C)(C)C	4525.5	Semi standard non polar	33892256
3'-Sialyllactosamine,2TMS,isomer #47	CC(=O)N[C@H]1C([C@H](O[Si](C)(C)C)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O	4527.2	Semi standard non polar	33892256
3'-Sialyllactosamine,2TMS,isomer #48	CC(=O)N[C@H]1C([C@H](O)[C@@H](CO)O[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O	4506.9	Semi standard non polar	33892256
3'-Sialyllactosamine,2TMS,isomer #49	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O	4487.6	Semi standard non polar	33892256
3'-Sialyllactosamine,2TMS,isomer #5	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO[Si](C)(C)C)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O[Si](C)(C)C	4486.7	Semi standard non polar	33892256
3'-Sialyllactosamine,2TMS,isomer #50	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O	4526.9	Semi standard non polar	33892256
3'-Sialyllactosamine,2TMS,isomer #51	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@@H]2O[Si](C)(C)C)(C(=O)O)C[C@@H]1O	4517.0	Semi standard non polar	33892256
3'-Sialyllactosamine,2TMS,isomer #52	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O[Si](C)(C)C)C[C@@H]1O	4461.0	Semi standard non polar	33892256
3'-Sialyllactosamine,2TMS,isomer #53	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C)[C@H](O)C(N)=CO[Si](C)(C)C)[C@@H]2O)(C(=O)O)C[C@@H]1O	4681.4	Semi standard non polar	33892256
3'-Sialyllactosamine,2TMS,isomer #54	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C)[C@H](O)[C@H](C=O)N[Si](C)(C)C)[C@@H]2O)(C(=O)O)C[C@@H]1O	4737.6	Semi standard non polar	33892256
3'-Sialyllactosamine,2TMS,isomer #55	CC(=O)N([C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O)[Si](C)(C)C	4522.1	Semi standard non polar	33892256
3'-Sialyllactosamine,2TMS,isomer #56	CC(=O)N[C@H]1C([C@H](O[Si](C)(C)C)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O[Si](C)(C)C)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O	4552.8	Semi standard non polar	33892256
3'-Sialyllactosamine,2TMS,isomer #57	CC(=O)N[C@H]1C([C@H](O)[C@@H](CO)O[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O[Si](C)(C)C)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O	4525.0	Semi standard non polar	33892256
3'-Sialyllactosamine,2TMS,isomer #58	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O[Si](C)(C)C)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O	4508.3	Semi standard non polar	33892256
3'-Sialyllactosamine,2TMS,isomer #59	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O[Si](C)(C)C)[C@@H](N)C=O)[C@@H]2O[Si](C)(C)C)(C(=O)O)C[C@@H]1O	4538.9	Semi standard non polar	33892256
3'-Sialyllactosamine,2TMS,isomer #6	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O[Si](C)(C)C	4512.4	Semi standard non polar	33892256
3'-Sialyllactosamine,2TMS,isomer #60	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O[Si](C)(C)C)[C@@H](N)C=O)[C@@H]2O)(C(=O)O[Si](C)(C)C)C[C@@H]1O	4493.3	Semi standard non polar	33892256
3'-Sialyllactosamine,2TMS,isomer #61	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O[Si](C)(C)C)C(N)=CO[Si](C)(C)C)[C@@H]2O)(C(=O)O)C[C@@H]1O	4680.4	Semi standard non polar	33892256
3'-Sialyllactosamine,2TMS,isomer #62	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O[Si](C)(C)C)[C@H](C=O)N[Si](C)(C)C)[C@@H]2O)(C(=O)O)C[C@@H]1O	4738.4	Semi standard non polar	33892256
3'-Sialyllactosamine,2TMS,isomer #63	CC(=O)N([C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O[Si](C)(C)C)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O)[Si](C)(C)C	4542.6	Semi standard non polar	33892256
3'-Sialyllactosamine,2TMS,isomer #64	CC(=O)N[C@H]1C([C@H](O[Si](C)(C)C)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O[Si](C)(C)C)(C(=O)O)C[C@@H]1O	4538.8	Semi standard non polar	33892256
3'-Sialyllactosamine,2TMS,isomer #65	CC(=O)N[C@H]1C([C@H](O)[C@@H](CO)O[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O[Si](C)(C)C)(C(=O)O)C[C@@H]1O	4511.8	Semi standard non polar	33892256
3'-Sialyllactosamine,2TMS,isomer #66	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O[Si](C)(C)C)(C(=O)O)C[C@@H]1O	4490.4	Semi standard non polar	33892256
3'-Sialyllactosamine,2TMS,isomer #67	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O[Si](C)(C)C)(C(=O)O[Si](C)(C)C)C[C@@H]1O	4452.8	Semi standard non polar	33892256
3'-Sialyllactosamine,2TMS,isomer #68	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)C(N)=CO[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)(C(=O)O)C[C@@H]1O	4668.3	Semi standard non polar	33892256
3'-Sialyllactosamine,2TMS,isomer #69	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@H](C=O)N[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)(C(=O)O)C[C@@H]1O	4752.8	Semi standard non polar	33892256
3'-Sialyllactosamine,2TMS,isomer #7	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O[Si](C)(C)C	4505.8	Semi standard non polar	33892256
3'-Sialyllactosamine,2TMS,isomer #70	CC(=O)N([C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O[Si](C)(C)C)(C(=O)O)C[C@@H]1O)[Si](C)(C)C	4524.5	Semi standard non polar	33892256
3'-Sialyllactosamine,2TMS,isomer #71	CC(=O)N[C@H]1C([C@H](O[Si](C)(C)C)[C@@H](CO)O[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O	4545.9	Semi standard non polar	33892256
3'-Sialyllactosamine,2TMS,isomer #72	CC(=O)N[C@H]1C([C@H](O[Si](C)(C)C)[C@H](O)CO[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O	4520.2	Semi standard non polar	33892256
3'-Sialyllactosamine,2TMS,isomer #73	CC(=O)N[C@H]1C([C@H](O[Si](C)(C)C)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O[Si](C)(C)C)C[C@@H]1O	4486.6	Semi standard non polar	33892256
3'-Sialyllactosamine,2TMS,isomer #74	CC(=O)N[C@H]1C([C@H](O[Si](C)(C)C)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)C(N)=CO[Si](C)(C)C)[C@@H]2O)(C(=O)O)C[C@@H]1O	4698.7	Semi standard non polar	33892256
3'-Sialyllactosamine,2TMS,isomer #75	CC(=O)N[C@H]1C([C@H](O[Si](C)(C)C)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@H](C=O)N[Si](C)(C)C)[C@@H]2O)(C(=O)O)C[C@@H]1O	4763.3	Semi standard non polar	33892256
3'-Sialyllactosamine,2TMS,isomer #76	CC(=O)N([C@H]1C([C@H](O[Si](C)(C)C)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O)[Si](C)(C)C	4542.1	Semi standard non polar	33892256
3'-Sialyllactosamine,2TMS,isomer #77	CC(=O)N[C@H]1C([C@H](O)[C@@H](CO[Si](C)(C)C)O[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O	4501.8	Semi standard non polar	33892256
3'-Sialyllactosamine,2TMS,isomer #78	CC(=O)N[C@H]1C([C@H](O)[C@@H](CO)O[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O[Si](C)(C)C)C[C@@H]1O	4465.0	Semi standard non polar	33892256
3'-Sialyllactosamine,2TMS,isomer #79	CC(=O)N[C@H]1C([C@H](O)[C@@H](CO)O[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)C(N)=CO[Si](C)(C)C)[C@@H]2O)(C(=O)O)C[C@@H]1O	4676.0	Semi standard non polar	33892256
3'-Sialyllactosamine,2TMS,isomer #8	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O[Si](C)(C)C)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O[Si](C)(C)C	4528.3	Semi standard non polar	33892256
3'-Sialyllactosamine,2TMS,isomer #80	CC(=O)N[C@H]1C([C@H](O)[C@@H](CO)O[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@H](C=O)N[Si](C)(C)C)[C@@H]2O)(C(=O)O)C[C@@H]1O	4734.7	Semi standard non polar	33892256
3'-Sialyllactosamine,2TMS,isomer #81	CC(=O)N([C@H]1C([C@H](O)[C@@H](CO)O[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O)[Si](C)(C)C	4513.0	Semi standard non polar	33892256
3'-Sialyllactosamine,2TMS,isomer #82	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O[Si](C)(C)C)C[C@@H]1O	4439.5	Semi standard non polar	33892256
3'-Sialyllactosamine,2TMS,isomer #83	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)C(N)=CO[Si](C)(C)C)[C@@H]2O)(C(=O)O)C[C@@H]1O	4669.9	Semi standard non polar	33892256
3'-Sialyllactosamine,2TMS,isomer #84	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@H](C=O)N[Si](C)(C)C)[C@@H]2O)(C(=O)O)C[C@@H]1O	4734.1	Semi standard non polar	33892256
3'-Sialyllactosamine,2TMS,isomer #85	CC(=O)N([C@H]1C([C@H](O)[C@H](O)CO[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O)[Si](C)(C)C	4509.8	Semi standard non polar	33892256
3'-Sialyllactosamine,2TMS,isomer #86	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)C(N)=CO[Si](C)(C)C)[C@@H]2O)(C(=O)O[Si](C)(C)C)C[C@@H]1O	4608.0	Semi standard non polar	33892256
3'-Sialyllactosamine,2TMS,isomer #87	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@H](C=O)N[Si](C)(C)C)[C@@H]2O)(C(=O)O[Si](C)(C)C)C[C@@H]1O	4701.3	Semi standard non polar	33892256
3'-Sialyllactosamine,2TMS,isomer #88	CC(=O)N([C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O[Si](C)(C)C)C[C@@H]1O)[Si](C)(C)C	4458.8	Semi standard non polar	33892256
3'-Sialyllactosamine,2TMS,isomer #89	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)C(=CO[Si](C)(C)C)N[Si](C)(C)C)[C@@H]2O)(C(=O)O)C[C@@H]1O	4909.7	Semi standard non polar	33892256
3'-Sialyllactosamine,2TMS,isomer #9	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O[Si](C)(C)C)(C(=O)O)C[C@@H]1O[Si](C)(C)C	4510.7	Semi standard non polar	33892256
3'-Sialyllactosamine,2TMS,isomer #90	CC(=O)N([C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)C(N)=CO[Si](C)(C)C)[C@@H]2O)(C(=O)O)C[C@@H]1O)[Si](C)(C)C	4692.8	Semi standard non polar	33892256
3'-Sialyllactosamine,2TMS,isomer #91	CC(=O)N([C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@H](C=O)N[Si](C)(C)C)[C@@H]2O)(C(=O)O)C[C@@H]1O)[Si](C)(C)C	4751.7	Semi standard non polar	33892256
3'-Sialyllactosamine,2TMS,isomer #92	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@H](C=O)N([Si](C)(C)C)[Si](C)(C)C)[C@@H]2O)(C(=O)O)C[C@@H]1O	4897.5	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #1	CC(=O)N[C@H]1C([C@H](O[Si](C)(C)C)[C@@H](CO)O[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O[Si](C)(C)C	4437.6	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #10	CC(=O)N[C@H]1C([C@H](O[Si](C)(C)C)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)C(N)=CO[Si](C)(C)C)[C@@H]2O)(C(=O)O)C[C@@H]1O[Si](C)(C)C	4576.3	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #100	CC(=O)N([C@H]1C([C@H](O)[C@@H](CO)O[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O[Si](C)(C)C)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O)[Si](C)(C)C	4402.3	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #101	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O[Si](C)(C)C)[C@@H](CO[Si](C)(C)C)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O	4367.3	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #102	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O[Si](C)(C)C)[C@@H](CO)O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O	4384.2	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #103	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O[Si](C)(C)C)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O	4381.1	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #104	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O[Si](C)(C)C)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O[Si](C)(C)C)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O	4397.2	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #105	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O[Si](C)(C)C)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O[Si](C)(C)C)(C(=O)O)C[C@@H]1O	4375.4	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #106	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O[Si](C)(C)C)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O[Si](C)(C)C)C[C@@H]1O	4337.1	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #107	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O[Si](C)(C)C)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)C(N)=CO[Si](C)(C)C)[C@@H]2O)(C(=O)O)C[C@@H]1O	4526.4	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #108	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O[Si](C)(C)C)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@H](C=O)N[Si](C)(C)C)[C@@H]2O)(C(=O)O)C[C@@H]1O	4600.9	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #109	CC(=O)N([C@H]1C([C@H](O)[C@H](O)CO[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O[Si](C)(C)C)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O)[Si](C)(C)C	4381.1	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #11	CC(=O)N[C@H]1C([C@H](O[Si](C)(C)C)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@H](C=O)N[Si](C)(C)C)[C@@H]2O)(C(=O)O)C[C@@H]1O[Si](C)(C)C	4652.9	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #110	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O[Si](C)(C)C)[C@@H](CO[Si](C)(C)C)O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O	4407.1	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #111	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O[Si](C)(C)C)[C@@H](CO[Si](C)(C)C)O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O	4396.2	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #112	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O[Si](C)(C)C)[C@@H](CO[Si](C)(C)C)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O[Si](C)(C)C)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O	4412.9	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #113	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O[Si](C)(C)C)[C@@H](CO[Si](C)(C)C)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O[Si](C)(C)C)(C(=O)O)C[C@@H]1O	4403.3	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #114	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O[Si](C)(C)C)[C@@H](CO[Si](C)(C)C)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O[Si](C)(C)C)C[C@@H]1O	4361.4	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #115	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O[Si](C)(C)C)[C@@H](CO[Si](C)(C)C)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)C(N)=CO[Si](C)(C)C)[C@@H]2O)(C(=O)O)C[C@@H]1O	4542.2	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #116	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O[Si](C)(C)C)[C@@H](CO[Si](C)(C)C)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@H](C=O)N[Si](C)(C)C)[C@@H]2O)(C(=O)O)C[C@@H]1O	4621.8	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #117	CC(=O)N([C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O[Si](C)(C)C)[C@@H](CO[Si](C)(C)C)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O)[Si](C)(C)C	4402.3	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #118	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O[Si](C)(C)C)[C@@H](CO)O[C@@H](O[C@H]([C@@H](CO[Si](C)(C)C)O[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O	4401.0	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #119	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O[Si](C)(C)C)[C@@H](CO)O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O	4436.6	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #12	CC(=O)N([C@H]1C([C@H](O[Si](C)(C)C)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O[Si](C)(C)C)[Si](C)(C)C	4451.9	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #120	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O[Si](C)(C)C)[C@@H](CO)O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@@H]2O[Si](C)(C)C)(C(=O)O)C[C@@H]1O	4421.5	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #121	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O[Si](C)(C)C)[C@@H](CO)O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O[Si](C)(C)C)C[C@@H]1O	4376.3	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #122	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O[Si](C)(C)C)[C@@H](CO)O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C)[C@H](O)C(N)=CO[Si](C)(C)C)[C@@H]2O)(C(=O)O)C[C@@H]1O	4566.7	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #123	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O[Si](C)(C)C)[C@@H](CO)O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C)[C@H](O)[C@H](C=O)N[Si](C)(C)C)[C@@H]2O)(C(=O)O)C[C@@H]1O	4624.7	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #124	CC(=O)N([C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O[Si](C)(C)C)[C@@H](CO)O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O)[Si](C)(C)C	4408.7	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #125	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O[Si](C)(C)C)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O	4419.6	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #126	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O[Si](C)(C)C)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@@H]2O[Si](C)(C)C)(C(=O)O)C[C@@H]1O	4403.3	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #127	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O[Si](C)(C)C)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O[Si](C)(C)C)C[C@@H]1O	4367.5	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #128	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O[Si](C)(C)C)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C)[C@H](O)C(N)=CO[Si](C)(C)C)[C@@H]2O)(C(=O)O)C[C@@H]1O	4556.3	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #129	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O[Si](C)(C)C)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C)[C@H](O)[C@H](C=O)N[Si](C)(C)C)[C@@H]2O)(C(=O)O)C[C@@H]1O	4616.4	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #13	CC(=O)N[C@H]1C([C@H](O)[C@@H](CO[Si](C)(C)C)O[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O[Si](C)(C)C	4390.9	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #130	CC(=O)N([C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O[Si](C)(C)C)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O)[Si](C)(C)C	4399.9	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #131	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O[Si](C)(C)C)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O[Si](C)(C)C)[C@@H](N)C=O)[C@@H]2O[Si](C)(C)C)(C(=O)O)C[C@@H]1O	4434.2	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #132	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O[Si](C)(C)C)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O[Si](C)(C)C)[C@@H](N)C=O)[C@@H]2O)(C(=O)O[Si](C)(C)C)C[C@@H]1O	4396.2	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #133	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O[Si](C)(C)C)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O[Si](C)(C)C)C(N)=CO[Si](C)(C)C)[C@@H]2O)(C(=O)O)C[C@@H]1O	4559.0	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #134	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O[Si](C)(C)C)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O[Si](C)(C)C)[C@H](C=O)N[Si](C)(C)C)[C@@H]2O)(C(=O)O)C[C@@H]1O	4614.7	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #135	CC(=O)N([C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O[Si](C)(C)C)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O[Si](C)(C)C)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O)[Si](C)(C)C	4424.7	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #136	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O[Si](C)(C)C)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O[Si](C)(C)C)(C(=O)O[Si](C)(C)C)C[C@@H]1O	4377.0	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #137	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O[Si](C)(C)C)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)C(N)=CO[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)(C(=O)O)C[C@@H]1O	4543.1	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #138	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O[Si](C)(C)C)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@H](C=O)N[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)(C(=O)O)C[C@@H]1O	4646.5	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #139	CC(=O)N([C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O[Si](C)(C)C)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O[Si](C)(C)C)(C(=O)O)C[C@@H]1O)[Si](C)(C)C	4409.5	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #14	CC(=O)N[C@H]1C([C@H](O)[C@@H](CO)O[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O[Si](C)(C)C)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O[Si](C)(C)C	4392.2	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #140	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O[Si](C)(C)C)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)C(N)=CO[Si](C)(C)C)[C@@H]2O)(C(=O)O[Si](C)(C)C)C[C@@H]1O	4483.1	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #141	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O[Si](C)(C)C)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@H](C=O)N[Si](C)(C)C)[C@@H]2O)(C(=O)O[Si](C)(C)C)C[C@@H]1O	4583.2	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #142	CC(=O)N([C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O[Si](C)(C)C)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O[Si](C)(C)C)C[C@@H]1O)[Si](C)(C)C	4359.9	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #143	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O[Si](C)(C)C)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)C(=CO[Si](C)(C)C)N[Si](C)(C)C)[C@@H]2O)(C(=O)O)C[C@@H]1O	4769.4	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #144	CC(=O)N([C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O[Si](C)(C)C)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)C(N)=CO[Si](C)(C)C)[C@@H]2O)(C(=O)O)C[C@@H]1O)[Si](C)(C)C	4542.2	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #145	CC(=O)N([C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O[Si](C)(C)C)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@H](C=O)N[Si](C)(C)C)[C@@H]2O)(C(=O)O)C[C@@H]1O)[Si](C)(C)C	4623.6	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #146	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O[Si](C)(C)C)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@H](C=O)N([Si](C)(C)C)[Si](C)(C)C)[C@@H]2O)(C(=O)O)C[C@@H]1O	4782.5	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #147	CC(=O)N[C@H]1C([C@H](O[Si](C)(C)C)[C@@H](CO)O[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO[Si](C)(C)C)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O	4426.2	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #148	CC(=O)N[C@H]1C([C@H](O[Si](C)(C)C)[C@H](O)CO[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO[Si](C)(C)C)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O	4401.6	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #149	CC(=O)N[C@H]1C([C@H](O[Si](C)(C)C)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO[Si](C)(C)C)O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O	4411.7	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #15	CC(=O)N[C@H]1C([C@H](O)[C@@H](CO)O[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO[Si](C)(C)C)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O[Si](C)(C)C	4384.5	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #150	CC(=O)N[C@H]1C([C@H](O[Si](C)(C)C)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO[Si](C)(C)C)O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O	4405.8	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #151	CC(=O)N[C@H]1C([C@H](O[Si](C)(C)C)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO[Si](C)(C)C)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O[Si](C)(C)C)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O	4423.0	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #152	CC(=O)N[C@H]1C([C@H](O[Si](C)(C)C)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO[Si](C)(C)C)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O[Si](C)(C)C)(C(=O)O)C[C@@H]1O	4406.9	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #153	CC(=O)N[C@H]1C([C@H](O[Si](C)(C)C)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO[Si](C)(C)C)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O[Si](C)(C)C)C[C@@H]1O	4375.5	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #154	CC(=O)N[C@H]1C([C@H](O[Si](C)(C)C)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO[Si](C)(C)C)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)C(N)=CO[Si](C)(C)C)[C@@H]2O)(C(=O)O)C[C@@H]1O	4560.7	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #155	CC(=O)N[C@H]1C([C@H](O[Si](C)(C)C)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO[Si](C)(C)C)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@H](C=O)N[Si](C)(C)C)[C@@H]2O)(C(=O)O)C[C@@H]1O	4638.0	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #156	CC(=O)N([C@H]1C([C@H](O[Si](C)(C)C)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO[Si](C)(C)C)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O)[Si](C)(C)C	4413.1	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #157	CC(=O)N[C@H]1C([C@H](O)[C@@H](CO[Si](C)(C)C)O[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO[Si](C)(C)C)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O	4377.7	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #158	CC(=O)N[C@H]1C([C@H](O)[C@@H](CO)O[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO[Si](C)(C)C)O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O	4405.6	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #159	CC(=O)N[C@H]1C([C@H](O)[C@@H](CO)O[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO[Si](C)(C)C)O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O	4401.6	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #16	CC(=O)N[C@H]1C([C@H](O)[C@@H](CO)O[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O[Si](C)(C)C	4417.6	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #160	CC(=O)N[C@H]1C([C@H](O)[C@@H](CO)O[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO[Si](C)(C)C)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O[Si](C)(C)C)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O	4413.8	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #161	CC(=O)N[C@H]1C([C@H](O)[C@@H](CO)O[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO[Si](C)(C)C)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O[Si](C)(C)C)(C(=O)O)C[C@@H]1O	4393.8	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #162	CC(=O)N[C@H]1C([C@H](O)[C@@H](CO)O[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO[Si](C)(C)C)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O[Si](C)(C)C)C[C@@H]1O	4367.8	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #163	CC(=O)N[C@H]1C([C@H](O)[C@@H](CO)O[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO[Si](C)(C)C)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)C(N)=CO[Si](C)(C)C)[C@@H]2O)(C(=O)O)C[C@@H]1O	4548.8	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #164	CC(=O)N[C@H]1C([C@H](O)[C@@H](CO)O[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO[Si](C)(C)C)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@H](C=O)N[Si](C)(C)C)[C@@H]2O)(C(=O)O)C[C@@H]1O	4613.3	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #165	CC(=O)N([C@H]1C([C@H](O)[C@@H](CO)O[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO[Si](C)(C)C)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O)[Si](C)(C)C	4402.6	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #166	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO[Si](C)(C)C)O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O	4381.6	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #167	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO[Si](C)(C)C)O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O	4376.8	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #168	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO[Si](C)(C)C)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O[Si](C)(C)C)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O	4387.6	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #169	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO[Si](C)(C)C)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O[Si](C)(C)C)(C(=O)O)C[C@@H]1O	4368.0	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #17	CC(=O)N[C@H]1C([C@H](O)[C@@H](CO)O[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O[Si](C)(C)C	4416.1	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #170	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO[Si](C)(C)C)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O[Si](C)(C)C)C[C@@H]1O	4337.1	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #171	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO[Si](C)(C)C)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)C(N)=CO[Si](C)(C)C)[C@@H]2O)(C(=O)O)C[C@@H]1O	4527.1	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #172	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO[Si](C)(C)C)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@H](C=O)N[Si](C)(C)C)[C@@H]2O)(C(=O)O)C[C@@H]1O	4601.2	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #173	CC(=O)N([C@H]1C([C@H](O)[C@H](O)CO[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO[Si](C)(C)C)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O)[Si](C)(C)C	4384.1	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #174	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO[Si](C)(C)C)O[C@@H](O[C@H]([C@@H](CO[Si](C)(C)C)O[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O	4398.4	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #175	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO[Si](C)(C)C)O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O	4426.7	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #176	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO[Si](C)(C)C)O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@@H]2O[Si](C)(C)C)(C(=O)O)C[C@@H]1O	4410.1	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #177	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO[Si](C)(C)C)O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O[Si](C)(C)C)C[C@@H]1O	4374.2	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #178	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO[Si](C)(C)C)O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C)[C@H](O)C(N)=CO[Si](C)(C)C)[C@@H]2O)(C(=O)O)C[C@@H]1O	4568.4	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #179	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO[Si](C)(C)C)O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C)[C@H](O)[C@H](C=O)N[Si](C)(C)C)[C@@H]2O)(C(=O)O)C[C@@H]1O	4626.4	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #18	CC(=O)N[C@H]1C([C@H](O)[C@@H](CO)O[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O[Si](C)(C)C)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O[Si](C)(C)C	4438.0	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #180	CC(=O)N([C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO[Si](C)(C)C)O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O)[Si](C)(C)C	4410.1	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #181	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO[Si](C)(C)C)O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O	4410.2	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #182	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO[Si](C)(C)C)O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@@H]2O[Si](C)(C)C)(C(=O)O)C[C@@H]1O	4395.4	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #183	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO[Si](C)(C)C)O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O[Si](C)(C)C)C[C@@H]1O	4367.3	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #184	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO[Si](C)(C)C)O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C)[C@H](O)C(N)=CO[Si](C)(C)C)[C@@H]2O)(C(=O)O)C[C@@H]1O	4560.4	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #185	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO[Si](C)(C)C)O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C)[C@H](O)[C@H](C=O)N[Si](C)(C)C)[C@@H]2O)(C(=O)O)C[C@@H]1O	4620.4	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #186	CC(=O)N([C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO[Si](C)(C)C)O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O)[Si](C)(C)C	4402.1	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #187	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO[Si](C)(C)C)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O[Si](C)(C)C)[C@@H](N)C=O)[C@@H]2O[Si](C)(C)C)(C(=O)O)C[C@@H]1O	4417.0	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #188	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO[Si](C)(C)C)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O[Si](C)(C)C)[C@@H](N)C=O)[C@@H]2O)(C(=O)O[Si](C)(C)C)C[C@@H]1O	4388.5	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #189	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO[Si](C)(C)C)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O[Si](C)(C)C)C(N)=CO[Si](C)(C)C)[C@@H]2O)(C(=O)O)C[C@@H]1O	4555.8	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #19	CC(=O)N[C@H]1C([C@H](O)[C@@H](CO)O[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O[Si](C)(C)C)(C(=O)O)C[C@@H]1O[Si](C)(C)C	4407.7	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #190	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO[Si](C)(C)C)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O[Si](C)(C)C)[C@H](C=O)N[Si](C)(C)C)[C@@H]2O)(C(=O)O)C[C@@H]1O	4608.2	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #191	CC(=O)N([C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO[Si](C)(C)C)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O[Si](C)(C)C)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O)[Si](C)(C)C	4421.2	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #192	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO[Si](C)(C)C)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O[Si](C)(C)C)(C(=O)O[Si](C)(C)C)C[C@@H]1O	4358.6	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #193	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO[Si](C)(C)C)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)C(N)=CO[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)(C(=O)O)C[C@@H]1O	4545.6	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #194	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO[Si](C)(C)C)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@H](C=O)N[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)(C(=O)O)C[C@@H]1O	4631.1	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #195	CC(=O)N([C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO[Si](C)(C)C)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O[Si](C)(C)C)(C(=O)O)C[C@@H]1O)[Si](C)(C)C	4402.3	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #196	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO[Si](C)(C)C)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)C(N)=CO[Si](C)(C)C)[C@@H]2O)(C(=O)O[Si](C)(C)C)C[C@@H]1O	4491.6	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #197	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO[Si](C)(C)C)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@H](C=O)N[Si](C)(C)C)[C@@H]2O)(C(=O)O[Si](C)(C)C)C[C@@H]1O	4585.1	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #198	CC(=O)N([C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO[Si](C)(C)C)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O[Si](C)(C)C)C[C@@H]1O)[Si](C)(C)C	4362.1	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #199	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO[Si](C)(C)C)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)C(=CO[Si](C)(C)C)N[Si](C)(C)C)[C@@H]2O)(C(=O)O)C[C@@H]1O	4783.2	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #2	CC(=O)N[C@H]1C([C@H](O[Si](C)(C)C)[C@H](O)CO[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O[Si](C)(C)C	4416.8	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #20	CC(=O)N[C@H]1C([C@H](O)[C@@H](CO)O[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O[Si](C)(C)C)C[C@@H]1O[Si](C)(C)C	4399.6	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #200	CC(=O)N([C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO[Si](C)(C)C)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)C(N)=CO[Si](C)(C)C)[C@@H]2O)(C(=O)O)C[C@@H]1O)[Si](C)(C)C	4552.6	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #201	CC(=O)N([C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO[Si](C)(C)C)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@H](C=O)N[Si](C)(C)C)[C@@H]2O)(C(=O)O)C[C@@H]1O)[Si](C)(C)C	4628.8	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #202	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO[Si](C)(C)C)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@H](C=O)N([Si](C)(C)C)[Si](C)(C)C)[C@@H]2O)(C(=O)O)C[C@@H]1O	4787.4	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #203	CC(=O)N[C@H]1C([C@H](O[Si](C)(C)C)[C@@H](CO)O[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O	4461.7	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #204	CC(=O)N[C@H]1C([C@H](O[Si](C)(C)C)[C@H](O)CO[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O	4440.6	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #205	CC(=O)N[C@H]1C([C@H](O[Si](C)(C)C)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@@H](CO[Si](C)(C)C)O[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O	4433.9	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #206	CC(=O)N[C@H]1C([C@H](O[Si](C)(C)C)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O	4463.5	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #207	CC(=O)N[C@H]1C([C@H](O[Si](C)(C)C)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@@H]2O[Si](C)(C)C)(C(=O)O)C[C@@H]1O	4438.9	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #208	CC(=O)N[C@H]1C([C@H](O[Si](C)(C)C)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O[Si](C)(C)C)C[C@@H]1O	4412.6	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #209	CC(=O)N[C@H]1C([C@H](O[Si](C)(C)C)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C)[C@H](O)C(N)=CO[Si](C)(C)C)[C@@H]2O)(C(=O)O)C[C@@H]1O	4596.2	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #21	CC(=O)N[C@H]1C([C@H](O)[C@@H](CO)O[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)C(N)=CO[Si](C)(C)C)[C@@H]2O)(C(=O)O)C[C@@H]1O[Si](C)(C)C	4570.6	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #210	CC(=O)N[C@H]1C([C@H](O[Si](C)(C)C)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C)[C@H](O)[C@H](C=O)N[Si](C)(C)C)[C@@H]2O)(C(=O)O)C[C@@H]1O	4653.2	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #211	CC(=O)N([C@H]1C([C@H](O[Si](C)(C)C)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O)[Si](C)(C)C	4435.1	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #212	CC(=O)N[C@H]1C([C@H](O)[C@@H](CO[Si](C)(C)C)O[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O	4413.1	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #213	CC(=O)N[C@H]1C([C@H](O)[C@@H](CO)O[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@@H](CO[Si](C)(C)C)O[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O	4425.8	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #214	CC(=O)N[C@H]1C([C@H](O)[C@@H](CO)O[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O	4455.7	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #215	CC(=O)N[C@H]1C([C@H](O)[C@@H](CO)O[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@@H]2O[Si](C)(C)C)(C(=O)O)C[C@@H]1O	4428.7	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #216	CC(=O)N[C@H]1C([C@H](O)[C@@H](CO)O[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O[Si](C)(C)C)C[C@@H]1O	4403.0	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #217	CC(=O)N[C@H]1C([C@H](O)[C@@H](CO)O[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C)[C@H](O)C(N)=CO[Si](C)(C)C)[C@@H]2O)(C(=O)O)C[C@@H]1O	4584.0	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #218	CC(=O)N[C@H]1C([C@H](O)[C@@H](CO)O[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C)[C@H](O)[C@H](C=O)N[Si](C)(C)C)[C@@H]2O)(C(=O)O)C[C@@H]1O	4627.4	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #219	CC(=O)N([C@H]1C([C@H](O)[C@@H](CO)O[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O)[Si](C)(C)C	4426.0	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #22	CC(=O)N[C@H]1C([C@H](O)[C@@H](CO)O[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@H](C=O)N[Si](C)(C)C)[C@@H]2O)(C(=O)O)C[C@@H]1O[Si](C)(C)C	4626.5	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #220	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@@H](CO[Si](C)(C)C)O[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O	4398.4	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #221	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O	4433.6	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #222	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@@H]2O[Si](C)(C)C)(C(=O)O)C[C@@H]1O	4400.3	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #223	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O[Si](C)(C)C)C[C@@H]1O	4373.7	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #224	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C)[C@H](O)C(N)=CO[Si](C)(C)C)[C@@H]2O)(C(=O)O)C[C@@H]1O	4562.8	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #225	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C)[C@H](O)[C@H](C=O)N[Si](C)(C)C)[C@@H]2O)(C(=O)O)C[C@@H]1O	4617.3	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #226	CC(=O)N([C@H]1C([C@H](O)[C@H](O)CO[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O)[Si](C)(C)C	4409.3	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #227	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@@H](CO[Si](C)(C)C)O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O	4454.7	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #228	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@@H](CO[Si](C)(C)C)O[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@@H]2O[Si](C)(C)C)(C(=O)O)C[C@@H]1O	4415.6	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #229	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@@H](CO[Si](C)(C)C)O[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O[Si](C)(C)C)C[C@@H]1O	4392.1	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #23	CC(=O)N([C@H]1C([C@H](O)[C@@H](CO)O[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O[Si](C)(C)C)[Si](C)(C)C	4438.4	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #230	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@@H](CO[Si](C)(C)C)O[Si](C)(C)C)[C@H](O)C(N)=CO[Si](C)(C)C)[C@@H]2O)(C(=O)O)C[C@@H]1O	4580.4	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #231	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@@H](CO[Si](C)(C)C)O[Si](C)(C)C)[C@H](O)[C@H](C=O)N[Si](C)(C)C)[C@@H]2O)(C(=O)O)C[C@@H]1O	4642.6	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #232	CC(=O)N([C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@@H](CO[Si](C)(C)C)O[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O)[Si](C)(C)C	4416.1	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #233	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](N)C=O)[C@@H]2O[Si](C)(C)C)(C(=O)O)C[C@@H]1O	4452.4	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #234	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](N)C=O)[C@@H]2O)(C(=O)O[Si](C)(C)C)C[C@@H]1O	4428.4	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #235	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C)[C@H](O[Si](C)(C)C)C(N)=CO[Si](C)(C)C)[C@@H]2O)(C(=O)O)C[C@@H]1O	4601.4	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #236	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](C=O)N[Si](C)(C)C)[C@@H]2O)(C(=O)O)C[C@@H]1O	4635.5	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #237	CC(=O)N([C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O)[Si](C)(C)C	4450.2	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #238	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@@H]2O[Si](C)(C)C)(C(=O)O[Si](C)(C)C)C[C@@H]1O	4396.1	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #239	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C)[C@H](O)C(N)=CO[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)(C(=O)O)C[C@@H]1O	4583.9	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #24	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O[Si](C)(C)C)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O[Si](C)(C)C	4362.0	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #240	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C)[C@H](O)[C@H](C=O)N[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)(C(=O)O)C[C@@H]1O	4645.0	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #241	CC(=O)N([C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@@H]2O[Si](C)(C)C)(C(=O)O)C[C@@H]1O)[Si](C)(C)C	4426.4	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #242	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C)[C@H](O)C(N)=CO[Si](C)(C)C)[C@@H]2O)(C(=O)O[Si](C)(C)C)C[C@@H]1O	4531.3	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #243	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C)[C@H](O)[C@H](C=O)N[Si](C)(C)C)[C@@H]2O)(C(=O)O[Si](C)(C)C)C[C@@H]1O	4605.1	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #244	CC(=O)N([C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O[Si](C)(C)C)C[C@@H]1O)[Si](C)(C)C	4389.1	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #245	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C)[C@H](O)C(=CO[Si](C)(C)C)N[Si](C)(C)C)[C@@H]2O)(C(=O)O)C[C@@H]1O	4804.0	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #246	CC(=O)N([C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C)[C@H](O)C(N)=CO[Si](C)(C)C)[C@@H]2O)(C(=O)O)C[C@@H]1O)[Si](C)(C)C	4579.5	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #247	CC(=O)N([C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C)[C@H](O)[C@H](C=O)N[Si](C)(C)C)[C@@H]2O)(C(=O)O)C[C@@H]1O)[Si](C)(C)C	4640.4	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #248	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C)[C@H](O)[C@H](C=O)N([Si](C)(C)C)[Si](C)(C)C)[C@@H]2O)(C(=O)O)C[C@@H]1O	4790.7	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #249	CC(=O)N[C@H]1C([C@H](O[Si](C)(C)C)[C@@H](CO)O[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O	4459.8	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #25	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO[Si](C)(C)C)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O[Si](C)(C)C	4353.8	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #250	CC(=O)N[C@H]1C([C@H](O[Si](C)(C)C)[C@H](O)CO[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O	4437.0	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #251	CC(=O)N[C@H]1C([C@H](O[Si](C)(C)C)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O	4450.5	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #252	CC(=O)N[C@H]1C([C@H](O[Si](C)(C)C)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@@H]2O[Si](C)(C)C)(C(=O)O)C[C@@H]1O	4427.0	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #253	CC(=O)N[C@H]1C([C@H](O[Si](C)(C)C)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O[Si](C)(C)C)C[C@@H]1O	4408.5	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #254	CC(=O)N[C@H]1C([C@H](O[Si](C)(C)C)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C)[C@H](O)C(N)=CO[Si](C)(C)C)[C@@H]2O)(C(=O)O)C[C@@H]1O	4588.2	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #255	CC(=O)N[C@H]1C([C@H](O[Si](C)(C)C)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C)[C@H](O)[C@H](C=O)N[Si](C)(C)C)[C@@H]2O)(C(=O)O)C[C@@H]1O	4645.3	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #256	CC(=O)N([C@H]1C([C@H](O[Si](C)(C)C)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O)[Si](C)(C)C	4428.2	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #257	CC(=O)N[C@H]1C([C@H](O)[C@@H](CO[Si](C)(C)C)O[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O	4409.6	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #258	CC(=O)N[C@H]1C([C@H](O)[C@@H](CO)O[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O	4442.5	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #259	CC(=O)N[C@H]1C([C@H](O)[C@@H](CO)O[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@@H]2O[Si](C)(C)C)(C(=O)O)C[C@@H]1O	4418.2	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #26	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O[Si](C)(C)C	4385.2	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #260	CC(=O)N[C@H]1C([C@H](O)[C@@H](CO)O[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O[Si](C)(C)C)C[C@@H]1O	4401.5	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #261	CC(=O)N[C@H]1C([C@H](O)[C@@H](CO)O[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C)[C@H](O)C(N)=CO[Si](C)(C)C)[C@@H]2O)(C(=O)O)C[C@@H]1O	4578.0	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #262	CC(=O)N[C@H]1C([C@H](O)[C@@H](CO)O[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C)[C@H](O)[C@H](C=O)N[Si](C)(C)C)[C@@H]2O)(C(=O)O)C[C@@H]1O	4623.7	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #263	CC(=O)N([C@H]1C([C@H](O)[C@@H](CO)O[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O)[Si](C)(C)C	4421.4	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #264	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O	4420.0	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #265	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@@H]2O[Si](C)(C)C)(C(=O)O)C[C@@H]1O	4389.8	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #266	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O[Si](C)(C)C)C[C@@H]1O	4370.8	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #267	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C)[C@H](O)C(N)=CO[Si](C)(C)C)[C@@H]2O)(C(=O)O)C[C@@H]1O	4554.8	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #268	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C)[C@H](O)[C@H](C=O)N[Si](C)(C)C)[C@@H]2O)(C(=O)O)C[C@@H]1O	4612.9	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #269	CC(=O)N([C@H]1C([C@H](O)[C@H](O)CO[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O)[Si](C)(C)C	4404.0	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #27	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O[Si](C)(C)C	4385.4	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #270	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](N)C=O)[C@@H]2O[Si](C)(C)C)(C(=O)O)C[C@@H]1O	4433.8	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #271	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](N)C=O)[C@@H]2O)(C(=O)O[Si](C)(C)C)C[C@@H]1O	4414.2	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #272	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)C(N)=CO[Si](C)(C)C)[C@@H]2O)(C(=O)O)C[C@@H]1O	4589.0	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #273	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](C=O)N[Si](C)(C)C)[C@@H]2O)(C(=O)O)C[C@@H]1O	4617.2	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #274	CC(=O)N([C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O)[Si](C)(C)C	4431.9	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #275	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@@H]2O[Si](C)(C)C)(C(=O)O[Si](C)(C)C)C[C@@H]1O	4378.7	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #276	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C)[C@H](O)C(N)=CO[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)(C(=O)O)C[C@@H]1O	4567.4	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #277	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C)[C@H](O)[C@H](C=O)N[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)(C(=O)O)C[C@@H]1O	4634.2	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #278	CC(=O)N([C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@@H]2O[Si](C)(C)C)(C(=O)O)C[C@@H]1O)[Si](C)(C)C	4412.0	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #279	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C)[C@H](O)C(N)=CO[Si](C)(C)C)[C@@H]2O)(C(=O)O[Si](C)(C)C)C[C@@H]1O	4525.0	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #28	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O[Si](C)(C)C)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O[Si](C)(C)C	4413.1	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #280	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C)[C@H](O)[C@H](C=O)N[Si](C)(C)C)[C@@H]2O)(C(=O)O[Si](C)(C)C)C[C@@H]1O	4595.6	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #281	CC(=O)N([C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O[Si](C)(C)C)C[C@@H]1O)[Si](C)(C)C	4380.1	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #282	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C)[C@H](O)C(=CO[Si](C)(C)C)N[Si](C)(C)C)[C@@H]2O)(C(=O)O)C[C@@H]1O	4799.0	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #283	CC(=O)N([C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C)[C@H](O)C(N)=CO[Si](C)(C)C)[C@@H]2O)(C(=O)O)C[C@@H]1O)[Si](C)(C)C	4570.7	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #284	CC(=O)N([C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C)[C@H](O)[C@H](C=O)N[Si](C)(C)C)[C@@H]2O)(C(=O)O)C[C@@H]1O)[Si](C)(C)C	4631.1	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #285	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C)[C@H](O)[C@H](C=O)N([Si](C)(C)C)[Si](C)(C)C)[C@@H]2O)(C(=O)O)C[C@@H]1O	4786.1	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #286	CC(=O)N[C@H]1C([C@H](O[Si](C)(C)C)[C@@H](CO)O[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O[Si](C)(C)C)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O	4473.2	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #287	CC(=O)N[C@H]1C([C@H](O[Si](C)(C)C)[C@H](O)CO[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O[Si](C)(C)C)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O	4449.6	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #288	CC(=O)N[C@H]1C([C@H](O[Si](C)(C)C)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O[Si](C)(C)C)[C@@H](N)C=O)[C@@H]2O[Si](C)(C)C)(C(=O)O)C[C@@H]1O	4457.3	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #289	CC(=O)N[C@H]1C([C@H](O[Si](C)(C)C)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O[Si](C)(C)C)[C@@H](N)C=O)[C@@H]2O)(C(=O)O[Si](C)(C)C)C[C@@H]1O	4431.6	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #29	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O[Si](C)(C)C)(C(=O)O)C[C@@H]1O[Si](C)(C)C	4374.6	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #290	CC(=O)N[C@H]1C([C@H](O[Si](C)(C)C)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O[Si](C)(C)C)C(N)=CO[Si](C)(C)C)[C@@H]2O)(C(=O)O)C[C@@H]1O	4588.3	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #291	CC(=O)N[C@H]1C([C@H](O[Si](C)(C)C)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O[Si](C)(C)C)[C@H](C=O)N[Si](C)(C)C)[C@@H]2O)(C(=O)O)C[C@@H]1O	4642.1	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #292	CC(=O)N([C@H]1C([C@H](O[Si](C)(C)C)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O[Si](C)(C)C)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O)[Si](C)(C)C	4451.3	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #293	CC(=O)N[C@H]1C([C@H](O)[C@@H](CO[Si](C)(C)C)O[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O[Si](C)(C)C)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O	4429.2	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #294	CC(=O)N[C@H]1C([C@H](O)[C@@H](CO)O[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O[Si](C)(C)C)[C@@H](N)C=O)[C@@H]2O[Si](C)(C)C)(C(=O)O)C[C@@H]1O	4438.6	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #295	CC(=O)N[C@H]1C([C@H](O)[C@@H](CO)O[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O[Si](C)(C)C)[C@@H](N)C=O)[C@@H]2O)(C(=O)O[Si](C)(C)C)C[C@@H]1O	4412.7	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #296	CC(=O)N[C@H]1C([C@H](O)[C@@H](CO)O[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O[Si](C)(C)C)C(N)=CO[Si](C)(C)C)[C@@H]2O)(C(=O)O)C[C@@H]1O	4579.6	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #297	CC(=O)N[C@H]1C([C@H](O)[C@@H](CO)O[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O[Si](C)(C)C)[C@H](C=O)N[Si](C)(C)C)[C@@H]2O)(C(=O)O)C[C@@H]1O	4613.7	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #298	CC(=O)N([C@H]1C([C@H](O)[C@@H](CO)O[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O[Si](C)(C)C)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O)[Si](C)(C)C	4435.5	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #299	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O[Si](C)(C)C)[C@@H](N)C=O)[C@@H]2O[Si](C)(C)C)(C(=O)O)C[C@@H]1O	4412.6	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #3	CC(=O)N[C@H]1C([C@H](O[Si](C)(C)C)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O[Si](C)(C)C)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O[Si](C)(C)C	4405.5	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #30	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O[Si](C)(C)C)C[C@@H]1O[Si](C)(C)C	4368.7	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #300	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O[Si](C)(C)C)[C@@H](N)C=O)[C@@H]2O)(C(=O)O[Si](C)(C)C)C[C@@H]1O	4391.5	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #301	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O[Si](C)(C)C)C(N)=CO[Si](C)(C)C)[C@@H]2O)(C(=O)O)C[C@@H]1O	4558.6	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #302	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O[Si](C)(C)C)[C@H](C=O)N[Si](C)(C)C)[C@@H]2O)(C(=O)O)C[C@@H]1O	4602.5	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #303	CC(=O)N([C@H]1C([C@H](O)[C@H](O)CO[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O[Si](C)(C)C)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O)[Si](C)(C)C	4420.3	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #304	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O[Si](C)(C)C)[C@@H](N)C=O)[C@@H]2O[Si](C)(C)C)(C(=O)O[Si](C)(C)C)C[C@@H]1O	4412.1	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #305	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O[Si](C)(C)C)C(N)=CO[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)(C(=O)O)C[C@@H]1O	4575.5	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #306	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O[Si](C)(C)C)[C@H](C=O)N[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)(C(=O)O)C[C@@H]1O	4635.4	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #307	CC(=O)N([C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O[Si](C)(C)C)[C@@H](N)C=O)[C@@H]2O[Si](C)(C)C)(C(=O)O)C[C@@H]1O)[Si](C)(C)C	4440.4	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #308	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O[Si](C)(C)C)C(N)=CO[Si](C)(C)C)[C@@H]2O)(C(=O)O[Si](C)(C)C)C[C@@H]1O	4525.3	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #309	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O[Si](C)(C)C)[C@H](C=O)N[Si](C)(C)C)[C@@H]2O)(C(=O)O[Si](C)(C)C)C[C@@H]1O	4598.6	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #31	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)C(N)=CO[Si](C)(C)C)[C@@H]2O)(C(=O)O)C[C@@H]1O[Si](C)(C)C	4542.4	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #310	CC(=O)N([C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O[Si](C)(C)C)[C@@H](N)C=O)[C@@H]2O)(C(=O)O[Si](C)(C)C)C[C@@H]1O)[Si](C)(C)C	4405.4	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #311	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O[Si](C)(C)C)C(=CO[Si](C)(C)C)N[Si](C)(C)C)[C@@H]2O)(C(=O)O)C[C@@H]1O	4799.1	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #312	CC(=O)N([C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O[Si](C)(C)C)C(N)=CO[Si](C)(C)C)[C@@H]2O)(C(=O)O)C[C@@H]1O)[Si](C)(C)C	4566.6	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #313	CC(=O)N([C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O[Si](C)(C)C)[C@H](C=O)N[Si](C)(C)C)[C@@H]2O)(C(=O)O)C[C@@H]1O)[Si](C)(C)C	4629.8	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #314	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O[Si](C)(C)C)[C@H](C=O)N([Si](C)(C)C)[Si](C)(C)C)[C@@H]2O)(C(=O)O)C[C@@H]1O	4791.0	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #315	CC(=O)N[C@H]1C([C@H](O[Si](C)(C)C)[C@@H](CO)O[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O[Si](C)(C)C)(C(=O)O)C[C@@H]1O	4451.5	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #316	CC(=O)N[C@H]1C([C@H](O[Si](C)(C)C)[C@H](O)CO[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O[Si](C)(C)C)(C(=O)O)C[C@@H]1O	4424.6	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #317	CC(=O)N[C@H]1C([C@H](O[Si](C)(C)C)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O[Si](C)(C)C)(C(=O)O[Si](C)(C)C)C[C@@H]1O	4395.8	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #318	CC(=O)N[C@H]1C([C@H](O[Si](C)(C)C)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)C(N)=CO[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)(C(=O)O)C[C@@H]1O	4574.4	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #319	CC(=O)N[C@H]1C([C@H](O[Si](C)(C)C)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@H](C=O)N[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)(C(=O)O)C[C@@H]1O	4666.5	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #32	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@H](C=O)N[Si](C)(C)C)[C@@H]2O)(C(=O)O)C[C@@H]1O[Si](C)(C)C	4613.5	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #320	CC(=O)N([C@H]1C([C@H](O[Si](C)(C)C)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O[Si](C)(C)C)(C(=O)O)C[C@@H]1O)[Si](C)(C)C	4431.2	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #321	CC(=O)N[C@H]1C([C@H](O)[C@@H](CO[Si](C)(C)C)O[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O[Si](C)(C)C)(C(=O)O)C[C@@H]1O	4394.0	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #322	CC(=O)N[C@H]1C([C@H](O)[C@@H](CO)O[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O[Si](C)(C)C)(C(=O)O[Si](C)(C)C)C[C@@H]1O	4383.0	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #323	CC(=O)N[C@H]1C([C@H](O)[C@@H](CO)O[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)C(N)=CO[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)(C(=O)O)C[C@@H]1O	4561.2	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #324	CC(=O)N[C@H]1C([C@H](O)[C@@H](CO)O[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@H](C=O)N[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)(C(=O)O)C[C@@H]1O	4634.0	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #325	CC(=O)N([C@H]1C([C@H](O)[C@@H](CO)O[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O[Si](C)(C)C)(C(=O)O)C[C@@H]1O)[Si](C)(C)C	4413.2	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #326	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O[Si](C)(C)C)(C(=O)O[Si](C)(C)C)C[C@@H]1O	4348.4	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #327	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)C(N)=CO[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)(C(=O)O)C[C@@H]1O	4536.2	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #328	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@H](C=O)N[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)(C(=O)O)C[C@@H]1O	4617.3	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #329	CC(=O)N([C@H]1C([C@H](O)[C@H](O)CO[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O[Si](C)(C)C)(C(=O)O)C[C@@H]1O)[Si](C)(C)C	4392.1	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #33	CC(=O)N([C@H]1C([C@H](O)[C@H](O)CO[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O[Si](C)(C)C)[Si](C)(C)C	4417.3	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #330	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)C(N)=CO[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)(C(=O)O[Si](C)(C)C)C[C@@H]1O	4495.4	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #331	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@H](C=O)N[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)(C(=O)O[Si](C)(C)C)C[C@@H]1O	4606.0	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #332	CC(=O)N([C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O[Si](C)(C)C)(C(=O)O[Si](C)(C)C)C[C@@H]1O)[Si](C)(C)C	4375.1	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #333	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)C(=CO[Si](C)(C)C)N[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)(C(=O)O)C[C@@H]1O	4791.0	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #334	CC(=O)N([C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)C(N)=CO[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)(C(=O)O)C[C@@H]1O)[Si](C)(C)C	4558.4	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #335	CC(=O)N([C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@H](C=O)N[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)(C(=O)O)C[C@@H]1O)[Si](C)(C)C	4641.6	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #336	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@H](C=O)N([Si](C)(C)C)[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)(C(=O)O)C[C@@H]1O	4803.0	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #337	CC(=O)N[C@H]1C([C@H](O[Si](C)(C)C)[C@@H](CO[Si](C)(C)C)O[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O	4438.8	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #338	CC(=O)N[C@H]1C([C@H](O[Si](C)(C)C)[C@@H](CO)O[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O[Si](C)(C)C)C[C@@H]1O	4426.9	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #339	CC(=O)N[C@H]1C([C@H](O[Si](C)(C)C)[C@@H](CO)O[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)C(N)=CO[Si](C)(C)C)[C@@H]2O)(C(=O)O)C[C@@H]1O	4600.2	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #34	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O[Si](C)(C)C)[C@@H](CO[Si](C)(C)C)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O[Si](C)(C)C	4384.7	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #340	CC(=O)N[C@H]1C([C@H](O[Si](C)(C)C)[C@@H](CO)O[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@H](C=O)N[Si](C)(C)C)[C@@H]2O)(C(=O)O)C[C@@H]1O	4658.9	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #341	CC(=O)N([C@H]1C([C@H](O[Si](C)(C)C)[C@@H](CO)O[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O)[Si](C)(C)C	4446.2	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #342	CC(=O)N[C@H]1C([C@H](O[Si](C)(C)C)[C@H](O)CO[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O[Si](C)(C)C)C[C@@H]1O	4407.0	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #343	CC(=O)N[C@H]1C([C@H](O[Si](C)(C)C)[C@H](O)CO[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)C(N)=CO[Si](C)(C)C)[C@@H]2O)(C(=O)O)C[C@@H]1O	4582.4	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #344	CC(=O)N[C@H]1C([C@H](O[Si](C)(C)C)[C@H](O)CO[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@H](C=O)N[Si](C)(C)C)[C@@H]2O)(C(=O)O)C[C@@H]1O	4638.0	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #345	CC(=O)N([C@H]1C([C@H](O[Si](C)(C)C)[C@H](O)CO[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O)[Si](C)(C)C	4429.2	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #346	CC(=O)N[C@H]1C([C@H](O[Si](C)(C)C)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)C(N)=CO[Si](C)(C)C)[C@@H]2O)(C(=O)O[Si](C)(C)C)C[C@@H]1O	4531.8	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #347	CC(=O)N[C@H]1C([C@H](O[Si](C)(C)C)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@H](C=O)N[Si](C)(C)C)[C@@H]2O)(C(=O)O[Si](C)(C)C)C[C@@H]1O	4623.9	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #348	CC(=O)N([C@H]1C([C@H](O[Si](C)(C)C)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O[Si](C)(C)C)C[C@@H]1O)[Si](C)(C)C	4406.3	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #349	CC(=O)N[C@H]1C([C@H](O[Si](C)(C)C)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)C(=CO[Si](C)(C)C)N[Si](C)(C)C)[C@@H]2O)(C(=O)O)C[C@@H]1O	4817.1	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #35	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O[Si](C)(C)C)[C@@H](CO)O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O[Si](C)(C)C	4394.0	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #350	CC(=O)N([C@H]1C([C@H](O[Si](C)(C)C)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)C(N)=CO[Si](C)(C)C)[C@@H]2O)(C(=O)O)C[C@@H]1O)[Si](C)(C)C	4583.3	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #351	CC(=O)N([C@H]1C([C@H](O[Si](C)(C)C)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@H](C=O)N[Si](C)(C)C)[C@@H]2O)(C(=O)O)C[C@@H]1O)[Si](C)(C)C	4654.9	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #352	CC(=O)N[C@H]1C([C@H](O[Si](C)(C)C)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@H](C=O)N([Si](C)(C)C)[Si](C)(C)C)[C@@H]2O)(C(=O)O)C[C@@H]1O	4815.4	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #353	CC(=O)N[C@H]1C([C@H](O)[C@@H](CO[Si](C)(C)C)O[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O[Si](C)(C)C)C[C@@H]1O	4373.8	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #354	CC(=O)N[C@H]1C([C@H](O)[C@@H](CO[Si](C)(C)C)O[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)C(N)=CO[Si](C)(C)C)[C@@H]2O)(C(=O)O)C[C@@H]1O	4549.1	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #355	CC(=O)N[C@H]1C([C@H](O)[C@@H](CO[Si](C)(C)C)O[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@H](C=O)N[Si](C)(C)C)[C@@H]2O)(C(=O)O)C[C@@H]1O	4619.0	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #356	CC(=O)N([C@H]1C([C@H](O)[C@@H](CO[Si](C)(C)C)O[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O)[Si](C)(C)C	4404.9	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #357	CC(=O)N[C@H]1C([C@H](O)[C@@H](CO)O[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)C(N)=CO[Si](C)(C)C)[C@@H]2O)(C(=O)O[Si](C)(C)C)C[C@@H]1O	4524.4	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #358	CC(=O)N[C@H]1C([C@H](O)[C@@H](CO)O[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@H](C=O)N[Si](C)(C)C)[C@@H]2O)(C(=O)O[Si](C)(C)C)C[C@@H]1O	4593.1	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #359	CC(=O)N([C@H]1C([C@H](O)[C@@H](CO)O[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O[Si](C)(C)C)C[C@@H]1O)[Si](C)(C)C	4381.6	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #36	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O[Si](C)(C)C)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O[Si](C)(C)C	4389.7	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #360	CC(=O)N[C@H]1C([C@H](O)[C@@H](CO)O[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)C(=CO[Si](C)(C)C)N[Si](C)(C)C)[C@@H]2O)(C(=O)O)C[C@@H]1O	4784.7	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #361	CC(=O)N([C@H]1C([C@H](O)[C@@H](CO)O[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)C(N)=CO[Si](C)(C)C)[C@@H]2O)(C(=O)O)C[C@@H]1O)[Si](C)(C)C	4562.2	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #362	CC(=O)N([C@H]1C([C@H](O)[C@@H](CO)O[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@H](C=O)N[Si](C)(C)C)[C@@H]2O)(C(=O)O)C[C@@H]1O)[Si](C)(C)C	4625.9	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #363	CC(=O)N[C@H]1C([C@H](O)[C@@H](CO)O[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@H](C=O)N([Si](C)(C)C)[Si](C)(C)C)[C@@H]2O)(C(=O)O)C[C@@H]1O	4791.2	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #364	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)C(N)=CO[Si](C)(C)C)[C@@H]2O)(C(=O)O[Si](C)(C)C)C[C@@H]1O	4498.1	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #365	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@H](C=O)N[Si](C)(C)C)[C@@H]2O)(C(=O)O[Si](C)(C)C)C[C@@H]1O	4581.7	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #366	CC(=O)N([C@H]1C([C@H](O)[C@H](O)CO[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O[Si](C)(C)C)C[C@@H]1O)[Si](C)(C)C	4362.3	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #367	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)C(=CO[Si](C)(C)C)N[Si](C)(C)C)[C@@H]2O)(C(=O)O)C[C@@H]1O	4782.4	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #368	CC(=O)N([C@H]1C([C@H](O)[C@H](O)CO[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)C(N)=CO[Si](C)(C)C)[C@@H]2O)(C(=O)O)C[C@@H]1O)[Si](C)(C)C	4548.2	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #369	CC(=O)N([C@H]1C([C@H](O)[C@H](O)CO[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@H](C=O)N[Si](C)(C)C)[C@@H]2O)(C(=O)O)C[C@@H]1O)[Si](C)(C)C	4623.1	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #37	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O[Si](C)(C)C)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O[Si](C)(C)C)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O[Si](C)(C)C	4417.3	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #370	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@H](C=O)N([Si](C)(C)C)[Si](C)(C)C)[C@@H]2O)(C(=O)O)C[C@@H]1O	4787.7	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #371	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)C(=CO[Si](C)(C)C)N[Si](C)(C)C)[C@@H]2O)(C(=O)O[Si](C)(C)C)C[C@@H]1O	4727.6	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #372	CC(=O)N([C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)C(N)=CO[Si](C)(C)C)[C@@H]2O)(C(=O)O[Si](C)(C)C)C[C@@H]1O)[Si](C)(C)C	4500.0	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #373	CC(=O)N([C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@H](C=O)N[Si](C)(C)C)[C@@H]2O)(C(=O)O[Si](C)(C)C)C[C@@H]1O)[Si](C)(C)C	4590.7	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #374	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@H](C=O)N([Si](C)(C)C)[Si](C)(C)C)[C@@H]2O)(C(=O)O[Si](C)(C)C)C[C@@H]1O	4742.0	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #375	CC(=O)N([C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)C(=CO[Si](C)(C)C)N[Si](C)(C)C)[C@@H]2O)(C(=O)O)C[C@@H]1O)[Si](C)(C)C	4792.6	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #376	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)C(=CO[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)[C@@H]2O)(C(=O)O)C[C@@H]1O	4815.3	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #377	CC(=O)N([C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@H](C=O)N([Si](C)(C)C)[Si](C)(C)C)[C@@H]2O)(C(=O)O)C[C@@H]1O)[Si](C)(C)C	4787.6	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #38	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O[Si](C)(C)C)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O[Si](C)(C)C)(C(=O)O)C[C@@H]1O[Si](C)(C)C	4402.4	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #39	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O[Si](C)(C)C)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O[Si](C)(C)C)C[C@@H]1O[Si](C)(C)C	4374.2	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #4	CC(=O)N[C@H]1C([C@H](O[Si](C)(C)C)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO[Si](C)(C)C)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O[Si](C)(C)C	4392.5	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #40	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O[Si](C)(C)C)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)C(N)=CO[Si](C)(C)C)[C@@H]2O)(C(=O)O)C[C@@H]1O[Si](C)(C)C	4539.1	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #41	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O[Si](C)(C)C)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@H](C=O)N[Si](C)(C)C)[C@@H]2O)(C(=O)O)C[C@@H]1O[Si](C)(C)C	4623.3	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #42	CC(=O)N([C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O[Si](C)(C)C)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O[Si](C)(C)C)[Si](C)(C)C	4421.6	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #43	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO[Si](C)(C)C)O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O[Si](C)(C)C	4386.7	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #44	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO[Si](C)(C)C)O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O[Si](C)(C)C	4381.8	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #45	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO[Si](C)(C)C)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O[Si](C)(C)C)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O[Si](C)(C)C	4403.1	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #46	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO[Si](C)(C)C)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O[Si](C)(C)C)(C(=O)O)C[C@@H]1O[Si](C)(C)C	4386.7	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #47	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO[Si](C)(C)C)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O[Si](C)(C)C)C[C@@H]1O[Si](C)(C)C	4371.0	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #48	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO[Si](C)(C)C)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)C(N)=CO[Si](C)(C)C)[C@@H]2O)(C(=O)O)C[C@@H]1O[Si](C)(C)C	4539.4	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #49	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO[Si](C)(C)C)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@H](C=O)N[Si](C)(C)C)[C@@H]2O)(C(=O)O)C[C@@H]1O[Si](C)(C)C	4617.3	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #5	CC(=O)N[C@H]1C([C@H](O[Si](C)(C)C)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O[Si](C)(C)C	4421.9	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #50	CC(=O)N([C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO[Si](C)(C)C)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O[Si](C)(C)C)[Si](C)(C)C	4423.6	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #51	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@@H](CO[Si](C)(C)C)O[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O[Si](C)(C)C	4406.0	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #52	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O[Si](C)(C)C	4444.3	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #53	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@@H]2O[Si](C)(C)C)(C(=O)O)C[C@@H]1O[Si](C)(C)C	4417.0	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #54	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O[Si](C)(C)C)C[C@@H]1O[Si](C)(C)C	4399.0	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #55	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C)[C@H](O)C(N)=CO[Si](C)(C)C)[C@@H]2O)(C(=O)O)C[C@@H]1O[Si](C)(C)C	4580.8	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #56	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C)[C@H](O)[C@H](C=O)N[Si](C)(C)C)[C@@H]2O)(C(=O)O)C[C@@H]1O[Si](C)(C)C	4633.6	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #57	CC(=O)N([C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O[Si](C)(C)C)[Si](C)(C)C	4449.1	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #58	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O[Si](C)(C)C	4429.7	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #59	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@@H]2O[Si](C)(C)C)(C(=O)O)C[C@@H]1O[Si](C)(C)C	4402.8	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #6	CC(=O)N[C@H]1C([C@H](O[Si](C)(C)C)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O[Si](C)(C)C	4418.3	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #60	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O[Si](C)(C)C)C[C@@H]1O[Si](C)(C)C	4392.4	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #61	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C)[C@H](O)C(N)=CO[Si](C)(C)C)[C@@H]2O)(C(=O)O)C[C@@H]1O[Si](C)(C)C	4569.6	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #62	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C)[C@H](O)[C@H](C=O)N[Si](C)(C)C)[C@@H]2O)(C(=O)O)C[C@@H]1O[Si](C)(C)C	4627.7	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #63	CC(=O)N([C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O[Si](C)(C)C)[Si](C)(C)C	4436.9	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #64	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O[Si](C)(C)C)[C@@H](N)C=O)[C@@H]2O[Si](C)(C)C)(C(=O)O)C[C@@H]1O[Si](C)(C)C	4434.5	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #65	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O[Si](C)(C)C)[C@@H](N)C=O)[C@@H]2O)(C(=O)O[Si](C)(C)C)C[C@@H]1O[Si](C)(C)C	4421.7	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #66	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O[Si](C)(C)C)C(N)=CO[Si](C)(C)C)[C@@H]2O)(C(=O)O)C[C@@H]1O[Si](C)(C)C	4570.7	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #67	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O[Si](C)(C)C)[C@H](C=O)N[Si](C)(C)C)[C@@H]2O)(C(=O)O)C[C@@H]1O[Si](C)(C)C	4621.6	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #68	CC(=O)N([C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O[Si](C)(C)C)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O[Si](C)(C)C)[Si](C)(C)C	4463.0	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #69	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O[Si](C)(C)C)(C(=O)O[Si](C)(C)C)C[C@@H]1O[Si](C)(C)C	4389.1	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #7	CC(=O)N[C@H]1C([C@H](O[Si](C)(C)C)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O[Si](C)(C)C)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O[Si](C)(C)C	4450.1	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #70	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)C(N)=CO[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)(C(=O)O)C[C@@H]1O[Si](C)(C)C	4553.9	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #71	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@H](C=O)N[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)(C(=O)O)C[C@@H]1O[Si](C)(C)C	4645.9	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #72	CC(=O)N([C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O[Si](C)(C)C)(C(=O)O)C[C@@H]1O[Si](C)(C)C)[Si](C)(C)C	4442.9	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #73	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)C(N)=CO[Si](C)(C)C)[C@@H]2O)(C(=O)O[Si](C)(C)C)C[C@@H]1O[Si](C)(C)C	4519.7	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #74	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@H](C=O)N[Si](C)(C)C)[C@@H]2O)(C(=O)O[Si](C)(C)C)C[C@@H]1O[Si](C)(C)C	4606.4	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #75	CC(=O)N([C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O[Si](C)(C)C)C[C@@H]1O[Si](C)(C)C)[Si](C)(C)C	4410.3	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #76	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)C(=CO[Si](C)(C)C)N[Si](C)(C)C)[C@@H]2O)(C(=O)O)C[C@@H]1O[Si](C)(C)C	4790.6	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #77	CC(=O)N([C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)C(N)=CO[Si](C)(C)C)[C@@H]2O)(C(=O)O)C[C@@H]1O[Si](C)(C)C)[Si](C)(C)C	4591.1	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #78	CC(=O)N([C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@H](C=O)N[Si](C)(C)C)[C@@H]2O)(C(=O)O)C[C@@H]1O[Si](C)(C)C)[Si](C)(C)C	4659.3	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #79	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@H](C=O)N([Si](C)(C)C)[Si](C)(C)C)[C@@H]2O)(C(=O)O)C[C@@H]1O[Si](C)(C)C	4789.5	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #8	CC(=O)N[C@H]1C([C@H](O[Si](C)(C)C)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O[Si](C)(C)C)(C(=O)O)C[C@@H]1O[Si](C)(C)C	4422.7	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #80	CC(=O)N[C@H]1C([C@H](O[Si](C)(C)C)[C@@H](CO)O[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O[Si](C)(C)C)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O	4434.3	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #81	CC(=O)N[C@H]1C([C@H](O[Si](C)(C)C)[C@H](O)CO[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O[Si](C)(C)C)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O	4410.4	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #82	CC(=O)N[C@H]1C([C@H](O[Si](C)(C)C)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O[Si](C)(C)C)[C@@H](CO[Si](C)(C)C)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O	4404.7	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #83	CC(=O)N[C@H]1C([C@H](O[Si](C)(C)C)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O[Si](C)(C)C)[C@@H](CO)O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O	4419.3	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #84	CC(=O)N[C@H]1C([C@H](O[Si](C)(C)C)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O[Si](C)(C)C)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O	4414.3	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #85	CC(=O)N[C@H]1C([C@H](O[Si](C)(C)C)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O[Si](C)(C)C)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O[Si](C)(C)C)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O	4438.8	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #86	CC(=O)N[C@H]1C([C@H](O[Si](C)(C)C)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O[Si](C)(C)C)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O[Si](C)(C)C)(C(=O)O)C[C@@H]1O	4424.0	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #87	CC(=O)N[C@H]1C([C@H](O[Si](C)(C)C)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O[Si](C)(C)C)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O[Si](C)(C)C)C[C@@H]1O	4381.6	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #88	CC(=O)N[C@H]1C([C@H](O[Si](C)(C)C)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O[Si](C)(C)C)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)C(N)=CO[Si](C)(C)C)[C@@H]2O)(C(=O)O)C[C@@H]1O	4560.1	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #89	CC(=O)N[C@H]1C([C@H](O[Si](C)(C)C)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O[Si](C)(C)C)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@H](C=O)N[Si](C)(C)C)[C@@H]2O)(C(=O)O)C[C@@H]1O	4645.1	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #9	CC(=O)N[C@H]1C([C@H](O[Si](C)(C)C)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O[Si](C)(C)C)C[C@@H]1O[Si](C)(C)C	4412.3	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #90	CC(=O)N([C@H]1C([C@H](O[Si](C)(C)C)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O[Si](C)(C)C)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O)[Si](C)(C)C	4414.1	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #91	CC(=O)N[C@H]1C([C@H](O)[C@@H](CO[Si](C)(C)C)O[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O[Si](C)(C)C)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O	4382.4	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #92	CC(=O)N[C@H]1C([C@H](O)[C@@H](CO)O[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O[Si](C)(C)C)[C@@H](CO[Si](C)(C)C)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O	4393.0	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #93	CC(=O)N[C@H]1C([C@H](O)[C@@H](CO)O[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O[Si](C)(C)C)[C@@H](CO)O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O	4410.1	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #94	CC(=O)N[C@H]1C([C@H](O)[C@@H](CO)O[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O[Si](C)(C)C)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O	4407.4	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #95	CC(=O)N[C@H]1C([C@H](O)[C@@H](CO)O[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O[Si](C)(C)C)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O[Si](C)(C)C)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O	4421.1	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #96	CC(=O)N[C@H]1C([C@H](O)[C@@H](CO)O[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O[Si](C)(C)C)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O[Si](C)(C)C)(C(=O)O)C[C@@H]1O	4406.3	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #97	CC(=O)N[C@H]1C([C@H](O)[C@@H](CO)O[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O[Si](C)(C)C)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O[Si](C)(C)C)C[C@@H]1O	4368.6	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #98	CC(=O)N[C@H]1C([C@H](O)[C@@H](CO)O[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O[Si](C)(C)C)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)C(N)=CO[Si](C)(C)C)[C@@H]2O)(C(=O)O)C[C@@H]1O	4550.0	Semi standard non polar	33892256
3'-Sialyllactosamine,3TMS,isomer #99	CC(=O)N[C@H]1C([C@H](O)[C@@H](CO)O[Si](C)(C)C)O[C@@](O[C@H]2[C@@H](O[Si](C)(C)C)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@H](C=O)N[Si](C)(C)C)[C@@H]2O)(C(=O)O)C[C@@H]1O	4616.0	Semi standard non polar	33892256
3'-Sialyllactosamine,1TBDMS,isomer #1	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O[Si](C)(C)C(C)(C)C	4801.7	Semi standard non polar	33892256
3'-Sialyllactosamine,1TBDMS,isomer #10	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO[Si](C)(C)C(C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O	4815.2	Semi standard non polar	33892256
3'-Sialyllactosamine,1TBDMS,isomer #11	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O[Si](C)(C)C(C)(C)C)C[C@@H]1O	4797.8	Semi standard non polar	33892256
3'-Sialyllactosamine,1TBDMS,isomer #12	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)C(N)=CO[Si](C)(C)C(C)(C)C)[C@@H]2O)(C(=O)O)C[C@@H]1O	4997.5	Semi standard non polar	33892256
3'-Sialyllactosamine,1TBDMS,isomer #13	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@H](C=O)N[Si](C)(C)C(C)(C)C)[C@@H]2O)(C(=O)O)C[C@@H]1O	5019.4	Semi standard non polar	33892256
3'-Sialyllactosamine,1TBDMS,isomer #14	CC(=O)N([C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O)[Si](C)(C)C(C)(C)C	4833.2	Semi standard non polar	33892256
3'-Sialyllactosamine,1TBDMS,isomer #2	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O	4790.9	Semi standard non polar	33892256
3'-Sialyllactosamine,1TBDMS,isomer #3	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO[Si](C)(C)C(C)(C)C)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O	4805.5	Semi standard non polar	33892256
3'-Sialyllactosamine,1TBDMS,isomer #4	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O	4810.4	Semi standard non polar	33892256
3'-Sialyllactosamine,1TBDMS,isomer #5	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O	4813.8	Semi standard non polar	33892256
3'-Sialyllactosamine,1TBDMS,isomer #6	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O	4836.8	Semi standard non polar	33892256
3'-Sialyllactosamine,1TBDMS,isomer #7	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O[Si](C)(C)C(C)(C)C)(C(=O)O)C[C@@H]1O	4814.8	Semi standard non polar	33892256
3'-Sialyllactosamine,1TBDMS,isomer #8	CC(=O)N[C@H]1C([C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O	4818.5	Semi standard non polar	33892256
3'-Sialyllactosamine,1TBDMS,isomer #9	CC(=O)N[C@H]1C([C@H](O)[C@@H](CO)O[Si](C)(C)C(C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O	4826.2	Semi standard non polar	33892256
3'-Sialyllactosamine,2TBDMS,isomer #1	CC(=O)N[C@H]1C([C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O[Si](C)(C)C(C)(C)C	4855.4	Semi standard non polar	33892256
3'-Sialyllactosamine,2TBDMS,isomer #10	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O[Si](C)(C)C(C)(C)C)C[C@@H]1O[Si](C)(C)C(C)(C)C	4842.0	Semi standard non polar	33892256
3'-Sialyllactosamine,2TBDMS,isomer #11	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)C(N)=CO[Si](C)(C)C(C)(C)C)[C@@H]2O)(C(=O)O)C[C@@H]1O[Si](C)(C)C(C)(C)C	5021.7	Semi standard non polar	33892256
3'-Sialyllactosamine,2TBDMS,isomer #12	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@H](C=O)N[Si](C)(C)C(C)(C)C)[C@@H]2O)(C(=O)O)C[C@@H]1O[Si](C)(C)C(C)(C)C	5055.5	Semi standard non polar	33892256
3'-Sialyllactosamine,2TBDMS,isomer #13	CC(=O)N([C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	4881.9	Semi standard non polar	33892256
3'-Sialyllactosamine,2TBDMS,isomer #14	CC(=O)N[C@H]1C([C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O	4845.4	Semi standard non polar	33892256
3'-Sialyllactosamine,2TBDMS,isomer #15	CC(=O)N[C@H]1C([C@H](O)[C@@H](CO)O[Si](C)(C)C(C)(C)C)O[C@@](O[C@H]2[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O	4857.1	Semi standard non polar	33892256
3'-Sialyllactosamine,2TBDMS,isomer #16	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO[Si](C)(C)C(C)(C)C)O[C@@](O[C@H]2[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O	4835.0	Semi standard non polar	33892256
3'-Sialyllactosamine,2TBDMS,isomer #17	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](CO[Si](C)(C)C(C)(C)C)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O	4838.0	Semi standard non polar	33892256
3'-Sialyllactosamine,2TBDMS,isomer #18	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](CO)O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O	4843.6	Semi standard non polar	33892256
3'-Sialyllactosamine,2TBDMS,isomer #19	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O	4843.0	Semi standard non polar	33892256
3'-Sialyllactosamine,2TBDMS,isomer #2	CC(=O)N[C@H]1C([C@H](O)[C@@H](CO)O[Si](C)(C)C(C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O[Si](C)(C)C(C)(C)C	4869.5	Semi standard non polar	33892256
3'-Sialyllactosamine,2TBDMS,isomer #20	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O	4862.6	Semi standard non polar	33892256
3'-Sialyllactosamine,2TBDMS,isomer #21	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O[Si](C)(C)C(C)(C)C)(C(=O)O)C[C@@H]1O	4836.9	Semi standard non polar	33892256
3'-Sialyllactosamine,2TBDMS,isomer #22	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O[Si](C)(C)C(C)(C)C)C[C@@H]1O	4812.0	Semi standard non polar	33892256
3'-Sialyllactosamine,2TBDMS,isomer #23	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)C(N)=CO[Si](C)(C)C(C)(C)C)[C@@H]2O)(C(=O)O)C[C@@H]1O	5009.9	Semi standard non polar	33892256
3'-Sialyllactosamine,2TBDMS,isomer #24	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@H](C=O)N[Si](C)(C)C(C)(C)C)[C@@H]2O)(C(=O)O)C[C@@H]1O	5045.4	Semi standard non polar	33892256
3'-Sialyllactosamine,2TBDMS,isomer #25	CC(=O)N([C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O)[Si](C)(C)C(C)(C)C	4833.0	Semi standard non polar	33892256
3'-Sialyllactosamine,2TBDMS,isomer #26	CC(=O)N[C@H]1C([C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO[Si](C)(C)C(C)(C)C)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O	4857.3	Semi standard non polar	33892256
3'-Sialyllactosamine,2TBDMS,isomer #27	CC(=O)N[C@H]1C([C@H](O)[C@@H](CO)O[Si](C)(C)C(C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO[Si](C)(C)C(C)(C)C)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O	4866.3	Semi standard non polar	33892256
3'-Sialyllactosamine,2TBDMS,isomer #28	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO[Si](C)(C)C(C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO[Si](C)(C)C(C)(C)C)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O	4847.6	Semi standard non polar	33892256
3'-Sialyllactosamine,2TBDMS,isomer #29	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO[Si](C)(C)C(C)(C)C)O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O	4856.7	Semi standard non polar	33892256
3'-Sialyllactosamine,2TBDMS,isomer #3	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO[Si](C)(C)C(C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O[Si](C)(C)C(C)(C)C	4845.8	Semi standard non polar	33892256
3'-Sialyllactosamine,2TBDMS,isomer #30	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO[Si](C)(C)C(C)(C)C)O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O	4855.7	Semi standard non polar	33892256
3'-Sialyllactosamine,2TBDMS,isomer #31	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO[Si](C)(C)C(C)(C)C)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O	4870.7	Semi standard non polar	33892256
3'-Sialyllactosamine,2TBDMS,isomer #32	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO[Si](C)(C)C(C)(C)C)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O[Si](C)(C)C(C)(C)C)(C(=O)O)C[C@@H]1O	4844.3	Semi standard non polar	33892256
3'-Sialyllactosamine,2TBDMS,isomer #33	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO[Si](C)(C)C(C)(C)C)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O[Si](C)(C)C(C)(C)C)C[C@@H]1O	4825.5	Semi standard non polar	33892256
3'-Sialyllactosamine,2TBDMS,isomer #34	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO[Si](C)(C)C(C)(C)C)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)C(N)=CO[Si](C)(C)C(C)(C)C)[C@@H]2O)(C(=O)O)C[C@@H]1O	5025.0	Semi standard non polar	33892256
3'-Sialyllactosamine,2TBDMS,isomer #35	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO[Si](C)(C)C(C)(C)C)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@H](C=O)N[Si](C)(C)C(C)(C)C)[C@@H]2O)(C(=O)O)C[C@@H]1O	5060.5	Semi standard non polar	33892256
3'-Sialyllactosamine,2TBDMS,isomer #36	CC(=O)N([C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO[Si](C)(C)C(C)(C)C)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O)[Si](C)(C)C(C)(C)C	4844.7	Semi standard non polar	33892256
3'-Sialyllactosamine,2TBDMS,isomer #37	CC(=O)N[C@H]1C([C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O	4870.4	Semi standard non polar	33892256
3'-Sialyllactosamine,2TBDMS,isomer #38	CC(=O)N[C@H]1C([C@H](O)[C@@H](CO)O[Si](C)(C)C(C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O	4880.9	Semi standard non polar	33892256
3'-Sialyllactosamine,2TBDMS,isomer #39	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO[Si](C)(C)C(C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O	4861.2	Semi standard non polar	33892256
3'-Sialyllactosamine,2TBDMS,isomer #4	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O[Si](C)(C)C(C)(C)C	4824.5	Semi standard non polar	33892256
3'-Sialyllactosamine,2TBDMS,isomer #40	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@@H](CO[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O	4857.8	Semi standard non polar	33892256
3'-Sialyllactosamine,2TBDMS,isomer #41	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O	4890.6	Semi standard non polar	33892256
3'-Sialyllactosamine,2TBDMS,isomer #42	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](N)C=O)[C@@H]2O[Si](C)(C)C(C)(C)C)(C(=O)O)C[C@@H]1O	4860.0	Semi standard non polar	33892256
3'-Sialyllactosamine,2TBDMS,isomer #43	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O[Si](C)(C)C(C)(C)C)C[C@@H]1O	4844.3	Semi standard non polar	33892256
3'-Sialyllactosamine,2TBDMS,isomer #44	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C(C)(C)C)[C@H](O)C(N)=CO[Si](C)(C)C(C)(C)C)[C@@H]2O)(C(=O)O)C[C@@H]1O	5042.4	Semi standard non polar	33892256
3'-Sialyllactosamine,2TBDMS,isomer #45	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H](C=O)N[Si](C)(C)C(C)(C)C)[C@@H]2O)(C(=O)O)C[C@@H]1O	5055.6	Semi standard non polar	33892256
3'-Sialyllactosamine,2TBDMS,isomer #46	CC(=O)N([C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O)[Si](C)(C)C(C)(C)C	4863.2	Semi standard non polar	33892256
3'-Sialyllactosamine,2TBDMS,isomer #47	CC(=O)N[C@H]1C([C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O	4872.7	Semi standard non polar	33892256
3'-Sialyllactosamine,2TBDMS,isomer #48	CC(=O)N[C@H]1C([C@H](O)[C@@H](CO)O[Si](C)(C)C(C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O	4882.6	Semi standard non polar	33892256
3'-Sialyllactosamine,2TBDMS,isomer #49	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO[Si](C)(C)C(C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O	4860.3	Semi standard non polar	33892256
3'-Sialyllactosamine,2TBDMS,isomer #5	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO[Si](C)(C)C(C)(C)C)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O[Si](C)(C)C(C)(C)C	4829.8	Semi standard non polar	33892256
3'-Sialyllactosamine,2TBDMS,isomer #50	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O	4886.4	Semi standard non polar	33892256
3'-Sialyllactosamine,2TBDMS,isomer #51	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](N)C=O)[C@@H]2O[Si](C)(C)C(C)(C)C)(C(=O)O)C[C@@H]1O	4856.2	Semi standard non polar	33892256
3'-Sialyllactosamine,2TBDMS,isomer #52	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O[Si](C)(C)C(C)(C)C)C[C@@H]1O	4847.3	Semi standard non polar	33892256
3'-Sialyllactosamine,2TBDMS,isomer #53	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C(C)(C)C)[C@H](O)C(N)=CO[Si](C)(C)C(C)(C)C)[C@@H]2O)(C(=O)O)C[C@@H]1O	5042.7	Semi standard non polar	33892256
3'-Sialyllactosamine,2TBDMS,isomer #54	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C(C)(C)C)[C@H](O)[C@H](C=O)N[Si](C)(C)C(C)(C)C)[C@@H]2O)(C(=O)O)C[C@@H]1O	5056.3	Semi standard non polar	33892256
3'-Sialyllactosamine,2TBDMS,isomer #55	CC(=O)N([C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O)[Si](C)(C)C(C)(C)C	4865.6	Semi standard non polar	33892256
3'-Sialyllactosamine,2TBDMS,isomer #56	CC(=O)N[C@H]1C([C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O	4892.0	Semi standard non polar	33892256
3'-Sialyllactosamine,2TBDMS,isomer #57	CC(=O)N[C@H]1C([C@H](O)[C@@H](CO)O[Si](C)(C)C(C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O	4902.1	Semi standard non polar	33892256
3'-Sialyllactosamine,2TBDMS,isomer #58	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO[Si](C)(C)C(C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O	4881.2	Semi standard non polar	33892256
3'-Sialyllactosamine,2TBDMS,isomer #59	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](N)C=O)[C@@H]2O[Si](C)(C)C(C)(C)C)(C(=O)O)C[C@@H]1O	4879.0	Semi standard non polar	33892256
3'-Sialyllactosamine,2TBDMS,isomer #6	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O[Si](C)(C)C(C)(C)C	4849.8	Semi standard non polar	33892256
3'-Sialyllactosamine,2TBDMS,isomer #60	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](N)C=O)[C@@H]2O)(C(=O)O[Si](C)(C)C(C)(C)C)C[C@@H]1O	4870.9	Semi standard non polar	33892256
3'-Sialyllactosamine,2TBDMS,isomer #61	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O[Si](C)(C)C(C)(C)C)C(N)=CO[Si](C)(C)C(C)(C)C)[C@@H]2O)(C(=O)O)C[C@@H]1O	5047.3	Semi standard non polar	33892256
3'-Sialyllactosamine,2TBDMS,isomer #62	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](C=O)N[Si](C)(C)C(C)(C)C)[C@@H]2O)(C(=O)O)C[C@@H]1O	5064.0	Semi standard non polar	33892256
3'-Sialyllactosamine,2TBDMS,isomer #63	CC(=O)N([C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O)[Si](C)(C)C(C)(C)C	4887.4	Semi standard non polar	33892256
3'-Sialyllactosamine,2TBDMS,isomer #64	CC(=O)N[C@H]1C([C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O[Si](C)(C)C(C)(C)C)(C(=O)O)C[C@@H]1O	4858.5	Semi standard non polar	33892256
3'-Sialyllactosamine,2TBDMS,isomer #65	CC(=O)N[C@H]1C([C@H](O)[C@@H](CO)O[Si](C)(C)C(C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O[Si](C)(C)C(C)(C)C)(C(=O)O)C[C@@H]1O	4868.4	Semi standard non polar	33892256
3'-Sialyllactosamine,2TBDMS,isomer #66	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO[Si](C)(C)C(C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O[Si](C)(C)C(C)(C)C)(C(=O)O)C[C@@H]1O	4847.1	Semi standard non polar	33892256
3'-Sialyllactosamine,2TBDMS,isomer #67	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O[Si](C)(C)C(C)(C)C)(C(=O)O[Si](C)(C)C(C)(C)C)C[C@@H]1O	4824.7	Semi standard non polar	33892256
3'-Sialyllactosamine,2TBDMS,isomer #68	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)C(N)=CO[Si](C)(C)C(C)(C)C)[C@@H]2O[Si](C)(C)C(C)(C)C)(C(=O)O)C[C@@H]1O	5030.1	Semi standard non polar	33892256
3'-Sialyllactosamine,2TBDMS,isomer #69	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@H](C=O)N[Si](C)(C)C(C)(C)C)[C@@H]2O[Si](C)(C)C(C)(C)C)(C(=O)O)C[C@@H]1O	5066.0	Semi standard non polar	33892256
3'-Sialyllactosamine,2TBDMS,isomer #7	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O[Si](C)(C)C(C)(C)C	4850.9	Semi standard non polar	33892256
3'-Sialyllactosamine,2TBDMS,isomer #70	CC(=O)N([C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O[Si](C)(C)C(C)(C)C)(C(=O)O)C[C@@H]1O)[Si](C)(C)C(C)(C)C	4850.6	Semi standard non polar	33892256
3'-Sialyllactosamine,2TBDMS,isomer #71	CC(=O)N[C@H]1C([C@H](O[Si](C)(C)C(C)(C)C)[C@@H](CO)O[Si](C)(C)C(C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O	4881.0	Semi standard non polar	33892256
3'-Sialyllactosamine,2TBDMS,isomer #72	CC(=O)N[C@H]1C([C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)CO[Si](C)(C)C(C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O	4869.0	Semi standard non polar	33892256
3'-Sialyllactosamine,2TBDMS,isomer #73	CC(=O)N[C@H]1C([C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O[Si](C)(C)C(C)(C)C)C[C@@H]1O	4850.8	Semi standard non polar	33892256
3'-Sialyllactosamine,2TBDMS,isomer #74	CC(=O)N[C@H]1C([C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)C(N)=CO[Si](C)(C)C(C)(C)C)[C@@H]2O)(C(=O)O)C[C@@H]1O	5030.8	Semi standard non polar	33892256
3'-Sialyllactosamine,2TBDMS,isomer #75	CC(=O)N[C@H]1C([C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@H](C=O)N[Si](C)(C)C(C)(C)C)[C@@H]2O)(C(=O)O)C[C@@H]1O	5070.3	Semi standard non polar	33892256
3'-Sialyllactosamine,2TBDMS,isomer #76	CC(=O)N([C@H]1C([C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O)[Si](C)(C)C(C)(C)C	4864.2	Semi standard non polar	33892256
3'-Sialyllactosamine,2TBDMS,isomer #77	CC(=O)N[C@H]1C([C@H](O)[C@@H](CO[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O	4855.0	Semi standard non polar	33892256
3'-Sialyllactosamine,2TBDMS,isomer #78	CC(=O)N[C@H]1C([C@H](O)[C@@H](CO)O[Si](C)(C)C(C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O[Si](C)(C)C(C)(C)C)C[C@@H]1O	4863.9	Semi standard non polar	33892256
3'-Sialyllactosamine,2TBDMS,isomer #79	CC(=O)N[C@H]1C([C@H](O)[C@@H](CO)O[Si](C)(C)C(C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)C(N)=CO[Si](C)(C)C(C)(C)C)[C@@H]2O)(C(=O)O)C[C@@H]1O	5046.3	Semi standard non polar	33892256
3'-Sialyllactosamine,2TBDMS,isomer #8	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O[Si](C)(C)C(C)(C)C	4874.3	Semi standard non polar	33892256
3'-Sialyllactosamine,2TBDMS,isomer #80	CC(=O)N[C@H]1C([C@H](O)[C@@H](CO)O[Si](C)(C)C(C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@H](C=O)N[Si](C)(C)C(C)(C)C)[C@@H]2O)(C(=O)O)C[C@@H]1O	5073.8	Semi standard non polar	33892256
3'-Sialyllactosamine,2TBDMS,isomer #81	CC(=O)N([C@H]1C([C@H](O)[C@@H](CO)O[Si](C)(C)C(C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O)[Si](C)(C)C(C)(C)C	4874.0	Semi standard non polar	33892256
3'-Sialyllactosamine,2TBDMS,isomer #82	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO[Si](C)(C)C(C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O[Si](C)(C)C(C)(C)C)C[C@@H]1O	4842.0	Semi standard non polar	33892256
3'-Sialyllactosamine,2TBDMS,isomer #83	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO[Si](C)(C)C(C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)C(N)=CO[Si](C)(C)C(C)(C)C)[C@@H]2O)(C(=O)O)C[C@@H]1O	5035.5	Semi standard non polar	33892256
3'-Sialyllactosamine,2TBDMS,isomer #84	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO[Si](C)(C)C(C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@H](C=O)N[Si](C)(C)C(C)(C)C)[C@@H]2O)(C(=O)O)C[C@@H]1O	5065.3	Semi standard non polar	33892256
3'-Sialyllactosamine,2TBDMS,isomer #85	CC(=O)N([C@H]1C([C@H](O)[C@H](O)CO[Si](C)(C)C(C)(C)C)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O)C[C@@H]1O)[Si](C)(C)C(C)(C)C	4865.7	Semi standard non polar	33892256
3'-Sialyllactosamine,2TBDMS,isomer #86	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)C(N)=CO[Si](C)(C)C(C)(C)C)[C@@H]2O)(C(=O)O[Si](C)(C)C(C)(C)C)C[C@@H]1O	5007.9	Semi standard non polar	33892256
3'-Sialyllactosamine,2TBDMS,isomer #87	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@H](C=O)N[Si](C)(C)C(C)(C)C)[C@@H]2O)(C(=O)O[Si](C)(C)C(C)(C)C)C[C@@H]1O	5036.9	Semi standard non polar	33892256
3'-Sialyllactosamine,2TBDMS,isomer #88	CC(=O)N([C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O)(C(=O)O[Si](C)(C)C(C)(C)C)C[C@@H]1O)[Si](C)(C)C(C)(C)C	4840.9	Semi standard non polar	33892256
3'-Sialyllactosamine,2TBDMS,isomer #89	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)C(=CO[Si](C)(C)C(C)(C)C)N[Si](C)(C)C(C)(C)C)[C@@H]2O)(C(=O)O)C[C@@H]1O	5237.0	Semi standard non polar	33892256
3'-Sialyllactosamine,2TBDMS,isomer #9	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@@H]2O[Si](C)(C)C(C)(C)C)(C(=O)O)C[C@@H]1O[Si](C)(C)C(C)(C)C	4834.8	Semi standard non polar	33892256
3'-Sialyllactosamine,2TBDMS,isomer #90	CC(=O)N([C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)C(N)=CO[Si](C)(C)C(C)(C)C)[C@@H]2O)(C(=O)O)C[C@@H]1O)[Si](C)(C)C(C)(C)C	5030.6	Semi standard non polar	33892256
3'-Sialyllactosamine,2TBDMS,isomer #91	CC(=O)N([C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@H](C=O)N[Si](C)(C)C(C)(C)C)[C@@H]2O)(C(=O)O)C[C@@H]1O)[Si](C)(C)C(C)(C)C	5069.5	Semi standard non polar	33892256
3'-Sialyllactosamine,2TBDMS,isomer #92	CC(=O)N[C@H]1C([C@H](O)[C@H](O)CO)O[C@@](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@H](C=O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[C@@H]2O)(C(=O)O)C[C@@H]1O	5189.0	Semi standard non polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - 3'-Sialyllactosamine GC-MS (Non-derivatized) - 70eV, Positive	splash10-044i-9110124000-46430d365f649b5f1e39	2017-09-01	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 3'-Sialyllactosamine GC-MS (TMS_1_1) - 70eV, Positive	Not Available	2021-10-17	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 3'-Sialyllactosamine GC-MS (TMS_1_2) - 70eV, Positive	Not Available	2021-10-17	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 3'-Sialyllactosamine GC-MS (TMS_1_3) - 70eV, Positive	Not Available	2021-10-17	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 3'-Sialyllactosamine GC-MS (TMS_1_4) - 70eV, Positive	Not Available	2021-10-17	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 3'-Sialyllactosamine GC-MS (TMS_1_5) - 70eV, Positive	Not Available	2021-10-17	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 3'-Sialyllactosamine GC-MS (TMS_1_6) - 70eV, Positive	Not Available	2021-10-17	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 3'-Sialyllactosamine GC-MS (TMS_1_7) - 70eV, Positive	Not Available	2021-10-17	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 3'-Sialyllactosamine GC-MS (TMS_1_8) - 70eV, Positive	Not Available	2021-10-17	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 3'-Sialyllactosamine GC-MS (TMS_1_9) - 70eV, Positive	Not Available	2021-10-17	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 3'-Sialyllactosamine GC-MS (TMS_1_10) - 70eV, Positive	Not Available	2021-10-17	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 3'-Sialyllactosamine GC-MS (TMS_1_11) - 70eV, Positive	Not Available	2021-10-17	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 3'-Sialyllactosamine GC-MS (TMS_1_12) - 70eV, Positive	Not Available	2021-10-17	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 3'-Sialyllactosamine GC-MS (TMS_1_13) - 70eV, Positive	Not Available	2021-10-17	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 3'-Sialyllactosamine GC-MS (TMS_1_14) - 70eV, Positive	Not Available	2021-10-17	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 3'-Sialyllactosamine GC-MS (TMS_2_1) - 70eV, Positive	Not Available	2021-10-17	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 3'-Sialyllactosamine GC-MS (TMS_2_2) - 70eV, Positive	Not Available	2021-10-17	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 3'-Sialyllactosamine GC-MS (TMS_2_3) - 70eV, Positive	Not Available	2021-10-17	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 3'-Sialyllactosamine GC-MS (TMS_2_4) - 70eV, Positive	Not Available	2021-10-17	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 3'-Sialyllactosamine GC-MS (TMS_2_5) - 70eV, Positive	Not Available	2021-10-17	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 3'-Sialyllactosamine GC-MS (TMS_2_6) - 70eV, Positive	Not Available	2021-10-17	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 3'-Sialyllactosamine GC-MS (TMS_2_7) - 70eV, Positive	Not Available	2021-10-17	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 3'-Sialyllactosamine GC-MS (TMS_2_8) - 70eV, Positive	Not Available	2021-10-17	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 3'-Sialyllactosamine GC-MS (TMS_2_9) - 70eV, Positive	Not Available	2021-10-17	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 3'-Sialyllactosamine GC-MS (TMS_2_10) - 70eV, Positive	Not Available	2021-10-17	Wishart Lab	View Spectrum

MS/MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 3'-Sialyllactosamine 10V, Positive-QTOF	splash10-02ha-1905068000-caeb7fb6634d6ab6fcd2	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 3'-Sialyllactosamine 20V, Positive-QTOF	splash10-075c-6609000000-146e3f2ef2d2e9aa1377	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 3'-Sialyllactosamine 40V, Positive-QTOF	splash10-03e9-9833000000-35c80a42471644c73f1e	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 3'-Sialyllactosamine 10V, Negative-QTOF	splash10-0h90-3910044000-8fc434a39a6ef1a08ae9	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 3'-Sialyllactosamine 20V, Negative-QTOF	splash10-0a73-8945010000-4f25fde98e0c37528451	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 3'-Sialyllactosamine 40V, Negative-QTOF	splash10-0a4i-9854000000-e406e044ac63b4da2ec7	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 3'-Sialyllactosamine 10V, Positive-QTOF	splash10-0fss-0500957000-7e0e4e1bc2c96cb7c918	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 3'-Sialyllactosamine 20V, Positive-QTOF	splash10-03el-8722392000-305b5bda4ed294df7dfb	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 3'-Sialyllactosamine 40V, Positive-QTOF	splash10-006x-9501300000-52e1a41de644356ab849	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 3'-Sialyllactosamine 10V, Negative-QTOF	splash10-0540-9000121000-9364dd99242c8e08a40c	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 3'-Sialyllactosamine 20V, Negative-QTOF	splash10-06r6-6000192000-b1046263cfeeb4fb790b	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 3'-Sialyllactosamine 40V, Negative-QTOF	splash10-0a4l-9100000000-3405e788c7e2ecec7aa5	2021-09-22	Wishart Lab	View Spectrum

NMR Spectra

Spectrum Type	Description	Deposition Date	Source	View
Predicted 1D NMR	¹³C NMR Spectrum (1D, 100 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 200 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 300 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 400 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 500 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 600 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 700 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 800 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 900 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum

Biological Properties

Cellular Locations

Not Available

Biospecimen Locations

Not Available

Tissue Locations

Not Available

Pathways

Not Available

Name	SMPDB/PathBank	KEGG

Normal Concentrations

Not Available

Abnormal Concentrations

Not Available

Associated Disorders and Diseases

Disease References

None

Associated OMIM IDs

None

External Links

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

FDB024000

KNApSAcK ID

Not Available

Chemspider ID

35016013

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

53477870

PDB ID

Not Available

ChEBI ID

168850

Food Biomarker Ontology

Not Available

VMH ID

Not Available

MarkerDB ID

Not Available

Good Scents ID

Not Available

References

Synthesis Reference

Not Available

Material Safety Data Sheet (MSDS)

Not Available

General References

Shen Z, Warren CD, Newburg DS: High-performance capillary electrophoresis of sialylated oligosaccharides of human milk. Anal Biochem. 2000 Mar 1;279(1):37-45. [PubMed:10683228 ]
Teneberg S, Jurstrand M, Karlsson KA, Danielsson D: Inhibition of nonopsonic Helicobacter pylori-induced activation of human neutrophils by sialylated oligosaccharides. Glycobiology. 2000 Nov;10(11):1171-81. [PubMed:11087709 ]

Showing metabocard for 3'-Sialyllactosamine (HMDB0006607)

MOL for HMDB0006607 (3'-Sialyllactosamine)

3D MOL for HMDB0006607 (3'-Sialyllactosamine)

3D SDF for HMDB0006607 (3'-Sialyllactosamine)

3D-SDF for HMDB0006607 (3'-Sialyllactosamine)

PDB for HMDB0006607 (3'-Sialyllactosamine)

3D PDB for HMDB0006607 (3'-Sialyllactosamine)

SMILES for HMDB0006607 (3'-Sialyllactosamine)

INCHI for HMDB0006607 (3'-Sialyllactosamine)

Structure for HMDB0006607 (3'-Sialyllactosamine)

3D Structure for HMDB0006607 (3'-Sialyllactosamine)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra

NMR Spectra