Hmdb loader

Showing metabocard for 3'-Sialyllactosamine (HMDB0006607)

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Record Information
Version5.0
StatusExpected but not Quantified
Creation Date2007-05-25 09:44:33 UTC
Update Date2021-09-14 15:46:06 UTC
HMDB IDHMDB0006607
Secondary Accession Numbers
  • HMDB06607
Metabolite Identification
Common Name3'-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
Data?1582752396
MOL3D MOLSDF3D SDFPDB3D PDBSMILESInChI

MOL for HMDB0006607 (3'-Sialyllactosamine)


  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
Download

3D MOL for HMDB0006607 (3'-Sialyllactosamine)

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
Download

3D SDF for HMDB0006607 (3'-Sialyllactosamine)


  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

$$$$
Download

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

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
Download

PDB for HMDB0006607 (3'-Sialyllactosamine)

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
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3D PDB for HMDB0006607 (3'-Sialyllactosamine)

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
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SMILES for HMDB0006607 (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
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INCHI for HMDB0006607 (3'-Sialyllactosamine)

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
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View in JSmolView NMR AssignmentsView Stereo Labels
Synonyms
ValueSource
3'-SLNHMDB
3-SialyllactosamineHMDB
O-(N-Acetyl-alpha-neuraminosyl)-(2->3)-O-beta-D-galactopyranosyl-(1->4)-2-amino-2-deoxy- D-glucoseHMDB
O-(N-Acetyl-alpha-neuraminosyl)-(2->3)-O-beta-delta-galactopyranosyl-(1->4)-2-amino-2-deoxy- D-glucoseHMDB
(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-carboxylateGenerator, HMDB
Chemical FormulaC23H40N2O18
Average Molecular Weight632.5663
Monoisotopic Molecular Weight632.227612486
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(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
CAS Registry Number126151-66-4
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 KeyMKNNYTWMAUAKMA-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.
KingdomOrganic compounds
Super ClassOrganic oxygen compounds
ClassOrganooxygen compounds
Sub ClassCarbohydrates and carbohydrate conjugates
Direct ParentN-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 FrameworkAliphatic heteromonocyclic compounds
External DescriptorsNot Available
Ontology
Not AvailableNot Available
Physical Properties
StateSolid
Experimental Molecular Properties
PropertyValueReference
Melting PointNot AvailableNot Available
Boiling PointNot AvailableNot Available
Water SolubilityNot AvailableNot Available
LogPNot AvailableNot Available
Experimental Chromatographic PropertiesNot Available
Predicted Molecular Properties
PropertyValueSource
Water Solubility79.6 g/LALOGPS
logP-3ALOGPS
logP-10ChemAxon
logS-0.9ALOGPS
pKa (Strongest Acidic)2.54ChemAxon
pKa (Strongest Basic)7.16ChemAxon
Physiological Charge0ChemAxon
Hydrogen Acceptor Count19ChemAxon
Hydrogen Donor Count13ChemAxon
Polar Surface Area348.71 ŲChemAxon
Rotatable Bond Count15ChemAxon
Refractivity131.69 m³·mol⁻¹ChemAxon
Polarizability58.98 ųChemAxon
Number of Rings2ChemAxon
BioavailabilityNoChemAxon
Rule of FiveNoChemAxon
Ghose FilterNoChemAxon
Veber's RuleNoChemAxon
MDDR-like RuleNoChemAxon
Predicted Chromatographic Properties

Predicted Collision Cross Sections

PredictorAdduct TypeCCS Value (Å2)Reference
DeepCCS[M+H]+235.16530932474
DeepCCS[M-H]-233.3630932474
DeepCCS[M-2H]-267.39430932474
DeepCCS[M+Na]+241.41330932474
AllCCS[M+H]+233.232859911
AllCCS[M+H-H2O]+232.432859911
AllCCS[M+NH4]+234.032859911
AllCCS[M+Na]+234.232859911
AllCCS[M-H]-230.332859911
AllCCS[M+Na-2H]-231.532859911
AllCCS[M+HCOO]-233.032859911

Predicted Kovats Retention Indices

Underivatized

MetaboliteSMILESKovats RI ValueColumn TypeReference
3'-SialyllactosamineCC(=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)=O3712.6Standard polar33892256
3'-SialyllactosamineCC(=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)=O4592.5Standard non polar33892256
3'-SialyllactosamineCC(=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)=O5042.7Semi standard non polar33892256

Derivatized

Derivative Name / StructureSMILESKovats RI ValueColumn TypeReference
3'-Sialyllactosamine,1TMS,isomer #1CC(=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)C4645.6Semi standard non polar33892256
3'-Sialyllactosamine,1TMS,isomer #10CC(=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]1O4641.4Semi standard non polar33892256
3'-Sialyllactosamine,1TMS,isomer #11CC(=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]1O4588.7Semi standard non polar33892256
3'-Sialyllactosamine,1TMS,isomer #12CC(=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]1O4804.8Semi standard non polar33892256
3'-Sialyllactosamine,1TMS,isomer #13CC(=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]1O4872.6Semi standard non polar33892256
3'-Sialyllactosamine,1TMS,isomer #14CC(=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)C4666.0Semi standard non polar33892256
3'-Sialyllactosamine,1TMS,isomer #2CC(=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]1O4637.2Semi standard non polar33892256
3'-Sialyllactosamine,1TMS,isomer #3CC(=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]1O4638.8Semi standard non polar33892256
3'-Sialyllactosamine,1TMS,isomer #4CC(=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]1O4658.3Semi standard non polar33892256
3'-Sialyllactosamine,1TMS,isomer #5CC(=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]1O4650.1Semi standard non polar33892256
3'-Sialyllactosamine,1TMS,isomer #6CC(=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]1O4674.3Semi standard non polar33892256
3'-Sialyllactosamine,1TMS,isomer #7CC(=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]1O4658.4Semi standard non polar33892256
3'-Sialyllactosamine,1TMS,isomer #8CC(=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]1O4676.5Semi standard non polar33892256
3'-Sialyllactosamine,1TMS,isomer #9CC(=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]1O4648.8Semi standard non polar33892256
3'-Sialyllactosamine,2TMS,isomer #1CC(=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)C4528.6Semi standard non polar33892256
3'-Sialyllactosamine,2TMS,isomer #10CC(=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)C4475.1Semi standard non polar33892256
3'-Sialyllactosamine,2TMS,isomer #11CC(=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)C4676.0Semi standard non polar33892256
3'-Sialyllactosamine,2TMS,isomer #12CC(=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)C4741.6Semi standard non polar33892256
3'-Sialyllactosamine,2TMS,isomer #13CC(=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)C4550.2Semi standard non polar33892256
3'-Sialyllactosamine,2TMS,isomer #14CC(=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]1O4514.4Semi standard non polar33892256
3'-Sialyllactosamine,2TMS,isomer #15CC(=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]1O4495.0Semi standard non polar33892256
3'-Sialyllactosamine,2TMS,isomer #16CC(=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]1O4473.8Semi standard non polar33892256
3'-Sialyllactosamine,2TMS,isomer #17CC(=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]1O4501.1Semi standard non polar33892256
3'-Sialyllactosamine,2TMS,isomer #18CC(=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]1O4507.5Semi standard non polar33892256
3'-Sialyllactosamine,2TMS,isomer #19CC(=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]1O4500.4Semi standard non polar33892256
3'-Sialyllactosamine,2TMS,isomer #2CC(=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)C4507.1Semi standard non polar33892256
3'-Sialyllactosamine,2TMS,isomer #20CC(=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]1O4518.1Semi standard non polar33892256
3'-Sialyllactosamine,2TMS,isomer #21CC(=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]1O4510.7Semi standard non polar33892256
3'-Sialyllactosamine,2TMS,isomer #22CC(=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]1O4438.2Semi standard non polar33892256
3'-Sialyllactosamine,2TMS,isomer #23CC(=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]1O4654.3Semi standard non polar33892256
3'-Sialyllactosamine,2TMS,isomer #24CC(=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]1O4730.9Semi standard non polar33892256
3'-Sialyllactosamine,2TMS,isomer #25CC(=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)C4506.9Semi standard non polar33892256
3'-Sialyllactosamine,2TMS,isomer #26CC(=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]1O4511.0Semi standard non polar33892256
3'-Sialyllactosamine,2TMS,isomer #27CC(=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]1O4492.2Semi standard non polar33892256
3'-Sialyllactosamine,2TMS,isomer #28CC(=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]1O4474.4Semi standard non polar33892256
3'-Sialyllactosamine,2TMS,isomer #29CC(=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]1O4506.5Semi standard non polar33892256
3'-Sialyllactosamine,2TMS,isomer #3CC(=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)C4486.3Semi standard non polar33892256
3'-Sialyllactosamine,2TMS,isomer #30CC(=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]1O4499.2Semi standard non polar33892256
3'-Sialyllactosamine,2TMS,isomer #31CC(=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]1O4511.7Semi standard non polar33892256
3'-Sialyllactosamine,2TMS,isomer #32CC(=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]1O4504.2Semi standard non polar33892256
3'-Sialyllactosamine,2TMS,isomer #33CC(=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]1O4435.6Semi standard non polar33892256
3'-Sialyllactosamine,2TMS,isomer #34CC(=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]1O4666.7Semi standard non polar33892256
3'-Sialyllactosamine,2TMS,isomer #35CC(=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]1O4739.6Semi standard non polar33892256
3'-Sialyllactosamine,2TMS,isomer #36CC(=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)C4518.8Semi standard non polar33892256
3'-Sialyllactosamine,2TMS,isomer #37CC(=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]1O4533.4Semi standard non polar33892256
3'-Sialyllactosamine,2TMS,isomer #38CC(=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]1O4510.8Semi standard non polar33892256
3'-Sialyllactosamine,2TMS,isomer #39CC(=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]1O4492.5Semi standard non polar33892256
3'-Sialyllactosamine,2TMS,isomer #4CC(=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)C4493.3Semi standard non polar33892256
3'-Sialyllactosamine,2TMS,isomer #40CC(=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]1O4525.6Semi standard non polar33892256
3'-Sialyllactosamine,2TMS,isomer #41CC(=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]1O4539.3Semi standard non polar33892256
3'-Sialyllactosamine,2TMS,isomer #42CC(=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]1O4529.1Semi standard non polar33892256
3'-Sialyllactosamine,2TMS,isomer #43CC(=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]1O4473.5Semi standard non polar33892256
3'-Sialyllactosamine,2TMS,isomer #44CC(=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]1O4685.0Semi standard non polar33892256
3'-Sialyllactosamine,2TMS,isomer #45CC(=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]1O4748.0Semi standard non polar33892256
3'-Sialyllactosamine,2TMS,isomer #46CC(=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)C4525.5Semi standard non polar33892256
3'-Sialyllactosamine,2TMS,isomer #47CC(=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]1O4527.2Semi standard non polar33892256
3'-Sialyllactosamine,2TMS,isomer #48CC(=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]1O4506.9Semi standard non polar33892256
3'-Sialyllactosamine,2TMS,isomer #49CC(=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]1O4487.6Semi standard non polar33892256
3'-Sialyllactosamine,2TMS,isomer #5CC(=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)C4486.7Semi standard non polar33892256
3'-Sialyllactosamine,2TMS,isomer #50CC(=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]1O4526.9Semi standard non polar33892256
3'-Sialyllactosamine,2TMS,isomer #51CC(=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]1O4517.0Semi standard non polar33892256
3'-Sialyllactosamine,2TMS,isomer #52CC(=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]1O4461.0Semi standard non polar33892256
3'-Sialyllactosamine,2TMS,isomer #53CC(=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]1O4681.4Semi standard non polar33892256
3'-Sialyllactosamine,2TMS,isomer #54CC(=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]1O4737.6Semi standard non polar33892256
3'-Sialyllactosamine,2TMS,isomer #55CC(=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)C4522.1Semi standard non polar33892256
3'-Sialyllactosamine,2TMS,isomer #56CC(=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]1O4552.8Semi standard non polar33892256
3'-Sialyllactosamine,2TMS,isomer #57CC(=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]1O4525.0Semi standard non polar33892256
3'-Sialyllactosamine,2TMS,isomer #58CC(=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]1O4508.3Semi standard non polar33892256
3'-Sialyllactosamine,2TMS,isomer #59CC(=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]1O4538.9Semi standard non polar33892256
3'-Sialyllactosamine,2TMS,isomer #6CC(=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)C4512.4Semi standard non polar33892256
3'-Sialyllactosamine,2TMS,isomer #60CC(=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]1O4493.3Semi standard non polar33892256
3'-Sialyllactosamine,2TMS,isomer #61CC(=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]1O4680.4Semi standard non polar33892256
3'-Sialyllactosamine,2TMS,isomer #62CC(=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]1O4738.4Semi standard non polar33892256
3'-Sialyllactosamine,2TMS,isomer #63CC(=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)C4542.6Semi standard non polar33892256
3'-Sialyllactosamine,2TMS,isomer #64CC(=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]1O4538.8Semi standard non polar33892256
3'-Sialyllactosamine,2TMS,isomer #65CC(=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]1O4511.8Semi standard non polar33892256
3'-Sialyllactosamine,2TMS,isomer #66CC(=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]1O4490.4Semi standard non polar33892256
3'-Sialyllactosamine,2TMS,isomer #67CC(=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]1O4452.8Semi standard non polar33892256
3'-Sialyllactosamine,2TMS,isomer #68CC(=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]1O4668.3Semi standard non polar33892256
3'-Sialyllactosamine,2TMS,isomer #69CC(=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]1O4752.8Semi standard non polar33892256
3'-Sialyllactosamine,2TMS,isomer #7CC(=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)C4505.8Semi standard non polar33892256
3'-Sialyllactosamine,2TMS,isomer #70CC(=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)C4524.5Semi standard non polar33892256
3'-Sialyllactosamine,2TMS,isomer #71CC(=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]1O4545.9Semi standard non polar33892256
3'-Sialyllactosamine,2TMS,isomer #72CC(=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]1O4520.2Semi standard non polar33892256
3'-Sialyllactosamine,2TMS,isomer #73CC(=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]1O4486.6Semi standard non polar33892256
3'-Sialyllactosamine,2TMS,isomer #74CC(=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]1O4698.7Semi standard non polar33892256
3'-Sialyllactosamine,2TMS,isomer #75CC(=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]1O4763.3Semi standard non polar33892256
3'-Sialyllactosamine,2TMS,isomer #76CC(=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)C4542.1Semi standard non polar33892256
3'-Sialyllactosamine,2TMS,isomer #77CC(=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]1O4501.8Semi standard non polar33892256
3'-Sialyllactosamine,2TMS,isomer #78CC(=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]1O4465.0Semi standard non polar33892256
3'-Sialyllactosamine,2TMS,isomer #79CC(=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]1O4676.0Semi standard non polar33892256
3'-Sialyllactosamine,2TMS,isomer #8CC(=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)C4528.3Semi standard non polar33892256
3'-Sialyllactosamine,2TMS,isomer #80CC(=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]1O4734.7Semi standard non polar33892256
3'-Sialyllactosamine,2TMS,isomer #81CC(=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)C4513.0Semi standard non polar33892256
3'-Sialyllactosamine,2TMS,isomer #82CC(=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]1O4439.5Semi standard non polar33892256
3'-Sialyllactosamine,2TMS,isomer #83CC(=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]1O4669.9Semi standard non polar33892256
3'-Sialyllactosamine,2TMS,isomer #84CC(=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]1O4734.1Semi standard non polar33892256
3'-Sialyllactosamine,2TMS,isomer #85CC(=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)C4509.8Semi standard non polar33892256
3'-Sialyllactosamine,2TMS,isomer #86CC(=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]1O4608.0Semi standard non polar33892256
3'-Sialyllactosamine,2TMS,isomer #87CC(=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]1O4701.3Semi standard non polar33892256
3'-Sialyllactosamine,2TMS,isomer #88CC(=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)C4458.8Semi standard non polar33892256
3'-Sialyllactosamine,2TMS,isomer #89CC(=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]1O4909.7Semi standard non polar33892256
3'-Sialyllactosamine,2TMS,isomer #9CC(=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)C4510.7Semi standard non polar33892256
3'-Sialyllactosamine,2TMS,isomer #90CC(=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)C4692.8Semi standard non polar33892256
3'-Sialyllactosamine,2TMS,isomer #91CC(=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)C4751.7Semi standard non polar33892256
3'-Sialyllactosamine,2TMS,isomer #92CC(=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]1O4897.5Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #1CC(=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)C4437.6Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #10CC(=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)C4576.3Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #100CC(=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)C4402.3Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #101CC(=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]1O4367.3Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #102CC(=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]1O4384.2Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #103CC(=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]1O4381.1Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #104CC(=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]1O4397.2Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #105CC(=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]1O4375.4Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #106CC(=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]1O4337.1Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #107CC(=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]1O4526.4Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #108CC(=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]1O4600.9Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #109CC(=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)C4381.1Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #11CC(=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)C4652.9Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #110CC(=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]1O4407.1Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #111CC(=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]1O4396.2Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #112CC(=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]1O4412.9Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #113CC(=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]1O4403.3Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #114CC(=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]1O4361.4Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #115CC(=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]1O4542.2Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #116CC(=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]1O4621.8Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #117CC(=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)C4402.3Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #118CC(=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]1O4401.0Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #119CC(=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]1O4436.6Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #12CC(=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)C4451.9Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #120CC(=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]1O4421.5Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #121CC(=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]1O4376.3Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #122CC(=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]1O4566.7Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #123CC(=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]1O4624.7Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #124CC(=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)C4408.7Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #125CC(=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]1O4419.6Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #126CC(=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]1O4403.3Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #127CC(=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]1O4367.5Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #128CC(=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]1O4556.3Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #129CC(=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]1O4616.4Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #13CC(=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)C4390.9Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #130CC(=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)C4399.9Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #131CC(=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]1O4434.2Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #132CC(=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]1O4396.2Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #133CC(=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]1O4559.0Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #134CC(=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]1O4614.7Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #135CC(=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)C4424.7Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #136CC(=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]1O4377.0Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #137CC(=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]1O4543.1Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #138CC(=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]1O4646.5Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #139CC(=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)C4409.5Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #14CC(=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)C4392.2Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #140CC(=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]1O4483.1Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #141CC(=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]1O4583.2Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #142CC(=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)C4359.9Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #143CC(=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]1O4769.4Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #144CC(=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)C4542.2Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #145CC(=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)C4623.6Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #146CC(=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]1O4782.5Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #147CC(=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]1O4426.2Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #148CC(=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]1O4401.6Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #149CC(=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]1O4411.7Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #15CC(=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)C4384.5Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #150CC(=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]1O4405.8Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #151CC(=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]1O4423.0Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #152CC(=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]1O4406.9Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #153CC(=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]1O4375.5Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #154CC(=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]1O4560.7Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #155CC(=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]1O4638.0Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #156CC(=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)C4413.1Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #157CC(=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]1O4377.7Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #158CC(=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]1O4405.6Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #159CC(=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]1O4401.6Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #16CC(=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)C4417.6Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #160CC(=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]1O4413.8Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #161CC(=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]1O4393.8Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #162CC(=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]1O4367.8Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #163CC(=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]1O4548.8Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #164CC(=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]1O4613.3Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #165CC(=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)C4402.6Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #166CC(=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]1O4381.6Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #167CC(=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]1O4376.8Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #168CC(=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]1O4387.6Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #169CC(=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]1O4368.0Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #17CC(=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)C4416.1Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #170CC(=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]1O4337.1Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #171CC(=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]1O4527.1Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #172CC(=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]1O4601.2Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #173CC(=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)C4384.1Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #174CC(=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]1O4398.4Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #175CC(=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]1O4426.7Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #176CC(=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]1O4410.1Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #177CC(=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]1O4374.2Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #178CC(=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]1O4568.4Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #179CC(=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]1O4626.4Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #18CC(=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)C4438.0Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #180CC(=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)C4410.1Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #181CC(=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]1O4410.2Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #182CC(=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]1O4395.4Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #183CC(=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]1O4367.3Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #184CC(=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]1O4560.4Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #185CC(=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]1O4620.4Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #186CC(=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)C4402.1Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #187CC(=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]1O4417.0Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #188CC(=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]1O4388.5Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #189CC(=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]1O4555.8Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #19CC(=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)C4407.7Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #190CC(=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]1O4608.2Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #191CC(=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)C4421.2Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #192CC(=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]1O4358.6Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #193CC(=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]1O4545.6Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #194CC(=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]1O4631.1Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #195CC(=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)C4402.3Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #196CC(=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]1O4491.6Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #197CC(=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]1O4585.1Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #198CC(=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)C4362.1Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #199CC(=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]1O4783.2Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #2CC(=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)C4416.8Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #20CC(=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)C4399.6Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #200CC(=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)C4552.6Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #201CC(=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)C4628.8Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #202CC(=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]1O4787.4Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #203CC(=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]1O4461.7Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #204CC(=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]1O4440.6Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #205CC(=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]1O4433.9Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #206CC(=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]1O4463.5Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #207CC(=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]1O4438.9Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #208CC(=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]1O4412.6Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #209CC(=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]1O4596.2Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #21CC(=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)C4570.6Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #210CC(=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]1O4653.2Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #211CC(=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)C4435.1Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #212CC(=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]1O4413.1Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #213CC(=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]1O4425.8Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #214CC(=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]1O4455.7Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #215CC(=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]1O4428.7Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #216CC(=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]1O4403.0Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #217CC(=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]1O4584.0Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #218CC(=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]1O4627.4Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #219CC(=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)C4426.0Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #22CC(=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)C4626.5Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #220CC(=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]1O4398.4Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #221CC(=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]1O4433.6Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #222CC(=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]1O4400.3Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #223CC(=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]1O4373.7Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #224CC(=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]1O4562.8Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #225CC(=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]1O4617.3Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #226CC(=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)C4409.3Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #227CC(=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]1O4454.7Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #228CC(=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]1O4415.6Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #229CC(=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]1O4392.1Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #23CC(=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)C4438.4Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #230CC(=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]1O4580.4Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #231CC(=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]1O4642.6Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #232CC(=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)C4416.1Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #233CC(=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]1O4452.4Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #234CC(=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]1O4428.4Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #235CC(=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]1O4601.4Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #236CC(=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]1O4635.5Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #237CC(=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)C4450.2Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #238CC(=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]1O4396.1Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #239CC(=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]1O4583.9Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #24CC(=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)C4362.0Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #240CC(=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]1O4645.0Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #241CC(=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)C4426.4Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #242CC(=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]1O4531.3Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #243CC(=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]1O4605.1Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #244CC(=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)C4389.1Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #245CC(=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]1O4804.0Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #246CC(=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)C4579.5Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #247CC(=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)C4640.4Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #248CC(=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]1O4790.7Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #249CC(=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]1O4459.8Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #25CC(=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)C4353.8Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #250CC(=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]1O4437.0Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #251CC(=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]1O4450.5Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #252CC(=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]1O4427.0Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #253CC(=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]1O4408.5Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #254CC(=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]1O4588.2Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #255CC(=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]1O4645.3Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #256CC(=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)C4428.2Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #257CC(=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]1O4409.6Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #258CC(=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]1O4442.5Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #259CC(=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]1O4418.2Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #26CC(=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)C4385.2Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #260CC(=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]1O4401.5Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #261CC(=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]1O4578.0Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #262CC(=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]1O4623.7Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #263CC(=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)C4421.4Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #264CC(=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]1O4420.0Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #265CC(=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]1O4389.8Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #266CC(=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]1O4370.8Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #267CC(=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]1O4554.8Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #268CC(=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]1O4612.9Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #269CC(=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)C4404.0Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #27CC(=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)C4385.4Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #270CC(=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]1O4433.8Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #271CC(=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]1O4414.2Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #272CC(=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]1O4589.0Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #273CC(=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]1O4617.2Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #274CC(=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)C4431.9Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #275CC(=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]1O4378.7Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #276CC(=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]1O4567.4Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #277CC(=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]1O4634.2Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #278CC(=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)C4412.0Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #279CC(=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]1O4525.0Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #28CC(=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)C4413.1Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #280CC(=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]1O4595.6Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #281CC(=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)C4380.1Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #282CC(=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]1O4799.0Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #283CC(=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)C4570.7Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #284CC(=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)C4631.1Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #285CC(=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]1O4786.1Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #286CC(=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]1O4473.2Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #287CC(=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]1O4449.6Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #288CC(=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]1O4457.3Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #289CC(=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]1O4431.6Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #29CC(=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)C4374.6Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #290CC(=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]1O4588.3Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #291CC(=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]1O4642.1Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #292CC(=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)C4451.3Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #293CC(=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]1O4429.2Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #294CC(=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]1O4438.6Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #295CC(=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]1O4412.7Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #296CC(=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]1O4579.6Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #297CC(=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]1O4613.7Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #298CC(=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)C4435.5Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #299CC(=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]1O4412.6Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #3CC(=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)C4405.5Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #30CC(=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)C4368.7Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #300CC(=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]1O4391.5Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #301CC(=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]1O4558.6Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #302CC(=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]1O4602.5Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #303CC(=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)C4420.3Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #304CC(=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]1O4412.1Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #305CC(=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]1O4575.5Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #306CC(=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]1O4635.4Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #307CC(=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)C4440.4Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #308CC(=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]1O4525.3Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #309CC(=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]1O4598.6Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #31CC(=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)C4542.4Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #310CC(=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)C4405.4Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #311CC(=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]1O4799.1Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #312CC(=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)C4566.6Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #313CC(=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)C4629.8Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #314CC(=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]1O4791.0Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #315CC(=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]1O4451.5Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #316CC(=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]1O4424.6Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #317CC(=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]1O4395.8Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #318CC(=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]1O4574.4Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #319CC(=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]1O4666.5Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #32CC(=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)C4613.5Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #320CC(=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)C4431.2Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #321CC(=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]1O4394.0Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #322CC(=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]1O4383.0Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #323CC(=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]1O4561.2Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #324CC(=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]1O4634.0Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #325CC(=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)C4413.2Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #326CC(=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]1O4348.4Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #327CC(=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]1O4536.2Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #328CC(=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]1O4617.3Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #329CC(=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)C4392.1Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #33CC(=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)C4417.3Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #330CC(=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]1O4495.4Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #331CC(=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]1O4606.0Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #332CC(=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)C4375.1Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #333CC(=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]1O4791.0Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #334CC(=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)C4558.4Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #335CC(=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)C4641.6Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #336CC(=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]1O4803.0Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #337CC(=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]1O4438.8Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #338CC(=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]1O4426.9Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #339CC(=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]1O4600.2Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #34CC(=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)C4384.7Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #340CC(=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]1O4658.9Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #341CC(=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)C4446.2Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #342CC(=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]1O4407.0Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #343CC(=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]1O4582.4Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #344CC(=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]1O4638.0Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #345CC(=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)C4429.2Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #346CC(=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]1O4531.8Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #347CC(=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]1O4623.9Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #348CC(=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)C4406.3Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #349CC(=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]1O4817.1Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #35CC(=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)C4394.0Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #350CC(=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)C4583.3Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #351CC(=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)C4654.9Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #352CC(=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]1O4815.4Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #353CC(=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]1O4373.8Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #354CC(=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]1O4549.1Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #355CC(=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]1O4619.0Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #356CC(=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)C4404.9Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #357CC(=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]1O4524.4Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #358CC(=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]1O4593.1Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #359CC(=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)C4381.6Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #36CC(=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)C4389.7Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #360CC(=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]1O4784.7Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #361CC(=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)C4562.2Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #362CC(=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)C4625.9Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #363CC(=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]1O4791.2Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #364CC(=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]1O4498.1Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #365CC(=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]1O4581.7Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #366CC(=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)C4362.3Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #367CC(=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]1O4782.4Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #368CC(=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)C4548.2Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #369CC(=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)C4623.1Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #37CC(=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)C4417.3Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #370CC(=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]1O4787.7Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #371CC(=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]1O4727.6Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #372CC(=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)C4500.0Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #373CC(=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)C4590.7Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #374CC(=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]1O4742.0Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #375CC(=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)C4792.6Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #376CC(=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]1O4815.3Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #377CC(=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)C4787.6Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #38CC(=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)C4402.4Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #39CC(=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)C4374.2Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #4CC(=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)C4392.5Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #40CC(=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)C4539.1Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #41CC(=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)C4623.3Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #42CC(=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)C4421.6Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #43CC(=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)C4386.7Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #44CC(=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)C4381.8Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #45CC(=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)C4403.1Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #46CC(=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)C4386.7Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #47CC(=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)C4371.0Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #48CC(=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)C4539.4Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #49CC(=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)C4617.3Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #5CC(=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)C4421.9Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #50CC(=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)C4423.6Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #51CC(=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)C4406.0Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #52CC(=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)C4444.3Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #53CC(=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)C4417.0Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #54CC(=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)C4399.0Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #55CC(=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)C4580.8Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #56CC(=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)C4633.6Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #57CC(=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)C4449.1Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #58CC(=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)C4429.7Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #59CC(=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)C4402.8Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #6CC(=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)C4418.3Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #60CC(=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)C4392.4Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #61CC(=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)C4569.6Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #62CC(=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)C4627.7Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #63CC(=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)C4436.9Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #64CC(=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)C4434.5Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #65CC(=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)C4421.7Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #66CC(=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)C4570.7Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #67CC(=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)C4621.6Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #68CC(=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)C4463.0Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #69CC(=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)C4389.1Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #7CC(=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)C4450.1Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #70CC(=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)C4553.9Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #71CC(=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)C4645.9Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #72CC(=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)C4442.9Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #73CC(=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)C4519.7Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #74CC(=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)C4606.4Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #75CC(=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)C4410.3Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #76CC(=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)C4790.6Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #77CC(=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)C4591.1Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #78CC(=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)C4659.3Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #79CC(=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)C4789.5Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #8CC(=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)C4422.7Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #80CC(=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]1O4434.3Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #81CC(=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]1O4410.4Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #82CC(=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]1O4404.7Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #83CC(=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]1O4419.3Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #84CC(=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]1O4414.3Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #85CC(=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]1O4438.8Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #86CC(=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]1O4424.0Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #87CC(=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]1O4381.6Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #88CC(=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]1O4560.1Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #89CC(=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]1O4645.1Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #9CC(=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)C4412.3Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #90CC(=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)C4414.1Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #91CC(=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]1O4382.4Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #92CC(=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]1O4393.0Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #93CC(=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]1O4410.1Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #94CC(=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]1O4407.4Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #95CC(=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]1O4421.1Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #96CC(=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]1O4406.3Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #97CC(=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]1O4368.6Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #98CC(=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]1O4550.0Semi standard non polar33892256
3'-Sialyllactosamine,3TMS,isomer #99CC(=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]1O4616.0Semi standard non polar33892256
3'-Sialyllactosamine,1TBDMS,isomer #1CC(=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)C4801.7Semi standard non polar33892256
3'-Sialyllactosamine,1TBDMS,isomer #10CC(=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]1O4815.2Semi standard non polar33892256
3'-Sialyllactosamine,1TBDMS,isomer #11CC(=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]1O4797.8Semi standard non polar33892256
3'-Sialyllactosamine,1TBDMS,isomer #12CC(=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]1O4997.5Semi standard non polar33892256
3'-Sialyllactosamine,1TBDMS,isomer #13CC(=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]1O5019.4Semi standard non polar33892256
3'-Sialyllactosamine,1TBDMS,isomer #14CC(=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)C4833.2Semi standard non polar33892256
3'-Sialyllactosamine,1TBDMS,isomer #2CC(=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]1O4790.9Semi standard non polar33892256
3'-Sialyllactosamine,1TBDMS,isomer #3CC(=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]1O4805.5Semi standard non polar33892256
3'-Sialyllactosamine,1TBDMS,isomer #4CC(=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]1O4810.4Semi standard non polar33892256
3'-Sialyllactosamine,1TBDMS,isomer #5CC(=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]1O4813.8Semi standard non polar33892256
3'-Sialyllactosamine,1TBDMS,isomer #6CC(=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]1O4836.8Semi standard non polar33892256
3'-Sialyllactosamine,1TBDMS,isomer #7CC(=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]1O4814.8Semi standard non polar33892256
3'-Sialyllactosamine,1TBDMS,isomer #8CC(=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]1O4818.5Semi standard non polar33892256
3'-Sialyllactosamine,1TBDMS,isomer #9CC(=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]1O4826.2Semi standard non polar33892256
3'-Sialyllactosamine,2TBDMS,isomer #1CC(=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)C4855.4Semi standard non polar33892256
3'-Sialyllactosamine,2TBDMS,isomer #10CC(=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)C4842.0Semi standard non polar33892256
3'-Sialyllactosamine,2TBDMS,isomer #11CC(=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)C5021.7Semi standard non polar33892256
3'-Sialyllactosamine,2TBDMS,isomer #12CC(=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)C5055.5Semi standard non polar33892256
3'-Sialyllactosamine,2TBDMS,isomer #13CC(=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)C4881.9Semi standard non polar33892256
3'-Sialyllactosamine,2TBDMS,isomer #14CC(=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]1O4845.4Semi standard non polar33892256
3'-Sialyllactosamine,2TBDMS,isomer #15CC(=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]1O4857.1Semi standard non polar33892256
3'-Sialyllactosamine,2TBDMS,isomer #16CC(=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]1O4835.0Semi standard non polar33892256
3'-Sialyllactosamine,2TBDMS,isomer #17CC(=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]1O4838.0Semi standard non polar33892256
3'-Sialyllactosamine,2TBDMS,isomer #18CC(=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]1O4843.6Semi standard non polar33892256
3'-Sialyllactosamine,2TBDMS,isomer #19CC(=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]1O4843.0Semi standard non polar33892256
3'-Sialyllactosamine,2TBDMS,isomer #2CC(=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)C4869.5Semi standard non polar33892256
3'-Sialyllactosamine,2TBDMS,isomer #20CC(=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]1O4862.6Semi standard non polar33892256
3'-Sialyllactosamine,2TBDMS,isomer #21CC(=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]1O4836.9Semi standard non polar33892256
3'-Sialyllactosamine,2TBDMS,isomer #22CC(=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]1O4812.0Semi standard non polar33892256
3'-Sialyllactosamine,2TBDMS,isomer #23CC(=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]1O5009.9Semi standard non polar33892256
3'-Sialyllactosamine,2TBDMS,isomer #24CC(=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]1O5045.4Semi standard non polar33892256
3'-Sialyllactosamine,2TBDMS,isomer #25CC(=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)C4833.0Semi standard non polar33892256
3'-Sialyllactosamine,2TBDMS,isomer #26CC(=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]1O4857.3Semi standard non polar33892256
3'-Sialyllactosamine,2TBDMS,isomer #27CC(=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]1O4866.3Semi standard non polar33892256
3'-Sialyllactosamine,2TBDMS,isomer #28CC(=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]1O4847.6Semi standard non polar33892256
3'-Sialyllactosamine,2TBDMS,isomer #29CC(=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]1O4856.7Semi standard non polar33892256
3'-Sialyllactosamine,2TBDMS,isomer #3CC(=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)C4845.8Semi standard non polar33892256
3'-Sialyllactosamine,2TBDMS,isomer #30CC(=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]1O4855.7Semi standard non polar33892256
3'-Sialyllactosamine,2TBDMS,isomer #31CC(=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]1O4870.7Semi standard non polar33892256
3'-Sialyllactosamine,2TBDMS,isomer #32CC(=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]1O4844.3Semi standard non polar33892256
3'-Sialyllactosamine,2TBDMS,isomer #33CC(=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]1O4825.5Semi standard non polar33892256
3'-Sialyllactosamine,2TBDMS,isomer #34CC(=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]1O5025.0Semi standard non polar33892256
3'-Sialyllactosamine,2TBDMS,isomer #35CC(=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]1O5060.5Semi standard non polar33892256
3'-Sialyllactosamine,2TBDMS,isomer #36CC(=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)C4844.7Semi standard non polar33892256
3'-Sialyllactosamine,2TBDMS,isomer #37CC(=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]1O4870.4Semi standard non polar33892256
3'-Sialyllactosamine,2TBDMS,isomer #38CC(=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]1O4880.9Semi standard non polar33892256
3'-Sialyllactosamine,2TBDMS,isomer #39CC(=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]1O4861.2Semi standard non polar33892256
3'-Sialyllactosamine,2TBDMS,isomer #4CC(=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)C4824.5Semi standard non polar33892256
3'-Sialyllactosamine,2TBDMS,isomer #40CC(=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]1O4857.8Semi standard non polar33892256
3'-Sialyllactosamine,2TBDMS,isomer #41CC(=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]1O4890.6Semi standard non polar33892256
3'-Sialyllactosamine,2TBDMS,isomer #42CC(=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]1O4860.0Semi standard non polar33892256
3'-Sialyllactosamine,2TBDMS,isomer #43CC(=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]1O4844.3Semi standard non polar33892256
3'-Sialyllactosamine,2TBDMS,isomer #44CC(=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]1O5042.4Semi standard non polar33892256
3'-Sialyllactosamine,2TBDMS,isomer #45CC(=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]1O5055.6Semi standard non polar33892256
3'-Sialyllactosamine,2TBDMS,isomer #46CC(=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)C4863.2Semi standard non polar33892256
3'-Sialyllactosamine,2TBDMS,isomer #47CC(=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]1O4872.7Semi standard non polar33892256
3'-Sialyllactosamine,2TBDMS,isomer #48CC(=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]1O4882.6Semi standard non polar33892256
3'-Sialyllactosamine,2TBDMS,isomer #49CC(=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]1O4860.3Semi standard non polar33892256
3'-Sialyllactosamine,2TBDMS,isomer #5CC(=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)C4829.8Semi standard non polar33892256
3'-Sialyllactosamine,2TBDMS,isomer #50CC(=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]1O4886.4Semi standard non polar33892256
3'-Sialyllactosamine,2TBDMS,isomer #51CC(=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]1O4856.2Semi standard non polar33892256
3'-Sialyllactosamine,2TBDMS,isomer #52CC(=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]1O4847.3Semi standard non polar33892256
3'-Sialyllactosamine,2TBDMS,isomer #53CC(=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]1O5042.7Semi standard non polar33892256
3'-Sialyllactosamine,2TBDMS,isomer #54CC(=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]1O5056.3Semi standard non polar33892256
3'-Sialyllactosamine,2TBDMS,isomer #55CC(=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)C4865.6Semi standard non polar33892256
3'-Sialyllactosamine,2TBDMS,isomer #56CC(=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]1O4892.0Semi standard non polar33892256
3'-Sialyllactosamine,2TBDMS,isomer #57CC(=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]1O4902.1Semi standard non polar33892256
3'-Sialyllactosamine,2TBDMS,isomer #58CC(=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]1O4881.2Semi standard non polar33892256
3'-Sialyllactosamine,2TBDMS,isomer #59CC(=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]1O4879.0Semi standard non polar33892256
3'-Sialyllactosamine,2TBDMS,isomer #6CC(=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)C4849.8Semi standard non polar33892256
3'-Sialyllactosamine,2TBDMS,isomer #60CC(=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]1O4870.9Semi standard non polar33892256
3'-Sialyllactosamine,2TBDMS,isomer #61CC(=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]1O5047.3Semi standard non polar33892256
3'-Sialyllactosamine,2TBDMS,isomer #62CC(=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]1O5064.0Semi standard non polar33892256
3'-Sialyllactosamine,2TBDMS,isomer #63CC(=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)C4887.4Semi standard non polar33892256
3'-Sialyllactosamine,2TBDMS,isomer #64CC(=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]1O4858.5Semi standard non polar33892256
3'-Sialyllactosamine,2TBDMS,isomer #65CC(=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]1O4868.4Semi standard non polar33892256
3'-Sialyllactosamine,2TBDMS,isomer #66CC(=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]1O4847.1Semi standard non polar33892256
3'-Sialyllactosamine,2TBDMS,isomer #67CC(=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]1O4824.7Semi standard non polar33892256
3'-Sialyllactosamine,2TBDMS,isomer #68CC(=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]1O5030.1Semi standard non polar33892256
3'-Sialyllactosamine,2TBDMS,isomer #69CC(=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]1O5066.0Semi standard non polar33892256
3'-Sialyllactosamine,2TBDMS,isomer #7CC(=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)C4850.9Semi standard non polar33892256
3'-Sialyllactosamine,2TBDMS,isomer #70CC(=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)C4850.6Semi standard non polar33892256
3'-Sialyllactosamine,2TBDMS,isomer #71CC(=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]1O4881.0Semi standard non polar33892256
3'-Sialyllactosamine,2TBDMS,isomer #72CC(=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]1O4869.0Semi standard non polar33892256
3'-Sialyllactosamine,2TBDMS,isomer #73CC(=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]1O4850.8Semi standard non polar33892256
3'-Sialyllactosamine,2TBDMS,isomer #74CC(=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]1O5030.8Semi standard non polar33892256
3'-Sialyllactosamine,2TBDMS,isomer #75CC(=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]1O5070.3Semi standard non polar33892256
3'-Sialyllactosamine,2TBDMS,isomer #76CC(=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)C4864.2Semi standard non polar33892256
3'-Sialyllactosamine,2TBDMS,isomer #77CC(=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]1O4855.0Semi standard non polar33892256
3'-Sialyllactosamine,2TBDMS,isomer #78CC(=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]1O4863.9Semi standard non polar33892256
3'-Sialyllactosamine,2TBDMS,isomer #79CC(=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]1O5046.3Semi standard non polar33892256
3'-Sialyllactosamine,2TBDMS,isomer #8CC(=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)C4874.3Semi standard non polar33892256
3'-Sialyllactosamine,2TBDMS,isomer #80CC(=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]1O5073.8Semi standard non polar33892256
3'-Sialyllactosamine,2TBDMS,isomer #81CC(=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)C4874.0Semi standard non polar33892256
3'-Sialyllactosamine,2TBDMS,isomer #82CC(=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]1O4842.0Semi standard non polar33892256
3'-Sialyllactosamine,2TBDMS,isomer #83CC(=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]1O5035.5Semi standard non polar33892256
3'-Sialyllactosamine,2TBDMS,isomer #84CC(=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]1O5065.3Semi standard non polar33892256
3'-Sialyllactosamine,2TBDMS,isomer #85CC(=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)C4865.7Semi standard non polar33892256
3'-Sialyllactosamine,2TBDMS,isomer #86CC(=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]1O5007.9Semi standard non polar33892256
3'-Sialyllactosamine,2TBDMS,isomer #87CC(=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]1O5036.9Semi standard non polar33892256
3'-Sialyllactosamine,2TBDMS,isomer #88CC(=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)C4840.9Semi standard non polar33892256
3'-Sialyllactosamine,2TBDMS,isomer #89CC(=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]1O5237.0Semi standard non polar33892256
3'-Sialyllactosamine,2TBDMS,isomer #9CC(=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)C4834.8Semi standard non polar33892256
3'-Sialyllactosamine,2TBDMS,isomer #90CC(=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)C5030.6Semi standard non polar33892256
3'-Sialyllactosamine,2TBDMS,isomer #91CC(=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)C5069.5Semi standard non polar33892256
3'-Sialyllactosamine,2TBDMS,isomer #92CC(=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]1O5189.0Semi standard non polar33892256
Spectra

GC-MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted GC-MSPredicted GC-MS Spectrum - 3'-Sialyllactosamine GC-MS (Non-derivatized) - 70eV, Positivesplash10-044i-9110124000-46430d365f649b5f1e392017-09-01Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - 3'-Sialyllactosamine GC-MS (TMS_1_1) - 70eV, PositiveNot Available2021-10-17Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - 3'-Sialyllactosamine GC-MS (TMS_1_2) - 70eV, PositiveNot Available2021-10-17Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - 3'-Sialyllactosamine GC-MS (TMS_1_3) - 70eV, PositiveNot Available2021-10-17Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - 3'-Sialyllactosamine GC-MS (TMS_1_4) - 70eV, PositiveNot Available2021-10-17Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - 3'-Sialyllactosamine GC-MS (TMS_1_5) - 70eV, PositiveNot Available2021-10-17Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - 3'-Sialyllactosamine GC-MS (TMS_1_6) - 70eV, PositiveNot Available2021-10-17Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - 3'-Sialyllactosamine GC-MS (TMS_1_7) - 70eV, PositiveNot Available2021-10-17Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - 3'-Sialyllactosamine GC-MS (TMS_1_8) - 70eV, PositiveNot Available2021-10-17Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - 3'-Sialyllactosamine GC-MS (TMS_1_9) - 70eV, PositiveNot Available2021-10-17Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - 3'-Sialyllactosamine GC-MS (TMS_1_10) - 70eV, PositiveNot Available2021-10-17Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - 3'-Sialyllactosamine GC-MS (TMS_1_11) - 70eV, PositiveNot Available2021-10-17Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - 3'-Sialyllactosamine GC-MS (TMS_1_12) - 70eV, PositiveNot Available2021-10-17Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - 3'-Sialyllactosamine GC-MS (TMS_1_13) - 70eV, PositiveNot Available2021-10-17Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - 3'-Sialyllactosamine GC-MS (TMS_1_14) - 70eV, PositiveNot Available2021-10-17Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - 3'-Sialyllactosamine GC-MS (TMS_2_1) - 70eV, PositiveNot Available2021-10-17Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - 3'-Sialyllactosamine GC-MS (TMS_2_2) - 70eV, PositiveNot Available2021-10-17Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - 3'-Sialyllactosamine GC-MS (TMS_2_3) - 70eV, PositiveNot Available2021-10-17Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - 3'-Sialyllactosamine GC-MS (TMS_2_4) - 70eV, PositiveNot Available2021-10-17Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - 3'-Sialyllactosamine GC-MS (TMS_2_5) - 70eV, PositiveNot Available2021-10-17Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - 3'-Sialyllactosamine GC-MS (TMS_2_6) - 70eV, PositiveNot Available2021-10-17Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - 3'-Sialyllactosamine GC-MS (TMS_2_7) - 70eV, PositiveNot Available2021-10-17Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - 3'-Sialyllactosamine GC-MS (TMS_2_8) - 70eV, PositiveNot Available2021-10-17Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - 3'-Sialyllactosamine GC-MS (TMS_2_9) - 70eV, PositiveNot Available2021-10-17Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - 3'-Sialyllactosamine GC-MS (TMS_2_10) - 70eV, PositiveNot Available2021-10-17Wishart LabView Spectrum

MS/MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 3'-Sialyllactosamine 10V, Positive-QTOFsplash10-02ha-1905068000-caeb7fb6634d6ab6fcd22017-09-01Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 3'-Sialyllactosamine 20V, Positive-QTOFsplash10-075c-6609000000-146e3f2ef2d2e9aa13772017-09-01Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 3'-Sialyllactosamine 40V, Positive-QTOFsplash10-03e9-9833000000-35c80a42471644c73f1e2017-09-01Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 3'-Sialyllactosamine 10V, Negative-QTOFsplash10-0h90-3910044000-8fc434a39a6ef1a08ae92017-09-01Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 3'-Sialyllactosamine 20V, Negative-QTOFsplash10-0a73-8945010000-4f25fde98e0c375284512017-09-01Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 3'-Sialyllactosamine 40V, Negative-QTOFsplash10-0a4i-9854000000-e406e044ac63b4da2ec72017-09-01Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 3'-Sialyllactosamine 10V, Positive-QTOFsplash10-0fss-0500957000-7e0e4e1bc2c96cb7c9182021-09-22Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 3'-Sialyllactosamine 20V, Positive-QTOFsplash10-03el-8722392000-305b5bda4ed294df7dfb2021-09-22Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 3'-Sialyllactosamine 40V, Positive-QTOFsplash10-006x-9501300000-52e1a41de644356ab8492021-09-22Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 3'-Sialyllactosamine 10V, Negative-QTOFsplash10-0540-9000121000-9364dd99242c8e08a40c2021-09-22Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 3'-Sialyllactosamine 20V, Negative-QTOFsplash10-06r6-6000192000-b1046263cfeeb4fb790b2021-09-22Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 3'-Sialyllactosamine 40V, Negative-QTOFsplash10-0a4l-9100000000-3405e788c7e2ecec7aa52021-09-22Wishart LabView Spectrum

NMR Spectra

Spectrum TypeDescriptionDeposition DateSourceView
Predicted 1D NMR13C NMR Spectrum (1D, 100 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 100 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 1000 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 1000 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 200 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 200 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 300 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 300 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 400 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 400 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 500 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 500 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 600 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 600 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 700 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 700 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 800 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 800 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 900 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 900 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Biological Properties
Cellular LocationsNot Available
Biospecimen LocationsNot Available
Tissue LocationsNot Available
Pathways
Normal Concentrations
Not Available
Abnormal Concentrations
Not Available
Associated Disorders and Diseases
Disease ReferencesNone
Associated OMIM IDsNone
DrugBank IDNot Available
Phenol Explorer Compound IDNot Available
FooDB IDFDB024000
KNApSAcK IDNot Available
Chemspider ID35016013
KEGG Compound IDNot Available
BioCyc IDNot Available
BiGG IDNot Available
Wikipedia LinkNot Available
METLIN IDNot Available
PubChem Compound53477870
PDB IDNot Available
ChEBI ID168850
Food Biomarker OntologyNot Available
VMH IDNot Available
MarkerDB IDNot Available
Good Scents IDNot Available
References
Synthesis ReferenceNot Available
Material Safety Data Sheet (MSDS)Not Available
General References
  1. 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 ]
  2. 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 ]