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Identification Taxonomy Ontology Physical properties Spectra Biological properties Concentrations Links References enzymes (8) Show 8 proteins XML

Record Information

Version

5.0

Status

Expected but not Quantified

Creation Date

2005-11-16 15:48:42 UTC

Update Date

2021-09-14 15:45:59 UTC

HMDB ID

HMDB0001542

Secondary Accession Numbers

HMDB01542

Metabolite Identification

Common Name

N-Acetyllactosamine

Description

N-Acetyllactosamine, also known as galb1-4glcnacb or lacnac, belongs to the class of organic compounds known as acylaminosugars. These are organic compounds containing a sugar linked to a chain through N-acyl group. N-Acetyllactosamine is an extremely weak basic (essentially neutral) compound (based on its pKa). N-Acetyllactosamine exists in all living organisms, ranging from bacteria to humans. A beta-D-galactopyranosyl-(1->4)-N-acetyl-D-glucosamine having beta-configuration at the reducing end anomeric centre.

Structure

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


  Mrv1652305271900222D          

 26 27  0  0  1  0            999 V2000
    0.5213    0.5892    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.5213    1.4202    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.2313    0.1700    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.1359    0.2757    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2313    1.8281    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1888    1.8281    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9528    0.5892    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.2313   -0.6535    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8460   -0.1359    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.9528    1.4202    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.9027    1.4202    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6666    0.1776    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5637    0.2720    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8460   -0.9670    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.6628    1.8318    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6666   -0.6421    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2775   -0.1359    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.5637   -1.3862    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.1322   -1.3786    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3804   -1.0500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9565   -1.0538    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2775   -0.9670    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.9877    0.2720    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5674   -2.2095    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9914   -1.3749    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6978   -0.1359    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  1  3  1  0  0  0  0
  1  4  1  6  0  0  0
  2  5  1  0  0  0  0
  2  6  1  1  0  0  0
  3  7  1  0  0  0  0
  3  8  1  1  0  0  0
  9  4  1  1  0  0  0
  5 10  1  0  0  0  0
  6 11  1  0  0  0  0
  7 12  1  6  0  0  0
  9 13  1  0  0  0  0
  9 14  1  0  0  0  0
 10 15  1  1  0  0  0
 12 16  1  0  0  0  0
 13 17  1  0  0  0  0
 14 18  1  0  0  0  0
 14 19  1  6  0  0  0
 16 20  1  0  0  0  0
 16 21  2  0  0  0  0
 17 22  1  0  0  0  0
 17 23  1  1  0  0  0
 18 24  1  1  0  0  0
 22 25  1  1  0  0  0
 23 26  1  0  0  0  0
  7 10  1  0  0  0  0
 18 22  1  0  0  0  0
M  END

HMDB0001542
     RDKit          3D
N-Acetyllactosamine
 51 52  0  0  0  0  0  0  0  0999 V2000
    4.7343    3.0595    2.5956 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0306    2.2756    1.5768 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0576    2.7089    0.3752 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3224    1.0633    1.8548 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.6580    0.3470    0.8200 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.2159   -1.0383    0.5974 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.5568   -0.8787    0.2497 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5869   -1.6355   -0.4887 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2025   -1.6698   -0.3392 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.5946   -2.5324   -1.3907 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1352   -3.8285   -1.2451 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6178   -0.2720   -0.3008 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.7212   -0.3510   -0.3860 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3342    0.2865   -1.4309 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.0727    1.3381   -0.9142 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2604    1.0349   -0.3294 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.0598    0.3950    1.0177 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3682    1.2136    1.8977 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1898    0.2023   -1.1615 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.3375   -0.1539   -0.4426 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4664   -1.0030   -1.6697 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.2827   -1.9776   -0.7243 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1891   -0.5310   -2.3249 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.6086    0.3317   -3.3701 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1336    0.3204    1.0090 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7121    1.6042    1.2133 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7786    4.1408    2.2751 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1951    3.0686    3.5672 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8056    2.7495    2.7106 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3080    0.7203    2.8400 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8008    0.8920   -0.1598 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1843   -1.6647    1.5054 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9520   -0.1892    0.8647 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9269   -2.1294    0.6560 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5095   -2.5817   -1.1565 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7968   -2.1044   -2.3849 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5795   -3.9233   -0.3548 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1228    0.3020   -1.1034 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5082    0.7691   -2.0291 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7613    2.0305   -0.1115 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0864    0.1670    1.4375 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5556   -0.5857    0.9948 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7229    0.6988    2.4613 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5520    0.8409   -1.9993 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9716   -0.5341   -1.0846 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0969   -1.3986   -2.5228 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4468   -2.9003   -1.0773 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6911   -1.3614   -2.8371 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4775    1.2706   -3.1459 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8358   -0.3468    1.8170 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4260    1.7597    2.1479 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
  6  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
  9 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 16 19  1  0
 19 20  1  0
 19 21  1  0
 21 22  1  0
 21 23  1  0
 23 24  1  0
 12 25  1  0
 25 26  1  0
 25  5  1  0
 23 14  1  0
  1 27  1  0
  1 28  1  0
  1 29  1  0
  4 30  1  0
  5 31  1  6
  6 32  1  1
  7 33  1  0
  9 34  1  1
 10 35  1  0
 10 36  1  0
 11 37  1  0
 12 38  1  6
 14 39  1  6
 16 40  1  1
 17 41  1  0
 17 42  1  0
 18 43  1  0
 19 44  1  6
 20 45  1  0
 21 46  1  6
 22 47  1  0
 23 48  1  6
 24 49  1  0
 25 50  1  1
 26 51  1  0
M  END


  Mrv1652305271900222D          

 26 27  0  0  1  0            999 V2000
    0.5213    0.5892    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.5213    1.4202    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.2313    0.1700    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.1359    0.2757    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2313    1.8281    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1888    1.8281    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9528    0.5892    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.2313   -0.6535    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8460   -0.1359    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.9528    1.4202    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.9027    1.4202    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6666    0.1776    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5637    0.2720    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8460   -0.9670    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.6628    1.8318    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6666   -0.6421    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2775   -0.1359    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.5637   -1.3862    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.1322   -1.3786    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3804   -1.0500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9565   -1.0538    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2775   -0.9670    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.9877    0.2720    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5674   -2.2095    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9914   -1.3749    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6978   -0.1359    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  1  3  1  0  0  0  0
  1  4  1  6  0  0  0
  2  5  1  0  0  0  0
  2  6  1  1  0  0  0
  3  7  1  0  0  0  0
  3  8  1  1  0  0  0
  9  4  1  1  0  0  0
  5 10  1  0  0  0  0
  6 11  1  0  0  0  0
  7 12  1  6  0  0  0
  9 13  1  0  0  0  0
  9 14  1  0  0  0  0
 10 15  1  1  0  0  0
 12 16  1  0  0  0  0
 13 17  1  0  0  0  0
 14 18  1  0  0  0  0
 14 19  1  6  0  0  0
 16 20  1  0  0  0  0
 16 21  2  0  0  0  0
 17 22  1  0  0  0  0
 17 23  1  1  0  0  0
 18 24  1  1  0  0  0
 22 25  1  1  0  0  0
 23 26  1  0  0  0  0
  7 10  1  0  0  0  0
 18 22  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0001542

> <DATABASE_NAME>
hmdb

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

> <INCHI_IDENTIFIER>
InChI=1S/C14H25NO11/c1-4(18)15-7-9(20)12(6(3-17)24-13(7)23)26-14-11(22)10(21)8(19)5(2-16)25-14/h5-14,16-17,19-23H,2-3H2,1H3,(H,15,18)/t5-,6-,7-,8+,9-,10+,11-,12-,13-,14+/m1/s1

> <INCHI_KEY>
KFEUJDWYNGMDBV-LODBTCKLSA-N

> <FORMULA>
C14H25NO11

> <MOLECULAR_WEIGHT>
383.3484

> <EXACT_MASS>
383.142760647

> <JCHEM_ACCEPTOR_COUNT>
11

> <JCHEM_ATOM_COUNT>
51

> <JCHEM_AVERAGE_POLARIZABILITY>
35.65701397378713

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
8

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
N-[(2R,3R,4R,5S,6R)-2,4-dihydroxy-6-(hydroxymethyl)-5-{[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}oxan-3-yl]acetamide

> <ALOGPS_LOGP>
-2.80

> <JCHEM_LOGP>
-4.991410057333334

> <ALOGPS_LOGS>
-0.17

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.231138627153623

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.501288100055472

> <JCHEM_PKA_STRONGEST_BASIC>
-2.981083565282729

> <JCHEM_POLAR_SURFACE_AREA>
198.39999999999998

> <JCHEM_REFRACTIVITY>
79.43799999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
2.59e+02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
N-acetyllactosamine

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0001542
     RDKit          3D
N-Acetyllactosamine
 51 52  0  0  0  0  0  0  0  0999 V2000
    4.7343    3.0595    2.5956 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0306    2.2756    1.5768 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0576    2.7089    0.3752 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3224    1.0633    1.8548 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.6580    0.3470    0.8200 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.2159   -1.0383    0.5974 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.5568   -0.8787    0.2497 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5869   -1.6355   -0.4887 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2025   -1.6698   -0.3392 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.5946   -2.5324   -1.3907 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1352   -3.8285   -1.2451 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6178   -0.2720   -0.3008 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.7212   -0.3510   -0.3860 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3342    0.2865   -1.4309 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.0727    1.3381   -0.9142 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2604    1.0349   -0.3294 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.0598    0.3950    1.0177 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3682    1.2136    1.8977 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1898    0.2023   -1.1615 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.3375   -0.1539   -0.4426 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4664   -1.0030   -1.6697 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.2827   -1.9776   -0.7243 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1891   -0.5310   -2.3249 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.6086    0.3317   -3.3701 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1336    0.3204    1.0090 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7121    1.6042    1.2133 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7786    4.1408    2.2751 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1951    3.0686    3.5672 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8056    2.7495    2.7106 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3080    0.7203    2.8400 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8008    0.8920   -0.1598 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1843   -1.6647    1.5054 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9520   -0.1892    0.8647 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9269   -2.1294    0.6560 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5095   -2.5817   -1.1565 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7968   -2.1044   -2.3849 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5795   -3.9233   -0.3548 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1228    0.3020   -1.1034 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5082    0.7691   -2.0291 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7613    2.0305   -0.1115 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0864    0.1670    1.4375 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5556   -0.5857    0.9948 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7229    0.6988    2.4613 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5520    0.8409   -1.9993 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9716   -0.5341   -1.0846 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0969   -1.3986   -2.5228 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4468   -2.9003   -1.0773 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6911   -1.3614   -2.8371 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4775    1.2706   -3.1459 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8358   -0.3468    1.8170 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4260    1.7597    2.1479 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
  6  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
  9 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 16 19  1  0
 19 20  1  0
 19 21  1  0
 21 22  1  0
 21 23  1  0
 23 24  1  0
 12 25  1  0
 25 26  1  0
 25  5  1  0
 23 14  1  0
  1 27  1  0
  1 28  1  0
  1 29  1  0
  4 30  1  0
  5 31  1  6
  6 32  1  1
  7 33  1  0
  9 34  1  1
 10 35  1  0
 10 36  1  0
 11 37  1  0
 12 38  1  6
 14 39  1  6
 16 40  1  1
 17 41  1  0
 17 42  1  0
 18 43  1  0
 19 44  1  6
 20 45  1  0
 21 46  1  6
 22 47  1  0
 23 48  1  6
 24 49  1  0
 25 50  1  1
 26 51  1  0
M  END

HEADER    PROTEIN                                 27-MAY-19   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   27-MAY-19         0                                  
HETATM    1  C   UNK     0       0.973   1.100   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       0.973   2.651   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       2.298   0.317   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0      -0.254   0.515   0.000  0.00  0.00           O+0
HETATM    5  O   UNK     0       2.298   3.412   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0      -0.352   3.412   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       3.645   1.100   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0       2.298  -1.220   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0      -1.579  -0.254   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       3.645   2.651   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0      -1.685   2.651   0.000  0.00  0.00           O+0
HETATM   12  N   UNK     0       4.978   0.332   0.000  0.00  0.00           N+0
HETATM   13  O   UNK     0      -2.919   0.508   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0      -1.579  -1.805   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       4.971   3.419   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       4.978  -1.199   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -4.251  -0.254   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -2.919  -2.588   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0      -0.247  -2.573   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       6.310  -1.960   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       3.652  -1.967   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0      -4.251  -1.805   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -5.577   0.508   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0      -2.926  -4.124   0.000  0.00  0.00           O+0
HETATM   25  O   UNK     0      -5.584  -2.566   0.000  0.00  0.00           O+0
HETATM   26  O   UNK     0      -6.903  -0.254   0.000  0.00  0.00           O+0
CONECT    1    2    3    4                                                  
CONECT    2    1    5    6                                                  
CONECT    3    1    7    8                                                  
CONECT    4    1    9                                                       
CONECT    5    2   10                                                       
CONECT    6    2   11                                                       
CONECT    7    3   12   10                                                  
CONECT    8    3                                                            
CONECT    9    4   13   14                                                  
CONECT   10    5   15    7                                                  
CONECT   11    6                                                            
CONECT   12    7   16                                                       
CONECT   13    9   17                                                       
CONECT   14    9   18   19                                                  
CONECT   15   10                                                            
CONECT   16   12   20   21                                                  
CONECT   17   13   22   23                                                  
CONECT   18   14   24   22                                                  
CONECT   19   14                                                            
CONECT   20   16                                                            
CONECT   21   16                                                            
CONECT   22   17   25   18                                                  
CONECT   23   17   26                                                       
CONECT   24   18                                                            
CONECT   25   22                                                            
CONECT   26   23                                                            
MASTER        0    0    0    0    0    0    0    0   26    0   54    0
END

COMPND    HMDB0001542
HETATM    1  C1  UNL     1       4.734   3.059   2.596  1.00  0.00           C  
HETATM    2  C2  UNL     1       4.031   2.276   1.577  1.00  0.00           C  
HETATM    3  O1  UNL     1       4.058   2.709   0.375  1.00  0.00           O  
HETATM    4  N1  UNL     1       3.322   1.063   1.855  1.00  0.00           N  
HETATM    5  C3  UNL     1       2.658   0.347   0.820  1.00  0.00           C  
HETATM    6  C4  UNL     1       3.216  -1.038   0.597  1.00  0.00           C  
HETATM    7  O2  UNL     1       4.557  -0.879   0.250  1.00  0.00           O  
HETATM    8  O3  UNL     1       2.587  -1.635  -0.489  1.00  0.00           O  
HETATM    9  C5  UNL     1       1.203  -1.670  -0.339  1.00  0.00           C  
HETATM   10  C6  UNL     1       0.595  -2.532  -1.391  1.00  0.00           C  
HETATM   11  O4  UNL     1       1.135  -3.829  -1.245  1.00  0.00           O  
HETATM   12  C7  UNL     1       0.618  -0.272  -0.301  1.00  0.00           C  
HETATM   13  O5  UNL     1      -0.721  -0.351  -0.386  1.00  0.00           O  
HETATM   14  C8  UNL     1      -1.334   0.287  -1.431  1.00  0.00           C  
HETATM   15  O6  UNL     1      -2.073   1.338  -0.914  1.00  0.00           O  
HETATM   16  C9  UNL     1      -3.260   1.035  -0.329  1.00  0.00           C  
HETATM   17  C10 UNL     1      -3.060   0.395   1.018  1.00  0.00           C  
HETATM   18  O7  UNL     1      -2.368   1.214   1.898  1.00  0.00           O  
HETATM   19  C11 UNL     1      -4.190   0.202  -1.161  1.00  0.00           C  
HETATM   20  O8  UNL     1      -5.338  -0.154  -0.443  1.00  0.00           O  
HETATM   21  C12 UNL     1      -3.466  -1.003  -1.670  1.00  0.00           C  
HETATM   22  O9  UNL     1      -3.283  -1.978  -0.724  1.00  0.00           O  
HETATM   23  C13 UNL     1      -2.189  -0.531  -2.325  1.00  0.00           C  
HETATM   24  O10 UNL     1      -2.609   0.332  -3.370  1.00  0.00           O  
HETATM   25  C14 UNL     1       1.134   0.320   1.009  1.00  0.00           C  
HETATM   26  O11 UNL     1       0.712   1.604   1.213  1.00  0.00           O  
HETATM   27  H1  UNL     1       4.779   4.141   2.275  1.00  0.00           H  
HETATM   28  H2  UNL     1       4.195   3.069   3.567  1.00  0.00           H  
HETATM   29  H3  UNL     1       5.806   2.749   2.711  1.00  0.00           H  
HETATM   30  H4  UNL     1       3.308   0.720   2.840  1.00  0.00           H  
HETATM   31  H5  UNL     1       2.801   0.892  -0.160  1.00  0.00           H  
HETATM   32  H6  UNL     1       3.184  -1.665   1.505  1.00  0.00           H  
HETATM   33  H7  UNL     1       4.952  -0.189   0.865  1.00  0.00           H  
HETATM   34  H8  UNL     1       0.927  -2.129   0.656  1.00  0.00           H  
HETATM   35  H9  UNL     1      -0.509  -2.582  -1.156  1.00  0.00           H  
HETATM   36  H10 UNL     1       0.797  -2.104  -2.385  1.00  0.00           H  
HETATM   37  H11 UNL     1       1.579  -3.923  -0.355  1.00  0.00           H  
HETATM   38  H12 UNL     1       1.123   0.302  -1.103  1.00  0.00           H  
HETATM   39  H13 UNL     1      -0.508   0.769  -2.029  1.00  0.00           H  
HETATM   40  H14 UNL     1      -3.761   2.030  -0.111  1.00  0.00           H  
HETATM   41  H15 UNL     1      -4.086   0.167   1.438  1.00  0.00           H  
HETATM   42  H16 UNL     1      -2.556  -0.586   0.995  1.00  0.00           H  
HETATM   43  H17 UNL     1      -1.723   0.699   2.461  1.00  0.00           H  
HETATM   44  H18 UNL     1      -4.552   0.841  -1.999  1.00  0.00           H  
HETATM   45  H19 UNL     1      -5.972  -0.534  -1.085  1.00  0.00           H  
HETATM   46  H20 UNL     1      -4.097  -1.399  -2.523  1.00  0.00           H  
HETATM   47  H21 UNL     1      -3.447  -2.900  -1.077  1.00  0.00           H  
HETATM   48  H22 UNL     1      -1.691  -1.361  -2.837  1.00  0.00           H  
HETATM   49  H23 UNL     1      -2.477   1.271  -3.146  1.00  0.00           H  
HETATM   50  H24 UNL     1       0.836  -0.347   1.817  1.00  0.00           H  
HETATM   51  H25 UNL     1       0.426   1.760   2.148  1.00  0.00           H  
CONECT    1    2   27   28   29
CONECT    2    3    3    4
CONECT    4    5   30
CONECT    5    6   25   31
CONECT    6    7    8   32
CONECT    7   33
CONECT    8    9
CONECT    9   10   12   34
CONECT   10   11   35   36
CONECT   11   37
CONECT   12   13   25   38
CONECT   13   14
CONECT   14   15   23   39
CONECT   15   16
CONECT   16   17   19   40
CONECT   17   18   41   42
CONECT   18   43
CONECT   19   20   21   44
CONECT   20   45
CONECT   21   22   23   46
CONECT   22   47
CONECT   23   24   48
CONECT   24   49
CONECT   25   26   50
CONECT   26   51
END

HMDB0001542
     RDKit          3D
N-Acetyllactosamine
 51 52  0  0  0  0  0  0  0  0999 V2000
    4.7343    3.0595    2.5956 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0306    2.2756    1.5768 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0576    2.7089    0.3752 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3224    1.0633    1.8548 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.6580    0.3470    0.8200 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.2159   -1.0383    0.5974 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.5568   -0.8787    0.2497 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5869   -1.6355   -0.4887 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2025   -1.6698   -0.3392 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.5946   -2.5324   -1.3907 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1352   -3.8285   -1.2451 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6178   -0.2720   -0.3008 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.7212   -0.3510   -0.3860 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3342    0.2865   -1.4309 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.0727    1.3381   -0.9142 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2604    1.0349   -0.3294 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.0598    0.3950    1.0177 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3682    1.2136    1.8977 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1898    0.2023   -1.1615 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.3375   -0.1539   -0.4426 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4664   -1.0030   -1.6697 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.2827   -1.9776   -0.7243 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1891   -0.5310   -2.3249 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.6086    0.3317   -3.3701 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1336    0.3204    1.0090 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7121    1.6042    1.2133 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7786    4.1408    2.2751 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1951    3.0686    3.5672 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8056    2.7495    2.7106 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3080    0.7203    2.8400 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8008    0.8920   -0.1598 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1843   -1.6647    1.5054 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9520   -0.1892    0.8647 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9269   -2.1294    0.6560 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5095   -2.5817   -1.1565 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7968   -2.1044   -2.3849 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5795   -3.9233   -0.3548 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1228    0.3020   -1.1034 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5082    0.7691   -2.0291 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7613    2.0305   -0.1115 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0864    0.1670    1.4375 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5556   -0.5857    0.9948 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7229    0.6988    2.4613 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5520    0.8409   -1.9993 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9716   -0.5341   -1.0846 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0969   -1.3986   -2.5228 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4468   -2.9003   -1.0773 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6911   -1.3614   -2.8371 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4775    1.2706   -3.1459 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8358   -0.3468    1.8170 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4260    1.7597    2.1479 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
  6  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
  9 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 16 19  1  0
 19 20  1  0
 19 21  1  0
 21 22  1  0
 21 23  1  0
 23 24  1  0
 12 25  1  0
 25 26  1  0
 25  5  1  0
 23 14  1  0
  1 27  1  0
  1 28  1  0
  1 29  1  0
  4 30  1  0
  5 31  1  6
  6 32  1  1
  7 33  1  0
  9 34  1  1
 10 35  1  0
 10 36  1  0
 11 37  1  0
 12 38  1  6
 14 39  1  6
 16 40  1  1
 17 41  1  0
 17 42  1  0
 18 43  1  0
 19 44  1  6
 20 45  1  0
 21 46  1  6
 22 47  1  0
 23 48  1  6
 24 49  1  0
 25 50  1  1
 26 51  1  0
M  END

View in JSmol View NMR Assignments View Stereo Labels

Synonyms

Value	Source
beta-D-Galactosyl-1,4-N-acetyl-D-glucosamine	ChEBI
Galb1-4glcnacb	ChEBI
Galbeta1-4glcnacbeta	ChEBI
LacNAc	ChEBI
N-Acetyl-beta-lactosamine	ChEBI
beta-D-Galactosyl-1,4-N-acetyl-beta-D-glucosamine	Kegg
b-D-Galactosyl-1,4-N-acetyl-D-glucosamine	Generator
Β-D-galactosyl-1,4-N-acetyl-D-glucosamine	Generator
N-Acetyl-b-lactosamine	Generator
N-Acetyl-β-lactosamine	Generator
b-D-Galactosyl-1,4-N-acetyl-b-D-glucosamine	Generator
Β-D-galactosyl-1,4-N-acetyl-β-D-glucosamine	Generator
beta-delta-Galactosyl-1,4-N-acetyl-beta-delta-glucosamine	HMDB
beta-delta-Galactosyl-1,4-N-acetyl-delta-glucosamine	HMDB
D-Galactopyranosyl	HMDB
delta-Galactopyranosyl	HMDB
N-Acetyl-lactosamine	HMDB
ACETYL lactosamine	HMDB

Chemical Formula

C₁₄H₂₅NO₁₁

Average Molecular Weight

383.3484

Monoisotopic Molecular Weight

383.142760647

IUPAC Name

N-[(2R,3R,4R,5S,6R)-2,4-dihydroxy-6-(hydroxymethyl)-5-{[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}oxan-3-yl]acetamide

Traditional Name

N-acetyllactosamine

CAS Registry Number

32181-59-2

SMILES

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

InChI Identifier

InChI=1S/C14H25NO11/c1-4(18)15-7-9(20)12(6(3-17)24-13(7)23)26-14-11(22)10(21)8(19)5(2-16)25-14/h5-14,16-17,19-23H,2-3H2,1H3,(H,15,18)/t5-,6-,7-,8+,9-,10+,11-,12-,13-,14+/m1/s1

InChI Key

KFEUJDWYNGMDBV-LODBTCKLSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as acylaminosugars. These are organic compounds containing a sugar linked to a chain through N-acyl group.

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Carbohydrates and carbohydrate conjugates

Direct Parent

Acylaminosugars

Alternative Parents

Substituents

Acylaminosugar
N-acyl-alpha-hexosamine
Disaccharide
Glycosyl compound
O-glycosyl compound
Oxane
Acetamide
Carboxamide group
Hemiacetal
Secondary carboxylic acid amide
Secondary alcohol
Acetal
Carboxylic acid derivative
Oxacycle
Organoheterocyclic compound
Polyol
Hydrocarbon derivative
Organic oxide
Organic nitrogen compound
Organopnictogen compound
Alcohol
Primary alcohol
Organonitrogen compound
Carbonyl group
Aliphatic heteromonocyclic compound

Molecular Framework

Aliphatic heteromonocyclic compounds

External Descriptors

beta-D-galactopyranosyl-(1->4)-N-acetyl-D-glucosamine (CHEBI:16153 )

Ontology

Not Available

Epidermis (HMDB: HMDB0001542)

Organ

Intestine (HMDB: HMDB0001542)
Spleen (HMDB: HMDB0001542)

Cellular substructure

Cytoplasm (HMDB: HMDB0001542)

Greylag goose (FooDB: FOOD00368)
Guinea hen (FooDB: FOOD00373)
Ostrich (FooDB: FOOD00422)
Velvet duck (FooDB: FOOD00427)
Pheasant (FooDB: FOOD00430)
Squab (FooDB: FOOD00481)
Turkey (FooDB: FOOD00494)
Quail (FooDB: FOOD00541)
Anatidae (FooDB: FOOD00576)
Rock ptarmigan (FooDB: FOOD00597)
Columbidae (Dove, Pigeon) (FooDB: FOOD00610)
Chicken (FooDB: FOOD00329)
Mallard duck (FooDB: FOOD00353)
Emu (FooDB: FOOD00360)

Equine

Horse (FooDB: FOOD00378)

Lagomorph

Ovis

Sheep (Mutton, Lamb) (FooDB: FOOD00473)

Bovine

Venison

Deer (FooDB: FOOD00524)
Mule deer (FooDB: FOOD00348)
Elk (FooDB: FOOD00359)

Caprae

Domestic goat (FooDB: FOOD00529)

Swine

Domestic pig (FooDB: FOOD00536)
Wild boar (FooDB: FOOD00307)

Process

Not Available

Role

Not Available

Physical Properties

State

Solid

Experimental Molecular Properties

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

Experimental Chromatographic Properties

Not Available

Predicted Molecular Properties

Property	Value	Source
Water Solubility	259 g/L	ALOGPS
logP	-2.8	ALOGPS
logP	-5	ChemAxon
logS	-0.17	ALOGPS
pKa (Strongest Acidic)	11.5	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	11	ChemAxon
Hydrogen Donor Count	8	ChemAxon
Polar Surface Area	198.4 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	79.44 m³·mol⁻¹	ChemAxon
Polarizability	35.66 Å³	ChemAxon
Number of Rings	2	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

Predicted Chromatographic Properties

Predicted Collision Cross Sections

Predictor	Adduct Type	CCS Value (Å²)	Reference
DarkChem	[M+H]+	183.604	31661259
DarkChem	[M-H]-	177.648	31661259
AllCCS	[M+H]+	186.627	32859911
AllCCS	[M-H]-	185.67	32859911
DeepCCS	[M+H]+	181.698	30932474
DeepCCS	[M-H]-	179.796	30932474
DeepCCS	[M-2H]-	213.248	30932474
DeepCCS	[M+Na]+	187.439	30932474
AllCCS	[M+H]+	186.6	32859911
AllCCS	[M+H-H2O]+	184.0	32859911
AllCCS	[M+NH4]+	189.0	32859911
AllCCS	[M+Na]+	189.7	32859911
AllCCS	[M-H]-	185.7	32859911
AllCCS	[M+Na-2H]-	185.4	32859911
AllCCS	[M+HCOO]-	185.3	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
N-Acetyllactosamine	CC(=O)N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O)[C@H]2O)[C@@H]1O	4168.5	Standard polar	33892256
N-Acetyllactosamine	CC(=O)N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O)[C@H]2O)[C@@H]1O	3118.3	Standard non polar	33892256
N-Acetyllactosamine	CC(=O)N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O)[C@H]2O)[C@@H]1O	3323.0	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
N-Acetyllactosamine,1TMS,isomer #1	CC(=O)N[C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O)[C@H]2O)[C@@H]1O	3019.9	Semi standard non polar	33892256
N-Acetyllactosamine,1TMS,isomer #2	CC(=O)N[C@H]1[C@H](O)O[C@H](CO[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O)[C@H]2O)[C@@H]1O	3000.5	Semi standard non polar	33892256
N-Acetyllactosamine,1TMS,isomer #3	CC(=O)N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]2O)[C@@H]1O	2987.4	Semi standard non polar	33892256
N-Acetyllactosamine,1TMS,isomer #4	CC(=O)N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)[C@@H]1O	3002.8	Semi standard non polar	33892256
N-Acetyllactosamine,1TMS,isomer #5	CC(=O)N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)[C@@H]1O	3013.5	Semi standard non polar	33892256
N-Acetyllactosamine,1TMS,isomer #6	CC(=O)N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)[C@@H]1O	3016.3	Semi standard non polar	33892256
N-Acetyllactosamine,1TMS,isomer #7	CC(=O)N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O)[C@H]2O)[C@@H]1O[Si](C)(C)C	3025.2	Semi standard non polar	33892256
N-Acetyllactosamine,1TMS,isomer #8	CC(=O)N([C@H]1[C@H](O)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O)[C@H]2O)[C@@H]1O)[Si](C)(C)C	2982.0	Semi standard non polar	33892256
N-Acetyllactosamine,2TMS,isomer #1	CC(=O)N[C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O)[C@H]2O)[C@@H]1O	2944.9	Semi standard non polar	33892256
N-Acetyllactosamine,2TMS,isomer #10	CC(=O)N[C@H]1[C@H](O)O[C@H](CO[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)[C@@H]1O	2944.1	Semi standard non polar	33892256
N-Acetyllactosamine,2TMS,isomer #11	CC(=O)N[C@H]1[C@H](O)O[C@H](CO[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)[C@@H]1O	2944.4	Semi standard non polar	33892256
N-Acetyllactosamine,2TMS,isomer #12	CC(=O)N[C@H]1[C@H](O)O[C@H](CO[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O)[C@H]2O)[C@@H]1O[Si](C)(C)C	2939.4	Semi standard non polar	33892256
N-Acetyllactosamine,2TMS,isomer #13	CC(=O)N([C@H]1[C@H](O)O[C@H](CO[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O)[C@H]2O)[C@@H]1O)[Si](C)(C)C	2989.0	Semi standard non polar	33892256
N-Acetyllactosamine,2TMS,isomer #14	CC(=O)N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)[C@@H]1O	2952.6	Semi standard non polar	33892256
N-Acetyllactosamine,2TMS,isomer #15	CC(=O)N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)[C@@H]1O	2934.5	Semi standard non polar	33892256
N-Acetyllactosamine,2TMS,isomer #16	CC(=O)N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)[C@@H]1O	2935.0	Semi standard non polar	33892256
N-Acetyllactosamine,2TMS,isomer #17	CC(=O)N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]2O)[C@@H]1O[Si](C)(C)C	2936.2	Semi standard non polar	33892256
N-Acetyllactosamine,2TMS,isomer #18	CC(=O)N([C@H]1[C@H](O)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]2O)[C@@H]1O)[Si](C)(C)C	2980.7	Semi standard non polar	33892256
N-Acetyllactosamine,2TMS,isomer #19	CC(=O)N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O)[C@@H]1O	2955.5	Semi standard non polar	33892256
N-Acetyllactosamine,2TMS,isomer #2	CC(=O)N[C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]2O)[C@@H]1O	2947.0	Semi standard non polar	33892256
N-Acetyllactosamine,2TMS,isomer #20	CC(=O)N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]2O[Si](C)(C)C)[C@@H]1O	2941.4	Semi standard non polar	33892256
N-Acetyllactosamine,2TMS,isomer #21	CC(=O)N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)[C@@H]1O[Si](C)(C)C	2943.4	Semi standard non polar	33892256
N-Acetyllactosamine,2TMS,isomer #22	CC(=O)N([C@H]1[C@H](O)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)[C@@H]1O)[Si](C)(C)C	2960.7	Semi standard non polar	33892256
N-Acetyllactosamine,2TMS,isomer #23	CC(=O)N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)[C@@H]1O	2943.7	Semi standard non polar	33892256
N-Acetyllactosamine,2TMS,isomer #24	CC(=O)N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)[C@@H]1O[Si](C)(C)C	2945.0	Semi standard non polar	33892256
N-Acetyllactosamine,2TMS,isomer #25	CC(=O)N([C@H]1[C@H](O)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)[C@@H]1O)[Si](C)(C)C	2960.4	Semi standard non polar	33892256
N-Acetyllactosamine,2TMS,isomer #26	CC(=O)N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2936.3	Semi standard non polar	33892256
N-Acetyllactosamine,2TMS,isomer #27	CC(=O)N([C@H]1[C@H](O)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)[C@@H]1O)[Si](C)(C)C	2963.3	Semi standard non polar	33892256
N-Acetyllactosamine,2TMS,isomer #28	CC(=O)N([C@H]1[C@H](O)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O)[C@H]2O)[C@@H]1O[Si](C)(C)C)[Si](C)(C)C	2971.2	Semi standard non polar	33892256
N-Acetyllactosamine,2TMS,isomer #3	CC(=O)N[C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)[C@@H]1O	2951.7	Semi standard non polar	33892256
N-Acetyllactosamine,2TMS,isomer #4	CC(=O)N[C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)[C@@H]1O	2945.9	Semi standard non polar	33892256
N-Acetyllactosamine,2TMS,isomer #5	CC(=O)N[C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)[C@@H]1O	2947.9	Semi standard non polar	33892256
N-Acetyllactosamine,2TMS,isomer #6	CC(=O)N[C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O)[C@H]2O)[C@@H]1O[Si](C)(C)C	2931.0	Semi standard non polar	33892256
N-Acetyllactosamine,2TMS,isomer #7	CC(=O)N([C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O)[C@H]2O)[C@@H]1O)[Si](C)(C)C	2973.0	Semi standard non polar	33892256
N-Acetyllactosamine,2TMS,isomer #8	CC(=O)N[C@H]1[C@H](O)O[C@H](CO[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]2O)[C@@H]1O	2956.7	Semi standard non polar	33892256
N-Acetyllactosamine,2TMS,isomer #9	CC(=O)N[C@H]1[C@H](O)O[C@H](CO[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)[C@@H]1O	2949.6	Semi standard non polar	33892256
N-Acetyllactosamine,3TMS,isomer #1	CC(=O)N[C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]2O)[C@@H]1O	2859.2	Semi standard non polar	33892256
N-Acetyllactosamine,3TMS,isomer #10	CC(=O)N[C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]2O)[C@@H]1O[Si](C)(C)C	2834.1	Semi standard non polar	33892256
N-Acetyllactosamine,3TMS,isomer #11	CC(=O)N([C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]2O)[C@@H]1O)[Si](C)(C)C	2911.4	Semi standard non polar	33892256
N-Acetyllactosamine,3TMS,isomer #12	CC(=O)N[C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O)[C@@H]1O	2927.7	Semi standard non polar	33892256
N-Acetyllactosamine,3TMS,isomer #13	CC(=O)N[C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]2O[Si](C)(C)C)[C@@H]1O	2917.3	Semi standard non polar	33892256
N-Acetyllactosamine,3TMS,isomer #14	CC(=O)N[C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)[C@@H]1O[Si](C)(C)C	2872.1	Semi standard non polar	33892256
N-Acetyllactosamine,3TMS,isomer #15	CC(=O)N([C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)[C@@H]1O)[Si](C)(C)C	2911.8	Semi standard non polar	33892256
N-Acetyllactosamine,3TMS,isomer #16	CC(=O)N[C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)[C@@H]1O	2903.9	Semi standard non polar	33892256
N-Acetyllactosamine,3TMS,isomer #17	CC(=O)N[C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)[C@@H]1O[Si](C)(C)C	2898.2	Semi standard non polar	33892256
N-Acetyllactosamine,3TMS,isomer #18	CC(=O)N([C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)[C@@H]1O)[Si](C)(C)C	2912.6	Semi standard non polar	33892256
N-Acetyllactosamine,3TMS,isomer #19	CC(=O)N[C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2854.7	Semi standard non polar	33892256
N-Acetyllactosamine,3TMS,isomer #2	CC(=O)N[C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)[C@@H]1O	2883.6	Semi standard non polar	33892256
N-Acetyllactosamine,3TMS,isomer #20	CC(=O)N([C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)[C@@H]1O)[Si](C)(C)C	2914.8	Semi standard non polar	33892256
N-Acetyllactosamine,3TMS,isomer #21	CC(=O)N([C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O)[C@H]2O)[C@@H]1O[Si](C)(C)C)[Si](C)(C)C	2932.0	Semi standard non polar	33892256
N-Acetyllactosamine,3TMS,isomer #22	CC(=O)N[C@H]1[C@H](O)O[C@H](CO[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)[C@@H]1O	2880.4	Semi standard non polar	33892256
N-Acetyllactosamine,3TMS,isomer #23	CC(=O)N[C@H]1[C@H](O)O[C@H](CO[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)[C@@H]1O	2896.7	Semi standard non polar	33892256
N-Acetyllactosamine,3TMS,isomer #24	CC(=O)N[C@H]1[C@H](O)O[C@H](CO[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)[C@@H]1O	2867.8	Semi standard non polar	33892256
N-Acetyllactosamine,3TMS,isomer #25	CC(=O)N[C@H]1[C@H](O)O[C@H](CO[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]2O)[C@@H]1O[Si](C)(C)C	2848.3	Semi standard non polar	33892256
N-Acetyllactosamine,3TMS,isomer #26	CC(=O)N([C@H]1[C@H](O)O[C@H](CO[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]2O)[C@@H]1O)[Si](C)(C)C	2930.9	Semi standard non polar	33892256
N-Acetyllactosamine,3TMS,isomer #27	CC(=O)N[C@H]1[C@H](O)O[C@H](CO[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O)[C@@H]1O	2918.1	Semi standard non polar	33892256
N-Acetyllactosamine,3TMS,isomer #28	CC(=O)N[C@H]1[C@H](O)O[C@H](CO[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]2O[Si](C)(C)C)[C@@H]1O	2900.8	Semi standard non polar	33892256
N-Acetyllactosamine,3TMS,isomer #29	CC(=O)N[C@H]1[C@H](O)O[C@H](CO[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)[C@@H]1O[Si](C)(C)C	2874.1	Semi standard non polar	33892256
N-Acetyllactosamine,3TMS,isomer #3	CC(=O)N[C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)[C@@H]1O	2906.6	Semi standard non polar	33892256
N-Acetyllactosamine,3TMS,isomer #30	CC(=O)N([C@H]1[C@H](O)O[C@H](CO[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)[C@@H]1O)[Si](C)(C)C	2908.6	Semi standard non polar	33892256
N-Acetyllactosamine,3TMS,isomer #31	CC(=O)N[C@H]1[C@H](O)O[C@H](CO[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)[C@@H]1O	2891.8	Semi standard non polar	33892256
N-Acetyllactosamine,3TMS,isomer #32	CC(=O)N[C@H]1[C@H](O)O[C@H](CO[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)[C@@H]1O[Si](C)(C)C	2898.2	Semi standard non polar	33892256
N-Acetyllactosamine,3TMS,isomer #33	CC(=O)N([C@H]1[C@H](O)O[C@H](CO[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)[C@@H]1O)[Si](C)(C)C	2906.5	Semi standard non polar	33892256
N-Acetyllactosamine,3TMS,isomer #34	CC(=O)N[C@H]1[C@H](O)O[C@H](CO[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2857.6	Semi standard non polar	33892256
N-Acetyllactosamine,3TMS,isomer #35	CC(=O)N([C@H]1[C@H](O)O[C@H](CO[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)[C@@H]1O)[Si](C)(C)C	2911.2	Semi standard non polar	33892256
N-Acetyllactosamine,3TMS,isomer #36	CC(=O)N([C@H]1[C@H](O)O[C@H](CO[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O)[C@H]2O)[C@@H]1O[Si](C)(C)C)[Si](C)(C)C	2919.7	Semi standard non polar	33892256
N-Acetyllactosamine,3TMS,isomer #37	CC(=O)N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O)[C@@H]1O	2913.4	Semi standard non polar	33892256
N-Acetyllactosamine,3TMS,isomer #38	CC(=O)N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]2O[Si](C)(C)C)[C@@H]1O	2914.8	Semi standard non polar	33892256
N-Acetyllactosamine,3TMS,isomer #39	CC(=O)N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)[C@@H]1O[Si](C)(C)C	2874.4	Semi standard non polar	33892256
N-Acetyllactosamine,3TMS,isomer #4	CC(=O)N[C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)[C@@H]1O	2870.8	Semi standard non polar	33892256
N-Acetyllactosamine,3TMS,isomer #40	CC(=O)N([C@H]1[C@H](O)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)[C@@H]1O)[Si](C)(C)C	2911.7	Semi standard non polar	33892256
N-Acetyllactosamine,3TMS,isomer #41	CC(=O)N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)[C@@H]1O	2894.0	Semi standard non polar	33892256
N-Acetyllactosamine,3TMS,isomer #42	CC(=O)N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)[C@@H]1O[Si](C)(C)C	2890.2	Semi standard non polar	33892256
N-Acetyllactosamine,3TMS,isomer #43	CC(=O)N([C@H]1[C@H](O)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)[C@@H]1O)[Si](C)(C)C	2905.3	Semi standard non polar	33892256
N-Acetyllactosamine,3TMS,isomer #44	CC(=O)N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2852.7	Semi standard non polar	33892256
N-Acetyllactosamine,3TMS,isomer #45	CC(=O)N([C@H]1[C@H](O)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)[C@@H]1O)[Si](C)(C)C	2898.1	Semi standard non polar	33892256
N-Acetyllactosamine,3TMS,isomer #46	CC(=O)N([C@H]1[C@H](O)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]2O)[C@@H]1O[Si](C)(C)C)[Si](C)(C)C	2910.4	Semi standard non polar	33892256
N-Acetyllactosamine,3TMS,isomer #47	CC(=O)N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)[C@@H]1O	2921.2	Semi standard non polar	33892256
N-Acetyllactosamine,3TMS,isomer #48	CC(=O)N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O)[C@@H]1O[Si](C)(C)C	2921.3	Semi standard non polar	33892256
N-Acetyllactosamine,3TMS,isomer #49	CC(=O)N([C@H]1[C@H](O)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O)[C@@H]1O)[Si](C)(C)C	2911.8	Semi standard non polar	33892256
N-Acetyllactosamine,3TMS,isomer #5	CC(=O)N[C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O)[C@H]2O)[C@@H]1O[Si](C)(C)C	2839.8	Semi standard non polar	33892256
N-Acetyllactosamine,3TMS,isomer #50	CC(=O)N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]2O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2908.0	Semi standard non polar	33892256
N-Acetyllactosamine,3TMS,isomer #51	CC(=O)N([C@H]1[C@H](O)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]2O[Si](C)(C)C)[C@@H]1O)[Si](C)(C)C	2908.6	Semi standard non polar	33892256
N-Acetyllactosamine,3TMS,isomer #52	CC(=O)N([C@H]1[C@H](O)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)[C@@H]1O[Si](C)(C)C)[Si](C)(C)C	2913.8	Semi standard non polar	33892256
N-Acetyllactosamine,3TMS,isomer #53	CC(=O)N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2900.0	Semi standard non polar	33892256
N-Acetyllactosamine,3TMS,isomer #54	CC(=O)N([C@H]1[C@H](O)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)[C@@H]1O)[Si](C)(C)C	2907.7	Semi standard non polar	33892256
N-Acetyllactosamine,3TMS,isomer #55	CC(=O)N([C@H]1[C@H](O)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)[C@@H]1O[Si](C)(C)C)[Si](C)(C)C	2911.8	Semi standard non polar	33892256
N-Acetyllactosamine,3TMS,isomer #56	CC(=O)N([C@H]1[C@H](O)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C)[Si](C)(C)C	2914.3	Semi standard non polar	33892256
N-Acetyllactosamine,3TMS,isomer #6	CC(=O)N([C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O)[C@H]2O)[C@@H]1O)[Si](C)(C)C	2914.5	Semi standard non polar	33892256
N-Acetyllactosamine,3TMS,isomer #7	CC(=O)N[C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)[C@@H]1O	2892.4	Semi standard non polar	33892256
N-Acetyllactosamine,3TMS,isomer #8	CC(=O)N[C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)[C@@H]1O	2902.2	Semi standard non polar	33892256
N-Acetyllactosamine,3TMS,isomer #9	CC(=O)N[C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)[C@@H]1O	2873.7	Semi standard non polar	33892256
N-Acetyllactosamine,4TMS,isomer #1	CC(=O)N[C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)[C@@H]1O	2878.1	Semi standard non polar	33892256
N-Acetyllactosamine,4TMS,isomer #10	CC(=O)N[C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)[C@@H]1O	2896.0	Semi standard non polar	33892256
N-Acetyllactosamine,4TMS,isomer #11	CC(=O)N[C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)[C@@H]1O[Si](C)(C)C	2904.1	Semi standard non polar	33892256
N-Acetyllactosamine,4TMS,isomer #12	CC(=O)N([C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)[C@@H]1O)[Si](C)(C)C	2893.0	Semi standard non polar	33892256
N-Acetyllactosamine,4TMS,isomer #13	CC(=O)N[C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2846.0	Semi standard non polar	33892256
N-Acetyllactosamine,4TMS,isomer #14	CC(=O)N([C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)[C@@H]1O)[Si](C)(C)C	2869.2	Semi standard non polar	33892256
N-Acetyllactosamine,4TMS,isomer #15	CC(=O)N([C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O)[C@H]2O)[C@@H]1O[Si](C)(C)C)[Si](C)(C)C	2890.9	Semi standard non polar	33892256
N-Acetyllactosamine,4TMS,isomer #16	CC(=O)N[C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O)[C@@H]1O	2921.5	Semi standard non polar	33892256
N-Acetyllactosamine,4TMS,isomer #17	CC(=O)N[C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]2O[Si](C)(C)C)[C@@H]1O	2924.9	Semi standard non polar	33892256
N-Acetyllactosamine,4TMS,isomer #18	CC(=O)N[C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)[C@@H]1O[Si](C)(C)C	2863.0	Semi standard non polar	33892256
N-Acetyllactosamine,4TMS,isomer #19	CC(=O)N([C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)[C@@H]1O)[Si](C)(C)C	2889.6	Semi standard non polar	33892256
N-Acetyllactosamine,4TMS,isomer #2	CC(=O)N[C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)[C@@H]1O	2899.0	Semi standard non polar	33892256
N-Acetyllactosamine,4TMS,isomer #20	CC(=O)N[C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)[C@@H]1O	2904.5	Semi standard non polar	33892256
N-Acetyllactosamine,4TMS,isomer #21	CC(=O)N[C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)[C@@H]1O[Si](C)(C)C	2889.1	Semi standard non polar	33892256
N-Acetyllactosamine,4TMS,isomer #22	CC(=O)N([C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)[C@@H]1O)[Si](C)(C)C	2894.0	Semi standard non polar	33892256
N-Acetyllactosamine,4TMS,isomer #23	CC(=O)N[C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2841.3	Semi standard non polar	33892256
N-Acetyllactosamine,4TMS,isomer #24	CC(=O)N([C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)[C@@H]1O)[Si](C)(C)C	2871.4	Semi standard non polar	33892256
N-Acetyllactosamine,4TMS,isomer #25	CC(=O)N([C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]2O)[C@@H]1O[Si](C)(C)C)[Si](C)(C)C	2893.3	Semi standard non polar	33892256
N-Acetyllactosamine,4TMS,isomer #26	CC(=O)N[C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)[C@@H]1O	2923.0	Semi standard non polar	33892256
N-Acetyllactosamine,4TMS,isomer #27	CC(=O)N[C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O)[C@@H]1O[Si](C)(C)C	2912.0	Semi standard non polar	33892256
N-Acetyllactosamine,4TMS,isomer #28	CC(=O)N([C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O)[C@@H]1O)[Si](C)(C)C	2913.0	Semi standard non polar	33892256
N-Acetyllactosamine,4TMS,isomer #29	CC(=O)N[C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]2O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2894.6	Semi standard non polar	33892256
N-Acetyllactosamine,4TMS,isomer #3	CC(=O)N[C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)[C@@H]1O	2858.9	Semi standard non polar	33892256
N-Acetyllactosamine,4TMS,isomer #30	CC(=O)N([C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]2O[Si](C)(C)C)[C@@H]1O)[Si](C)(C)C	2902.3	Semi standard non polar	33892256
N-Acetyllactosamine,4TMS,isomer #31	CC(=O)N([C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)[C@@H]1O[Si](C)(C)C)[Si](C)(C)C	2921.6	Semi standard non polar	33892256
N-Acetyllactosamine,4TMS,isomer #32	CC(=O)N[C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2893.4	Semi standard non polar	33892256
N-Acetyllactosamine,4TMS,isomer #33	CC(=O)N([C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)[C@@H]1O)[Si](C)(C)C	2898.3	Semi standard non polar	33892256
N-Acetyllactosamine,4TMS,isomer #34	CC(=O)N([C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)[C@@H]1O[Si](C)(C)C)[Si](C)(C)C	2928.7	Semi standard non polar	33892256
N-Acetyllactosamine,4TMS,isomer #35	CC(=O)N([C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C)[Si](C)(C)C	2912.7	Semi standard non polar	33892256
N-Acetyllactosamine,4TMS,isomer #36	CC(=O)N[C@H]1[C@H](O)O[C@H](CO[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O)[C@@H]1O	2912.8	Semi standard non polar	33892256
N-Acetyllactosamine,4TMS,isomer #37	CC(=O)N[C@H]1[C@H](O)O[C@H](CO[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]2O[Si](C)(C)C)[C@@H]1O	2917.4	Semi standard non polar	33892256
N-Acetyllactosamine,4TMS,isomer #38	CC(=O)N[C@H]1[C@H](O)O[C@H](CO[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)[C@@H]1O[Si](C)(C)C	2872.8	Semi standard non polar	33892256
N-Acetyllactosamine,4TMS,isomer #39	CC(=O)N([C@H]1[C@H](O)O[C@H](CO[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)[C@@H]1O)[Si](C)(C)C	2887.8	Semi standard non polar	33892256
N-Acetyllactosamine,4TMS,isomer #4	CC(=O)N[C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]2O)[C@@H]1O[Si](C)(C)C	2823.2	Semi standard non polar	33892256
N-Acetyllactosamine,4TMS,isomer #40	CC(=O)N[C@H]1[C@H](O)O[C@H](CO[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)[C@@H]1O	2894.6	Semi standard non polar	33892256
N-Acetyllactosamine,4TMS,isomer #41	CC(=O)N[C@H]1[C@H](O)O[C@H](CO[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)[C@@H]1O[Si](C)(C)C	2892.6	Semi standard non polar	33892256
N-Acetyllactosamine,4TMS,isomer #42	CC(=O)N([C@H]1[C@H](O)O[C@H](CO[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)[C@@H]1O)[Si](C)(C)C	2895.5	Semi standard non polar	33892256
N-Acetyllactosamine,4TMS,isomer #43	CC(=O)N[C@H]1[C@H](O)O[C@H](CO[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2852.8	Semi standard non polar	33892256
N-Acetyllactosamine,4TMS,isomer #44	CC(=O)N([C@H]1[C@H](O)O[C@H](CO[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)[C@@H]1O)[Si](C)(C)C	2874.4	Semi standard non polar	33892256
N-Acetyllactosamine,4TMS,isomer #45	CC(=O)N([C@H]1[C@H](O)O[C@H](CO[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]2O)[C@@H]1O[Si](C)(C)C)[Si](C)(C)C	2873.3	Semi standard non polar	33892256
N-Acetyllactosamine,4TMS,isomer #46	CC(=O)N[C@H]1[C@H](O)O[C@H](CO[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)[C@@H]1O	2913.5	Semi standard non polar	33892256
N-Acetyllactosamine,4TMS,isomer #47	CC(=O)N[C@H]1[C@H](O)O[C@H](CO[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O)[C@@H]1O[Si](C)(C)C	2918.9	Semi standard non polar	33892256
N-Acetyllactosamine,4TMS,isomer #48	CC(=O)N([C@H]1[C@H](O)O[C@H](CO[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O)[C@@H]1O)[Si](C)(C)C	2901.7	Semi standard non polar	33892256
N-Acetyllactosamine,4TMS,isomer #49	CC(=O)N[C@H]1[C@H](O)O[C@H](CO[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]2O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2901.9	Semi standard non polar	33892256
N-Acetyllactosamine,4TMS,isomer #5	CC(=O)N([C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]2O)[C@@H]1O)[Si](C)(C)C	2866.5	Semi standard non polar	33892256
N-Acetyllactosamine,4TMS,isomer #50	CC(=O)N([C@H]1[C@H](O)O[C@H](CO[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]2O[Si](C)(C)C)[C@@H]1O)[Si](C)(C)C	2893.0	Semi standard non polar	33892256
N-Acetyllactosamine,4TMS,isomer #51	CC(=O)N([C@H]1[C@H](O)O[C@H](CO[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)[C@@H]1O[Si](C)(C)C)[Si](C)(C)C	2882.0	Semi standard non polar	33892256
N-Acetyllactosamine,4TMS,isomer #52	CC(=O)N[C@H]1[C@H](O)O[C@H](CO[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2894.7	Semi standard non polar	33892256
N-Acetyllactosamine,4TMS,isomer #53	CC(=O)N([C@H]1[C@H](O)O[C@H](CO[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)[C@@H]1O)[Si](C)(C)C	2887.6	Semi standard non polar	33892256
N-Acetyllactosamine,4TMS,isomer #54	CC(=O)N([C@H]1[C@H](O)O[C@H](CO[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)[C@@H]1O[Si](C)(C)C)[Si](C)(C)C	2897.7	Semi standard non polar	33892256
N-Acetyllactosamine,4TMS,isomer #55	CC(=O)N([C@H]1[C@H](O)O[C@H](CO[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C)[Si](C)(C)C	2873.4	Semi standard non polar	33892256
N-Acetyllactosamine,4TMS,isomer #56	CC(=O)N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)[C@@H]1O	2918.9	Semi standard non polar	33892256
N-Acetyllactosamine,4TMS,isomer #57	CC(=O)N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O)[C@@H]1O[Si](C)(C)C	2910.6	Semi standard non polar	33892256
N-Acetyllactosamine,4TMS,isomer #58	CC(=O)N([C@H]1[C@H](O)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O)[C@@H]1O)[Si](C)(C)C	2904.0	Semi standard non polar	33892256
N-Acetyllactosamine,4TMS,isomer #59	CC(=O)N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]2O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2913.1	Semi standard non polar	33892256
N-Acetyllactosamine,4TMS,isomer #6	CC(=O)N[C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O)[C@@H]1O	2923.5	Semi standard non polar	33892256
N-Acetyllactosamine,4TMS,isomer #60	CC(=O)N([C@H]1[C@H](O)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]2O[Si](C)(C)C)[C@@H]1O)[Si](C)(C)C	2898.3	Semi standard non polar	33892256
N-Acetyllactosamine,4TMS,isomer #61	CC(=O)N([C@H]1[C@H](O)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)[C@@H]1O[Si](C)(C)C)[Si](C)(C)C	2888.3	Semi standard non polar	33892256
N-Acetyllactosamine,4TMS,isomer #62	CC(=O)N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2891.9	Semi standard non polar	33892256
N-Acetyllactosamine,4TMS,isomer #63	CC(=O)N([C@H]1[C@H](O)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)[C@@H]1O)[Si](C)(C)C	2886.3	Semi standard non polar	33892256
N-Acetyllactosamine,4TMS,isomer #64	CC(=O)N([C@H]1[C@H](O)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)[C@@H]1O[Si](C)(C)C)[Si](C)(C)C	2892.7	Semi standard non polar	33892256
N-Acetyllactosamine,4TMS,isomer #65	CC(=O)N([C@H]1[C@H](O)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C)[Si](C)(C)C	2871.6	Semi standard non polar	33892256
N-Acetyllactosamine,4TMS,isomer #66	CC(=O)N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2905.4	Semi standard non polar	33892256
N-Acetyllactosamine,4TMS,isomer #67	CC(=O)N([C@H]1[C@H](O)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)[C@@H]1O)[Si](C)(C)C	2905.4	Semi standard non polar	33892256
N-Acetyllactosamine,4TMS,isomer #68	CC(=O)N([C@H]1[C@H](O)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O)[C@@H]1O[Si](C)(C)C)[Si](C)(C)C	2914.4	Semi standard non polar	33892256
N-Acetyllactosamine,4TMS,isomer #69	CC(=O)N([C@H]1[C@H](O)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]2O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C)[Si](C)(C)C	2899.9	Semi standard non polar	33892256
N-Acetyllactosamine,4TMS,isomer #7	CC(=O)N[C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]2O[Si](C)(C)C)[C@@H]1O	2906.3	Semi standard non polar	33892256
N-Acetyllactosamine,4TMS,isomer #70	CC(=O)N([C@H]1[C@H](O)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C)[Si](C)(C)C	2904.2	Semi standard non polar	33892256
N-Acetyllactosamine,4TMS,isomer #8	CC(=O)N[C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)[C@@H]1O[Si](C)(C)C	2869.5	Semi standard non polar	33892256
N-Acetyllactosamine,4TMS,isomer #9	CC(=O)N([C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)[C@@H]1O)[Si](C)(C)C	2877.3	Semi standard non polar	33892256
N-Acetyllactosamine,5TMS,isomer #1	CC(=O)N[C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O)[C@@H]1O	2887.2	Semi standard non polar	33892256
N-Acetyllactosamine,5TMS,isomer #10	CC(=O)N([C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]2O)[C@@H]1O[Si](C)(C)C)[Si](C)(C)C	2908.7	Semi standard non polar	33892256
N-Acetyllactosamine,5TMS,isomer #11	CC(=O)N[C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)[C@@H]1O	2872.7	Semi standard non polar	33892256
N-Acetyllactosamine,5TMS,isomer #12	CC(=O)N[C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O)[C@@H]1O[Si](C)(C)C	2877.3	Semi standard non polar	33892256
N-Acetyllactosamine,5TMS,isomer #13	CC(=O)N([C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O)[C@@H]1O)[Si](C)(C)C	2911.7	Semi standard non polar	33892256
N-Acetyllactosamine,5TMS,isomer #14	CC(=O)N[C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]2O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2860.9	Semi standard non polar	33892256
N-Acetyllactosamine,5TMS,isomer #15	CC(=O)N([C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]2O[Si](C)(C)C)[C@@H]1O)[Si](C)(C)C	2894.2	Semi standard non polar	33892256
N-Acetyllactosamine,5TMS,isomer #16	CC(=O)N([C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)[C@@H]1O[Si](C)(C)C)[Si](C)(C)C	2924.6	Semi standard non polar	33892256
N-Acetyllactosamine,5TMS,isomer #17	CC(=O)N[C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2851.7	Semi standard non polar	33892256
N-Acetyllactosamine,5TMS,isomer #18	CC(=O)N([C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)[C@@H]1O)[Si](C)(C)C	2894.3	Semi standard non polar	33892256
N-Acetyllactosamine,5TMS,isomer #19	CC(=O)N([C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)[C@@H]1O[Si](C)(C)C)[Si](C)(C)C	2921.0	Semi standard non polar	33892256
N-Acetyllactosamine,5TMS,isomer #2	CC(=O)N[C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]2O[Si](C)(C)C)[C@@H]1O	2881.3	Semi standard non polar	33892256
N-Acetyllactosamine,5TMS,isomer #20	CC(=O)N([C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C)[Si](C)(C)C	2909.4	Semi standard non polar	33892256
N-Acetyllactosamine,5TMS,isomer #21	CC(=O)N[C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)[C@@H]1O	2869.6	Semi standard non polar	33892256
N-Acetyllactosamine,5TMS,isomer #22	CC(=O)N[C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O)[C@@H]1O[Si](C)(C)C	2871.8	Semi standard non polar	33892256
N-Acetyllactosamine,5TMS,isomer #23	CC(=O)N([C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O)[C@@H]1O)[Si](C)(C)C	2908.4	Semi standard non polar	33892256
N-Acetyllactosamine,5TMS,isomer #24	CC(=O)N[C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]2O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2863.9	Semi standard non polar	33892256
N-Acetyllactosamine,5TMS,isomer #25	CC(=O)N([C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]2O[Si](C)(C)C)[C@@H]1O)[Si](C)(C)C	2899.6	Semi standard non polar	33892256
N-Acetyllactosamine,5TMS,isomer #26	CC(=O)N([C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)[C@@H]1O[Si](C)(C)C)[Si](C)(C)C	2917.2	Semi standard non polar	33892256
N-Acetyllactosamine,5TMS,isomer #27	CC(=O)N[C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2847.2	Semi standard non polar	33892256
N-Acetyllactosamine,5TMS,isomer #28	CC(=O)N([C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)[C@@H]1O)[Si](C)(C)C	2891.5	Semi standard non polar	33892256
N-Acetyllactosamine,5TMS,isomer #29	CC(=O)N([C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)[C@@H]1O[Si](C)(C)C)[Si](C)(C)C	2908.2	Semi standard non polar	33892256
N-Acetyllactosamine,5TMS,isomer #3	CC(=O)N[C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)[C@@H]1O[Si](C)(C)C	2854.6	Semi standard non polar	33892256
N-Acetyllactosamine,5TMS,isomer #30	CC(=O)N([C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C)[Si](C)(C)C	2903.2	Semi standard non polar	33892256
N-Acetyllactosamine,5TMS,isomer #31	CC(=O)N[C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2866.8	Semi standard non polar	33892256
N-Acetyllactosamine,5TMS,isomer #32	CC(=O)N([C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)[C@@H]1O)[Si](C)(C)C	2919.4	Semi standard non polar	33892256
N-Acetyllactosamine,5TMS,isomer #33	CC(=O)N([C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O)[C@@H]1O[Si](C)(C)C)[Si](C)(C)C	2940.8	Semi standard non polar	33892256
N-Acetyllactosamine,5TMS,isomer #34	CC(=O)N([C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]2O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C)[Si](C)(C)C	2923.7	Semi standard non polar	33892256
N-Acetyllactosamine,5TMS,isomer #35	CC(=O)N([C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C)[Si](C)(C)C	2924.8	Semi standard non polar	33892256
N-Acetyllactosamine,5TMS,isomer #36	CC(=O)N[C@H]1[C@H](O)O[C@H](CO[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)[C@@H]1O	2890.6	Semi standard non polar	33892256
N-Acetyllactosamine,5TMS,isomer #37	CC(=O)N[C@H]1[C@H](O)O[C@H](CO[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O)[C@@H]1O[Si](C)(C)C	2888.8	Semi standard non polar	33892256
N-Acetyllactosamine,5TMS,isomer #38	CC(=O)N([C@H]1[C@H](O)O[C@H](CO[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O)[C@@H]1O)[Si](C)(C)C	2917.1	Semi standard non polar	33892256
N-Acetyllactosamine,5TMS,isomer #39	CC(=O)N[C@H]1[C@H](O)O[C@H](CO[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]2O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2883.6	Semi standard non polar	33892256
N-Acetyllactosamine,5TMS,isomer #4	CC(=O)N([C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)[C@@H]1O)[Si](C)(C)C	2900.4	Semi standard non polar	33892256
N-Acetyllactosamine,5TMS,isomer #40	CC(=O)N([C@H]1[C@H](O)O[C@H](CO[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]2O[Si](C)(C)C)[C@@H]1O)[Si](C)(C)C	2910.6	Semi standard non polar	33892256
N-Acetyllactosamine,5TMS,isomer #41	CC(=O)N([C@H]1[C@H](O)O[C@H](CO[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)[C@@H]1O[Si](C)(C)C)[Si](C)(C)C	2902.0	Semi standard non polar	33892256
N-Acetyllactosamine,5TMS,isomer #42	CC(=O)N[C@H]1[C@H](O)O[C@H](CO[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2869.1	Semi standard non polar	33892256
N-Acetyllactosamine,5TMS,isomer #43	CC(=O)N([C@H]1[C@H](O)O[C@H](CO[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)[C@@H]1O)[Si](C)(C)C	2900.1	Semi standard non polar	33892256
N-Acetyllactosamine,5TMS,isomer #44	CC(=O)N([C@H]1[C@H](O)O[C@H](CO[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)[C@@H]1O[Si](C)(C)C)[Si](C)(C)C	2902.5	Semi standard non polar	33892256
N-Acetyllactosamine,5TMS,isomer #45	CC(=O)N([C@H]1[C@H](O)O[C@H](CO[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C)[Si](C)(C)C	2889.0	Semi standard non polar	33892256
N-Acetyllactosamine,5TMS,isomer #46	CC(=O)N[C@H]1[C@H](O)O[C@H](CO[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2860.5	Semi standard non polar	33892256
N-Acetyllactosamine,5TMS,isomer #47	CC(=O)N([C@H]1[C@H](O)O[C@H](CO[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)[C@@H]1O)[Si](C)(C)C	2908.0	Semi standard non polar	33892256
N-Acetyllactosamine,5TMS,isomer #48	CC(=O)N([C@H]1[C@H](O)O[C@H](CO[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O)[C@@H]1O[Si](C)(C)C)[Si](C)(C)C	2913.8	Semi standard non polar	33892256
N-Acetyllactosamine,5TMS,isomer #49	CC(=O)N([C@H]1[C@H](O)O[C@H](CO[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]2O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C)[Si](C)(C)C	2893.2	Semi standard non polar	33892256
N-Acetyllactosamine,5TMS,isomer #5	CC(=O)N[C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)[C@@H]1O	2869.8	Semi standard non polar	33892256
N-Acetyllactosamine,5TMS,isomer #50	CC(=O)N([C@H]1[C@H](O)O[C@H](CO[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C)[Si](C)(C)C	2896.9	Semi standard non polar	33892256
N-Acetyllactosamine,5TMS,isomer #51	CC(=O)N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2865.0	Semi standard non polar	33892256
N-Acetyllactosamine,5TMS,isomer #52	CC(=O)N([C@H]1[C@H](O)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)[C@@H]1O)[Si](C)(C)C	2899.4	Semi standard non polar	33892256
N-Acetyllactosamine,5TMS,isomer #53	CC(=O)N([C@H]1[C@H](O)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O)[C@@H]1O[Si](C)(C)C)[Si](C)(C)C	2907.9	Semi standard non polar	33892256
N-Acetyllactosamine,5TMS,isomer #54	CC(=O)N([C@H]1[C@H](O)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]2O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C)[Si](C)(C)C	2898.2	Semi standard non polar	33892256
N-Acetyllactosamine,5TMS,isomer #55	CC(=O)N([C@H]1[C@H](O)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C)[Si](C)(C)C	2892.9	Semi standard non polar	33892256
N-Acetyllactosamine,5TMS,isomer #56	CC(=O)N([C@H]1[C@H](O)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C)[Si](C)(C)C	2917.4	Semi standard non polar	33892256
N-Acetyllactosamine,5TMS,isomer #6	CC(=O)N[C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)[C@@H]1O[Si](C)(C)C	2870.0	Semi standard non polar	33892256
N-Acetyllactosamine,5TMS,isomer #7	CC(=O)N([C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)[C@@H]1O)[Si](C)(C)C	2900.6	Semi standard non polar	33892256
N-Acetyllactosamine,5TMS,isomer #8	CC(=O)N[C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2830.0	Semi standard non polar	33892256
N-Acetyllactosamine,5TMS,isomer #9	CC(=O)N([C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)[C@@H]1O)[Si](C)(C)C	2888.4	Semi standard non polar	33892256
N-Acetyllactosamine,6TMS,isomer #1	CC(=O)N[C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)[C@@H]1O	2861.2	Semi standard non polar	33892256
N-Acetyllactosamine,6TMS,isomer #10	CC(=O)N([C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C)[Si](C)(C)C	2913.5	Semi standard non polar	33892256
N-Acetyllactosamine,6TMS,isomer #11	CC(=O)N[C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2849.0	Semi standard non polar	33892256
N-Acetyllactosamine,6TMS,isomer #12	CC(=O)N([C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)[C@@H]1O)[Si](C)(C)C	2938.6	Semi standard non polar	33892256
N-Acetyllactosamine,6TMS,isomer #13	CC(=O)N([C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O)[C@@H]1O[Si](C)(C)C)[Si](C)(C)C	2947.0	Semi standard non polar	33892256
N-Acetyllactosamine,6TMS,isomer #14	CC(=O)N([C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]2O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C)[Si](C)(C)C	2926.7	Semi standard non polar	33892256
N-Acetyllactosamine,6TMS,isomer #15	CC(=O)N([C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C)[Si](C)(C)C	2920.5	Semi standard non polar	33892256
N-Acetyllactosamine,6TMS,isomer #16	CC(=O)N[C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2854.3	Semi standard non polar	33892256
N-Acetyllactosamine,6TMS,isomer #17	CC(=O)N([C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)[C@@H]1O)[Si](C)(C)C	2931.7	Semi standard non polar	33892256
N-Acetyllactosamine,6TMS,isomer #18	CC(=O)N([C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O)[C@@H]1O[Si](C)(C)C)[Si](C)(C)C	2937.1	Semi standard non polar	33892256
N-Acetyllactosamine,6TMS,isomer #19	CC(=O)N([C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]2O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C)[Si](C)(C)C	2917.9	Semi standard non polar	33892256
N-Acetyllactosamine,6TMS,isomer #2	CC(=O)N[C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O)[C@@H]1O[Si](C)(C)C	2861.7	Semi standard non polar	33892256
N-Acetyllactosamine,6TMS,isomer #20	CC(=O)N([C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C)[Si](C)(C)C	2917.6	Semi standard non polar	33892256
N-Acetyllactosamine,6TMS,isomer #21	CC(=O)N([C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C)[Si](C)(C)C	2945.9	Semi standard non polar	33892256
N-Acetyllactosamine,6TMS,isomer #22	CC(=O)N[C@H]1[C@H](O)O[C@H](CO[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2857.6	Semi standard non polar	33892256
N-Acetyllactosamine,6TMS,isomer #23	CC(=O)N([C@H]1[C@H](O)O[C@H](CO[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)[C@@H]1O)[Si](C)(C)C	2925.5	Semi standard non polar	33892256
N-Acetyllactosamine,6TMS,isomer #24	CC(=O)N([C@H]1[C@H](O)O[C@H](CO[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O)[C@@H]1O[Si](C)(C)C)[Si](C)(C)C	2933.3	Semi standard non polar	33892256
N-Acetyllactosamine,6TMS,isomer #25	CC(=O)N([C@H]1[C@H](O)O[C@H](CO[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]2O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C)[Si](C)(C)C	2915.9	Semi standard non polar	33892256
N-Acetyllactosamine,6TMS,isomer #26	CC(=O)N([C@H]1[C@H](O)O[C@H](CO[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C)[Si](C)(C)C	2917.4	Semi standard non polar	33892256
N-Acetyllactosamine,6TMS,isomer #27	CC(=O)N([C@H]1[C@H](O)O[C@H](CO[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C)[Si](C)(C)C	2929.9	Semi standard non polar	33892256
N-Acetyllactosamine,6TMS,isomer #28	CC(=O)N([C@H]1[C@H](O)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C)[Si](C)(C)C	2927.2	Semi standard non polar	33892256
N-Acetyllactosamine,6TMS,isomer #3	CC(=O)N([C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O)[C@@H]1O)[Si](C)(C)C	2936.6	Semi standard non polar	33892256
N-Acetyllactosamine,6TMS,isomer #4	CC(=O)N[C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]2O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2843.2	Semi standard non polar	33892256
N-Acetyllactosamine,6TMS,isomer #5	CC(=O)N([C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]2O[Si](C)(C)C)[C@@H]1O)[Si](C)(C)C	2916.2	Semi standard non polar	33892256
N-Acetyllactosamine,6TMS,isomer #6	CC(=O)N([C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)[C@@H]1O[Si](C)(C)C)[Si](C)(C)C	2930.0	Semi standard non polar	33892256
N-Acetyllactosamine,6TMS,isomer #7	CC(=O)N[C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2841.8	Semi standard non polar	33892256
N-Acetyllactosamine,6TMS,isomer #8	CC(=O)N([C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)[C@@H]1O)[Si](C)(C)C	2921.0	Semi standard non polar	33892256
N-Acetyllactosamine,6TMS,isomer #9	CC(=O)N([C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)[C@@H]1O[Si](C)(C)C)[Si](C)(C)C	2922.8	Semi standard non polar	33892256
N-Acetyllactosamine,7TMS,isomer #1	CC(=O)N[C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2870.4	Semi standard non polar	33892256
N-Acetyllactosamine,7TMS,isomer #2	CC(=O)N([C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)[C@@H]1O)[Si](C)(C)C	2960.1	Semi standard non polar	33892256
N-Acetyllactosamine,7TMS,isomer #3	CC(=O)N([C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O)[C@@H]1O[Si](C)(C)C)[Si](C)(C)C	2959.1	Semi standard non polar	33892256
N-Acetyllactosamine,7TMS,isomer #4	CC(=O)N([C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]2O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C)[Si](C)(C)C	2943.7	Semi standard non polar	33892256
N-Acetyllactosamine,7TMS,isomer #5	CC(=O)N([C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C)[Si](C)(C)C	2937.2	Semi standard non polar	33892256
N-Acetyllactosamine,7TMS,isomer #6	CC(=O)N([C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C)[Si](C)(C)C	2948.7	Semi standard non polar	33892256
N-Acetyllactosamine,7TMS,isomer #7	CC(=O)N([C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C)[Si](C)(C)C	2946.0	Semi standard non polar	33892256
N-Acetyllactosamine,7TMS,isomer #8	CC(=O)N([C@H]1[C@H](O)O[C@H](CO[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C)[Si](C)(C)C	2952.4	Semi standard non polar	33892256
N-Acetyllactosamine,1TBDMS,isomer #1	CC(=O)N[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O)[C@H]2O)[C@@H]1O	3258.6	Semi standard non polar	33892256
N-Acetyllactosamine,1TBDMS,isomer #2	CC(=O)N[C@H]1[C@H](O)O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O)[C@H]2O)[C@@H]1O	3259.5	Semi standard non polar	33892256
N-Acetyllactosamine,1TBDMS,isomer #3	CC(=O)N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C(C)(C)C)[C@H](O)[C@H](O)[C@H]2O)[C@@H]1O	3246.1	Semi standard non polar	33892256
N-Acetyllactosamine,1TBDMS,isomer #4	CC(=O)N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]2O)[C@@H]1O	3255.7	Semi standard non polar	33892256
N-Acetyllactosamine,1TBDMS,isomer #5	CC(=O)N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)[C@@H]1O	3261.9	Semi standard non polar	33892256
N-Acetyllactosamine,1TBDMS,isomer #6	CC(=O)N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)[C@@H]1O	3267.2	Semi standard non polar	33892256
N-Acetyllactosamine,1TBDMS,isomer #7	CC(=O)N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O)[C@H]2O)[C@@H]1O[Si](C)(C)C(C)(C)C	3273.7	Semi standard non polar	33892256
N-Acetyllactosamine,1TBDMS,isomer #8	CC(=O)N([C@H]1[C@H](O)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O)[C@H]2O)[C@@H]1O)[Si](C)(C)C(C)(C)C	3238.7	Semi standard non polar	33892256
N-Acetyllactosamine,2TBDMS,isomer #1	CC(=O)N[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O)[C@H]2O)[C@@H]1O	3426.6	Semi standard non polar	33892256
N-Acetyllactosamine,2TBDMS,isomer #10	CC(=O)N[C@H]1[C@H](O)O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)[C@@H]1O	3448.2	Semi standard non polar	33892256
N-Acetyllactosamine,2TBDMS,isomer #11	CC(=O)N[C@H]1[C@H](O)O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)[C@@H]1O	3451.8	Semi standard non polar	33892256
N-Acetyllactosamine,2TBDMS,isomer #12	CC(=O)N[C@H]1[C@H](O)O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O)[C@H]2O)[C@@H]1O[Si](C)(C)C(C)(C)C	3438.9	Semi standard non polar	33892256
N-Acetyllactosamine,2TBDMS,isomer #13	CC(=O)N([C@H]1[C@H](O)O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O)[C@H]2O)[C@@H]1O)[Si](C)(C)C(C)(C)C	3444.0	Semi standard non polar	33892256
N-Acetyllactosamine,2TBDMS,isomer #14	CC(=O)N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]2O)[C@@H]1O	3434.0	Semi standard non polar	33892256
N-Acetyllactosamine,2TBDMS,isomer #15	CC(=O)N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C(C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)[C@@H]1O	3439.0	Semi standard non polar	33892256
N-Acetyllactosamine,2TBDMS,isomer #16	CC(=O)N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C(C)(C)C)[C@H](O)[C@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)[C@@H]1O	3434.0	Semi standard non polar	33892256
N-Acetyllactosamine,2TBDMS,isomer #17	CC(=O)N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C(C)(C)C)[C@H](O)[C@H](O)[C@H]2O)[C@@H]1O[Si](C)(C)C(C)(C)C	3424.4	Semi standard non polar	33892256
N-Acetyllactosamine,2TBDMS,isomer #18	CC(=O)N([C@H]1[C@H](O)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C(C)(C)C)[C@H](O)[C@H](O)[C@H]2O)[C@@H]1O)[Si](C)(C)C(C)(C)C	3434.7	Semi standard non polar	33892256
N-Acetyllactosamine,2TBDMS,isomer #19	CC(=O)N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)[C@@H]1O	3435.8	Semi standard non polar	33892256
N-Acetyllactosamine,2TBDMS,isomer #2	CC(=O)N[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C(C)(C)C)[C@H](O)[C@H](O)[C@H]2O)[C@@H]1O	3428.1	Semi standard non polar	33892256
N-Acetyllactosamine,2TBDMS,isomer #20	CC(=O)N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)[C@@H]1O	3430.7	Semi standard non polar	33892256
N-Acetyllactosamine,2TBDMS,isomer #21	CC(=O)N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]2O)[C@@H]1O[Si](C)(C)C(C)(C)C	3437.8	Semi standard non polar	33892256
N-Acetyllactosamine,2TBDMS,isomer #22	CC(=O)N([C@H]1[C@H](O)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]2O)[C@@H]1O)[Si](C)(C)C(C)(C)C	3431.2	Semi standard non polar	33892256
N-Acetyllactosamine,2TBDMS,isomer #23	CC(=O)N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O[Si](C)(C)C(C)(C)C)[C@@H]1O	3442.4	Semi standard non polar	33892256
N-Acetyllactosamine,2TBDMS,isomer #24	CC(=O)N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)[C@@H]1O[Si](C)(C)C(C)(C)C	3442.7	Semi standard non polar	33892256
N-Acetyllactosamine,2TBDMS,isomer #25	CC(=O)N([C@H]1[C@H](O)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)[C@@H]1O)[Si](C)(C)C(C)(C)C	3425.3	Semi standard non polar	33892256
N-Acetyllactosamine,2TBDMS,isomer #26	CC(=O)N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C	3450.2	Semi standard non polar	33892256
N-Acetyllactosamine,2TBDMS,isomer #27	CC(=O)N([C@H]1[C@H](O)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)[C@@H]1O)[Si](C)(C)C(C)(C)C	3437.3	Semi standard non polar	33892256
N-Acetyllactosamine,2TBDMS,isomer #28	CC(=O)N([C@H]1[C@H](O)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O)[C@H]2O)[C@@H]1O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3439.4	Semi standard non polar	33892256
N-Acetyllactosamine,2TBDMS,isomer #3	CC(=O)N[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]2O)[C@@H]1O	3435.6	Semi standard non polar	33892256
N-Acetyllactosamine,2TBDMS,isomer #4	CC(=O)N[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)[C@@H]1O	3440.8	Semi standard non polar	33892256
N-Acetyllactosamine,2TBDMS,isomer #5	CC(=O)N[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)[C@@H]1O	3446.7	Semi standard non polar	33892256
N-Acetyllactosamine,2TBDMS,isomer #6	CC(=O)N[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O)[C@H]2O)[C@@H]1O[Si](C)(C)C(C)(C)C	3420.8	Semi standard non polar	33892256
N-Acetyllactosamine,2TBDMS,isomer #7	CC(=O)N([C@H]1[C@H](O[Si](C)(C)C(C)(C)C)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O)[C@H]2O)[C@@H]1O)[Si](C)(C)C(C)(C)C	3434.4	Semi standard non polar	33892256
N-Acetyllactosamine,2TBDMS,isomer #8	CC(=O)N[C@H]1[C@H](O)O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C(C)(C)C)[C@H](O)[C@H](O)[C@H]2O)[C@@H]1O	3446.7	Semi standard non polar	33892256
N-Acetyllactosamine,2TBDMS,isomer #9	CC(=O)N[C@H]1[C@H](O)O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]2O)[C@@H]1O	3445.0	Semi standard non polar	33892256
N-Acetyllactosamine,3TBDMS,isomer #1	CC(=O)N[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C(C)(C)C)[C@H](O)[C@H](O)[C@H]2O)[C@@H]1O	3600.7	Semi standard non polar	33892256
N-Acetyllactosamine,3TBDMS,isomer #10	CC(=O)N[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C(C)(C)C)[C@H](O)[C@H](O)[C@H]2O)[C@@H]1O[Si](C)(C)C(C)(C)C	3579.0	Semi standard non polar	33892256
N-Acetyllactosamine,3TBDMS,isomer #11	CC(=O)N([C@H]1[C@H](O[Si](C)(C)C(C)(C)C)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C(C)(C)C)[C@H](O)[C@H](O)[C@H]2O)[C@@H]1O)[Si](C)(C)C(C)(C)C	3594.8	Semi standard non polar	33892256
N-Acetyllactosamine,3TBDMS,isomer #12	CC(=O)N[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)[C@@H]1O	3603.2	Semi standard non polar	33892256
N-Acetyllactosamine,3TBDMS,isomer #13	CC(=O)N[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)[C@@H]1O	3610.2	Semi standard non polar	33892256
N-Acetyllactosamine,3TBDMS,isomer #14	CC(=O)N[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]2O)[C@@H]1O[Si](C)(C)C(C)(C)C	3592.0	Semi standard non polar	33892256
N-Acetyllactosamine,3TBDMS,isomer #15	CC(=O)N([C@H]1[C@H](O[Si](C)(C)C(C)(C)C)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]2O)[C@@H]1O)[Si](C)(C)C(C)(C)C	3604.9	Semi standard non polar	33892256
N-Acetyllactosamine,3TBDMS,isomer #16	CC(=O)N[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O[Si](C)(C)C(C)(C)C)[C@@H]1O	3609.2	Semi standard non polar	33892256
N-Acetyllactosamine,3TBDMS,isomer #17	CC(=O)N[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)[C@@H]1O[Si](C)(C)C(C)(C)C	3600.2	Semi standard non polar	33892256
N-Acetyllactosamine,3TBDMS,isomer #18	CC(=O)N([C@H]1[C@H](O[Si](C)(C)C(C)(C)C)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)[C@@H]1O)[Si](C)(C)C(C)(C)C	3603.5	Semi standard non polar	33892256
N-Acetyllactosamine,3TBDMS,isomer #19	CC(=O)N[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C	3601.9	Semi standard non polar	33892256
N-Acetyllactosamine,3TBDMS,isomer #2	CC(=O)N[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]2O)[C@@H]1O	3599.0	Semi standard non polar	33892256
N-Acetyllactosamine,3TBDMS,isomer #20	CC(=O)N([C@H]1[C@H](O[Si](C)(C)C(C)(C)C)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)[C@@H]1O)[Si](C)(C)C(C)(C)C	3610.5	Semi standard non polar	33892256
N-Acetyllactosamine,3TBDMS,isomer #21	CC(=O)N([C@H]1[C@H](O[Si](C)(C)C(C)(C)C)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O)[C@H]2O)[C@@H]1O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3614.0	Semi standard non polar	33892256
N-Acetyllactosamine,3TBDMS,isomer #22	CC(=O)N[C@H]1[C@H](O)O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]2O)[C@@H]1O	3616.4	Semi standard non polar	33892256
N-Acetyllactosamine,3TBDMS,isomer #23	CC(=O)N[C@H]1[C@H](O)O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C(C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)[C@@H]1O	3613.5	Semi standard non polar	33892256
N-Acetyllactosamine,3TBDMS,isomer #24	CC(=O)N[C@H]1[C@H](O)O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C(C)(C)C)[C@H](O)[C@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)[C@@H]1O	3621.0	Semi standard non polar	33892256
N-Acetyllactosamine,3TBDMS,isomer #25	CC(=O)N[C@H]1[C@H](O)O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C(C)(C)C)[C@H](O)[C@H](O)[C@H]2O)[C@@H]1O[Si](C)(C)C(C)(C)C	3596.9	Semi standard non polar	33892256
N-Acetyllactosamine,3TBDMS,isomer #26	CC(=O)N([C@H]1[C@H](O)O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C(C)(C)C)[C@H](O)[C@H](O)[C@H]2O)[C@@H]1O)[Si](C)(C)C(C)(C)C	3605.6	Semi standard non polar	33892256
N-Acetyllactosamine,3TBDMS,isomer #27	CC(=O)N[C@H]1[C@H](O)O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)[C@@H]1O	3600.0	Semi standard non polar	33892256
N-Acetyllactosamine,3TBDMS,isomer #28	CC(=O)N[C@H]1[C@H](O)O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)[C@@H]1O	3604.1	Semi standard non polar	33892256
N-Acetyllactosamine,3TBDMS,isomer #29	CC(=O)N[C@H]1[C@H](O)O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]2O)[C@@H]1O[Si](C)(C)C(C)(C)C	3597.0	Semi standard non polar	33892256
N-Acetyllactosamine,3TBDMS,isomer #3	CC(=O)N[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)[C@@H]1O	3610.4	Semi standard non polar	33892256
N-Acetyllactosamine,3TBDMS,isomer #30	CC(=O)N([C@H]1[C@H](O)O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]2O)[C@@H]1O)[Si](C)(C)C(C)(C)C	3610.7	Semi standard non polar	33892256
N-Acetyllactosamine,3TBDMS,isomer #31	CC(=O)N[C@H]1[C@H](O)O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O[Si](C)(C)C(C)(C)C)[C@@H]1O	3608.3	Semi standard non polar	33892256
N-Acetyllactosamine,3TBDMS,isomer #32	CC(=O)N[C@H]1[C@H](O)O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)[C@@H]1O[Si](C)(C)C(C)(C)C	3608.1	Semi standard non polar	33892256
N-Acetyllactosamine,3TBDMS,isomer #33	CC(=O)N([C@H]1[C@H](O)O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)[C@@H]1O)[Si](C)(C)C(C)(C)C	3609.9	Semi standard non polar	33892256
N-Acetyllactosamine,3TBDMS,isomer #34	CC(=O)N[C@H]1[C@H](O)O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C	3610.3	Semi standard non polar	33892256
N-Acetyllactosamine,3TBDMS,isomer #35	CC(=O)N([C@H]1[C@H](O)O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)[C@@H]1O)[Si](C)(C)C(C)(C)C	3615.7	Semi standard non polar	33892256
N-Acetyllactosamine,3TBDMS,isomer #36	CC(=O)N([C@H]1[C@H](O)O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O)[C@H]2O)[C@@H]1O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3604.2	Semi standard non polar	33892256
N-Acetyllactosamine,3TBDMS,isomer #37	CC(=O)N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)[C@@H]1O	3600.4	Semi standard non polar	33892256
N-Acetyllactosamine,3TBDMS,isomer #38	CC(=O)N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)[C@@H]1O	3607.8	Semi standard non polar	33892256
N-Acetyllactosamine,3TBDMS,isomer #39	CC(=O)N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]2O)[C@@H]1O[Si](C)(C)C(C)(C)C	3598.4	Semi standard non polar	33892256
N-Acetyllactosamine,3TBDMS,isomer #4	CC(=O)N[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)[C@@H]1O	3612.4	Semi standard non polar	33892256
N-Acetyllactosamine,3TBDMS,isomer #40	CC(=O)N([C@H]1[C@H](O)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]2O)[C@@H]1O)[Si](C)(C)C(C)(C)C	3601.5	Semi standard non polar	33892256
N-Acetyllactosamine,3TBDMS,isomer #41	CC(=O)N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C(C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O[Si](C)(C)C(C)(C)C)[C@@H]1O	3599.2	Semi standard non polar	33892256
N-Acetyllactosamine,3TBDMS,isomer #42	CC(=O)N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C(C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)[C@@H]1O[Si](C)(C)C(C)(C)C	3599.7	Semi standard non polar	33892256
N-Acetyllactosamine,3TBDMS,isomer #43	CC(=O)N([C@H]1[C@H](O)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C(C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)[C@@H]1O)[Si](C)(C)C(C)(C)C	3599.7	Semi standard non polar	33892256
N-Acetyllactosamine,3TBDMS,isomer #44	CC(=O)N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C(C)(C)C)[C@H](O)[C@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C	3604.9	Semi standard non polar	33892256
N-Acetyllactosamine,3TBDMS,isomer #45	CC(=O)N([C@H]1[C@H](O)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C(C)(C)C)[C@H](O)[C@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)[C@@H]1O)[Si](C)(C)C(C)(C)C	3607.3	Semi standard non polar	33892256
N-Acetyllactosamine,3TBDMS,isomer #46	CC(=O)N([C@H]1[C@H](O)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C(C)(C)C)[C@H](O)[C@H](O)[C@H]2O)[C@@H]1O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3590.8	Semi standard non polar	33892256
N-Acetyllactosamine,3TBDMS,isomer #47	CC(=O)N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O[Si](C)(C)C(C)(C)C)[C@@H]1O	3596.1	Semi standard non polar	33892256
N-Acetyllactosamine,3TBDMS,isomer #48	CC(=O)N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)[C@@H]1O[Si](C)(C)C(C)(C)C	3593.2	Semi standard non polar	33892256
N-Acetyllactosamine,3TBDMS,isomer #49	CC(=O)N([C@H]1[C@H](O)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)[C@@H]1O)[Si](C)(C)C(C)(C)C	3595.4	Semi standard non polar	33892256
N-Acetyllactosamine,3TBDMS,isomer #5	CC(=O)N[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O)[C@H]2O)[C@@H]1O[Si](C)(C)C(C)(C)C	3587.8	Semi standard non polar	33892256
N-Acetyllactosamine,3TBDMS,isomer #50	CC(=O)N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C	3605.8	Semi standard non polar	33892256
N-Acetyllactosamine,3TBDMS,isomer #51	CC(=O)N([C@H]1[C@H](O)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)[C@@H]1O)[Si](C)(C)C(C)(C)C	3601.4	Semi standard non polar	33892256
N-Acetyllactosamine,3TBDMS,isomer #52	CC(=O)N([C@H]1[C@H](O)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]2O)[C@@H]1O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3600.6	Semi standard non polar	33892256
N-Acetyllactosamine,3TBDMS,isomer #53	CC(=O)N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C	3600.9	Semi standard non polar	33892256
N-Acetyllactosamine,3TBDMS,isomer #54	CC(=O)N([C@H]1[C@H](O)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O[Si](C)(C)C(C)(C)C)[C@@H]1O)[Si](C)(C)C(C)(C)C	3593.6	Semi standard non polar	33892256
N-Acetyllactosamine,3TBDMS,isomer #55	CC(=O)N([C@H]1[C@H](O)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)[C@@H]1O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3602.1	Semi standard non polar	33892256
N-Acetyllactosamine,3TBDMS,isomer #56	CC(=O)N([C@H]1[C@H](O)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3609.3	Semi standard non polar	33892256
N-Acetyllactosamine,3TBDMS,isomer #6	CC(=O)N([C@H]1[C@H](O[Si](C)(C)C(C)(C)C)O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O)[C@H]2O)[C@@H]1O)[Si](C)(C)C(C)(C)C	3595.0	Semi standard non polar	33892256
N-Acetyllactosamine,3TBDMS,isomer #7	CC(=O)N[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]2O)[C@@H]1O	3605.8	Semi standard non polar	33892256
N-Acetyllactosamine,3TBDMS,isomer #8	CC(=O)N[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C(C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)[C@@H]1O	3608.7	Semi standard non polar	33892256
N-Acetyllactosamine,3TBDMS,isomer #9	CC(=O)N[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C(C)(C)C)[C@H](O)[C@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)[C@@H]1O	3613.7	Semi standard non polar	33892256
N-Acetyllactosamine,4TBDMS,isomer #1	CC(=O)N[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]2O)[C@@H]1O	3753.7	Semi standard non polar	33892256
N-Acetyllactosamine,4TBDMS,isomer #10	CC(=O)N[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O[Si](C)(C)C(C)(C)C)[C@@H]1O	3751.0	Semi standard non polar	33892256
N-Acetyllactosamine,4TBDMS,isomer #11	CC(=O)N[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)[C@@H]1O[Si](C)(C)C(C)(C)C	3740.4	Semi standard non polar	33892256
N-Acetyllactosamine,4TBDMS,isomer #12	CC(=O)N([C@H]1[C@H](O[Si](C)(C)C(C)(C)C)O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)[C@@H]1O)[Si](C)(C)C(C)(C)C	3784.3	Semi standard non polar	33892256
N-Acetyllactosamine,4TBDMS,isomer #13	CC(=O)N[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C	3741.5	Semi standard non polar	33892256
N-Acetyllactosamine,4TBDMS,isomer #14	CC(=O)N([C@H]1[C@H](O[Si](C)(C)C(C)(C)C)O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)[C@@H]1O)[Si](C)(C)C(C)(C)C	3777.6	Semi standard non polar	33892256
N-Acetyllactosamine,4TBDMS,isomer #15	CC(=O)N([C@H]1[C@H](O[Si](C)(C)C(C)(C)C)O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O)[C@H]2O)[C@@H]1O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3773.2	Semi standard non polar	33892256
N-Acetyllactosamine,4TBDMS,isomer #16	CC(=O)N[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)[C@@H]1O	3767.1	Semi standard non polar	33892256
N-Acetyllactosamine,4TBDMS,isomer #17	CC(=O)N[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)[C@@H]1O	3771.0	Semi standard non polar	33892256
N-Acetyllactosamine,4TBDMS,isomer #18	CC(=O)N[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]2O)[C@@H]1O[Si](C)(C)C(C)(C)C	3736.4	Semi standard non polar	33892256
N-Acetyllactosamine,4TBDMS,isomer #19	CC(=O)N([C@H]1[C@H](O[Si](C)(C)C(C)(C)C)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]2O)[C@@H]1O)[Si](C)(C)C(C)(C)C	3779.2	Semi standard non polar	33892256
N-Acetyllactosamine,4TBDMS,isomer #2	CC(=O)N[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C(C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)[C@@H]1O	3763.9	Semi standard non polar	33892256
N-Acetyllactosamine,4TBDMS,isomer #20	CC(=O)N[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C(C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O[Si](C)(C)C(C)(C)C)[C@@H]1O	3764.7	Semi standard non polar	33892256
N-Acetyllactosamine,4TBDMS,isomer #21	CC(=O)N[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C(C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)[C@@H]1O[Si](C)(C)C(C)(C)C	3737.3	Semi standard non polar	33892256
N-Acetyllactosamine,4TBDMS,isomer #22	CC(=O)N([C@H]1[C@H](O[Si](C)(C)C(C)(C)C)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C(C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)[C@@H]1O)[Si](C)(C)C(C)(C)C	3787.8	Semi standard non polar	33892256
N-Acetyllactosamine,4TBDMS,isomer #23	CC(=O)N[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C(C)(C)C)[C@H](O)[C@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C	3741.0	Semi standard non polar	33892256
N-Acetyllactosamine,4TBDMS,isomer #24	CC(=O)N([C@H]1[C@H](O[Si](C)(C)C(C)(C)C)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C(C)(C)C)[C@H](O)[C@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)[C@@H]1O)[Si](C)(C)C(C)(C)C	3781.8	Semi standard non polar	33892256
N-Acetyllactosamine,4TBDMS,isomer #25	CC(=O)N([C@H]1[C@H](O[Si](C)(C)C(C)(C)C)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C(C)(C)C)[C@H](O)[C@H](O)[C@H]2O)[C@@H]1O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3766.5	Semi standard non polar	33892256
N-Acetyllactosamine,4TBDMS,isomer #26	CC(=O)N[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O[Si](C)(C)C(C)(C)C)[C@@H]1O	3755.2	Semi standard non polar	33892256
N-Acetyllactosamine,4TBDMS,isomer #27	CC(=O)N[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)[C@@H]1O[Si](C)(C)C(C)(C)C	3735.9	Semi standard non polar	33892256
N-Acetyllactosamine,4TBDMS,isomer #28	CC(=O)N([C@H]1[C@H](O[Si](C)(C)C(C)(C)C)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)[C@@H]1O)[Si](C)(C)C(C)(C)C	3788.4	Semi standard non polar	33892256
N-Acetyllactosamine,4TBDMS,isomer #29	CC(=O)N[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C	3736.1	Semi standard non polar	33892256
N-Acetyllactosamine,4TBDMS,isomer #3	CC(=O)N[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C(C)(C)C)[C@H](O)[C@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)[C@@H]1O	3763.5	Semi standard non polar	33892256
N-Acetyllactosamine,4TBDMS,isomer #30	CC(=O)N([C@H]1[C@H](O[Si](C)(C)C(C)(C)C)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)[C@@H]1O)[Si](C)(C)C(C)(C)C	3797.9	Semi standard non polar	33892256
N-Acetyllactosamine,4TBDMS,isomer #31	CC(=O)N([C@H]1[C@H](O[Si](C)(C)C(C)(C)C)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]2O)[C@@H]1O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3796.6	Semi standard non polar	33892256
N-Acetyllactosamine,4TBDMS,isomer #32	CC(=O)N[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C	3739.6	Semi standard non polar	33892256
N-Acetyllactosamine,4TBDMS,isomer #33	CC(=O)N([C@H]1[C@H](O[Si](C)(C)C(C)(C)C)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O[Si](C)(C)C(C)(C)C)[C@@H]1O)[Si](C)(C)C(C)(C)C	3785.8	Semi standard non polar	33892256
N-Acetyllactosamine,4TBDMS,isomer #34	CC(=O)N([C@H]1[C@H](O[Si](C)(C)C(C)(C)C)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)[C@@H]1O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3799.3	Semi standard non polar	33892256
N-Acetyllactosamine,4TBDMS,isomer #35	CC(=O)N([C@H]1[C@H](O[Si](C)(C)C(C)(C)C)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3795.3	Semi standard non polar	33892256
N-Acetyllactosamine,4TBDMS,isomer #36	CC(=O)N[C@H]1[C@H](O)O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)[C@@H]1O	3779.2	Semi standard non polar	33892256
N-Acetyllactosamine,4TBDMS,isomer #37	CC(=O)N[C@H]1[C@H](O)O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)[C@@H]1O	3789.4	Semi standard non polar	33892256
N-Acetyllactosamine,4TBDMS,isomer #38	CC(=O)N[C@H]1[C@H](O)O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]2O)[C@@H]1O[Si](C)(C)C(C)(C)C	3749.2	Semi standard non polar	33892256
N-Acetyllactosamine,4TBDMS,isomer #39	CC(=O)N([C@H]1[C@H](O)O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]2O)[C@@H]1O)[Si](C)(C)C(C)(C)C	3783.2	Semi standard non polar	33892256
N-Acetyllactosamine,4TBDMS,isomer #4	CC(=O)N[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C(C)(C)C)[C@H](O)[C@H](O)[C@H]2O)[C@@H]1O[Si](C)(C)C(C)(C)C	3728.1	Semi standard non polar	33892256
N-Acetyllactosamine,4TBDMS,isomer #40	CC(=O)N[C@H]1[C@H](O)O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C(C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O[Si](C)(C)C(C)(C)C)[C@@H]1O	3775.0	Semi standard non polar	33892256
N-Acetyllactosamine,4TBDMS,isomer #41	CC(=O)N[C@H]1[C@H](O)O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C(C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)[C@@H]1O[Si](C)(C)C(C)(C)C	3756.1	Semi standard non polar	33892256
N-Acetyllactosamine,4TBDMS,isomer #42	CC(=O)N([C@H]1[C@H](O)O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C(C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)[C@@H]1O)[Si](C)(C)C(C)(C)C	3791.8	Semi standard non polar	33892256
N-Acetyllactosamine,4TBDMS,isomer #43	CC(=O)N[C@H]1[C@H](O)O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C(C)(C)C)[C@H](O)[C@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C	3758.6	Semi standard non polar	33892256
N-Acetyllactosamine,4TBDMS,isomer #44	CC(=O)N([C@H]1[C@H](O)O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C(C)(C)C)[C@H](O)[C@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)[C@@H]1O)[Si](C)(C)C(C)(C)C	3786.5	Semi standard non polar	33892256
N-Acetyllactosamine,4TBDMS,isomer #45	CC(=O)N([C@H]1[C@H](O)O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C(C)(C)C)[C@H](O)[C@H](O)[C@H]2O)[C@@H]1O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3766.5	Semi standard non polar	33892256
N-Acetyllactosamine,4TBDMS,isomer #46	CC(=O)N[C@H]1[C@H](O)O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O[Si](C)(C)C(C)(C)C)[C@@H]1O	3760.9	Semi standard non polar	33892256
N-Acetyllactosamine,4TBDMS,isomer #47	CC(=O)N[C@H]1[C@H](O)O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)[C@@H]1O[Si](C)(C)C(C)(C)C	3749.2	Semi standard non polar	33892256
N-Acetyllactosamine,4TBDMS,isomer #48	CC(=O)N([C@H]1[C@H](O)O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)[C@@H]1O)[Si](C)(C)C(C)(C)C	3789.7	Semi standard non polar	33892256
N-Acetyllactosamine,4TBDMS,isomer #49	CC(=O)N[C@H]1[C@H](O)O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C	3753.2	Semi standard non polar	33892256
N-Acetyllactosamine,4TBDMS,isomer #5	CC(=O)N([C@H]1[C@H](O[Si](C)(C)C(C)(C)C)O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C(C)(C)C)[C@H](O)[C@H](O)[C@H]2O)[C@@H]1O)[Si](C)(C)C(C)(C)C	3755.3	Semi standard non polar	33892256
N-Acetyllactosamine,4TBDMS,isomer #50	CC(=O)N([C@H]1[C@H](O)O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)[C@@H]1O)[Si](C)(C)C(C)(C)C	3797.4	Semi standard non polar	33892256
N-Acetyllactosamine,4TBDMS,isomer #51	CC(=O)N([C@H]1[C@H](O)O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]2O)[C@@H]1O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3784.2	Semi standard non polar	33892256
N-Acetyllactosamine,4TBDMS,isomer #52	CC(=O)N[C@H]1[C@H](O)O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C	3753.1	Semi standard non polar	33892256
N-Acetyllactosamine,4TBDMS,isomer #53	CC(=O)N([C@H]1[C@H](O)O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O[Si](C)(C)C(C)(C)C)[C@@H]1O)[Si](C)(C)C(C)(C)C	3781.2	Semi standard non polar	33892256
N-Acetyllactosamine,4TBDMS,isomer #54	CC(=O)N([C@H]1[C@H](O)O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)[C@@H]1O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3789.5	Semi standard non polar	33892256
N-Acetyllactosamine,4TBDMS,isomer #55	CC(=O)N([C@H]1[C@H](O)O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3784.7	Semi standard non polar	33892256
N-Acetyllactosamine,4TBDMS,isomer #56	CC(=O)N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O[Si](C)(C)C(C)(C)C)[C@@H]1O	3773.1	Semi standard non polar	33892256
N-Acetyllactosamine,4TBDMS,isomer #57	CC(=O)N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)[C@@H]1O[Si](C)(C)C(C)(C)C	3756.0	Semi standard non polar	33892256
N-Acetyllactosamine,4TBDMS,isomer #58	CC(=O)N([C@H]1[C@H](O)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)[C@@H]1O)[Si](C)(C)C(C)(C)C	3792.4	Semi standard non polar	33892256
N-Acetyllactosamine,4TBDMS,isomer #59	CC(=O)N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C	3765.1	Semi standard non polar	33892256
N-Acetyllactosamine,4TBDMS,isomer #6	CC(=O)N[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)[C@@H]1O	3753.3	Semi standard non polar	33892256
N-Acetyllactosamine,4TBDMS,isomer #60	CC(=O)N([C@H]1[C@H](O)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)[C@@H]1O)[Si](C)(C)C(C)(C)C	3798.6	Semi standard non polar	33892256
N-Acetyllactosamine,4TBDMS,isomer #61	CC(=O)N([C@H]1[C@H](O)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]2O)[C@@H]1O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3773.7	Semi standard non polar	33892256
N-Acetyllactosamine,4TBDMS,isomer #62	CC(=O)N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C(C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C	3756.4	Semi standard non polar	33892256
N-Acetyllactosamine,4TBDMS,isomer #63	CC(=O)N([C@H]1[C@H](O)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C(C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O[Si](C)(C)C(C)(C)C)[C@@H]1O)[Si](C)(C)C(C)(C)C	3783.9	Semi standard non polar	33892256
N-Acetyllactosamine,4TBDMS,isomer #64	CC(=O)N([C@H]1[C@H](O)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C(C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)[C@@H]1O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3785.2	Semi standard non polar	33892256
N-Acetyllactosamine,4TBDMS,isomer #65	CC(=O)N([C@H]1[C@H](O)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C(C)(C)C)[C@H](O)[C@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3777.2	Semi standard non polar	33892256
N-Acetyllactosamine,4TBDMS,isomer #66	CC(=O)N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C	3746.4	Semi standard non polar	33892256
N-Acetyllactosamine,4TBDMS,isomer #67	CC(=O)N([C@H]1[C@H](O)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O[Si](C)(C)C(C)(C)C)[C@@H]1O)[Si](C)(C)C(C)(C)C	3774.8	Semi standard non polar	33892256
N-Acetyllactosamine,4TBDMS,isomer #68	CC(=O)N([C@H]1[C@H](O)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)[C@@H]1O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3782.5	Semi standard non polar	33892256
N-Acetyllactosamine,4TBDMS,isomer #69	CC(=O)N([C@H]1[C@H](O)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3790.9	Semi standard non polar	33892256
N-Acetyllactosamine,4TBDMS,isomer #7	CC(=O)N[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)[C@@H]1O	3754.1	Semi standard non polar	33892256
N-Acetyllactosamine,4TBDMS,isomer #70	CC(=O)N([C@H]1[C@H](O)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3781.0	Semi standard non polar	33892256
N-Acetyllactosamine,4TBDMS,isomer #8	CC(=O)N[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]2O)[C@@H]1O[Si](C)(C)C(C)(C)C	3735.0	Semi standard non polar	33892256
N-Acetyllactosamine,4TBDMS,isomer #9	CC(=O)N([C@H]1[C@H](O[Si](C)(C)C(C)(C)C)O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]2O)[C@@H]1O)[Si](C)(C)C(C)(C)C	3778.3	Semi standard non polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - N-Acetyllactosamine GC-MS (Non-derivatized) - 70eV, Positive	splash10-0uy3-5539000000-9001b4ffdf2686f61fdb	2017-09-01	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - N-Acetyllactosamine GC-MS (4 TMS) - 70eV, Positive	splash10-0a4i-3410139000-490a44b54a788af499ad	2017-10-06	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - N-Acetyllactosamine GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum

MS/MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Experimental LC-MS/MS	LC-MS/MS Spectrum - N-Acetyllactosamine Quattro_QQQ 10V, Positive-QTOF (Annotated)	splash10-0g4i-0294000000-eba3eabd1634e1f899d6	2012-07-24	HMDB team, MONA	View Spectrum
Experimental LC-MS/MS	LC-MS/MS Spectrum - N-Acetyllactosamine Quattro_QQQ 25V, Positive-QTOF (Annotated)	splash10-002r-0900000000-65d60bd6a084f5fb8a03	2012-07-24	HMDB team, MONA	View Spectrum
Experimental LC-MS/MS	LC-MS/MS Spectrum - N-Acetyllactosamine Quattro_QQQ 40V, Positive-QTOF (Annotated)	splash10-0019-9800000000-5cfef19dd8c8707bef7a	2012-07-24	HMDB team, MONA	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - N-Acetyllactosamine 10V, Positive-QTOF	splash10-00yi-0179000000-d117b299438bee3a1a40	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - N-Acetyllactosamine 20V, Positive-QTOF	splash10-0uk9-0592000000-db6f5abfab26c98d8af4	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - N-Acetyllactosamine 40V, Positive-QTOF	splash10-0wbc-5960000000-915e1f050484eedb63d2	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - N-Acetyllactosamine 10V, Negative-QTOF	splash10-0udi-2492000000-1208b9128bdb1fd8688e	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - N-Acetyllactosamine 20V, Negative-QTOF	splash10-0h90-7984000000-2636a4af2a05389c39e5	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - N-Acetyllactosamine 40V, Negative-QTOF	splash10-0pb9-7910000000-dce1bda7d8788ebd90af	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - N-Acetyllactosamine 10V, Negative-QTOF	splash10-003r-1169000000-37af2930ba0a18fdfe2d	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - N-Acetyllactosamine 20V, Negative-QTOF	splash10-0bu3-9317000000-05676e3bb792b14a9ea9	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - N-Acetyllactosamine 40V, Negative-QTOF	splash10-0a4l-9410000000-9f5dbeeb51b744740d72	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - N-Acetyllactosamine 10V, Positive-QTOF	splash10-0f8a-0659000000-98f0c5a2f817d77728ac	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - N-Acetyllactosamine 20V, Positive-QTOF	splash10-0uk9-0951000000-f475151e03af91aeeac3	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - N-Acetyllactosamine 40V, Positive-QTOF	splash10-006w-9410000000-abd7ef88c6f0a3d44980	2021-09-23	Wishart Lab	View Spectrum

NMR Spectra

Spectrum Type	Description	Deposition Date	Source	View
Predicted 1D NMR	¹³C NMR Spectrum (1D, 100 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 200 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 300 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 400 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 500 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 600 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 700 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 800 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 900 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Experimental 2D NMR	[¹H, ¹³C]-HSQC NMR Spectrum (2D, 600 MHz, H₂O, experimental)	2012-12-05	Wishart Lab	View Spectrum

Biological Properties

Cellular Locations

Cytoplasm (predicted from logP)

Biospecimen Locations

Not Available

Tissue Locations

Epidermis
Intestine
Spleen

Pathways

Not Available

Name	SMPDB/PathBank	KEGG

Normal Concentrations

Not Available

Abnormal Concentrations

Not Available

Associated Disorders and Diseases

Disease References

None

Associated OMIM IDs

None

External Links

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

FDB019860

KNApSAcK ID

Not Available

Chemspider ID

388404

KEGG Compound ID

C00611

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

N-Acetyllactosamine

METLIN ID

4231

PubChem Compound

439271

PDB ID

Not Available

ChEBI ID

16153

Food Biomarker Ontology

Not Available

VMH ID

Not Available

MarkerDB ID

Not Available

Good Scents ID

Not Available

References

Synthesis Reference

Dekany, Gyula; Agoston, Karoly; Bajza, Istvan; Boejstrup, Marie; Kroeger, Lars. Process for the large-scale preparation of N-acetyllactosamine, lactosamine, lactosamine salts and lactosamine-containing oligosaccharides. PCT Int. Appl. (2007), 44pp.

Material Safety Data Sheet (MSDS)

Download (PDF)

General References

Jung SK, Fujimoto D: A novel beta-galactoside-binding lectin in adult rat kidney. J Biochem. 1994 Sep;116(3):547-53. [PubMed:7852273 ]
Mollicone R, Candelier JJ, Mennesson B, Couillin P, Venot AP, Oriol R: Five specificity patterns of (1----3)-alpha-L-fucosyltransferase activity defined by use of synthetic oligosaccharide acceptors. Differential expression of the enzymes during human embryonic development and in adult tissues. Carbohydr Res. 1992 Apr 10;228(1):265-76. [PubMed:1366057 ]
Yu LC, Twu YC, Chang CY, Lin M: Molecular basis of the adult i phenotype and the gene responsible for the expression of the human blood group I antigen. Blood. 2001 Dec 15;98(13):3840-5. [PubMed:11739194 ]
Dabelsteen E, Buschard K, Hakomori S, Young WW: Pattern of distribution of blood group antigens on human epidermal cells during maturation. J Invest Dermatol. 1984 Jan;82(1):13-7. [PubMed:6361167 ]
Ahmed H, Pohl J, Fink NE, Strobel F, Vasta GR: The primary structure and carbohydrate specificity of a beta-galactosyl-binding lectin from toad (Bufo arenarum Hensel) ovary reveal closer similarities to the mammalian galectin-1 than to the galectin from the clawed frog Xenopus laevis. J Biol Chem. 1996 Dec 20;271(51):33083-94. [PubMed:8955156 ]
Hosomi O, Takeya A: The relationship between the (beta 1-3) N-acetylglucosaminyltransferase and the presence of oligosaccharides containing lacto-N-triose II structure in bovine and human milk. Nihon Juigaku Zasshi. 1989 Feb;51(1):1-6. [PubMed:2522567 ]
Jinno K, Moriwaki S, Govindarajan S, Okada Y, Tsuji T: Blood group antigens in the intrahepatic biliary tree. II. Type 1 chain N-acetyllactosamine-related carbohydrate antigens in the proliferated bile ductules. J Hepatol. 1989 May;8(3):330-7. [PubMed:2732447 ]
Takeya A, Hosomi O, Kogure T: The presence of N-acetyllactosamine and lactose: beta (1-3)N-acetylglucosaminyltransferase activity in human urine. Jpn J Med Sci Biol. 1985 Feb;38(1):1-8. [PubMed:3160874 ]
Draberova L, Cerna H, Brodska H, Boubelik M, Watt SM, Stanners CP, Draber P: Soluble isoforms of CEACAM1 containing the A2 domain: increased serum levels in patients with obstructive jaundice and differences in 3-fucosyl-N-acetyl-lactosamine moiety. Immunology. 2000 Oct;101(2):279-87. [PubMed:11012782 ]
Kojima S, Eguchi H, Ookawara T, Fujiwara N, Yasuda J, Nakagawa K, Yamamura T, Suzuki K: Clostridium botulinum type A progenitor toxin binds to Intestine-407 cells via N-acetyllactosamine moiety. Biochem Biophys Res Commun. 2005 Jun 3;331(2):571-6. [PubMed:15850798 ]
Hosomi O, Takeya A, Kogure T: Human serum contains N-acetyllactosamine: beta 1-3 N-acetylglucosaminyltransferase activity. J Biochem. 1984 Jun;95(6):1655-9. [PubMed:6236210 ]
Dabelsteen E, Holbrook K, Clausen H, Hakomori S: Cell surface carbohydrate changes during embryonic and fetal skin development. J Invest Dermatol. 1986 Jul;87(1):81-5. [PubMed:3522754 ]
Argueso P, Spurr-Michaud S, Tisdale A, Gipson IK: Variation in the amount of T antigen and N-acetyllactosamine oligosaccharides in human cervical mucus secretions with the menstrual cycle. J Clin Endocrinol Metab. 2002 Dec;87(12):5641-8. [PubMed:12466366 ]

Enzymes

Enzyme Details

1. Carbohydrate sulfotransferase 3

General function:: Involved in sulfotransferase activity
Specific function:: Sulfotransferase that utilizes 3'-phospho-5'-adenylyl sulfate (PAPS) as sulfonate donor to catalyze the transfer of sulfate to position 6 of the N-acetylgalactosamine (GalNAc) residue of chondroitin. Chondroitin sulfate constitutes the predominant proteoglycan present in cartilage and is distributed on the surfaces of many cells and extracellular matrices. Can also sulfate Gal residues of keratan sulfate, another glycosaminoglycan, and the Gal residues in sialyl N-acetyllactosamine (sialyl LacNAc) oligosaccharides. May play a role in the maintenance of naive T-lymphocytes in the spleen.
Gene Name:: CHST3
Uniprot ID:: Q7LGC8
Molecular weight:: 54705.5

Enzyme Details

2. Carbohydrate sulfotransferase 1

General function:: Involved in sulfotransferase activity
Specific function:: Sulfotransferase that utilizes 3'-phospho-5'-adenylyl sulfate (PAPS) as sulfonate donor to catalyze the transfer of sulfate to position 6 of galactose (Gal) residues of keratan. Has a preference for sulfating keratan sulfate, but it also transfers sulfate to the unsulfated polymer. The sulfotransferase activity on sialyl LacNAc structures is much higher than the corresponding desialylated substrate, and only internal Gal residues are sulfated. May function in the sulfation of sialyl N-acetyllactosamine oligosaccharide chains attached to glycoproteins. Participates in biosynthesis of selectin ligands. Selectin ligands are present in high endothelial cells (HEVs) and play a central role in lymphocyte homing at sites of inflammation.
Gene Name:: CHST1
Uniprot ID:: O43916
Molecular weight:: 46714.21

Enzyme Details

3. Beta-1,4-galactosyltransferase 2

General function:: Involved in transferase activity, transferring glycosyl groups
Specific function:: Responsible for the synthesis of complex-type N-linked oligosaccharides in many glycoproteins as well as the carbohydrate moieties of glycolipids. Can produce lactose.
Gene Name:: B4GALT2
Uniprot ID:: O60909
Molecular weight:: 41971.815

Reactions

Uridine diphosphategalactose + N-Acetyl-D-glucosamine → Uridine 5'-diphosphate + N-Acetyllactosamine	details

Enzyme Details

4. Beta-1,4-galactosyltransferase 1

General function:: Involved in transferase activity, transferring glycosyl groups
Specific function:: The Golgi complex form catalyzes the production of lactose in the lactating mammary gland and could also be responsible for the synthesis of complex-type N-linked oligosaccharides in many glycoproteins as well as the carbohydrate moieties of glycolipids. The cell surface form functions as a recognition molecule during a variety of cell to cell and cell to matrix interactions, as those occurring during development and egg fertilization, by binding to specific oligosaccharide ligands on opposing cells or in the extracellular matrix.
Gene Name:: B4GALT1
Uniprot ID:: P15291
Molecular weight:: 43919.895

Reactions

Uridine diphosphategalactose + N-Acetyl-D-glucosamine → Uridine 5'-diphosphate + N-Acetyllactosamine	details

Enzyme Details

5. Carbohydrate sulfotransferase 7

General function:: Involved in sulfotransferase activity
Specific function:: Sulfotransferase that utilizes 3'-phospho-5'-adenylyl sulfate (PAPS) as sulfonate donor to catalyze the transfer of sulfate to position 6 of non-reducing N-acetylglucosamine (GlcNAc) residues. Preferentially acts on mannose-linked GlcNAc. Also able to catalyze the transfer of sulfate to position 6 of the N-acetylgalactosamine (GalNAc) residue of chondroitin. Also acts on core 2 mucin-type oligosaccharide and N-acetyllactosamine oligomer with a lower efficiency. Has weak or no activity toward keratan sulfate and oligosaccharides containing the Galbeta1-4GlcNAc. Catalyzes 6-O-sulfation of beta-benzyl GlcNAc but not alpha- or beta-benzyl GalNAc.
Gene Name:: CHST7
Uniprot ID:: Q9NS84
Molecular weight:: 54265.635

Enzyme Details

6. Beta-1,4-galactosyltransferase 3

General function:: Involved in transferase activity, transferring glycosyl groups
Specific function:: Responsible for the synthesis of complex-type N-linked oligosaccharides in many glycoproteins as well as the carbohydrate moieties of glycolipids.
Gene Name:: B4GALT3
Uniprot ID:: O60512
Molecular weight:: 43927.63

Reactions

Uridine diphosphategalactose + N-Acetyl-D-glucosamine → Uridine 5'-diphosphate + N-Acetyllactosamine	details

Enzyme Details

7. Beta-1,4-galactosyltransferase 4

General function:: Involved in transferase activity, transferring glycosyl groups
Specific function:: Responsible for the synthesis of complex-type N-linked oligosaccharides in many glycoproteins as well as the carbohydrate moieties of glycolipids.
Gene Name:: B4GALT4
Uniprot ID:: O60513
Molecular weight:: 40040.865

Reactions

Uridine diphosphategalactose + N-Acetyl-D-glucosamine → Uridine 5'-diphosphate + N-Acetyllactosamine	details

Enzyme Details

8. Killer cell lectin-like receptor subfamily B member 1

General function:: Involved in binding
Specific function:: Plays an inhibitory role on natural killer (NK) cells cytotoxicity. Activation results in specific acid sphingomyelinase/SMPD1 stimulation with subsequent marked elevation of intracellular ceramide. Activation also leads to AKT1/PKB and RPS6KA1/RSK1 kinases stimulation as well as markedly enhanced T-cell proliferation induced by anti-CD3. Acts as a lectin that binds to the terminal carbohydrate Gal-alpha(1,3)Gal epitope as well as to the N-acetyllactosamine epitope. Binds also to CLEC2D/LLT1 as a ligand and inhibits NK cell-mediated cytotoxicity as well as interferon-gamma secretion in target cells
Gene Name:: KLRB1
Uniprot ID:: Q12918
Molecular weight:: 25414.6

Showing metabocard for N-Acetyllactosamine (HMDB0001542)

MOL for HMDB0001542 (N-Acetyllactosamine)

3D MOL for HMDB0001542 (N-Acetyllactosamine)

3D SDF for HMDB0001542 (N-Acetyllactosamine)

3D-SDF for HMDB0001542 (N-Acetyllactosamine)

PDB for HMDB0001542 (N-Acetyllactosamine)

3D PDB for HMDB0001542 (N-Acetyllactosamine)

SMILES for HMDB0001542 (N-Acetyllactosamine)

INCHI for HMDB0001542 (N-Acetyllactosamine)

Structure for HMDB0001542 (N-Acetyllactosamine)

3D Structure for HMDB0001542 (N-Acetyllactosamine)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra

NMR Spectra

Enzymes

Reactions

Reactions

Reactions

Reactions