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Record Information

Version

5.0

Status

Expected but not Quantified

Creation Date

2006-05-22 14:17:42 UTC

Update Date

2021-10-13 04:38:16 UTC

HMDB ID

HMDB0002220

Secondary Accession Numbers

HMDB02220

Metabolite Identification

Common Name

N-Acetyl-6-O-L-fucosyl-D-glucosamine

Description

N-Acetyl-6-O-L-fucosyl-D-glucosamine belongs to the class of organic compounds known as fatty acyl glycosides of mono- and disaccharides. Fatty acyl glycosides of mono- and disaccharides are compounds composed of a mono- or disaccharide moiety linked to one hydroxyl group of a fatty alcohol or of a phosphorylated alcohol (phosphoprenols), a hydroxy fatty acid or to one carboxyl group of a fatty acid (ester linkage) or to an amino alcohol. Based on a literature review very few articles have been published on N-Acetyl-6-O-L-fucosyl-D-glucosamine.

Structure

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

HMDB0002220
     RDKit          3D
N-Acetyl-6-O-L-fucosyl-D-glucosamine
 50 50  0  0  0  0  0  0  0  0999 V2000
    6.1097    1.3356   -1.3235 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0490    0.3383   -1.1125 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6734   -0.4259   -2.0556 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4333    0.2173    0.1432 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.3674   -0.7626    0.4100 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.8904   -1.7132    1.4151 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0221   -1.5724    1.8901 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1650   -0.0401    0.9155 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.7829    0.8669   -0.1112 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0185   -0.9197    1.2942 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.2799   -1.8265    2.2888 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4224   -1.5293    0.0411 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3063   -2.5021   -0.4519 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9011   -2.1618    0.2852 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8166   -1.2549    0.7542 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0963   -0.2907   -0.2109 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6807    0.9605    0.1499 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3516    1.9214   -0.5752 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.2789    1.8022   -2.0548 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7702    2.0361   -0.0503 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.5113    2.9185   -0.8300 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4134    0.6775    0.0926 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.6252    0.7028   -0.5962 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5715   -0.4106   -0.5225 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.0526   -1.6432   -0.0873 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.1219    0.8858   -1.2834 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9409    1.7944   -2.3234 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9929    2.1421   -0.5559 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7112    0.8219    0.9385 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2221   -1.2938   -0.5352 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3567   -2.5695    1.8002 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4508    0.6060    1.7957 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0537    1.4407    0.2020 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1768   -0.2662    1.7294 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5182   -2.0529    2.8602 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3513   -0.7321   -0.6978 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2399   -2.5199   -1.4199 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2143   -2.6006   -0.7144 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8367   -3.0684    0.9372 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5156   -0.5721   -1.1147 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8379    2.8995   -0.3022 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8497    0.8788   -2.4557 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8346    2.7144   -2.5096 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3472    1.8112   -2.4319 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7003    2.4789    0.9628 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3446    2.5414   -1.1774 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6485    0.4243    1.1467 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1131   -0.1509   -0.4150 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6900   -0.4140   -1.6245 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6548   -1.9229    0.7788 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  2  0
  5  8  1  0
  8  9  1  0
  8 10  1  0
 10 11  1  0
 10 12  1  0
 12 13  1  0
 12 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 18 20  1  0
 20 21  1  0
 20 22  1  0
 22 23  1  0
 22 24  1  0
 24 25  1  0
 24 16  1  0
  1 26  1  0
  1 27  1  0
  1 28  1  0
  4 29  1  0
  5 30  1  6
  6 31  1  0
  8 32  1  1
  9 33  1  0
 10 34  1  1
 11 35  1  0
 12 36  1  0
 13 37  1  0
 14 38  1  0
 14 39  1  0
 16 40  1  0
 18 41  1  6
 19 42  1  0
 19 43  1  0
 19 44  1  0
 20 45  1  1
 21 46  1  0
 22 47  1  1
 23 48  1  0
 24 49  1  6
 25 50  1  0
M  END


  Mrv0541 02231219262D          

 25 25  0  0  1  0            999 V2000
   16.7229  -11.3968    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   16.3105  -10.6823    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   17.5479  -11.3968    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   16.7229   -9.9679    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   17.9605  -10.6823    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.5479   -9.9679    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   16.3105  -12.1112    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.4855  -10.6823    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   16.3105   -9.2533    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   17.9605   -9.2533    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   18.7855  -10.6823    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   19.1979  -11.3968    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.0229  -11.3968    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.4355  -10.6823    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   21.2605  -10.6823    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   21.6729   -9.9679    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   22.4979   -9.9679    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.4355  -12.1112    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   20.0229   -9.9679    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   21.6729  -11.3968    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   21.2605   -9.2533    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   21.6729   -8.5389    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   21.2605   -7.8244    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   22.4979   -8.5389    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   22.9105  -10.6823    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
  2  4  1  0  0  0  0
  3  5  1  0  0  0  0
  4  6  1  0  0  0  0
  5  6  1  0  0  0  0
  1  7  1  1  0  0  0
  2  8  1  1  0  0  0
  4  9  1  1  0  0  0
  6 10  1  6  0  0  0
  5 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 14 13  1  0  0  0  0
 15 14  1  0  0  0  0
 16 15  1  0  0  0  0
 17 16  1  0  0  0  0
 18 13  1  6  0  0  0
 14 19  1  1  0  0  0
 15 20  1  1  0  0  0
 16 21  1  1  0  0  0
 23 22  2  0  0  0  0
 24 22  1  0  0  0  0
 21 22  1  0  0  0  0
 25 17  2  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0002220

> <DATABASE_NAME>
hmdb

> <SMILES>
C[C@@H]1OC(OCC(O)[C@@H](O)[C@H](O)[C@@H](NC(C)=O)C=O)[C@@H](O)[C@H](O)[C@@H]1O

> <INCHI_IDENTIFIER>
InChI=1S/C14H25NO10/c1-5-9(19)12(22)13(23)14(25-5)24-4-8(18)11(21)10(20)7(3-16)15-6(2)17/h3,5,7-14,18-23H,4H2,1-2H3,(H,15,17)/t5-,7-,8?,9+,10+,11+,12+,13-,14?/m0/s1

> <INCHI_KEY>
YBWAUUBLHOFOPK-SOHGFDPZSA-N

> <FORMULA>
C14H25NO10

> <MOLECULAR_WEIGHT>
367.349

> <EXACT_MASS>
367.147846025

> <JCHEM_ACCEPTOR_COUNT>
10

> <JCHEM_AVERAGE_POLARIZABILITY>
34.993932527370866

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
7

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
N-[(2R,3R,4S)-3,4,5-trihydroxy-1-oxo-6-{[(3S,4R,5S,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}hexan-2-yl]acetamide

> <ALOGPS_LOGP>
-2.01

> <JCHEM_LOGP>
-4.580321435666667

> <ALOGPS_LOGS>
-0.56

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.190371883416958

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.422072460879455

> <JCHEM_PKA_STRONGEST_BASIC>
-3.521618047550593

> <JCHEM_POLAR_SURFACE_AREA>
186.01

> <JCHEM_REFRACTIVITY>
79.31649999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
8

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.02e+02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
N-[(2R,3R,4S)-3,4,5-trihydroxy-1-oxo-6-{[(3S,4R,5S,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}hexan-2-yl]acetamide

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0002220
     RDKit          3D
N-Acetyl-6-O-L-fucosyl-D-glucosamine
 50 50  0  0  0  0  0  0  0  0999 V2000
    6.1097    1.3356   -1.3235 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0490    0.3383   -1.1125 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6734   -0.4259   -2.0556 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4333    0.2173    0.1432 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.3674   -0.7626    0.4100 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.8904   -1.7132    1.4151 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0221   -1.5724    1.8901 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1650   -0.0401    0.9155 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.7829    0.8669   -0.1112 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0185   -0.9197    1.2942 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.2799   -1.8265    2.2888 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4224   -1.5293    0.0411 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3063   -2.5021   -0.4519 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9011   -2.1618    0.2852 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8166   -1.2549    0.7542 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0963   -0.2907   -0.2109 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6807    0.9605    0.1499 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3516    1.9214   -0.5752 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.2789    1.8022   -2.0548 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7702    2.0361   -0.0503 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.5113    2.9185   -0.8300 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4134    0.6775    0.0926 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.6252    0.7028   -0.5962 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5715   -0.4106   -0.5225 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.0526   -1.6432   -0.0873 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.1219    0.8858   -1.2834 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9409    1.7944   -2.3234 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9929    2.1421   -0.5559 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7112    0.8219    0.9385 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2221   -1.2938   -0.5352 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3567   -2.5695    1.8002 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4508    0.6060    1.7957 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0537    1.4407    0.2020 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1768   -0.2662    1.7294 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5182   -2.0529    2.8602 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3513   -0.7321   -0.6978 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2399   -2.5199   -1.4199 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2143   -2.6006   -0.7144 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8367   -3.0684    0.9372 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5156   -0.5721   -1.1147 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8379    2.8995   -0.3022 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8497    0.8788   -2.4557 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8346    2.7144   -2.5096 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3472    1.8112   -2.4319 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7003    2.4789    0.9628 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3446    2.5414   -1.1774 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6485    0.4243    1.1467 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1131   -0.1509   -0.4150 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6900   -0.4140   -1.6245 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6548   -1.9229    0.7788 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  2  0
  5  8  1  0
  8  9  1  0
  8 10  1  0
 10 11  1  0
 10 12  1  0
 12 13  1  0
 12 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 18 20  1  0
 20 21  1  0
 20 22  1  0
 22 23  1  0
 22 24  1  0
 24 25  1  0
 24 16  1  0
  1 26  1  0
  1 27  1  0
  1 28  1  0
  4 29  1  0
  5 30  1  6
  6 31  1  0
  8 32  1  1
  9 33  1  0
 10 34  1  1
 11 35  1  0
 12 36  1  0
 13 37  1  0
 14 38  1  0
 14 39  1  0
 16 40  1  0
 18 41  1  6
 19 42  1  0
 19 43  1  0
 19 44  1  0
 20 45  1  1
 21 46  1  0
 22 47  1  1
 23 48  1  0
 24 49  1  6
 25 50  1  0
M  END

HEADER    PROTEIN                                 23-FEB-12   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   23-FEB-12         0                                  
HETATM    1  C   UNK     0      31.216 -21.274   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      30.446 -19.940   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0      32.756 -21.274   0.000  0.00  0.00           O+0
HETATM    4  C   UNK     0      31.216 -18.607   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      33.526 -19.940   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      32.756 -18.607   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      30.446 -22.608   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0      28.906 -19.940   0.000  0.00  0.00           O+0
HETATM    9  O   UNK     0      30.446 -17.273   0.000  0.00  0.00           O+0
HETATM   10  O   UNK     0      33.526 -17.273   0.000  0.00  0.00           O+0
HETATM   11  O   UNK     0      35.066 -19.940   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0      35.836 -21.274   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      37.376 -21.274   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      38.146 -19.940   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      39.686 -19.940   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      40.456 -18.607   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      41.996 -18.607   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0      38.146 -22.608   0.000  0.00  0.00           O+0
HETATM   19  O   UNK     0      37.376 -18.607   0.000  0.00  0.00           O+0
HETATM   20  O   UNK     0      40.456 -21.274   0.000  0.00  0.00           O+0
HETATM   21  N   UNK     0      39.686 -17.273   0.000  0.00  0.00           N+0
HETATM   22  C   UNK     0      40.456 -15.939   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      39.686 -14.605   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0      41.996 -15.939   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0      42.766 -19.940   0.000  0.00  0.00           O+0
CONECT    1    2    3    7                                                  
CONECT    2    1    4    8                                                  
CONECT    3    1    5                                                       
CONECT    4    2    6    9                                                  
CONECT    5    3    6   11                                                  
CONECT    6    4    5   10                                                  
CONECT    7    1                                                            
CONECT    8    2                                                            
CONECT    9    4                                                            
CONECT   10    6                                                            
CONECT   11    5   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14   18                                                  
CONECT   14   13   15   19                                                  
CONECT   15   14   16   20                                                  
CONECT   16   15   17   21                                                  
CONECT   17   16   25                                                       
CONECT   18   13                                                            
CONECT   19   14                                                            
CONECT   20   15                                                            
CONECT   21   16   22                                                       
CONECT   22   23   24   21                                                  
CONECT   23   22                                                            
CONECT   24   22                                                            
CONECT   25   17                                                            
MASTER        0    0    0    0    0    0    0    0   25    0   50    0
END

COMPND    HMDB0002220
HETATM    1  C1  UNL     1       6.110   1.336  -1.324  1.00  0.00           C  
HETATM    2  C2  UNL     1       5.049   0.338  -1.113  1.00  0.00           C  
HETATM    3  O1  UNL     1       4.673  -0.426  -2.056  1.00  0.00           O  
HETATM    4  N1  UNL     1       4.433   0.217   0.143  1.00  0.00           N  
HETATM    5  C3  UNL     1       3.367  -0.763   0.410  1.00  0.00           C  
HETATM    6  C4  UNL     1       3.890  -1.713   1.415  1.00  0.00           C  
HETATM    7  O2  UNL     1       5.022  -1.572   1.890  1.00  0.00           O  
HETATM    8  C5  UNL     1       2.165  -0.040   0.915  1.00  0.00           C  
HETATM    9  O3  UNL     1       1.783   0.867  -0.111  1.00  0.00           O  
HETATM   10  C6  UNL     1       1.019  -0.920   1.294  1.00  0.00           C  
HETATM   11  O4  UNL     1       1.280  -1.826   2.289  1.00  0.00           O  
HETATM   12  C7  UNL     1       0.422  -1.529   0.041  1.00  0.00           C  
HETATM   13  O5  UNL     1       1.306  -2.502  -0.452  1.00  0.00           O  
HETATM   14  C8  UNL     1      -0.901  -2.162   0.285  1.00  0.00           C  
HETATM   15  O6  UNL     1      -1.817  -1.255   0.754  1.00  0.00           O  
HETATM   16  C9  UNL     1      -2.096  -0.291  -0.211  1.00  0.00           C  
HETATM   17  O7  UNL     1      -1.681   0.961   0.150  1.00  0.00           O  
HETATM   18  C10 UNL     1      -2.352   1.921  -0.575  1.00  0.00           C  
HETATM   19  C11 UNL     1      -2.279   1.802  -2.055  1.00  0.00           C  
HETATM   20  C12 UNL     1      -3.770   2.036  -0.050  1.00  0.00           C  
HETATM   21  O8  UNL     1      -4.511   2.919  -0.830  1.00  0.00           O  
HETATM   22  C13 UNL     1      -4.413   0.677   0.093  1.00  0.00           C  
HETATM   23  O9  UNL     1      -5.625   0.703  -0.596  1.00  0.00           O  
HETATM   24  C14 UNL     1      -3.571  -0.411  -0.523  1.00  0.00           C  
HETATM   25  O10 UNL     1      -4.053  -1.643  -0.087  1.00  0.00           O  
HETATM   26  H1  UNL     1       7.122   0.886  -1.283  1.00  0.00           H  
HETATM   27  H2  UNL     1       5.941   1.794  -2.323  1.00  0.00           H  
HETATM   28  H3  UNL     1       5.993   2.142  -0.556  1.00  0.00           H  
HETATM   29  H4  UNL     1       4.711   0.822   0.939  1.00  0.00           H  
HETATM   30  H5  UNL     1       3.222  -1.294  -0.535  1.00  0.00           H  
HETATM   31  H6  UNL     1       3.357  -2.570   1.800  1.00  0.00           H  
HETATM   32  H7  UNL     1       2.451   0.606   1.796  1.00  0.00           H  
HETATM   33  H8  UNL     1       1.054   1.441   0.202  1.00  0.00           H  
HETATM   34  H9  UNL     1       0.177  -0.266   1.729  1.00  0.00           H  
HETATM   35  H10 UNL     1       0.518  -2.053   2.860  1.00  0.00           H  
HETATM   36  H11 UNL     1       0.351  -0.732  -0.698  1.00  0.00           H  
HETATM   37  H12 UNL     1       1.240  -2.520  -1.420  1.00  0.00           H  
HETATM   38  H13 UNL     1      -1.214  -2.601  -0.714  1.00  0.00           H  
HETATM   39  H14 UNL     1      -0.837  -3.068   0.937  1.00  0.00           H  
HETATM   40  H15 UNL     1      -1.516  -0.572  -1.115  1.00  0.00           H  
HETATM   41  H16 UNL     1      -1.838   2.900  -0.302  1.00  0.00           H  
HETATM   42  H17 UNL     1      -1.850   0.879  -2.456  1.00  0.00           H  
HETATM   43  H18 UNL     1      -1.835   2.714  -2.510  1.00  0.00           H  
HETATM   44  H19 UNL     1      -3.347   1.811  -2.432  1.00  0.00           H  
HETATM   45  H20 UNL     1      -3.700   2.479   0.963  1.00  0.00           H  
HETATM   46  H21 UNL     1      -5.345   2.541  -1.177  1.00  0.00           H  
HETATM   47  H22 UNL     1      -4.649   0.424   1.147  1.00  0.00           H  
HETATM   48  H23 UNL     1      -6.113  -0.151  -0.415  1.00  0.00           H  
HETATM   49  H24 UNL     1      -3.690  -0.414  -1.625  1.00  0.00           H  
HETATM   50  H25 UNL     1      -3.655  -1.923   0.779  1.00  0.00           H  
CONECT    1    2   26   27   28
CONECT    2    3    3    4
CONECT    4    5   29
CONECT    5    6    8   30
CONECT    6    7    7   31
CONECT    8    9   10   32
CONECT    9   33
CONECT   10   11   12   34
CONECT   11   35
CONECT   12   13   14   36
CONECT   13   37
CONECT   14   15   38   39
CONECT   15   16
CONECT   16   17   24   40
CONECT   17   18
CONECT   18   19   20   41
CONECT   19   42   43   44
CONECT   20   21   22   45
CONECT   21   46
CONECT   22   23   24   47
CONECT   23   48
CONECT   24   25   49
CONECT   25   50
END

HMDB0002220
     RDKit          3D
N-Acetyl-6-O-L-fucosyl-D-glucosamine
 50 50  0  0  0  0  0  0  0  0999 V2000
    6.1097    1.3356   -1.3235 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0490    0.3383   -1.1125 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6734   -0.4259   -2.0556 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4333    0.2173    0.1432 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.3674   -0.7626    0.4100 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.8904   -1.7132    1.4151 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0221   -1.5724    1.8901 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1650   -0.0401    0.9155 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.7829    0.8669   -0.1112 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0185   -0.9197    1.2942 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.2799   -1.8265    2.2888 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4224   -1.5293    0.0411 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3063   -2.5021   -0.4519 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9011   -2.1618    0.2852 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8166   -1.2549    0.7542 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0963   -0.2907   -0.2109 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6807    0.9605    0.1499 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3516    1.9214   -0.5752 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.2789    1.8022   -2.0548 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7702    2.0361   -0.0503 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.5113    2.9185   -0.8300 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4134    0.6775    0.0926 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.6252    0.7028   -0.5962 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5715   -0.4106   -0.5225 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.0526   -1.6432   -0.0873 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.1219    0.8858   -1.2834 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9409    1.7944   -2.3234 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9929    2.1421   -0.5559 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7112    0.8219    0.9385 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2221   -1.2938   -0.5352 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3567   -2.5695    1.8002 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4508    0.6060    1.7957 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0537    1.4407    0.2020 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1768   -0.2662    1.7294 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5182   -2.0529    2.8602 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3513   -0.7321   -0.6978 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2399   -2.5199   -1.4199 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2143   -2.6006   -0.7144 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8367   -3.0684    0.9372 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5156   -0.5721   -1.1147 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8379    2.8995   -0.3022 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8497    0.8788   -2.4557 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8346    2.7144   -2.5096 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3472    1.8112   -2.4319 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7003    2.4789    0.9628 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3446    2.5414   -1.1774 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6485    0.4243    1.1467 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1131   -0.1509   -0.4150 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6900   -0.4140   -1.6245 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6548   -1.9229    0.7788 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  2  0
  5  8  1  0
  8  9  1  0
  8 10  1  0
 10 11  1  0
 10 12  1  0
 12 13  1  0
 12 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 18 20  1  0
 20 21  1  0
 20 22  1  0
 22 23  1  0
 22 24  1  0
 24 25  1  0
 24 16  1  0
  1 26  1  0
  1 27  1  0
  1 28  1  0
  4 29  1  0
  5 30  1  6
  6 31  1  0
  8 32  1  1
  9 33  1  0
 10 34  1  1
 11 35  1  0
 12 36  1  0
 13 37  1  0
 14 38  1  0
 14 39  1  0
 16 40  1  0
 18 41  1  6
 19 42  1  0
 19 43  1  0
 19 44  1  0
 20 45  1  1
 21 46  1  0
 22 47  1  1
 23 48  1  0
 24 49  1  6
 25 50  1  0
M  END

View in JSmol View NMR Assignments View Stereo Labels

Synonyms

Value	Source
2-(acetylamino)-2-Deoxy-6-O-(6-deoxy-L-galactopyranosyl)-D-glucose	HMDB
N-[(2R,3R,4S)-3,4,5-Trihydroxy-1-oxo-6-{[(3S,4R,5S,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}hexan-2-yl]ethanimidate	Generator, HMDB

Chemical Formula

C₁₄H₂₅NO₁₀

Average Molecular Weight

367.349

Monoisotopic Molecular Weight

367.147846025

IUPAC Name

N-[(2R,3R,4S)-3,4,5-trihydroxy-1-oxo-6-{[(3S,4R,5S,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}hexan-2-yl]acetamide

Traditional Name

N-[(2R,3R,4S)-3,4,5-trihydroxy-1-oxo-6-{[(3S,4R,5S,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}hexan-2-yl]acetamide

CAS Registry Number

109582-58-3

SMILES

C[C@@H]1OC(OCC(O)[C@@H](O)[C@H](O)[C@@H](NC(C)=O)C=O)[C@@H](O)[C@H](O)[C@@H]1O

InChI Identifier

InChI=1S/C14H25NO10/c1-5-9(19)12(22)13(23)14(25-5)24-4-8(18)11(21)10(20)7(3-16)15-6(2)17/h3,5,7-14,18-23H,4H2,1-2H3,(H,15,17)/t5-,7-,8?,9+,10+,11+,12+,13-,14?/m0/s1

InChI Key

YBWAUUBLHOFOPK-SOHGFDPZSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as fatty acyl glycosides of mono- and disaccharides. Fatty acyl glycosides of mono- and disaccharides are compounds composed of a mono- or disaccharide moiety linked to one hydroxyl group of a fatty alcohol or of a phosphorylated alcohol (phosphoprenols), a hydroxy fatty acid or to one carboxyl group of a fatty acid (ester linkage) or to an amino alcohol.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Fatty Acyls

Sub Class

Fatty acyl glycosides

Direct Parent

Fatty acyl glycosides of mono- and disaccharides

Alternative Parents

Substituents

Fatty acyl glycoside of mono- or disaccharide
Alkyl glycoside
Hexose monosaccharide
Glycosyl compound
O-glycosyl compound
Amino saccharide
Beta-hydroxy aldehyde
Monosaccharide
Oxane
Acetamide
Carboxamide group
Secondary carboxylic acid amide
Secondary alcohol
Acetal
Carboxylic acid derivative
Oxacycle
Organoheterocyclic compound
Polyol
Hydrocarbon derivative
Organic oxide
Alcohol
Organopnictogen compound
Carbonyl group
Organic oxygen compound
Aldehyde
Organic nitrogen compound
Organonitrogen compound
Organooxygen compound
Aliphatic heteromonocyclic compound

Molecular Framework

Aliphatic heteromonocyclic compounds

External Descriptors

Not Available

Ontology

Physiological effect

Not Available

Disposition

Biological location

Cytoplasm (HMDB: HMDB0002220)
Cell membrane (HMDB: HMDB0002220)

Biofluid or Excreta

Urine (HMDB: HMDB0002220)

Route of exposure

Enteral

Ingestion (HMDB: HMDB0002220)

Source

Endogenous

Endogenous (HMDB: HMDB0002220)

Animal

Animal (HMDB: HMDB0002220)

Exogenous

Food

Food (HMDB: HMDB0002220)

Animal origin

Poultry

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

Naturally occurring process

Biological process

Chemical reaction

Lipid peroxidation (HMDB: HMDB0002220)

Biochemical process

Fatty acid metabolism (HMDB: HMDB0002220)

Biochemical pathway

Lipid metabolism pathway (HMDB: HMDB0002220)

Role

Biological role

Membrane stabilizer (HMDB: HMDB0002220)

Nutrient

Nutrient (HMDB: HMDB0002220)

Physical Properties

State

Solid

Experimental Molecular Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	1000000 mg/L @ 25 °C (est)	The Good Scents Company Information System
LogP	Not Available	Not Available

Experimental Chromatographic Properties

Not Available

Predicted Molecular Properties

Property	Value	Source
Water Solubility	102 g/L	ALOGPS
logP	-2	ALOGPS
logP	-4.6	ChemAxon
logS	-0.56	ALOGPS
pKa (Strongest Acidic)	11.42	ChemAxon
pKa (Strongest Basic)	-3.5	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	10	ChemAxon
Hydrogen Donor Count	7	ChemAxon
Polar Surface Area	186.01 Å²	ChemAxon
Rotatable Bond Count	8	ChemAxon
Refractivity	79.32 m³·mol⁻¹	ChemAxon
Polarizability	34.99 Å³	ChemAxon
Number of Rings	1	ChemAxon
Bioavailability	Yes	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]+	182.659	31661259
DarkChem	[M-H]-	178.812	31661259
DeepCCS	[M+H]+	183.643	30932474
DeepCCS	[M-H]-	181.247	30932474
DeepCCS	[M-2H]-	214.633	30932474
DeepCCS	[M+Na]+	189.555	30932474
AllCCS	[M+H]+	182.8	32859911
AllCCS	[M+H-H2O]+	180.4	32859911
AllCCS	[M+NH4]+	185.1	32859911
AllCCS	[M+Na]+	185.7	32859911
AllCCS	[M-H]-	184.5	32859911
AllCCS	[M+Na-2H]-	184.6	32859911
AllCCS	[M+HCOO]-	184.8	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
N-Acetyl-6-O-L-fucosyl-D-glucosamine	C[C@@H]1OC(OCC(O)[C@@H](O)[C@H](O)[C@@H](NC(C)=O)C=O)[C@@H](O)[C@H](O)[C@@H]1O	4080.4	Standard polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine	C[C@@H]1OC(OCC(O)[C@@H](O)[C@H](O)[C@@H](NC(C)=O)C=O)[C@@H](O)[C@H](O)[C@@H]1O	2758.1	Standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine	C[C@@H]1OC(OCC(O)[C@@H](O)[C@H](O)[C@@H](NC(C)=O)C=O)[C@@H](O)[C@H](O)[C@@H]1O	3049.9	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
N-Acetyl-6-O-L-fucosyl-D-glucosamine,1TMS,isomer #1	CC(=O)N[C@@H](C=O)[C@@H](O)[C@H](O)C(COC1O[C@@H](C)[C@@H](O)[C@@H](O)[C@@H]1O)O[Si](C)(C)C	2812.3	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,1TMS,isomer #2	CC(=O)N[C@@H](C=O)[C@@H](O)[C@H](O[Si](C)(C)C)C(O)COC1O[C@@H](C)[C@@H](O)[C@@H](O)[C@@H]1O	2814.7	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,1TMS,isomer #3	CC(=O)N[C@@H](C=O)[C@@H](O[Si](C)(C)C)[C@H](O)C(O)COC1O[C@@H](C)[C@@H](O)[C@@H](O)[C@@H]1O	2810.0	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,1TMS,isomer #4	CC(=O)N[C@@H](C=O)[C@@H](O)[C@H](O)C(O)COC1O[C@@H](C)[C@@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	2806.7	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,1TMS,isomer #5	CC(=O)N[C@@H](C=O)[C@@H](O)[C@H](O)C(O)COC1O[C@@H](C)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	2778.9	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,1TMS,isomer #6	CC(=O)N[C@@H](C=O)[C@@H](O)[C@H](O)C(O)COC1O[C@@H](C)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	2807.2	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,1TMS,isomer #7	CC(=O)NC(=CO[Si](C)(C)C)[C@@H](O)[C@H](O)C(O)COC1O[C@@H](C)[C@@H](O)[C@@H](O)[C@@H]1O	2971.1	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,1TMS,isomer #8	CC(=O)N([C@@H](C=O)[C@@H](O)[C@H](O)C(O)COC1O[C@@H](C)[C@@H](O)[C@@H](O)[C@@H]1O)[Si](C)(C)C	2865.0	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,2TMS,isomer #1	CC(=O)N[C@@H](C=O)[C@@H](O[Si](C)(C)C)[C@H](O)C(COC1O[C@@H](C)[C@@H](O)[C@@H](O)[C@@H]1O)O[Si](C)(C)C	2801.5	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,2TMS,isomer #10	CC(=O)N[C@@H](C=O)[C@@H](O)[C@H](O[Si](C)(C)C)C(O)COC1O[C@@H](C)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	2772.5	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,2TMS,isomer #11	CC(=O)N[C@@H](C=O)[C@@H](O)[C@H](O[Si](C)(C)C)C(O)COC1O[C@@H](C)[C@@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	2800.2	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,2TMS,isomer #12	CC(=O)NC(=CO[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)C(O)COC1O[C@@H](C)[C@@H](O)[C@@H](O)[C@@H]1O	2956.3	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,2TMS,isomer #13	CC(=O)N([C@@H](C=O)[C@@H](O)[C@H](O[Si](C)(C)C)C(O)COC1O[C@@H](C)[C@@H](O)[C@@H](O)[C@@H]1O)[Si](C)(C)C	2883.3	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,2TMS,isomer #14	CC(=O)N[C@@H](C=O)[C@@H](O[Si](C)(C)C)[C@H](O)C(O)COC1O[C@@H](C)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	2777.5	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,2TMS,isomer #15	CC(=O)N[C@@H](C=O)[C@@H](O[Si](C)(C)C)[C@H](O)C(O)COC1O[C@@H](C)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	2772.9	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,2TMS,isomer #16	CC(=O)N[C@@H](C=O)[C@@H](O[Si](C)(C)C)[C@H](O)C(O)COC1O[C@@H](C)[C@@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	2800.1	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,2TMS,isomer #17	CC(=O)NC(=CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)C(O)COC1O[C@@H](C)[C@@H](O)[C@@H](O)[C@@H]1O	2965.8	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,2TMS,isomer #18	CC(=O)N([C@@H](C=O)[C@@H](O[Si](C)(C)C)[C@H](O)C(O)COC1O[C@@H](C)[C@@H](O)[C@@H](O)[C@@H]1O)[Si](C)(C)C	2837.3	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,2TMS,isomer #19	CC(=O)N[C@@H](C=O)[C@@H](O)[C@H](O)C(O)COC1O[C@@H](C)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C	2792.0	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,2TMS,isomer #2	CC(=O)N[C@@H](C=O)[C@@H](O)[C@H](O[Si](C)(C)C)C(COC1O[C@@H](C)[C@@H](O)[C@@H](O)[C@@H]1O)O[Si](C)(C)C	2822.5	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,2TMS,isomer #20	CC(=O)N[C@@H](C=O)[C@@H](O)[C@H](O)C(O)COC1O[C@@H](C)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2787.7	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,2TMS,isomer #21	CC(=O)NC(=CO[Si](C)(C)C)[C@@H](O)[C@H](O)C(O)COC1O[C@@H](C)[C@@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	2971.9	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,2TMS,isomer #22	CC(=O)N([C@@H](C=O)[C@@H](O)[C@H](O)C(O)COC1O[C@@H](C)[C@@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C)[Si](C)(C)C	2882.2	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,2TMS,isomer #23	CC(=O)N[C@@H](C=O)[C@@H](O)[C@H](O)C(O)COC1O[C@@H](C)[C@@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O	2750.7	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,2TMS,isomer #24	CC(=O)NC(=CO[Si](C)(C)C)[C@@H](O)[C@H](O)C(O)COC1O[C@@H](C)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	2939.6	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,2TMS,isomer #25	CC(=O)N([C@@H](C=O)[C@@H](O)[C@H](O)C(O)COC1O[C@@H](C)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O)[Si](C)(C)C	2851.1	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,2TMS,isomer #26	CC(=O)NC(=CO[Si](C)(C)C)[C@@H](O)[C@H](O)C(O)COC1O[C@@H](C)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	2952.3	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,2TMS,isomer #27	CC(=O)N([C@@H](C=O)[C@@H](O)[C@H](O)C(O)COC1O[C@@H](C)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O)[Si](C)(C)C	2868.5	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,2TMS,isomer #28	CC(=O)N(C(=CO[Si](C)(C)C)[C@@H](O)[C@H](O)C(O)COC1O[C@@H](C)[C@@H](O)[C@@H](O)[C@@H]1O)[Si](C)(C)C	2956.5	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,2TMS,isomer #3	CC(=O)N[C@@H](C=O)[C@@H](O)[C@H](O)C(COC1O[C@@H](C)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O)O[Si](C)(C)C	2807.6	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,2TMS,isomer #4	CC(=O)N[C@@H](C=O)[C@@H](O)[C@H](O)C(COC1O[C@@H](C)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O)O[Si](C)(C)C	2795.2	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,2TMS,isomer #5	CC(=O)N[C@@H](C=O)[C@@H](O)[C@H](O)C(COC1O[C@@H](C)[C@@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C)O[Si](C)(C)C	2833.0	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,2TMS,isomer #6	CC(=O)NC(=CO[Si](C)(C)C)[C@@H](O)[C@H](O)C(COC1O[C@@H](C)[C@@H](O)[C@@H](O)[C@@H]1O)O[Si](C)(C)C	2976.5	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,2TMS,isomer #7	CC(=O)N([C@@H](C=O)[C@@H](O)[C@H](O)C(COC1O[C@@H](C)[C@@H](O)[C@@H](O)[C@@H]1O)O[Si](C)(C)C)[Si](C)(C)C	2873.7	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,2TMS,isomer #8	CC(=O)N[C@@H](C=O)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)C(O)COC1O[C@@H](C)[C@@H](O)[C@@H](O)[C@@H]1O	2779.8	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,2TMS,isomer #9	CC(=O)N[C@@H](C=O)[C@@H](O)[C@H](O[Si](C)(C)C)C(O)COC1O[C@@H](C)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	2779.8	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,3TMS,isomer #1	CC(=O)N[C@@H](C=O)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)C(COC1O[C@@H](C)[C@@H](O)[C@@H](O)[C@@H]1O)O[Si](C)(C)C	2766.8	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,3TMS,isomer #10	CC(=O)NC(=CO[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)C(COC1O[C@@H](C)[C@@H](O)[C@@H](O)[C@@H]1O)O[Si](C)(C)C	2957.6	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,3TMS,isomer #11	CC(=O)N([C@@H](C=O)[C@@H](O)[C@H](O[Si](C)(C)C)C(COC1O[C@@H](C)[C@@H](O)[C@@H](O)[C@@H]1O)O[Si](C)(C)C)[Si](C)(C)C	2859.9	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,3TMS,isomer #12	CC(=O)N[C@@H](C=O)[C@@H](O)[C@H](O)C(COC1O[C@@H](C)[C@@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O)O[Si](C)(C)C	2766.6	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,3TMS,isomer #13	CC(=O)N[C@@H](C=O)[C@@H](O)[C@H](O)C(COC1O[C@@H](C)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C)O[Si](C)(C)C	2804.7	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,3TMS,isomer #14	CC(=O)NC(=CO[Si](C)(C)C)[C@@H](O)[C@H](O)C(COC1O[C@@H](C)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O)O[Si](C)(C)C	2939.6	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,3TMS,isomer #15	CC(=O)N([C@@H](C=O)[C@@H](O)[C@H](O)C(COC1O[C@@H](C)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O)O[Si](C)(C)C)[Si](C)(C)C	2840.3	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,3TMS,isomer #16	CC(=O)N[C@@H](C=O)[C@@H](O)[C@H](O)C(COC1O[C@@H](C)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C)O[Si](C)(C)C	2785.2	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,3TMS,isomer #17	CC(=O)NC(=CO[Si](C)(C)C)[C@@H](O)[C@H](O)C(COC1O[C@@H](C)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O)O[Si](C)(C)C	2932.3	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,3TMS,isomer #18	CC(=O)N([C@@H](C=O)[C@@H](O)[C@H](O)C(COC1O[C@@H](C)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O)O[Si](C)(C)C)[Si](C)(C)C	2831.2	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,3TMS,isomer #19	CC(=O)NC(=CO[Si](C)(C)C)[C@@H](O)[C@H](O)C(COC1O[C@@H](C)[C@@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C)O[Si](C)(C)C	2970.8	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,3TMS,isomer #2	CC(=O)N[C@@H](C=O)[C@@H](O[Si](C)(C)C)[C@H](O)C(COC1O[C@@H](C)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O)O[Si](C)(C)C	2781.4	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,3TMS,isomer #20	CC(=O)N([C@@H](C=O)[C@@H](O)[C@H](O)C(COC1O[C@@H](C)[C@@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C)O[Si](C)(C)C)[Si](C)(C)C	2866.6	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,3TMS,isomer #21	CC(=O)N(C(=CO[Si](C)(C)C)[C@@H](O)[C@H](O)C(COC1O[C@@H](C)[C@@H](O)[C@@H](O)[C@@H]1O)O[Si](C)(C)C)[Si](C)(C)C	2898.6	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,3TMS,isomer #22	CC(=O)N[C@@H](C=O)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)C(O)COC1O[C@@H](C)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	2797.9	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,3TMS,isomer #23	CC(=O)N[C@@H](C=O)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)C(O)COC1O[C@@H](C)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	2803.0	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,3TMS,isomer #24	CC(=O)N[C@@H](C=O)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)C(O)COC1O[C@@H](C)[C@@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	2798.2	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,3TMS,isomer #25	CC(=O)NC(=CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)C(O)COC1O[C@@H](C)[C@@H](O)[C@@H](O)[C@@H]1O	2925.3	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,3TMS,isomer #26	CC(=O)N([C@@H](C=O)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)C(O)COC1O[C@@H](C)[C@@H](O)[C@@H](O)[C@@H]1O)[Si](C)(C)C	2823.4	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,3TMS,isomer #27	CC(=O)N[C@@H](C=O)[C@@H](O)[C@H](O[Si](C)(C)C)C(O)COC1O[C@@H](C)[C@@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O	2789.0	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,3TMS,isomer #28	CC(=O)N[C@@H](C=O)[C@@H](O)[C@H](O[Si](C)(C)C)C(O)COC1O[C@@H](C)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C	2822.3	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,3TMS,isomer #29	CC(=O)NC(=CO[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)C(O)COC1O[C@@H](C)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	2913.7	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,3TMS,isomer #3	CC(=O)N[C@@H](C=O)[C@@H](O[Si](C)(C)C)[C@H](O)C(COC1O[C@@H](C)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O)O[Si](C)(C)C	2783.6	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,3TMS,isomer #30	CC(=O)N([C@@H](C=O)[C@@H](O)[C@H](O[Si](C)(C)C)C(O)COC1O[C@@H](C)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O)[Si](C)(C)C	2854.3	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,3TMS,isomer #31	CC(=O)N[C@@H](C=O)[C@@H](O)[C@H](O[Si](C)(C)C)C(O)COC1O[C@@H](C)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2790.8	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,3TMS,isomer #32	CC(=O)NC(=CO[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)C(O)COC1O[C@@H](C)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	2912.5	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,3TMS,isomer #33	CC(=O)N([C@@H](C=O)[C@@H](O)[C@H](O[Si](C)(C)C)C(O)COC1O[C@@H](C)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O)[Si](C)(C)C	2841.6	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,3TMS,isomer #34	CC(=O)NC(=CO[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)C(O)COC1O[C@@H](C)[C@@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	2934.4	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,3TMS,isomer #35	CC(=O)N([C@@H](C=O)[C@@H](O)[C@H](O[Si](C)(C)C)C(O)COC1O[C@@H](C)[C@@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C)[Si](C)(C)C	2868.8	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,3TMS,isomer #36	CC(=O)N(C(=CO[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)C(O)COC1O[C@@H](C)[C@@H](O)[C@@H](O)[C@@H]1O)[Si](C)(C)C	2903.3	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,3TMS,isomer #37	CC(=O)N[C@@H](C=O)[C@@H](O[Si](C)(C)C)[C@H](O)C(O)COC1O[C@@H](C)[C@@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O	2771.2	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,3TMS,isomer #38	CC(=O)N[C@@H](C=O)[C@@H](O[Si](C)(C)C)[C@H](O)C(O)COC1O[C@@H](C)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C	2804.7	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,3TMS,isomer #39	CC(=O)NC(=CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)C(O)COC1O[C@@H](C)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	2922.8	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,3TMS,isomer #4	CC(=O)N[C@@H](C=O)[C@@H](O[Si](C)(C)C)[C@H](O)C(COC1O[C@@H](C)[C@@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C)O[Si](C)(C)C	2787.0	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,3TMS,isomer #40	CC(=O)N([C@@H](C=O)[C@@H](O[Si](C)(C)C)[C@H](O)C(O)COC1O[C@@H](C)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O)[Si](C)(C)C	2814.0	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,3TMS,isomer #41	CC(=O)N[C@@H](C=O)[C@@H](O[Si](C)(C)C)[C@H](O)C(O)COC1O[C@@H](C)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2768.9	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,3TMS,isomer #42	CC(=O)NC(=CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)C(O)COC1O[C@@H](C)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	2909.7	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,3TMS,isomer #43	CC(=O)N([C@@H](C=O)[C@@H](O[Si](C)(C)C)[C@H](O)C(O)COC1O[C@@H](C)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O)[Si](C)(C)C	2804.2	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,3TMS,isomer #44	CC(=O)NC(=CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)C(O)COC1O[C@@H](C)[C@@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	2945.6	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,3TMS,isomer #45	CC(=O)N([C@@H](C=O)[C@@H](O[Si](C)(C)C)[C@H](O)C(O)COC1O[C@@H](C)[C@@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C)[Si](C)(C)C	2820.0	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,3TMS,isomer #46	CC(=O)N(C(=CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)C(O)COC1O[C@@H](C)[C@@H](O)[C@@H](O)[C@@H]1O)[Si](C)(C)C	2882.0	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,3TMS,isomer #47	CC(=O)N[C@@H](C=O)[C@@H](O)[C@H](O)C(O)COC1O[C@@H](C)[C@@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2767.9	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,3TMS,isomer #48	CC(=O)NC(=CO[Si](C)(C)C)[C@@H](O)[C@H](O)C(O)COC1O[C@@H](C)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C	2916.2	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,3TMS,isomer #49	CC(=O)N([C@@H](C=O)[C@@H](O)[C@H](O)C(O)COC1O[C@@H](C)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C)[Si](C)(C)C	2840.6	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,3TMS,isomer #5	CC(=O)NC(=CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)C(COC1O[C@@H](C)[C@@H](O)[C@@H](O)[C@@H]1O)O[Si](C)(C)C	2962.5	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,3TMS,isomer #50	CC(=O)NC(=CO[Si](C)(C)C)[C@@H](O)[C@H](O)C(O)COC1O[C@@H](C)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2902.4	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,3TMS,isomer #51	CC(=O)N([C@@H](C=O)[C@@H](O)[C@H](O)C(O)COC1O[C@@H](C)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C)[Si](C)(C)C	2840.4	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,3TMS,isomer #52	CC(=O)N(C(=CO[Si](C)(C)C)[C@@H](O)[C@H](O)C(O)COC1O[C@@H](C)[C@@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C)[Si](C)(C)C	2885.0	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,3TMS,isomer #53	CC(=O)NC(=CO[Si](C)(C)C)[C@@H](O)[C@H](O)C(O)COC1O[C@@H](C)[C@@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O	2865.9	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,3TMS,isomer #54	CC(=O)N([C@@H](C=O)[C@@H](O)[C@H](O)C(O)COC1O[C@@H](C)[C@@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O)[Si](C)(C)C	2810.6	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,3TMS,isomer #55	CC(=O)N(C(=CO[Si](C)(C)C)[C@@H](O)[C@H](O)C(O)COC1O[C@@H](C)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O)[Si](C)(C)C	2856.7	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,3TMS,isomer #56	CC(=O)N(C(=CO[Si](C)(C)C)[C@@H](O)[C@H](O)C(O)COC1O[C@@H](C)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O)[Si](C)(C)C	2869.2	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,3TMS,isomer #6	CC(=O)N([C@@H](C=O)[C@@H](O[Si](C)(C)C)[C@H](O)C(COC1O[C@@H](C)[C@@H](O)[C@@H](O)[C@@H]1O)O[Si](C)(C)C)[Si](C)(C)C	2805.8	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,3TMS,isomer #7	CC(=O)N[C@@H](C=O)[C@@H](O)[C@H](O[Si](C)(C)C)C(COC1O[C@@H](C)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O)O[Si](C)(C)C	2786.8	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,3TMS,isomer #8	CC(=O)N[C@@H](C=O)[C@@H](O)[C@H](O[Si](C)(C)C)C(COC1O[C@@H](C)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O)O[Si](C)(C)C	2782.0	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,3TMS,isomer #9	CC(=O)N[C@@H](C=O)[C@@H](O)[C@H](O[Si](C)(C)C)C(COC1O[C@@H](C)[C@@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C)O[Si](C)(C)C	2807.4	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,4TMS,isomer #1	CC(=O)N[C@@H](C=O)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)C(COC1O[C@@H](C)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O)O[Si](C)(C)C	2833.5	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,4TMS,isomer #10	CC(=O)N[C@@H](C=O)[C@@H](O[Si](C)(C)C)[C@H](O)C(COC1O[C@@H](C)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C)O[Si](C)(C)C	2826.8	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,4TMS,isomer #11	CC(=O)NC(=CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)C(COC1O[C@@H](C)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O)O[Si](C)(C)C	2953.6	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,4TMS,isomer #12	CC(=O)N([C@@H](C=O)[C@@H](O[Si](C)(C)C)[C@H](O)C(COC1O[C@@H](C)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O)O[Si](C)(C)C)[Si](C)(C)C	2839.3	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,4TMS,isomer #13	CC(=O)NC(=CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)C(COC1O[C@@H](C)[C@@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C)O[Si](C)(C)C	2937.1	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,4TMS,isomer #14	CC(=O)N([C@@H](C=O)[C@@H](O[Si](C)(C)C)[C@H](O)C(COC1O[C@@H](C)[C@@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C)O[Si](C)(C)C)[Si](C)(C)C	2845.5	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,4TMS,isomer #15	CC(=O)N(C(=CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)C(COC1O[C@@H](C)[C@@H](O)[C@@H](O)[C@@H]1O)O[Si](C)(C)C)[Si](C)(C)C	2878.9	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,4TMS,isomer #16	CC(=O)N[C@@H](C=O)[C@@H](O)[C@H](O[Si](C)(C)C)C(COC1O[C@@H](C)[C@@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O)O[Si](C)(C)C	2820.9	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,4TMS,isomer #17	CC(=O)N[C@@H](C=O)[C@@H](O)[C@H](O[Si](C)(C)C)C(COC1O[C@@H](C)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C)O[Si](C)(C)C	2846.9	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,4TMS,isomer #18	CC(=O)NC(=CO[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)C(COC1O[C@@H](C)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O)O[Si](C)(C)C	2914.0	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,4TMS,isomer #19	CC(=O)N([C@@H](C=O)[C@@H](O)[C@H](O[Si](C)(C)C)C(COC1O[C@@H](C)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O)O[Si](C)(C)C)[Si](C)(C)C	2847.6	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,4TMS,isomer #2	CC(=O)N[C@@H](C=O)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)C(COC1O[C@@H](C)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O)O[Si](C)(C)C	2836.9	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,4TMS,isomer #20	CC(=O)N[C@@H](C=O)[C@@H](O)[C@H](O[Si](C)(C)C)C(COC1O[C@@H](C)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C)O[Si](C)(C)C	2822.2	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,4TMS,isomer #21	CC(=O)NC(=CO[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)C(COC1O[C@@H](C)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O)O[Si](C)(C)C	2915.1	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,4TMS,isomer #22	CC(=O)N([C@@H](C=O)[C@@H](O)[C@H](O[Si](C)(C)C)C(COC1O[C@@H](C)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O)O[Si](C)(C)C)[Si](C)(C)C	2842.3	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,4TMS,isomer #23	CC(=O)NC(=CO[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)C(COC1O[C@@H](C)[C@@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C)O[Si](C)(C)C	2908.0	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,4TMS,isomer #24	CC(=O)N([C@@H](C=O)[C@@H](O)[C@H](O[Si](C)(C)C)C(COC1O[C@@H](C)[C@@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C)O[Si](C)(C)C)[Si](C)(C)C	2859.9	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,4TMS,isomer #25	CC(=O)N(C(=CO[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)C(COC1O[C@@H](C)[C@@H](O)[C@@H](O)[C@@H]1O)O[Si](C)(C)C)[Si](C)(C)C	2895.1	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,4TMS,isomer #26	CC(=O)N[C@@H](C=O)[C@@H](O)[C@H](O)C(COC1O[C@@H](C)[C@@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C)O[Si](C)(C)C	2806.7	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,4TMS,isomer #27	CC(=O)NC(=CO[Si](C)(C)C)[C@@H](O)[C@H](O)C(COC1O[C@@H](C)[C@@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O)O[Si](C)(C)C	2881.7	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,4TMS,isomer #28	CC(=O)N([C@@H](C=O)[C@@H](O)[C@H](O)C(COC1O[C@@H](C)[C@@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O)O[Si](C)(C)C)[Si](C)(C)C	2821.9	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,4TMS,isomer #29	CC(=O)NC(=CO[Si](C)(C)C)[C@@H](O)[C@H](O)C(COC1O[C@@H](C)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C)O[Si](C)(C)C	2920.1	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,4TMS,isomer #3	CC(=O)N[C@@H](C=O)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)C(COC1O[C@@H](C)[C@@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C)O[Si](C)(C)C	2814.6	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,4TMS,isomer #30	CC(=O)N([C@@H](C=O)[C@@H](O)[C@H](O)C(COC1O[C@@H](C)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C)O[Si](C)(C)C)[Si](C)(C)C	2842.4	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,4TMS,isomer #31	CC(=O)N(C(=CO[Si](C)(C)C)[C@@H](O)[C@H](O)C(COC1O[C@@H](C)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O)O[Si](C)(C)C)[Si](C)(C)C	2871.3	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,4TMS,isomer #32	CC(=O)NC(=CO[Si](C)(C)C)[C@@H](O)[C@H](O)C(COC1O[C@@H](C)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C)O[Si](C)(C)C	2894.4	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,4TMS,isomer #33	CC(=O)N([C@@H](C=O)[C@@H](O)[C@H](O)C(COC1O[C@@H](C)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C)O[Si](C)(C)C)[Si](C)(C)C	2843.0	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,4TMS,isomer #34	CC(=O)N(C(=CO[Si](C)(C)C)[C@@H](O)[C@H](O)C(COC1O[C@@H](C)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O)O[Si](C)(C)C)[Si](C)(C)C	2863.8	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,4TMS,isomer #35	CC(=O)N(C(=CO[Si](C)(C)C)[C@@H](O)[C@H](O)C(COC1O[C@@H](C)[C@@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C)O[Si](C)(C)C)[Si](C)(C)C	2873.2	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,4TMS,isomer #36	CC(=O)N[C@@H](C=O)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)C(O)COC1O[C@@H](C)[C@@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O	2866.0	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,4TMS,isomer #37	CC(=O)N[C@@H](C=O)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)C(O)COC1O[C@@H](C)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C	2882.9	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,4TMS,isomer #38	CC(=O)NC(=CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)C(O)COC1O[C@@H](C)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	2958.9	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,4TMS,isomer #39	CC(=O)N([C@@H](C=O)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)C(O)COC1O[C@@H](C)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O)[Si](C)(C)C	2865.6	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,4TMS,isomer #4	CC(=O)NC(=CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)C(COC1O[C@@H](C)[C@@H](O)[C@@H](O)[C@@H]1O)O[Si](C)(C)C	2917.3	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,4TMS,isomer #40	CC(=O)N[C@@H](C=O)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)C(O)COC1O[C@@H](C)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2856.1	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,4TMS,isomer #41	CC(=O)NC(=CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)C(O)COC1O[C@@H](C)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	2956.0	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,4TMS,isomer #42	CC(=O)N([C@@H](C=O)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)C(O)COC1O[C@@H](C)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O)[Si](C)(C)C	2864.1	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,4TMS,isomer #43	CC(=O)NC(=CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)C(O)COC1O[C@@H](C)[C@@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	2941.2	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,4TMS,isomer #44	CC(=O)N([C@@H](C=O)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)C(O)COC1O[C@@H](C)[C@@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C)[Si](C)(C)C	2864.9	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,4TMS,isomer #45	CC(=O)N(C(=CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)C(O)COC1O[C@@H](C)[C@@H](O)[C@@H](O)[C@@H]1O)[Si](C)(C)C	2873.5	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,4TMS,isomer #46	CC(=O)N[C@@H](C=O)[C@@H](O)[C@H](O[Si](C)(C)C)C(O)COC1O[C@@H](C)[C@@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2835.2	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,4TMS,isomer #47	CC(=O)NC(=CO[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)C(O)COC1O[C@@H](C)[C@@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O	2911.0	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,4TMS,isomer #48	CC(=O)N([C@@H](C=O)[C@@H](O)[C@H](O[Si](C)(C)C)C(O)COC1O[C@@H](C)[C@@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O)[Si](C)(C)C	2844.6	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,4TMS,isomer #49	CC(=O)NC(=CO[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)C(O)COC1O[C@@H](C)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C	2940.7	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,4TMS,isomer #5	CC(=O)N([C@@H](C=O)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)C(COC1O[C@@H](C)[C@@H](O)[C@@H](O)[C@@H]1O)O[Si](C)(C)C)[Si](C)(C)C	2842.6	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,4TMS,isomer #50	CC(=O)N([C@@H](C=O)[C@@H](O)[C@H](O[Si](C)(C)C)C(O)COC1O[C@@H](C)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C)[Si](C)(C)C	2862.2	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,4TMS,isomer #51	CC(=O)N(C(=CO[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)C(O)COC1O[C@@H](C)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O)[Si](C)(C)C	2900.3	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,4TMS,isomer #52	CC(=O)NC(=CO[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)C(O)COC1O[C@@H](C)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2914.3	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,4TMS,isomer #53	CC(=O)N([C@@H](C=O)[C@@H](O)[C@H](O[Si](C)(C)C)C(O)COC1O[C@@H](C)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C)[Si](C)(C)C	2863.0	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,4TMS,isomer #54	CC(=O)N(C(=CO[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)C(O)COC1O[C@@H](C)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O)[Si](C)(C)C	2896.3	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,4TMS,isomer #55	CC(=O)N(C(=CO[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)C(O)COC1O[C@@H](C)[C@@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C)[Si](C)(C)C	2903.3	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,4TMS,isomer #56	CC(=O)N[C@@H](C=O)[C@@H](O[Si](C)(C)C)[C@H](O)C(O)COC1O[C@@H](C)[C@@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2838.4	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,4TMS,isomer #57	CC(=O)NC(=CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)C(O)COC1O[C@@H](C)[C@@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O	2920.2	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,4TMS,isomer #58	CC(=O)N([C@@H](C=O)[C@@H](O[Si](C)(C)C)[C@H](O)C(O)COC1O[C@@H](C)[C@@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O)[Si](C)(C)C	2840.4	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,4TMS,isomer #59	CC(=O)NC(=CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)C(O)COC1O[C@@H](C)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C	2948.5	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,4TMS,isomer #6	CC(=O)N[C@@H](C=O)[C@@H](O[Si](C)(C)C)[C@H](O)C(COC1O[C@@H](C)[C@@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O)O[Si](C)(C)C	2833.8	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,4TMS,isomer #60	CC(=O)N([C@@H](C=O)[C@@H](O[Si](C)(C)C)[C@H](O)C(O)COC1O[C@@H](C)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C)[Si](C)(C)C	2852.5	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,4TMS,isomer #61	CC(=O)N(C(=CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)C(O)COC1O[C@@H](C)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O)[Si](C)(C)C	2869.7	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,4TMS,isomer #62	CC(=O)NC(=CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)C(O)COC1O[C@@H](C)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2920.4	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,4TMS,isomer #63	CC(=O)N([C@@H](C=O)[C@@H](O[Si](C)(C)C)[C@H](O)C(O)COC1O[C@@H](C)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C)[Si](C)(C)C	2853.8	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,4TMS,isomer #64	CC(=O)N(C(=CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)C(O)COC1O[C@@H](C)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O)[Si](C)(C)C	2855.4	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,4TMS,isomer #65	CC(=O)N(C(=CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)C(O)COC1O[C@@H](C)[C@@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C)[Si](C)(C)C	2863.8	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,4TMS,isomer #66	CC(=O)NC(=CO[Si](C)(C)C)[C@@H](O)[C@H](O)C(O)COC1O[C@@H](C)[C@@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2870.6	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,4TMS,isomer #67	CC(=O)N([C@@H](C=O)[C@@H](O)[C@H](O)C(O)COC1O[C@@H](C)[C@@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C)[Si](C)(C)C	2830.4	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,4TMS,isomer #68	CC(=O)N(C(=CO[Si](C)(C)C)[C@@H](O)[C@H](O)C(O)COC1O[C@@H](C)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C)[Si](C)(C)C	2878.4	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,4TMS,isomer #69	CC(=O)N(C(=CO[Si](C)(C)C)[C@@H](O)[C@H](O)C(O)COC1O[C@@H](C)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C)[Si](C)(C)C	2868.5	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,4TMS,isomer #7	CC(=O)N[C@@H](C=O)[C@@H](O[Si](C)(C)C)[C@H](O)C(COC1O[C@@H](C)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C)O[Si](C)(C)C	2855.8	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,4TMS,isomer #70	CC(=O)N(C(=CO[Si](C)(C)C)[C@@H](O)[C@H](O)C(O)COC1O[C@@H](C)[C@@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O)[Si](C)(C)C	2852.8	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,4TMS,isomer #8	CC(=O)NC(=CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)C(COC1O[C@@H](C)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O)O[Si](C)(C)C	2955.9	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,4TMS,isomer #9	CC(=O)N([C@@H](C=O)[C@@H](O[Si](C)(C)C)[C@H](O)C(COC1O[C@@H](C)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O)O[Si](C)(C)C)[Si](C)(C)C	2837.5	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,5TMS,isomer #1	CC(=O)N[C@@H](C=O)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)C(COC1O[C@@H](C)[C@@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O)O[Si](C)(C)C	2874.7	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,5TMS,isomer #10	CC(=O)N(C(=CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)C(COC1O[C@@H](C)[C@@H](O)[C@@H](O)[C@@H]1O)O[Si](C)(C)C)[Si](C)(C)C	2908.6	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,5TMS,isomer #11	CC(=O)N[C@@H](C=O)[C@@H](O[Si](C)(C)C)[C@H](O)C(COC1O[C@@H](C)[C@@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C)O[Si](C)(C)C	2877.9	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,5TMS,isomer #12	CC(=O)NC(=CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)C(COC1O[C@@H](C)[C@@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O)O[Si](C)(C)C	2956.9	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,5TMS,isomer #13	CC(=O)N([C@@H](C=O)[C@@H](O[Si](C)(C)C)[C@H](O)C(COC1O[C@@H](C)[C@@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O)O[Si](C)(C)C)[Si](C)(C)C	2859.7	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,5TMS,isomer #14	CC(=O)NC(=CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)C(COC1O[C@@H](C)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C)O[Si](C)(C)C	2980.0	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,5TMS,isomer #15	CC(=O)N([C@@H](C=O)[C@@H](O[Si](C)(C)C)[C@H](O)C(COC1O[C@@H](C)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C)O[Si](C)(C)C)[Si](C)(C)C	2875.5	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,5TMS,isomer #16	CC(=O)N(C(=CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)C(COC1O[C@@H](C)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O)O[Si](C)(C)C)[Si](C)(C)C	2915.7	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,5TMS,isomer #17	CC(=O)NC(=CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)C(COC1O[C@@H](C)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C)O[Si](C)(C)C	2963.1	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,5TMS,isomer #18	CC(=O)N([C@@H](C=O)[C@@H](O[Si](C)(C)C)[C@H](O)C(COC1O[C@@H](C)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C)O[Si](C)(C)C)[Si](C)(C)C	2880.6	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,5TMS,isomer #19	CC(=O)N(C(=CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)C(COC1O[C@@H](C)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O)O[Si](C)(C)C)[Si](C)(C)C	2907.7	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,5TMS,isomer #2	CC(=O)N[C@@H](C=O)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)C(COC1O[C@@H](C)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C)O[Si](C)(C)C	2888.3	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,5TMS,isomer #20	CC(=O)N(C(=CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)C(COC1O[C@@H](C)[C@@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C)O[Si](C)(C)C)[Si](C)(C)C	2920.9	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,5TMS,isomer #21	CC(=O)N[C@@H](C=O)[C@@H](O)[C@H](O[Si](C)(C)C)C(COC1O[C@@H](C)[C@@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C)O[Si](C)(C)C	2866.7	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,5TMS,isomer #22	CC(=O)NC(=CO[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)C(COC1O[C@@H](C)[C@@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O)O[Si](C)(C)C	2917.4	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,5TMS,isomer #23	CC(=O)N([C@@H](C=O)[C@@H](O)[C@H](O[Si](C)(C)C)C(COC1O[C@@H](C)[C@@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O)O[Si](C)(C)C)[Si](C)(C)C	2864.7	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,5TMS,isomer #24	CC(=O)NC(=CO[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)C(COC1O[C@@H](C)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C)O[Si](C)(C)C	2946.9	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,5TMS,isomer #25	CC(=O)N([C@@H](C=O)[C@@H](O)[C@H](O[Si](C)(C)C)C(COC1O[C@@H](C)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C)O[Si](C)(C)C)[Si](C)(C)C	2883.0	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,5TMS,isomer #26	CC(=O)N(C(=CO[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)C(COC1O[C@@H](C)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O)O[Si](C)(C)C)[Si](C)(C)C	2929.1	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,5TMS,isomer #27	CC(=O)NC(=CO[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)C(COC1O[C@@H](C)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C)O[Si](C)(C)C	2935.0	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,5TMS,isomer #28	CC(=O)N([C@@H](C=O)[C@@H](O)[C@H](O[Si](C)(C)C)C(COC1O[C@@H](C)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C)O[Si](C)(C)C)[Si](C)(C)C	2882.8	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,5TMS,isomer #29	CC(=O)N(C(=CO[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)C(COC1O[C@@H](C)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O)O[Si](C)(C)C)[Si](C)(C)C	2925.3	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,5TMS,isomer #3	CC(=O)NC(=CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)C(COC1O[C@@H](C)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O)O[Si](C)(C)C	2953.8	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,5TMS,isomer #30	CC(=O)N(C(=CO[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)C(COC1O[C@@H](C)[C@@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C)O[Si](C)(C)C)[Si](C)(C)C	2941.3	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,5TMS,isomer #31	CC(=O)NC(=CO[Si](C)(C)C)[C@@H](O)[C@H](O)C(COC1O[C@@H](C)[C@@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C)O[Si](C)(C)C	2909.0	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,5TMS,isomer #32	CC(=O)N([C@@H](C=O)[C@@H](O)[C@H](O)C(COC1O[C@@H](C)[C@@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C)O[Si](C)(C)C)[Si](C)(C)C	2861.0	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,5TMS,isomer #33	CC(=O)N(C(=CO[Si](C)(C)C)[C@@H](O)[C@H](O)C(COC1O[C@@H](C)[C@@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O)O[Si](C)(C)C)[Si](C)(C)C	2893.0	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,5TMS,isomer #34	CC(=O)N(C(=CO[Si](C)(C)C)[C@@H](O)[C@H](O)C(COC1O[C@@H](C)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C)O[Si](C)(C)C)[Si](C)(C)C	2917.2	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,5TMS,isomer #35	CC(=O)N(C(=CO[Si](C)(C)C)[C@@H](O)[C@H](O)C(COC1O[C@@H](C)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C)O[Si](C)(C)C)[Si](C)(C)C	2916.4	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,5TMS,isomer #36	CC(=O)N[C@@H](C=O)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)C(O)COC1O[C@@H](C)[C@@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2902.1	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,5TMS,isomer #37	CC(=O)NC(=CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)C(O)COC1O[C@@H](C)[C@@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O	2958.5	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,5TMS,isomer #38	CC(=O)N([C@@H](C=O)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)C(O)COC1O[C@@H](C)[C@@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O)[Si](C)(C)C	2887.8	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,5TMS,isomer #39	CC(=O)NC(=CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)C(O)COC1O[C@@H](C)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C	2986.9	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,5TMS,isomer #4	CC(=O)N([C@@H](C=O)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)C(COC1O[C@@H](C)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O)O[Si](C)(C)C)[Si](C)(C)C	2890.3	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,5TMS,isomer #40	CC(=O)N([C@@H](C=O)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)C(O)COC1O[C@@H](C)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C)[Si](C)(C)C	2898.7	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,5TMS,isomer #41	CC(=O)N(C(=CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)C(O)COC1O[C@@H](C)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O)[Si](C)(C)C	2917.6	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,5TMS,isomer #42	CC(=O)NC(=CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)C(O)COC1O[C@@H](C)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2964.9	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,5TMS,isomer #43	CC(=O)N([C@@H](C=O)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)C(O)COC1O[C@@H](C)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C)[Si](C)(C)C	2902.4	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,5TMS,isomer #44	CC(=O)N(C(=CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)C(O)COC1O[C@@H](C)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O)[Si](C)(C)C	2904.7	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,5TMS,isomer #45	CC(=O)N(C(=CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)C(O)COC1O[C@@H](C)[C@@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C)[Si](C)(C)C	2912.7	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,5TMS,isomer #46	CC(=O)NC(=CO[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)C(O)COC1O[C@@H](C)[C@@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2935.0	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,5TMS,isomer #47	CC(=O)N([C@@H](C=O)[C@@H](O)[C@H](O[Si](C)(C)C)C(O)COC1O[C@@H](C)[C@@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C)[Si](C)(C)C	2880.6	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,5TMS,isomer #48	CC(=O)N(C(=CO[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)C(O)COC1O[C@@H](C)[C@@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O)[Si](C)(C)C	2918.0	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,5TMS,isomer #49	CC(=O)N(C(=CO[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)C(O)COC1O[C@@H](C)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C)[Si](C)(C)C	2937.1	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,5TMS,isomer #5	CC(=O)N[C@@H](C=O)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)C(COC1O[C@@H](C)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C)O[Si](C)(C)C	2884.4	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,5TMS,isomer #50	CC(=O)N(C(=CO[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)C(O)COC1O[C@@H](C)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C)[Si](C)(C)C	2937.0	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,5TMS,isomer #51	CC(=O)NC(=CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)C(O)COC1O[C@@H](C)[C@@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2950.3	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,5TMS,isomer #52	CC(=O)N([C@@H](C=O)[C@@H](O[Si](C)(C)C)[C@H](O)C(O)COC1O[C@@H](C)[C@@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C)[Si](C)(C)C	2883.3	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,5TMS,isomer #53	CC(=O)N(C(=CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)C(O)COC1O[C@@H](C)[C@@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O)[Si](C)(C)C	2894.6	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,5TMS,isomer #54	CC(=O)N(C(=CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)C(O)COC1O[C@@H](C)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C)[Si](C)(C)C	2923.3	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,5TMS,isomer #55	CC(=O)N(C(=CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)C(O)COC1O[C@@H](C)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C)[Si](C)(C)C	2904.2	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,5TMS,isomer #56	CC(=O)N(C(=CO[Si](C)(C)C)[C@@H](O)[C@H](O)C(O)COC1O[C@@H](C)[C@@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C)[Si](C)(C)C	2888.9	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,5TMS,isomer #6	CC(=O)NC(=CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)C(COC1O[C@@H](C)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O)O[Si](C)(C)C	2952.0	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,5TMS,isomer #7	CC(=O)N([C@@H](C=O)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)C(COC1O[C@@H](C)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O)O[Si](C)(C)C)[Si](C)(C)C	2883.5	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,5TMS,isomer #8	CC(=O)NC(=CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)C(COC1O[C@@H](C)[C@@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C)O[Si](C)(C)C	2939.9	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,5TMS,isomer #9	CC(=O)N([C@@H](C=O)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)C(COC1O[C@@H](C)[C@@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C)O[Si](C)(C)C)[Si](C)(C)C	2898.2	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,6TMS,isomer #1	CC(=O)N[C@@H](C=O)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)C(COC1O[C@@H](C)[C@@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C)O[Si](C)(C)C	2924.2	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,6TMS,isomer #10	CC(=O)N(C(=CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)C(COC1O[C@@H](C)[C@@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C)O[Si](C)(C)C)[Si](C)(C)C	2952.6	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,6TMS,isomer #11	CC(=O)NC(=CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)C(COC1O[C@@H](C)[C@@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C)O[Si](C)(C)C	2956.4	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,6TMS,isomer #12	CC(=O)N([C@@H](C=O)[C@@H](O[Si](C)(C)C)[C@H](O)C(COC1O[C@@H](C)[C@@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C)O[Si](C)(C)C)[Si](C)(C)C	2894.6	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,6TMS,isomer #13	CC(=O)N(C(=CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)C(COC1O[C@@H](C)[C@@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O)O[Si](C)(C)C)[Si](C)(C)C	2929.2	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,6TMS,isomer #14	CC(=O)N(C(=CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)C(COC1O[C@@H](C)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C)O[Si](C)(C)C)[Si](C)(C)C	2950.4	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,6TMS,isomer #15	CC(=O)N(C(=CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)C(COC1O[C@@H](C)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C)O[Si](C)(C)C)[Si](C)(C)C	2949.5	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,6TMS,isomer #16	CC(=O)NC(=CO[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)C(COC1O[C@@H](C)[C@@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C)O[Si](C)(C)C	2954.4	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,6TMS,isomer #17	CC(=O)N([C@@H](C=O)[C@@H](O)[C@H](O[Si](C)(C)C)C(COC1O[C@@H](C)[C@@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C)O[Si](C)(C)C)[Si](C)(C)C	2905.3	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,6TMS,isomer #18	CC(=O)N(C(=CO[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)C(COC1O[C@@H](C)[C@@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O)O[Si](C)(C)C)[Si](C)(C)C	2935.3	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,6TMS,isomer #19	CC(=O)N(C(=CO[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)C(COC1O[C@@H](C)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C)O[Si](C)(C)C)[Si](C)(C)C	2954.2	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,6TMS,isomer #2	CC(=O)NC(=CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)C(COC1O[C@@H](C)[C@@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O)O[Si](C)(C)C	2952.3	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,6TMS,isomer #20	CC(=O)N(C(=CO[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)C(COC1O[C@@H](C)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C)O[Si](C)(C)C)[Si](C)(C)C	2964.5	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,6TMS,isomer #21	CC(=O)N(C(=CO[Si](C)(C)C)[C@@H](O)[C@H](O)C(COC1O[C@@H](C)[C@@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C)O[Si](C)(C)C)[Si](C)(C)C	2919.7	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,6TMS,isomer #22	CC(=O)NC(=CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)C(O)COC1O[C@@H](C)[C@@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2961.2	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,6TMS,isomer #23	CC(=O)N([C@@H](C=O)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)C(O)COC1O[C@@H](C)[C@@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C)[Si](C)(C)C	2917.5	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,6TMS,isomer #24	CC(=O)N(C(=CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)C(O)COC1O[C@@H](C)[C@@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O)[Si](C)(C)C	2927.3	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,6TMS,isomer #25	CC(=O)N(C(=CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)C(O)COC1O[C@@H](C)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C)[Si](C)(C)C	2946.0	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,6TMS,isomer #26	CC(=O)N(C(=CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)C(O)COC1O[C@@H](C)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C)[Si](C)(C)C	2942.4	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,6TMS,isomer #27	CC(=O)N(C(=CO[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)C(O)COC1O[C@@H](C)[C@@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C)[Si](C)(C)C	2924.2	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,6TMS,isomer #28	CC(=O)N(C(=CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)C(O)COC1O[C@@H](C)[C@@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C)[Si](C)(C)C	2925.4	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,6TMS,isomer #3	CC(=O)N([C@@H](C=O)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)C(COC1O[C@@H](C)[C@@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O)O[Si](C)(C)C)[Si](C)(C)C	2910.9	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,6TMS,isomer #4	CC(=O)NC(=CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)C(COC1O[C@@H](C)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C)O[Si](C)(C)C	2963.2	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,6TMS,isomer #5	CC(=O)N([C@@H](C=O)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)C(COC1O[C@@H](C)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C)O[Si](C)(C)C)[Si](C)(C)C	2919.7	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,6TMS,isomer #6	CC(=O)N(C(=CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)C(COC1O[C@@H](C)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O)O[Si](C)(C)C)[Si](C)(C)C	2952.2	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,6TMS,isomer #7	CC(=O)NC(=CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)C(COC1O[C@@H](C)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C)O[Si](C)(C)C	2964.0	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,6TMS,isomer #8	CC(=O)N([C@@H](C=O)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)C(COC1O[C@@H](C)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C)O[Si](C)(C)C)[Si](C)(C)C	2923.6	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,6TMS,isomer #9	CC(=O)N(C(=CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)C(COC1O[C@@H](C)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O)O[Si](C)(C)C)[Si](C)(C)C	2941.2	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,7TMS,isomer #1	CC(=O)NC(=CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)C(COC1O[C@@H](C)[C@@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C)O[Si](C)(C)C	2999.3	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,7TMS,isomer #1	CC(=O)NC(=CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)C(COC1O[C@@H](C)[C@@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C)O[Si](C)(C)C	2915.8	Standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,7TMS,isomer #1	CC(=O)NC(=CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)C(COC1O[C@@H](C)[C@@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C)O[Si](C)(C)C	3372.8	Standard polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,7TMS,isomer #2	CC(=O)N([C@@H](C=O)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)C(COC1O[C@@H](C)[C@@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C)O[Si](C)(C)C)[Si](C)(C)C	2950.8	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,7TMS,isomer #2	CC(=O)N([C@@H](C=O)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)C(COC1O[C@@H](C)[C@@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C)O[Si](C)(C)C)[Si](C)(C)C	2949.7	Standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,7TMS,isomer #2	CC(=O)N([C@@H](C=O)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)C(COC1O[C@@H](C)[C@@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C)O[Si](C)(C)C)[Si](C)(C)C	3069.3	Standard polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,7TMS,isomer #3	CC(=O)N(C(=CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)C(COC1O[C@@H](C)[C@@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O)O[Si](C)(C)C)[Si](C)(C)C	2969.1	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,7TMS,isomer #3	CC(=O)N(C(=CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)C(COC1O[C@@H](C)[C@@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O)O[Si](C)(C)C)[Si](C)(C)C	2931.0	Standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,7TMS,isomer #3	CC(=O)N(C(=CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)C(COC1O[C@@H](C)[C@@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O)O[Si](C)(C)C)[Si](C)(C)C	3314.9	Standard polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,7TMS,isomer #4	CC(=O)N(C(=CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)C(COC1O[C@@H](C)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C)O[Si](C)(C)C)[Si](C)(C)C	2972.1	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,7TMS,isomer #4	CC(=O)N(C(=CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)C(COC1O[C@@H](C)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C)O[Si](C)(C)C)[Si](C)(C)C	2946.7	Standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,7TMS,isomer #4	CC(=O)N(C(=CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)C(COC1O[C@@H](C)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C)O[Si](C)(C)C)[Si](C)(C)C	3353.1	Standard polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,7TMS,isomer #5	CC(=O)N(C(=CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)C(COC1O[C@@H](C)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C)O[Si](C)(C)C)[Si](C)(C)C	2980.8	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,7TMS,isomer #5	CC(=O)N(C(=CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)C(COC1O[C@@H](C)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C)O[Si](C)(C)C)[Si](C)(C)C	2913.6	Standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,7TMS,isomer #5	CC(=O)N(C(=CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)C(COC1O[C@@H](C)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C)O[Si](C)(C)C)[Si](C)(C)C	3378.7	Standard polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,7TMS,isomer #6	CC(=O)N(C(=CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)C(COC1O[C@@H](C)[C@@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C)O[Si](C)(C)C)[Si](C)(C)C	2960.3	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,7TMS,isomer #6	CC(=O)N(C(=CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)C(COC1O[C@@H](C)[C@@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C)O[Si](C)(C)C)[Si](C)(C)C	2942.4	Standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,7TMS,isomer #6	CC(=O)N(C(=CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)C(COC1O[C@@H](C)[C@@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C)O[Si](C)(C)C)[Si](C)(C)C	3306.4	Standard polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,7TMS,isomer #7	CC(=O)N(C(=CO[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)C(COC1O[C@@H](C)[C@@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C)O[Si](C)(C)C)[Si](C)(C)C	2955.9	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,7TMS,isomer #7	CC(=O)N(C(=CO[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)C(COC1O[C@@H](C)[C@@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C)O[Si](C)(C)C)[Si](C)(C)C	2942.1	Standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,7TMS,isomer #7	CC(=O)N(C(=CO[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)C(COC1O[C@@H](C)[C@@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C)O[Si](C)(C)C)[Si](C)(C)C	3338.3	Standard polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,7TMS,isomer #8	CC(=O)N(C(=CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)C(O)COC1O[C@@H](C)[C@@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C)[Si](C)(C)C	2952.7	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,7TMS,isomer #8	CC(=O)N(C(=CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)C(O)COC1O[C@@H](C)[C@@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C)[Si](C)(C)C	2930.5	Standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,7TMS,isomer #8	CC(=O)N(C(=CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)C(O)COC1O[C@@H](C)[C@@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C)[Si](C)(C)C	3275.3	Standard polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,1TBDMS,isomer #1	CC(=O)N[C@@H](C=O)[C@@H](O)[C@H](O)C(COC1O[C@@H](C)[C@@H](O)[C@@H](O)[C@@H]1O)O[Si](C)(C)C(C)(C)C	3073.6	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,1TBDMS,isomer #2	CC(=O)N[C@@H](C=O)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)C(O)COC1O[C@@H](C)[C@@H](O)[C@@H](O)[C@@H]1O	3059.5	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,1TBDMS,isomer #3	CC(=O)N[C@@H](C=O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)C(O)COC1O[C@@H](C)[C@@H](O)[C@@H](O)[C@@H]1O	3077.7	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,1TBDMS,isomer #4	CC(=O)N[C@@H](C=O)[C@@H](O)[C@H](O)C(O)COC1O[C@@H](C)[C@@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C	3041.2	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,1TBDMS,isomer #5	CC(=O)N[C@@H](C=O)[C@@H](O)[C@H](O)C(O)COC1O[C@@H](C)[C@@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O	3030.0	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,1TBDMS,isomer #6	CC(=O)N[C@@H](C=O)[C@@H](O)[C@H](O)C(O)COC1O[C@@H](C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O	3049.8	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,1TBDMS,isomer #7	CC(=O)NC(=CO[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O)C(O)COC1O[C@@H](C)[C@@H](O)[C@@H](O)[C@@H]1O	3218.6	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,1TBDMS,isomer #8	CC(=O)N([C@@H](C=O)[C@@H](O)[C@H](O)C(O)COC1O[C@@H](C)[C@@H](O)[C@@H](O)[C@@H]1O)[Si](C)(C)C(C)(C)C	3108.7	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,2TBDMS,isomer #1	CC(=O)N[C@@H](C=O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)C(COC1O[C@@H](C)[C@@H](O)[C@@H](O)[C@@H]1O)O[Si](C)(C)C(C)(C)C	3295.2	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,2TBDMS,isomer #10	CC(=O)N[C@@H](C=O)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)C(O)COC1O[C@@H](C)[C@@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O	3260.1	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,2TBDMS,isomer #11	CC(=O)N[C@@H](C=O)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)C(O)COC1O[C@@H](C)[C@@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C	3261.0	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,2TBDMS,isomer #12	CC(=O)NC(=CO[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)C(O)COC1O[C@@H](C)[C@@H](O)[C@@H](O)[C@@H]1O	3377.3	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,2TBDMS,isomer #13	CC(=O)N([C@@H](C=O)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)C(O)COC1O[C@@H](C)[C@@H](O)[C@@H](O)[C@@H]1O)[Si](C)(C)C(C)(C)C	3343.5	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,2TBDMS,isomer #14	CC(=O)N[C@@H](C=O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)C(O)COC1O[C@@H](C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O	3287.6	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,2TBDMS,isomer #15	CC(=O)N[C@@H](C=O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)C(O)COC1O[C@@H](C)[C@@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O	3292.8	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,2TBDMS,isomer #16	CC(=O)N[C@@H](C=O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)C(O)COC1O[C@@H](C)[C@@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C	3293.1	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,2TBDMS,isomer #17	CC(=O)NC(=CO[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)C(O)COC1O[C@@H](C)[C@@H](O)[C@@H](O)[C@@H]1O	3388.1	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,2TBDMS,isomer #18	CC(=O)N([C@@H](C=O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)C(O)COC1O[C@@H](C)[C@@H](O)[C@@H](O)[C@@H]1O)[Si](C)(C)C(C)(C)C	3323.9	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,2TBDMS,isomer #19	CC(=O)N[C@@H](C=O)[C@@H](O)[C@H](O)C(O)COC1O[C@@H](C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C	3227.0	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,2TBDMS,isomer #2	CC(=O)N[C@@H](C=O)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)C(COC1O[C@@H](C)[C@@H](O)[C@@H](O)[C@@H]1O)O[Si](C)(C)C(C)(C)C	3257.9	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,2TBDMS,isomer #20	CC(=O)N[C@@H](C=O)[C@@H](O)[C@H](O)C(O)COC1O[C@@H](C)[C@@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C	3224.0	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,2TBDMS,isomer #21	CC(=O)NC(=CO[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O)C(O)COC1O[C@@H](C)[C@@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C	3361.6	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,2TBDMS,isomer #22	CC(=O)N([C@@H](C=O)[C@@H](O)[C@H](O)C(O)COC1O[C@@H](C)[C@@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3322.9	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,2TBDMS,isomer #23	CC(=O)N[C@@H](C=O)[C@@H](O)[C@H](O)C(O)COC1O[C@@H](C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O	3212.2	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,2TBDMS,isomer #24	CC(=O)NC(=CO[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O)C(O)COC1O[C@@H](C)[C@@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O	3346.0	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,2TBDMS,isomer #25	CC(=O)N([C@@H](C=O)[C@@H](O)[C@H](O)C(O)COC1O[C@@H](C)[C@@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O)[Si](C)(C)C(C)(C)C	3308.5	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,2TBDMS,isomer #26	CC(=O)NC(=CO[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O)C(O)COC1O[C@@H](C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O	3358.4	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,2TBDMS,isomer #27	CC(=O)N([C@@H](C=O)[C@@H](O)[C@H](O)C(O)COC1O[C@@H](C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O)[Si](C)(C)C(C)(C)C	3324.2	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,2TBDMS,isomer #28	CC(=O)N(C(=CO[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O)C(O)COC1O[C@@H](C)[C@@H](O)[C@@H](O)[C@@H]1O)[Si](C)(C)C(C)(C)C	3389.7	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,2TBDMS,isomer #3	CC(=O)N[C@@H](C=O)[C@@H](O)[C@H](O)C(COC1O[C@@H](C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O)O[Si](C)(C)C(C)(C)C	3260.0	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,2TBDMS,isomer #4	CC(=O)N[C@@H](C=O)[C@@H](O)[C@H](O)C(COC1O[C@@H](C)[C@@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O)O[Si](C)(C)C(C)(C)C	3245.0	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,2TBDMS,isomer #5	CC(=O)N[C@@H](C=O)[C@@H](O)[C@H](O)C(COC1O[C@@H](C)[C@@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	3260.5	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,2TBDMS,isomer #6	CC(=O)NC(=CO[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O)C(COC1O[C@@H](C)[C@@H](O)[C@@H](O)[C@@H]1O)O[Si](C)(C)C(C)(C)C	3393.3	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,2TBDMS,isomer #7	CC(=O)N([C@@H](C=O)[C@@H](O)[C@H](O)C(COC1O[C@@H](C)[C@@H](O)[C@@H](O)[C@@H]1O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3334.0	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,2TBDMS,isomer #8	CC(=O)N[C@@H](C=O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)C(O)COC1O[C@@H](C)[C@@H](O)[C@@H](O)[C@@H]1O	3292.0	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,2TBDMS,isomer #9	CC(=O)N[C@@H](C=O)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)C(O)COC1O[C@@H](C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O	3260.8	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,3TBDMS,isomer #1	CC(=O)N[C@@H](C=O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)C(COC1O[C@@H](C)[C@@H](O)[C@@H](O)[C@@H]1O)O[Si](C)(C)C(C)(C)C	3484.7	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,3TBDMS,isomer #10	CC(=O)NC(=CO[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)C(COC1O[C@@H](C)[C@@H](O)[C@@H](O)[C@@H]1O)O[Si](C)(C)C(C)(C)C	3555.4	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,3TBDMS,isomer #11	CC(=O)N([C@@H](C=O)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)C(COC1O[C@@H](C)[C@@H](O)[C@@H](O)[C@@H]1O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3536.9	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,3TBDMS,isomer #12	CC(=O)N[C@@H](C=O)[C@@H](O)[C@H](O)C(COC1O[C@@H](C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O)O[Si](C)(C)C(C)(C)C	3420.0	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,3TBDMS,isomer #13	CC(=O)N[C@@H](C=O)[C@@H](O)[C@H](O)C(COC1O[C@@H](C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	3442.5	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,3TBDMS,isomer #14	CC(=O)NC(=CO[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O)C(COC1O[C@@H](C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O)O[Si](C)(C)C(C)(C)C	3535.5	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,3TBDMS,isomer #15	CC(=O)N([C@@H](C=O)[C@@H](O)[C@H](O)C(COC1O[C@@H](C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3519.8	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,3TBDMS,isomer #16	CC(=O)N[C@@H](C=O)[C@@H](O)[C@H](O)C(COC1O[C@@H](C)[C@@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	3435.7	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,3TBDMS,isomer #17	CC(=O)NC(=CO[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O)C(COC1O[C@@H](C)[C@@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O)O[Si](C)(C)C(C)(C)C	3523.6	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,3TBDMS,isomer #18	CC(=O)N([C@@H](C=O)[C@@H](O)[C@H](O)C(COC1O[C@@H](C)[C@@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3501.6	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,3TBDMS,isomer #19	CC(=O)NC(=CO[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O)C(COC1O[C@@H](C)[C@@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	3534.3	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,3TBDMS,isomer #2	CC(=O)N[C@@H](C=O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)C(COC1O[C@@H](C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O)O[Si](C)(C)C(C)(C)C	3507.7	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,3TBDMS,isomer #20	CC(=O)N([C@@H](C=O)[C@@H](O)[C@H](O)C(COC1O[C@@H](C)[C@@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3513.3	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,3TBDMS,isomer #21	CC(=O)N(C(=CO[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O)C(COC1O[C@@H](C)[C@@H](O)[C@@H](O)[C@@H]1O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3548.8	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,3TBDMS,isomer #22	CC(=O)N[C@@H](C=O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)C(O)COC1O[C@@H](C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O	3512.3	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,3TBDMS,isomer #23	CC(=O)N[C@@H](C=O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)C(O)COC1O[C@@H](C)[C@@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O	3493.9	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,3TBDMS,isomer #24	CC(=O)N[C@@H](C=O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)C(O)COC1O[C@@H](C)[C@@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C	3490.3	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,3TBDMS,isomer #25	CC(=O)NC(=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(O)COC1O[C@@H](C)[C@@H](O)[C@@H](O)[C@@H]1O	3560.3	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,3TBDMS,isomer #26	CC(=O)N([C@@H](C=O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)C(O)COC1O[C@@H](C)[C@@H](O)[C@@H](O)[C@@H]1O)[Si](C)(C)C(C)(C)C	3527.8	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,3TBDMS,isomer #27	CC(=O)N[C@@H](C=O)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)C(O)COC1O[C@@H](C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O	3444.9	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,3TBDMS,isomer #28	CC(=O)N[C@@H](C=O)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)C(O)COC1O[C@@H](C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C	3466.8	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,3TBDMS,isomer #29	CC(=O)NC(=CO[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)C(O)COC1O[C@@H](C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O	3550.9	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,3TBDMS,isomer #3	CC(=O)N[C@@H](C=O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)C(COC1O[C@@H](C)[C@@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O)O[Si](C)(C)C(C)(C)C	3499.8	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,3TBDMS,isomer #30	CC(=O)N([C@@H](C=O)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)C(O)COC1O[C@@H](C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O)[Si](C)(C)C(C)(C)C	3539.3	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,3TBDMS,isomer #31	CC(=O)N[C@@H](C=O)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)C(O)COC1O[C@@H](C)[C@@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C	3453.2	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,3TBDMS,isomer #32	CC(=O)NC(=CO[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)C(O)COC1O[C@@H](C)[C@@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O	3545.1	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,3TBDMS,isomer #33	CC(=O)N([C@@H](C=O)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)C(O)COC1O[C@@H](C)[C@@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O)[Si](C)(C)C(C)(C)C	3519.0	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,3TBDMS,isomer #34	CC(=O)NC(=CO[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)C(O)COC1O[C@@H](C)[C@@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C	3550.1	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,3TBDMS,isomer #35	CC(=O)N([C@@H](C=O)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)C(O)COC1O[C@@H](C)[C@@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3533.8	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,3TBDMS,isomer #36	CC(=O)N(C(=CO[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)C(O)COC1O[C@@H](C)[C@@H](O)[C@@H](O)[C@@H]1O)[Si](C)(C)C(C)(C)C	3578.4	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,3TBDMS,isomer #37	CC(=O)N[C@@H](C=O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)C(O)COC1O[C@@H](C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O	3470.9	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,3TBDMS,isomer #38	CC(=O)N[C@@H](C=O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)C(O)COC1O[C@@H](C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C	3489.6	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,3TBDMS,isomer #39	CC(=O)NC(=CO[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)C(O)COC1O[C@@H](C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O	3563.2	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,3TBDMS,isomer #4	CC(=O)N[C@@H](C=O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)C(COC1O[C@@H](C)[C@@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	3498.2	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,3TBDMS,isomer #40	CC(=O)N([C@@H](C=O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)C(O)COC1O[C@@H](C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O)[Si](C)(C)C(C)(C)C	3526.6	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,3TBDMS,isomer #41	CC(=O)N[C@@H](C=O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)C(O)COC1O[C@@H](C)[C@@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C	3471.9	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,3TBDMS,isomer #42	CC(=O)NC(=CO[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)C(O)COC1O[C@@H](C)[C@@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O	3558.2	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,3TBDMS,isomer #43	CC(=O)N([C@@H](C=O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)C(O)COC1O[C@@H](C)[C@@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O)[Si](C)(C)C(C)(C)C	3504.7	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,3TBDMS,isomer #44	CC(=O)NC(=CO[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)C(O)COC1O[C@@H](C)[C@@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C	3555.0	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,3TBDMS,isomer #45	CC(=O)N([C@@H](C=O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)C(O)COC1O[C@@H](C)[C@@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3520.4	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,3TBDMS,isomer #46	CC(=O)N(C(=CO[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)C(O)COC1O[C@@H](C)[C@@H](O)[C@@H](O)[C@@H]1O)[Si](C)(C)C(C)(C)C	3558.6	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,3TBDMS,isomer #47	CC(=O)N[C@@H](C=O)[C@@H](O)[C@H](O)C(O)COC1O[C@@H](C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C	3417.6	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,3TBDMS,isomer #48	CC(=O)NC(=CO[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O)C(O)COC1O[C@@H](C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C	3511.2	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,3TBDMS,isomer #49	CC(=O)N([C@@H](C=O)[C@@H](O)[C@H](O)C(O)COC1O[C@@H](C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3493.0	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,3TBDMS,isomer #5	CC(=O)NC(=CO[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)C(COC1O[C@@H](C)[C@@H](O)[C@@H](O)[C@@H]1O)O[Si](C)(C)C(C)(C)C	3587.2	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,3TBDMS,isomer #50	CC(=O)NC(=CO[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O)C(O)COC1O[C@@H](C)[C@@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C	3498.3	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,3TBDMS,isomer #51	CC(=O)N([C@@H](C=O)[C@@H](O)[C@H](O)C(O)COC1O[C@@H](C)[C@@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3488.8	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,3TBDMS,isomer #52	CC(=O)N(C(=CO[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O)C(O)COC1O[C@@H](C)[C@@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3544.2	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,3TBDMS,isomer #53	CC(=O)NC(=CO[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O)C(O)COC1O[C@@H](C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O	3488.9	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,3TBDMS,isomer #54	CC(=O)N([C@@H](C=O)[C@@H](O)[C@H](O)C(O)COC1O[C@@H](C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O)[Si](C)(C)C(C)(C)C	3486.1	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,3TBDMS,isomer #55	CC(=O)N(C(=CO[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O)C(O)COC1O[C@@H](C)[C@@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O)[Si](C)(C)C(C)(C)C	3529.7	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,3TBDMS,isomer #56	CC(=O)N(C(=CO[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O)C(O)COC1O[C@@H](C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O)[Si](C)(C)C(C)(C)C	3540.7	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,3TBDMS,isomer #6	CC(=O)N([C@@H](C=O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)C(COC1O[C@@H](C)[C@@H](O)[C@@H](O)[C@@H]1O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3513.3	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,3TBDMS,isomer #7	CC(=O)N[C@@H](C=O)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)C(COC1O[C@@H](C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O)O[Si](C)(C)C(C)(C)C	3461.8	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,3TBDMS,isomer #8	CC(=O)N[C@@H](C=O)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)C(COC1O[C@@H](C)[C@@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O)O[Si](C)(C)C(C)(C)C	3456.8	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,3TBDMS,isomer #9	CC(=O)N[C@@H](C=O)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)C(COC1O[C@@H](C)[C@@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	3463.7	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,4TBDMS,isomer #1	CC(=O)N[C@@H](C=O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)C(COC1O[C@@H](C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O)O[Si](C)(C)C(C)(C)C	3716.5	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,4TBDMS,isomer #10	CC(=O)N[C@@H](C=O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)C(COC1O[C@@H](C)[C@@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	3687.7	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,4TBDMS,isomer #11	CC(=O)NC(=CO[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)C(COC1O[C@@H](C)[C@@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O)O[Si](C)(C)C(C)(C)C	3781.2	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,4TBDMS,isomer #12	CC(=O)N([C@@H](C=O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)C(COC1O[C@@H](C)[C@@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3711.2	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,4TBDMS,isomer #13	CC(=O)NC(=CO[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)C(COC1O[C@@H](C)[C@@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	3768.4	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,4TBDMS,isomer #14	CC(=O)N([C@@H](C=O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)C(COC1O[C@@H](C)[C@@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3707.8	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,4TBDMS,isomer #15	CC(=O)N(C(=CO[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)C(COC1O[C@@H](C)[C@@H](O)[C@@H](O)[C@@H]1O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3745.1	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,4TBDMS,isomer #16	CC(=O)N[C@@H](C=O)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)C(COC1O[C@@H](C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O)O[Si](C)(C)C(C)(C)C	3668.7	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,4TBDMS,isomer #17	CC(=O)N[C@@H](C=O)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)C(COC1O[C@@H](C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	3684.5	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,4TBDMS,isomer #18	CC(=O)NC(=CO[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)C(COC1O[C@@H](C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O)O[Si](C)(C)C(C)(C)C	3735.0	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,4TBDMS,isomer #19	CC(=O)N([C@@H](C=O)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)C(COC1O[C@@H](C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3742.7	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,4TBDMS,isomer #2	CC(=O)N[C@@H](C=O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)C(COC1O[C@@H](C)[C@@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O)O[Si](C)(C)C(C)(C)C	3697.9	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,4TBDMS,isomer #20	CC(=O)N[C@@H](C=O)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)C(COC1O[C@@H](C)[C@@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	3663.0	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,4TBDMS,isomer #21	CC(=O)NC(=CO[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)C(COC1O[C@@H](C)[C@@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O)O[Si](C)(C)C(C)(C)C	3730.0	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,4TBDMS,isomer #22	CC(=O)N([C@@H](C=O)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)C(COC1O[C@@H](C)[C@@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3721.6	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,4TBDMS,isomer #23	CC(=O)NC(=CO[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)C(COC1O[C@@H](C)[C@@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	3729.2	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,4TBDMS,isomer #24	CC(=O)N([C@@H](C=O)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)C(COC1O[C@@H](C)[C@@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3722.5	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,4TBDMS,isomer #25	CC(=O)N(C(=CO[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)C(COC1O[C@@H](C)[C@@H](O)[C@@H](O)[C@@H]1O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3748.3	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,4TBDMS,isomer #26	CC(=O)N[C@@H](C=O)[C@@H](O)[C@H](O)C(COC1O[C@@H](C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	3636.1	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,4TBDMS,isomer #27	CC(=O)NC(=CO[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O)C(COC1O[C@@H](C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O)O[Si](C)(C)C(C)(C)C	3700.5	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,4TBDMS,isomer #28	CC(=O)N([C@@H](C=O)[C@@H](O)[C@H](O)C(COC1O[C@@H](C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3701.7	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,4TBDMS,isomer #29	CC(=O)NC(=CO[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O)C(COC1O[C@@H](C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	3712.8	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,4TBDMS,isomer #3	CC(=O)N[C@@H](C=O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)C(COC1O[C@@H](C)[C@@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	3690.3	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,4TBDMS,isomer #30	CC(=O)N([C@@H](C=O)[C@@H](O)[C@H](O)C(COC1O[C@@H](C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3707.5	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,4TBDMS,isomer #31	CC(=O)N(C(=CO[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O)C(COC1O[C@@H](C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3733.2	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,4TBDMS,isomer #32	CC(=O)NC(=CO[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O)C(COC1O[C@@H](C)[C@@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	3702.5	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,4TBDMS,isomer #33	CC(=O)N([C@@H](C=O)[C@@H](O)[C@H](O)C(COC1O[C@@H](C)[C@@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3694.2	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,4TBDMS,isomer #34	CC(=O)N(C(=CO[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O)C(COC1O[C@@H](C)[C@@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3720.5	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,4TBDMS,isomer #35	CC(=O)N(C(=CO[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O)C(COC1O[C@@H](C)[C@@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3715.6	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,4TBDMS,isomer #36	CC(=O)N[C@@H](C=O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)C(O)COC1O[C@@H](C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O	3693.3	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,4TBDMS,isomer #37	CC(=O)N[C@@H](C=O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)C(O)COC1O[C@@H](C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C	3707.8	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,4TBDMS,isomer #38	CC(=O)NC(=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(O)COC1O[C@@H](C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O	3775.2	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,4TBDMS,isomer #39	CC(=O)N([C@@H](C=O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)C(O)COC1O[C@@H](C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O)[Si](C)(C)C(C)(C)C	3740.2	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,4TBDMS,isomer #4	CC(=O)NC(=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(COC1O[C@@H](C)[C@@H](O)[C@@H](O)[C@@H]1O)O[Si](C)(C)C(C)(C)C	3774.0	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,4TBDMS,isomer #40	CC(=O)N[C@@H](C=O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)C(O)COC1O[C@@H](C)[C@@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C	3687.7	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,4TBDMS,isomer #41	CC(=O)NC(=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(O)COC1O[C@@H](C)[C@@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O	3767.2	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,4TBDMS,isomer #42	CC(=O)N([C@@H](C=O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)C(O)COC1O[C@@H](C)[C@@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O)[Si](C)(C)C(C)(C)C	3719.7	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,4TBDMS,isomer #43	CC(=O)NC(=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(O)COC1O[C@@H](C)[C@@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C	3755.7	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,4TBDMS,isomer #44	CC(=O)N([C@@H](C=O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)C(O)COC1O[C@@H](C)[C@@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3711.8	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,4TBDMS,isomer #45	CC(=O)N(C(=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(O)COC1O[C@@H](C)[C@@H](O)[C@@H](O)[C@@H]1O)[Si](C)(C)C(C)(C)C	3745.7	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,4TBDMS,isomer #46	CC(=O)N[C@@H](C=O)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)C(O)COC1O[C@@H](C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C	3670.4	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,4TBDMS,isomer #47	CC(=O)NC(=CO[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)C(O)COC1O[C@@H](C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O	3716.6	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,4TBDMS,isomer #48	CC(=O)N([C@@H](C=O)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)C(O)COC1O[C@@H](C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O)[Si](C)(C)C(C)(C)C	3725.1	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,4TBDMS,isomer #49	CC(=O)NC(=CO[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)C(O)COC1O[C@@H](C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C	3733.1	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,4TBDMS,isomer #5	CC(=O)N([C@@H](C=O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)C(COC1O[C@@H](C)[C@@H](O)[C@@H](O)[C@@H]1O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3711.3	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,4TBDMS,isomer #50	CC(=O)N([C@@H](C=O)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)C(O)COC1O[C@@H](C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3731.4	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,4TBDMS,isomer #51	CC(=O)N(C(=CO[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)C(O)COC1O[C@@H](C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O)[Si](C)(C)C(C)(C)C	3759.3	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,4TBDMS,isomer #52	CC(=O)NC(=CO[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)C(O)COC1O[C@@H](C)[C@@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C	3716.9	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,4TBDMS,isomer #53	CC(=O)N([C@@H](C=O)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)C(O)COC1O[C@@H](C)[C@@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3715.6	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,4TBDMS,isomer #54	CC(=O)N(C(=CO[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)C(O)COC1O[C@@H](C)[C@@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O)[Si](C)(C)C(C)(C)C	3744.9	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,4TBDMS,isomer #55	CC(=O)N(C(=CO[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)C(O)COC1O[C@@H](C)[C@@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3739.2	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,4TBDMS,isomer #56	CC(=O)N[C@@H](C=O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)C(O)COC1O[C@@H](C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C	3681.1	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,4TBDMS,isomer #57	CC(=O)NC(=CO[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)C(O)COC1O[C@@H](C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O	3753.4	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,4TBDMS,isomer #58	CC(=O)N([C@@H](C=O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)C(O)COC1O[C@@H](C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O)[Si](C)(C)C(C)(C)C	3703.3	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,4TBDMS,isomer #59	CC(=O)NC(=CO[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)C(O)COC1O[C@@H](C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C	3765.7	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,4TBDMS,isomer #6	CC(=O)N[C@@H](C=O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)C(COC1O[C@@H](C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O)O[Si](C)(C)C(C)(C)C	3696.4	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,4TBDMS,isomer #60	CC(=O)N([C@@H](C=O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)C(O)COC1O[C@@H](C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3709.5	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,4TBDMS,isomer #61	CC(=O)N(C(=CO[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)C(O)COC1O[C@@H](C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O)[Si](C)(C)C(C)(C)C	3751.6	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,4TBDMS,isomer #62	CC(=O)NC(=CO[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)C(O)COC1O[C@@H](C)[C@@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C	3747.2	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,4TBDMS,isomer #63	CC(=O)N([C@@H](C=O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)C(O)COC1O[C@@H](C)[C@@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3696.2	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,4TBDMS,isomer #64	CC(=O)N(C(=CO[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)C(O)COC1O[C@@H](C)[C@@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O)[Si](C)(C)C(C)(C)C	3735.5	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,4TBDMS,isomer #65	CC(=O)N(C(=CO[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)C(O)COC1O[C@@H](C)[C@@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3730.0	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,4TBDMS,isomer #66	CC(=O)NC(=CO[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O)C(O)COC1O[C@@H](C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C	3685.4	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,4TBDMS,isomer #67	CC(=O)N([C@@H](C=O)[C@@H](O)[C@H](O)C(O)COC1O[C@@H](C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3680.9	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,4TBDMS,isomer #68	CC(=O)N(C(=CO[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O)C(O)COC1O[C@@H](C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3708.4	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,4TBDMS,isomer #69	CC(=O)N(C(=CO[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O)C(O)COC1O[C@@H](C)[C@@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3698.0	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,4TBDMS,isomer #7	CC(=O)N[C@@H](C=O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)C(COC1O[C@@H](C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	3710.8	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,4TBDMS,isomer #70	CC(=O)N(C(=CO[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O)C(O)COC1O[C@@H](C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O)[Si](C)(C)C(C)(C)C	3702.5	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,4TBDMS,isomer #8	CC(=O)NC(=CO[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)C(COC1O[C@@H](C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O)O[Si](C)(C)C(C)(C)C	3787.1	Semi standard non polar	33892256
N-Acetyl-6-O-L-fucosyl-D-glucosamine,4TBDMS,isomer #9	CC(=O)N([C@@H](C=O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)C(COC1O[C@@H](C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3730.0	Semi standard non polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - N-Acetyl-6-O-L-fucosyl-D-glucosamine GC-MS (Non-derivatized) - 70eV, Positive	splash10-0lxt-8977000000-a2bb860c76008c8ba468	2017-09-01	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - N-Acetyl-6-O-L-fucosyl-D-glucosamine GC-MS (4 TMS) - 70eV, Positive	splash10-0006-6422319000-91030c99372ae17b724c	2017-10-06	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - N-Acetyl-6-O-L-fucosyl-D-glucosamine GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - N-Acetyl-6-O-L-fucosyl-D-glucosamine 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
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - N-Acetyl-6-O-L-fucosyl-D-glucosamine 10V, Positive-QTOF	splash10-0uxr-1219000000-f15747e1b5ccf9e81e65	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - N-Acetyl-6-O-L-fucosyl-D-glucosamine 20V, Positive-QTOF	splash10-0pb9-9720000000-19137fd08ea152aadd6d	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - N-Acetyl-6-O-L-fucosyl-D-glucosamine 40V, Positive-QTOF	splash10-0w29-8900000000-f71c7291db908ebd248e	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - N-Acetyl-6-O-L-fucosyl-D-glucosamine 10V, Negative-QTOF	splash10-0cea-1923000000-caffbe52ec84c868cb4d	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - N-Acetyl-6-O-L-fucosyl-D-glucosamine 20V, Negative-QTOF	splash10-052b-4921000000-71facf6e0f221fb8e3d4	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - N-Acetyl-6-O-L-fucosyl-D-glucosamine 40V, Negative-QTOF	splash10-0a4i-9710000000-c1d713140c972dfce842	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - N-Acetyl-6-O-L-fucosyl-D-glucosamine 10V, Negative-QTOF	splash10-0a4i-9315000000-e449249c04bae5502537	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - N-Acetyl-6-O-L-fucosyl-D-glucosamine 20V, Negative-QTOF	splash10-0a4i-9300000000-494e7c53dfe677c9151e	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - N-Acetyl-6-O-L-fucosyl-D-glucosamine 40V, Negative-QTOF	splash10-0a4l-9100000000-e1289f85de752e1143d5	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - N-Acetyl-6-O-L-fucosyl-D-glucosamine 10V, Positive-QTOF	splash10-014i-0229000000-899d186fea014b0d7629	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - N-Acetyl-6-O-L-fucosyl-D-glucosamine 20V, Positive-QTOF	splash10-0kh9-9411000000-2a9b99c9e48ef6125eb2	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - N-Acetyl-6-O-L-fucosyl-D-glucosamine 40V, Positive-QTOF	splash10-0ac0-9320000000-466625b9719e971e162a	2021-09-22	Wishart Lab	View Spectrum

NMR Spectra

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

Biological Properties

Cellular Locations

Not Available

Biospecimen Locations

Not Available

Tissue Locations

Not Available

Pathways

Not Available

Name	SMPDB/PathBank	KEGG

Normal Concentrations

Not Available

Abnormal Concentrations

Not Available

Associated Disorders and Diseases

Disease References

None

Associated OMIM IDs

None

External Links

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

FDB022914

KNApSAcK ID

Not Available

Chemspider ID

17216173

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

22833588

PDB ID

Not Available

ChEBI ID

172599

Food Biomarker Ontology

Not Available

VMH ID

Not Available

MarkerDB ID

Not Available

Good Scents ID

rw1902051

References

Synthesis Reference

Not Available

Material Safety Data Sheet (MSDS)

Not Available

General References

Not Available

Showing metabocard for N-Acetyl-6-O-L-fucosyl-D-glucosamine (HMDB0002220)

MOL for HMDB0002220 (N-Acetyl-6-O-L-fucosyl-D-glucosamine)

3D MOL for HMDB0002220 (N-Acetyl-6-O-L-fucosyl-D-glucosamine)

3D SDF for HMDB0002220 (N-Acetyl-6-O-L-fucosyl-D-glucosamine)

3D-SDF for HMDB0002220 (N-Acetyl-6-O-L-fucosyl-D-glucosamine)

PDB for HMDB0002220 (N-Acetyl-6-O-L-fucosyl-D-glucosamine)

3D PDB for HMDB0002220 (N-Acetyl-6-O-L-fucosyl-D-glucosamine)

SMILES for HMDB0002220 (N-Acetyl-6-O-L-fucosyl-D-glucosamine)

INCHI for HMDB0002220 (N-Acetyl-6-O-L-fucosyl-D-glucosamine)

Structure for HMDB0002220 (N-Acetyl-6-O-L-fucosyl-D-glucosamine)

3D Structure for HMDB0002220 (N-Acetyl-6-O-L-fucosyl-D-glucosamine)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra

NMR Spectra