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Record Information
Version5.0
StatusExpected but not Quantified
Creation Date2005-11-16 15:48:42 UTC
Update Date2021-09-14 15:40:13 UTC
HMDB IDHMDB0001095
Secondary Accession Numbers
  • HMDB0062554
  • HMDB01095
  • HMDB62554
Metabolite Identification
Common NameGDP-L-fucose
DescriptionGDP-L-fucose is a sugar nucleotide and a readily available source of fucose. Fucose is a deoxyhexose that is found in nearly all plant and animal species. The monosaccharide plays several important metabolic roles in complex carbohydrates and in glycoproteins. Fucosylated oligosaccharides are involved in cell-cell recognition, selectin-mediated leukocyte-endothelial adhesion, and mouse embryogenesis. They form the basis of the Lewis-type blood group antigens, are involved in the formation of atherosclerosis, and mediate host-bacterial interactions. A decrease in the availability of fucose is associated with leukocyte adhesion deficiency type-II disorder, and fucosylated glycoproteins have been implicated in memory processes. Fucose is made available during the synthesis of fucosylated glycolipids, oligosaccharides, and glycoproteins via a sugar nucleotide intermediate, specifically GDP-L-fucose. GTP-L-fucose pyrophosphorylase (GFPP, E. C. 2.7.7.30) catalyzes the reversible condensation of guanosine triphosphate and beta-L-fucose-1-phosphate to form the nucleotide-sugar GDP-L-fucose. The enzyme functions primarily in the mammalian liver and kidney to salvage free L-fucose during the breakdown of glycolipids and glycoproteins. (PMID: 16086588 ).
Structure
Data?1582752176
Synonyms
ValueSource
(6-Deoxy-beta-L-galactopyranosyl) esterHMDB
GDP FucoseHMDB
GDP-beta-L-FucoseHMDB
Guanosine diphosphate fucoseHMDB
Guanosine diphosphofucoseHMDB
Diphosphate fucose, guanosineHMDB
Diphosphofucose, guanosineHMDB
Fucose, GDPHMDB
Fucose, guanosine diphosphateHMDB
GDP-FucoseHMDB
GDP-Β-L-fucoseHMDB
Guanosine 5'-diphosphate L-fucoseHMDB
Guanosine 5'-diphospho-fucoseHMDB
Guanosine 5'-diphosphofucoseHMDB
Guanosine 5’-diphosphate L-fucoseHMDB
Guanosine 5’-diphospho-fucoseHMDB
Guanosine 5’-diphosphofucoseHMDB
GDP-L-fucoseHMDB
Chemical FormulaC16H25N5O15P2
Average Molecular Weight589.3417
Monoisotopic Molecular Weight589.082238179
IUPAC Name[({[(2R,3S,4R,5R)-5-(2-amino-6-oxo-6,9-dihydro-1H-purin-9-yl)-3,4-dihydroxyoxolan-2-yl]methoxy}(hydroxy)phosphoryl)oxy]({[(3S,4R,5S,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy})phosphinic acid
Traditional Namegdp-L-fucose
CAS Registry Number15839-70-0
SMILES
C[C@@H]1OC(OP(O)(=O)OP(O)(=O)OC[C@H]2O[C@H]([C@H](O)[C@@H]2O)N2C=NC3=C2N=C(N)NC3=O)[C@@H](O)[C@H](O)[C@@H]1O
InChI Identifier
InChI=1S/C16H25N5O15P2/c1-4-7(22)9(24)11(26)15(33-4)35-38(30,31)36-37(28,29)32-2-5-8(23)10(25)14(34-5)21-3-18-6-12(21)19-16(17)20-13(6)27/h3-5,7-11,14-15,22-26H,2H2,1H3,(H,28,29)(H,30,31)(H3,17,19,20,27)/t4-,5+,7+,8+,9+,10+,11-,14+,15?/m0/s1
InChI KeyLQEBEXMHBLQMDB-QIXZNPMTSA-N
Chemical Taxonomy
Description Belongs to the class of organic compounds known as purine nucleotide sugars. These are purine nucleotides bound to a saccharide derivative through the terminal phosphate group.
KingdomOrganic compounds
Super ClassNucleosides, nucleotides, and analogues
ClassPurine nucleotides
Sub ClassPurine nucleotide sugars
Direct ParentPurine nucleotide sugars
Alternative Parents
Substituents
  • Purine nucleotide sugar
  • Purine ribonucleoside diphosphate
  • Purine ribonucleoside monophosphate
  • Pentose phosphate
  • Pentose-5-phosphate
  • Glycosyl compound
  • N-glycosyl compound
  • 6-oxopurine
  • Hypoxanthine
  • Monosaccharide phosphate
  • Organic pyrophosphate
  • Imidazopyrimidine
  • Purine
  • Aminopyrimidine
  • Monoalkyl phosphate
  • Pyrimidone
  • Pyrimidine
  • Monosaccharide
  • N-substituted imidazole
  • Organic phosphoric acid derivative
  • Oxane
  • Phosphoric acid ester
  • Alkyl phosphate
  • Tetrahydrofuran
  • Vinylogous amide
  • Azole
  • Imidazole
  • Heteroaromatic compound
  • Secondary alcohol
  • Organoheterocyclic compound
  • Azacycle
  • Polyol
  • Oxacycle
  • Hydrocarbon derivative
  • Organooxygen compound
  • Organic oxide
  • Organopnictogen compound
  • Alcohol
  • Primary amine
  • Organonitrogen compound
  • Amine
  • Organic oxygen compound
  • Organic nitrogen compound
  • Aromatic heteropolycyclic compound
Molecular FrameworkAromatic heteropolycyclic compounds
External Descriptors
Ontology
Disposition

Biological location

Source

Process

Naturally occurring process

Physical Properties
StateSolid
Experimental Molecular Properties
PropertyValueReference
Melting PointNot AvailableNot Available
Boiling PointNot AvailableNot Available
Water SolubilityNot AvailableNot Available
LogPNot AvailableNot Available
Experimental Chromatographic Properties

Experimental Collision Cross Sections

Adduct TypeData SourceCCS Value (Å2)Reference
[M-H]-MetCCS_train_neg206.72430932474
[M+H]+MetCCS_train_pos217.19130932474
[M-H]-Not Available206.724http://allccs.zhulab.cn/database/detail?ID=AllCCS00000115
[M+H]+Not Available217.916http://allccs.zhulab.cn/database/detail?ID=AllCCS00000115
Predicted Molecular Properties
PropertyValueSource
Water Solubility7.04 g/LALOGPS
logP-1.7ALOGPS
logP-4.2ChemAxon
logS-1.9ALOGPS
pKa (Strongest Acidic)1.73ChemAxon
pKa (Strongest Basic)-3.6ChemAxon
Physiological Charge-2ChemAxon
Hydrogen Acceptor Count15ChemAxon
Hydrogen Donor Count9ChemAxon
Polar Surface Area307.2 ŲChemAxon
Rotatable Bond Count8ChemAxon
Refractivity116.97 m³·mol⁻¹ChemAxon
Polarizability48.22 ųChemAxon
Number of Rings4ChemAxon
BioavailabilityNoChemAxon
Rule of FiveNoChemAxon
Ghose FilterNoChemAxon
Veber's RuleNoChemAxon
MDDR-like RuleYesChemAxon
Predicted Chromatographic Properties

Predicted Collision Cross Sections

PredictorAdduct TypeCCS Value (Å2)Reference
AllCCS[M+H]+217.07532859911
AllCCS[M-H]-212.61632859911
DeepCCS[M+H]+203.23830932474
DeepCCS[M-H]-200.84230932474
DeepCCS[M-2H]-234.75630932474
DeepCCS[M+Na]+209.32730932474
AllCCS[M+H]+217.132859911
AllCCS[M+H-H2O]+215.932859911
AllCCS[M+NH4]+218.232859911
AllCCS[M+Na]+218.532859911
AllCCS[M-H]-212.632859911
AllCCS[M+Na-2H]-213.832859911
AllCCS[M+HCOO]-215.232859911

Predicted Kovats Retention Indices

Underivatized

MetaboliteSMILESKovats RI ValueColumn TypeReference
GDP-L-fucoseC[C@@H]1OC(OP(O)(=O)OP(O)(=O)OC[C@H]2O[C@H]([C@H](O)[C@@H]2O)N2C=NC3=C2N=C(N)NC3=O)[C@@H](O)[C@H](O)[C@@H]1O4608.4Standard polar33892256
GDP-L-fucoseC[C@@H]1OC(OP(O)(=O)OP(O)(=O)OC[C@H]2O[C@H]([C@H](O)[C@@H]2O)N2C=NC3=C2N=C(N)NC3=O)[C@@H](O)[C@H](O)[C@@H]1O3240.3Standard non polar33892256
GDP-L-fucoseC[C@@H]1OC(OP(O)(=O)OP(O)(=O)OC[C@H]2O[C@H]([C@H](O)[C@@H]2O)N2C=NC3=C2N=C(N)NC3=O)[C@@H](O)[C@H](O)[C@@H]1O5156.6Semi standard non polar33892256

Derivatized

Derivative Name / StructureSMILESKovats RI ValueColumn TypeReference
GDP-L-fucose,1TMS,isomer #1C[C@@H]1OC(OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)[NH]C4=O)[C@H](O[Si](C)(C)C)[C@@H]2O)[C@@H](O)[C@H](O)[C@@H]1O4560.2Semi standard non polar33892256
GDP-L-fucose,1TMS,isomer #2C[C@@H]1OC(OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)[NH]C4=O)[C@H](O)[C@@H]2O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@@H]1O4566.1Semi standard non polar33892256
GDP-L-fucose,1TMS,isomer #3C[C@@H]1OC(OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)[NH]C4=O)[C@H](O)[C@@H]2O)[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H]1O4569.5Semi standard non polar33892256
GDP-L-fucose,1TMS,isomer #4C[C@@H]1OC(OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)[NH]C4=O)[C@H](O)[C@@H]2O)[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H]1O4513.6Semi standard non polar33892256
GDP-L-fucose,1TMS,isomer #5C[C@@H]1OC(OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)[NH]C4=O)[C@H](O)[C@@H]2O)[C@@H](O)[C@H](O)[C@@H]1O[Si](C)(C)C4554.7Semi standard non polar33892256
GDP-L-fucose,1TMS,isomer #6C[C@@H]1OC(OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)[NH]C4=O)[C@H](O)[C@@H]2O)[C@@H](O)[C@H](O)[C@@H]1O4631.5Semi standard non polar33892256
GDP-L-fucose,1TMS,isomer #7C[C@@H]1OC(OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)[NH]C4=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@@H]1O4619.6Semi standard non polar33892256
GDP-L-fucose,1TMS,isomer #8C[C@@H]1OC(OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N[Si](C)(C)C)[NH]C4=O)[C@H](O)[C@@H]2O)[C@@H](O)[C@H](O)[C@@H]1O4567.1Semi standard non polar33892256
GDP-L-fucose,1TMS,isomer #9C[C@@H]1OC(OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)N([Si](C)(C)C)C4=O)[C@H](O)[C@@H]2O)[C@@H](O)[C@H](O)[C@@H]1O4570.0Semi standard non polar33892256
GDP-L-fucose,2TMS,isomer #1C[C@@H]1OC(OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)[NH]C4=O)[C@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@@H]1O4402.2Semi standard non polar33892256
GDP-L-fucose,2TMS,isomer #10C[C@@H]1OC(OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)[NH]C4=O)[C@H](O)[C@@H]2O[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H]1O4323.2Semi standard non polar33892256
GDP-L-fucose,2TMS,isomer #11C[C@@H]1OC(OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)[NH]C4=O)[C@H](O)[C@@H]2O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@@H]1O[Si](C)(C)C4374.7Semi standard non polar33892256
GDP-L-fucose,2TMS,isomer #12C[C@@H]1OC(OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)[NH]C4=O)[C@H](O)[C@@H]2O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@@H]1O4456.9Semi standard non polar33892256
GDP-L-fucose,2TMS,isomer #13C[C@@H]1OC(OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)[NH]C4=O)[C@H](O)[C@@H]2O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@@H]1O4447.1Semi standard non polar33892256
GDP-L-fucose,2TMS,isomer #14C[C@@H]1OC(OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N[Si](C)(C)C)[NH]C4=O)[C@H](O)[C@@H]2O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@@H]1O4444.5Semi standard non polar33892256
GDP-L-fucose,2TMS,isomer #15C[C@@H]1OC(OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)N([Si](C)(C)C)C4=O)[C@H](O)[C@@H]2O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@@H]1O4450.8Semi standard non polar33892256
GDP-L-fucose,2TMS,isomer #16C[C@@H]1OC(OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)[NH]C4=O)[C@H](O)[C@@H]2O)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H]1O4397.3Semi standard non polar33892256
GDP-L-fucose,2TMS,isomer #17C[C@@H]1OC(OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)[NH]C4=O)[C@H](O)[C@@H]2O)[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H]1O[Si](C)(C)C4409.4Semi standard non polar33892256
GDP-L-fucose,2TMS,isomer #18C[C@@H]1OC(OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)[NH]C4=O)[C@H](O)[C@@H]2O)[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H]1O4488.6Semi standard non polar33892256
GDP-L-fucose,2TMS,isomer #19C[C@@H]1OC(OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)[NH]C4=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H]1O4479.3Semi standard non polar33892256
GDP-L-fucose,2TMS,isomer #2C[C@@H]1OC(OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)[NH]C4=O)[C@H](O[Si](C)(C)C)[C@@H]2O)[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H]1O4409.3Semi standard non polar33892256
GDP-L-fucose,2TMS,isomer #20C[C@@H]1OC(OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N[Si](C)(C)C)[NH]C4=O)[C@H](O)[C@@H]2O)[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H]1O4478.9Semi standard non polar33892256
GDP-L-fucose,2TMS,isomer #21C[C@@H]1OC(OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)N([Si](C)(C)C)C4=O)[C@H](O)[C@@H]2O)[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H]1O4478.6Semi standard non polar33892256
GDP-L-fucose,2TMS,isomer #22C[C@@H]1OC(OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)[NH]C4=O)[C@H](O)[C@@H]2O)[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C4350.0Semi standard non polar33892256
GDP-L-fucose,2TMS,isomer #23C[C@@H]1OC(OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)[NH]C4=O)[C@H](O)[C@@H]2O)[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H]1O4409.1Semi standard non polar33892256
GDP-L-fucose,2TMS,isomer #24C[C@@H]1OC(OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)[NH]C4=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H]1O4399.4Semi standard non polar33892256
GDP-L-fucose,2TMS,isomer #25C[C@@H]1OC(OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N[Si](C)(C)C)[NH]C4=O)[C@H](O)[C@@H]2O)[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H]1O4412.1Semi standard non polar33892256
GDP-L-fucose,2TMS,isomer #26C[C@@H]1OC(OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)N([Si](C)(C)C)C4=O)[C@H](O)[C@@H]2O)[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H]1O4414.6Semi standard non polar33892256
GDP-L-fucose,2TMS,isomer #27C[C@@H]1OC(OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)[NH]C4=O)[C@H](O)[C@@H]2O)[C@@H](O)[C@H](O)[C@@H]1O[Si](C)(C)C4456.4Semi standard non polar33892256
GDP-L-fucose,2TMS,isomer #28C[C@@H]1OC(OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)[NH]C4=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@@H]1O[Si](C)(C)C4447.4Semi standard non polar33892256
GDP-L-fucose,2TMS,isomer #29C[C@@H]1OC(OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N[Si](C)(C)C)[NH]C4=O)[C@H](O)[C@@H]2O)[C@@H](O)[C@H](O)[C@@H]1O[Si](C)(C)C4444.7Semi standard non polar33892256
GDP-L-fucose,2TMS,isomer #3C[C@@H]1OC(OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)[NH]C4=O)[C@H](O[Si](C)(C)C)[C@@H]2O)[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H]1O4316.7Semi standard non polar33892256
GDP-L-fucose,2TMS,isomer #30C[C@@H]1OC(OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)N([Si](C)(C)C)C4=O)[C@H](O)[C@@H]2O)[C@@H](O)[C@H](O)[C@@H]1O[Si](C)(C)C4445.3Semi standard non polar33892256
GDP-L-fucose,2TMS,isomer #31C[C@@H]1OC(OP(=O)(O[Si](C)(C)C)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)[NH]C4=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@@H]1O4515.5Semi standard non polar33892256
GDP-L-fucose,2TMS,isomer #32C[C@@H]1OC(OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N[Si](C)(C)C)[NH]C4=O)[C@H](O)[C@@H]2O)[C@@H](O)[C@H](O)[C@@H]1O4522.0Semi standard non polar33892256
GDP-L-fucose,2TMS,isomer #33C[C@@H]1OC(OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)N([Si](C)(C)C)C4=O)[C@H](O)[C@@H]2O)[C@@H](O)[C@H](O)[C@@H]1O4521.4Semi standard non polar33892256
GDP-L-fucose,2TMS,isomer #34C[C@@H]1OC(OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N[Si](C)(C)C)[NH]C4=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@@H]1O4511.5Semi standard non polar33892256
GDP-L-fucose,2TMS,isomer #35C[C@@H]1OC(OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)N([Si](C)(C)C)C4=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@@H]1O4502.5Semi standard non polar33892256
GDP-L-fucose,2TMS,isomer #36C[C@@H]1OC(OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N[Si](C)(C)C)N([Si](C)(C)C)C4=O)[C@H](O)[C@@H]2O)[C@@H](O)[C@H](O)[C@@H]1O4541.0Semi standard non polar33892256
GDP-L-fucose,2TMS,isomer #37C[C@@H]1OC(OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]C4=O)[C@H](O)[C@@H]2O)[C@@H](O)[C@H](O)[C@@H]1O4536.4Semi standard non polar33892256
GDP-L-fucose,2TMS,isomer #4C[C@@H]1OC(OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)[NH]C4=O)[C@H](O[Si](C)(C)C)[C@@H]2O)[C@@H](O)[C@H](O)[C@@H]1O[Si](C)(C)C4368.9Semi standard non polar33892256
GDP-L-fucose,2TMS,isomer #5C[C@@H]1OC(OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)[NH]C4=O)[C@H](O[Si](C)(C)C)[C@@H]2O)[C@@H](O)[C@H](O)[C@@H]1O4450.2Semi standard non polar33892256
GDP-L-fucose,2TMS,isomer #6C[C@@H]1OC(OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)[NH]C4=O)[C@H](O[Si](C)(C)C)[C@@H]2O)O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@@H]1O4442.4Semi standard non polar33892256
GDP-L-fucose,2TMS,isomer #7C[C@@H]1OC(OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N[Si](C)(C)C)[NH]C4=O)[C@H](O[Si](C)(C)C)[C@@H]2O)[C@@H](O)[C@H](O)[C@@H]1O4449.5Semi standard non polar33892256
GDP-L-fucose,2TMS,isomer #8C[C@@H]1OC(OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)N([Si](C)(C)C)C4=O)[C@H](O[Si](C)(C)C)[C@@H]2O)[C@@H](O)[C@H](O)[C@@H]1O4448.3Semi standard non polar33892256
GDP-L-fucose,2TMS,isomer #9C[C@@H]1OC(OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)[NH]C4=O)[C@H](O)[C@@H]2O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H]1O4413.2Semi standard non polar33892256
GDP-L-fucose,3TMS,isomer #1C[C@@H]1OC(OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)[NH]C4=O)[C@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H]1O4254.0Semi standard non polar33892256
GDP-L-fucose,3TMS,isomer #10C[C@@H]1OC(OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)[NH]C4=O)[C@H](O[Si](C)(C)C)[C@@H]2O)[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H]1O4280.3Semi standard non polar33892256
GDP-L-fucose,3TMS,isomer #11C[C@@H]1OC(OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)[NH]C4=O)[C@H](O[Si](C)(C)C)[C@@H]2O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H]1O4270.4Semi standard non polar33892256
GDP-L-fucose,3TMS,isomer #12C[C@@H]1OC(OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N[Si](C)(C)C)[NH]C4=O)[C@H](O[Si](C)(C)C)[C@@H]2O)[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H]1O4321.0Semi standard non polar33892256
GDP-L-fucose,3TMS,isomer #13C[C@@H]1OC(OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)N([Si](C)(C)C)C4=O)[C@H](O[Si](C)(C)C)[C@@H]2O)[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H]1O4324.3Semi standard non polar33892256
GDP-L-fucose,3TMS,isomer #14C[C@@H]1OC(OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)[NH]C4=O)[C@H](O[Si](C)(C)C)[C@@H]2O)[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C4175.3Semi standard non polar33892256
GDP-L-fucose,3TMS,isomer #15C[C@@H]1OC(OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)[NH]C4=O)[C@H](O[Si](C)(C)C)[C@@H]2O)[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H]1O4212.8Semi standard non polar33892256
GDP-L-fucose,3TMS,isomer #16C[C@@H]1OC(OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)[NH]C4=O)[C@H](O[Si](C)(C)C)[C@@H]2O)O[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H]1O4204.0Semi standard non polar33892256
GDP-L-fucose,3TMS,isomer #17C[C@@H]1OC(OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N[Si](C)(C)C)[NH]C4=O)[C@H](O[Si](C)(C)C)[C@@H]2O)[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H]1O4259.3Semi standard non polar33892256
GDP-L-fucose,3TMS,isomer #18C[C@@H]1OC(OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)N([Si](C)(C)C)C4=O)[C@H](O[Si](C)(C)C)[C@@H]2O)[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H]1O4259.7Semi standard non polar33892256
GDP-L-fucose,3TMS,isomer #19C[C@@H]1OC(OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)[NH]C4=O)[C@H](O[Si](C)(C)C)[C@@H]2O)[C@@H](O)[C@H](O)[C@@H]1O[Si](C)(C)C4253.6Semi standard non polar33892256
GDP-L-fucose,3TMS,isomer #2C[C@@H]1OC(OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)[NH]C4=O)[C@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H]1O4182.4Semi standard non polar33892256
GDP-L-fucose,3TMS,isomer #20C[C@@H]1OC(OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)[NH]C4=O)[C@H](O[Si](C)(C)C)[C@@H]2O)O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@@H]1O[Si](C)(C)C4243.1Semi standard non polar33892256
GDP-L-fucose,3TMS,isomer #21C[C@@H]1OC(OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N[Si](C)(C)C)[NH]C4=O)[C@H](O[Si](C)(C)C)[C@@H]2O)[C@@H](O)[C@H](O)[C@@H]1O[Si](C)(C)C4286.7Semi standard non polar33892256
GDP-L-fucose,3TMS,isomer #22C[C@@H]1OC(OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)N([Si](C)(C)C)C4=O)[C@H](O[Si](C)(C)C)[C@@H]2O)[C@@H](O)[C@H](O)[C@@H]1O[Si](C)(C)C4284.7Semi standard non polar33892256
GDP-L-fucose,3TMS,isomer #23C[C@@H]1OC(OP(=O)(O[Si](C)(C)C)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)[NH]C4=O)[C@H](O[Si](C)(C)C)[C@@H]2O)O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@@H]1O4302.4Semi standard non polar33892256
GDP-L-fucose,3TMS,isomer #24C[C@@H]1OC(OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N[Si](C)(C)C)[NH]C4=O)[C@H](O[Si](C)(C)C)[C@@H]2O)[C@@H](O)[C@H](O)[C@@H]1O4355.2Semi standard non polar33892256
GDP-L-fucose,3TMS,isomer #25C[C@@H]1OC(OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)N([Si](C)(C)C)C4=O)[C@H](O[Si](C)(C)C)[C@@H]2O)[C@@H](O)[C@H](O)[C@@H]1O4346.4Semi standard non polar33892256
GDP-L-fucose,3TMS,isomer #26C[C@@H]1OC(OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N[Si](C)(C)C)[NH]C4=O)[C@H](O[Si](C)(C)C)[C@@H]2O)O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@@H]1O4349.6Semi standard non polar33892256
GDP-L-fucose,3TMS,isomer #27C[C@@H]1OC(OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)N([Si](C)(C)C)C4=O)[C@H](O[Si](C)(C)C)[C@@H]2O)O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@@H]1O4337.3Semi standard non polar33892256
GDP-L-fucose,3TMS,isomer #28C[C@@H]1OC(OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N[Si](C)(C)C)N([Si](C)(C)C)C4=O)[C@H](O[Si](C)(C)C)[C@@H]2O)[C@@H](O)[C@H](O)[C@@H]1O4404.1Semi standard non polar33892256
GDP-L-fucose,3TMS,isomer #29C[C@@H]1OC(OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]C4=O)[C@H](O[Si](C)(C)C)[C@@H]2O)[C@@H](O)[C@H](O)[C@@H]1O4371.8Semi standard non polar33892256
GDP-L-fucose,3TMS,isomer #3C[C@@H]1OC(OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)[NH]C4=O)[C@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@@H]1O[Si](C)(C)C4225.5Semi standard non polar33892256
GDP-L-fucose,3TMS,isomer #30C[C@@H]1OC(OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)[NH]C4=O)[C@H](O)[C@@H]2O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H]1O4209.4Semi standard non polar33892256
GDP-L-fucose,3TMS,isomer #31C[C@@H]1OC(OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)[NH]C4=O)[C@H](O)[C@@H]2O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H]1O[Si](C)(C)C4222.1Semi standard non polar33892256
GDP-L-fucose,3TMS,isomer #32C[C@@H]1OC(OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)[NH]C4=O)[C@H](O)[C@@H]2O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H]1O4285.3Semi standard non polar33892256
GDP-L-fucose,3TMS,isomer #33C[C@@H]1OC(OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)[NH]C4=O)[C@H](O)[C@@H]2O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H]1O4274.0Semi standard non polar33892256
GDP-L-fucose,3TMS,isomer #34C[C@@H]1OC(OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N[Si](C)(C)C)[NH]C4=O)[C@H](O)[C@@H]2O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H]1O4320.7Semi standard non polar33892256
GDP-L-fucose,3TMS,isomer #35C[C@@H]1OC(OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)N([Si](C)(C)C)C4=O)[C@H](O)[C@@H]2O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H]1O4333.1Semi standard non polar33892256
GDP-L-fucose,3TMS,isomer #36C[C@@H]1OC(OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)[NH]C4=O)[C@H](O)[C@@H]2O[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C4183.7Semi standard non polar33892256
GDP-L-fucose,3TMS,isomer #37C[C@@H]1OC(OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)[NH]C4=O)[C@H](O)[C@@H]2O[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H]1O4224.2Semi standard non polar33892256
GDP-L-fucose,3TMS,isomer #38C[C@@H]1OC(OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)[NH]C4=O)[C@H](O)[C@@H]2O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H]1O4213.5Semi standard non polar33892256
GDP-L-fucose,3TMS,isomer #39C[C@@H]1OC(OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N[Si](C)(C)C)[NH]C4=O)[C@H](O)[C@@H]2O[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H]1O4258.2Semi standard non polar33892256
GDP-L-fucose,3TMS,isomer #4C[C@@H]1OC(OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)[NH]C4=O)[C@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@@H]1O4276.3Semi standard non polar33892256
GDP-L-fucose,3TMS,isomer #40C[C@@H]1OC(OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)N([Si](C)(C)C)C4=O)[C@H](O)[C@@H]2O[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H]1O4269.4Semi standard non polar33892256
GDP-L-fucose,3TMS,isomer #41C[C@@H]1OC(OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)[NH]C4=O)[C@H](O)[C@@H]2O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@@H]1O[Si](C)(C)C4263.8Semi standard non polar33892256
GDP-L-fucose,3TMS,isomer #42C[C@@H]1OC(OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)[NH]C4=O)[C@H](O)[C@@H]2O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@@H]1O[Si](C)(C)C4253.0Semi standard non polar33892256
GDP-L-fucose,3TMS,isomer #43C[C@@H]1OC(OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N[Si](C)(C)C)[NH]C4=O)[C@H](O)[C@@H]2O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@@H]1O[Si](C)(C)C4285.2Semi standard non polar33892256
GDP-L-fucose,3TMS,isomer #44C[C@@H]1OC(OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)N([Si](C)(C)C)C4=O)[C@H](O)[C@@H]2O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@@H]1O[Si](C)(C)C4294.7Semi standard non polar33892256
GDP-L-fucose,3TMS,isomer #45C[C@@H]1OC(OP(=O)(O[Si](C)(C)C)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)[NH]C4=O)[C@H](O)[C@@H]2O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@@H]1O4305.1Semi standard non polar33892256
GDP-L-fucose,3TMS,isomer #46C[C@@H]1OC(OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N[Si](C)(C)C)[NH]C4=O)[C@H](O)[C@@H]2O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@@H]1O4352.9Semi standard non polar33892256
GDP-L-fucose,3TMS,isomer #47C[C@@H]1OC(OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)N([Si](C)(C)C)C4=O)[C@H](O)[C@@H]2O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@@H]1O4352.2Semi standard non polar33892256
GDP-L-fucose,3TMS,isomer #48C[C@@H]1OC(OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N[Si](C)(C)C)[NH]C4=O)[C@H](O)[C@@H]2O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@@H]1O4345.9Semi standard non polar33892256
GDP-L-fucose,3TMS,isomer #49C[C@@H]1OC(OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)N([Si](C)(C)C)C4=O)[C@H](O)[C@@H]2O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@@H]1O4344.1Semi standard non polar33892256
GDP-L-fucose,3TMS,isomer #5C[C@@H]1OC(OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)[NH]C4=O)[C@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@@H]1O4267.7Semi standard non polar33892256
GDP-L-fucose,3TMS,isomer #50C[C@@H]1OC(OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N[Si](C)(C)C)N([Si](C)(C)C)C4=O)[C@H](O)[C@@H]2O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@@H]1O4405.1Semi standard non polar33892256
GDP-L-fucose,3TMS,isomer #51C[C@@H]1OC(OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]C4=O)[C@H](O)[C@@H]2O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@@H]1O4372.6Semi standard non polar33892256
GDP-L-fucose,3TMS,isomer #52C[C@@H]1OC(OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)[NH]C4=O)[C@H](O)[C@@H]2O)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C4252.3Semi standard non polar33892256
GDP-L-fucose,3TMS,isomer #53C[C@@H]1OC(OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)[NH]C4=O)[C@H](O)[C@@H]2O)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H]1O4274.6Semi standard non polar33892256
GDP-L-fucose,3TMS,isomer #54C[C@@H]1OC(OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)[NH]C4=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H]1O4264.4Semi standard non polar33892256
GDP-L-fucose,3TMS,isomer #55C[C@@H]1OC(OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N[Si](C)(C)C)[NH]C4=O)[C@H](O)[C@@H]2O)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H]1O4306.2Semi standard non polar33892256
GDP-L-fucose,3TMS,isomer #56C[C@@H]1OC(OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)N([Si](C)(C)C)C4=O)[C@H](O)[C@@H]2O)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H]1O4317.2Semi standard non polar33892256
GDP-L-fucose,3TMS,isomer #57C[C@@H]1OC(OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)[NH]C4=O)[C@H](O)[C@@H]2O)[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H]1O[Si](C)(C)C4288.0Semi standard non polar33892256
GDP-L-fucose,3TMS,isomer #58C[C@@H]1OC(OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)[NH]C4=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H]1O[Si](C)(C)C4275.9Semi standard non polar33892256
GDP-L-fucose,3TMS,isomer #59C[C@@H]1OC(OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N[Si](C)(C)C)[NH]C4=O)[C@H](O)[C@@H]2O)[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H]1O[Si](C)(C)C4308.9Semi standard non polar33892256
GDP-L-fucose,3TMS,isomer #6C[C@@H]1OC(OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N[Si](C)(C)C)[NH]C4=O)[C@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@@H]1O4321.3Semi standard non polar33892256
GDP-L-fucose,3TMS,isomer #60C[C@@H]1OC(OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)N([Si](C)(C)C)C4=O)[C@H](O)[C@@H]2O)[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H]1O[Si](C)(C)C4324.9Semi standard non polar33892256
GDP-L-fucose,3TMS,isomer #61C[C@@H]1OC(OP(=O)(O[Si](C)(C)C)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)[NH]C4=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H]1O4337.8Semi standard non polar33892256
GDP-L-fucose,3TMS,isomer #62C[C@@H]1OC(OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N[Si](C)(C)C)[NH]C4=O)[C@H](O)[C@@H]2O)[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H]1O4385.3Semi standard non polar33892256
GDP-L-fucose,3TMS,isomer #63C[C@@H]1OC(OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)N([Si](C)(C)C)C4=O)[C@H](O)[C@@H]2O)[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H]1O4394.0Semi standard non polar33892256
GDP-L-fucose,3TMS,isomer #64C[C@@H]1OC(OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N[Si](C)(C)C)[NH]C4=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H]1O4377.1Semi standard non polar33892256
GDP-L-fucose,3TMS,isomer #65C[C@@H]1OC(OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)N([Si](C)(C)C)C4=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H]1O4383.6Semi standard non polar33892256
GDP-L-fucose,3TMS,isomer #66C[C@@H]1OC(OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N[Si](C)(C)C)N([Si](C)(C)C)C4=O)[C@H](O)[C@@H]2O)[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H]1O4444.7Semi standard non polar33892256
GDP-L-fucose,3TMS,isomer #67C[C@@H]1OC(OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]C4=O)[C@H](O)[C@@H]2O)[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H]1O4412.0Semi standard non polar33892256
GDP-L-fucose,3TMS,isomer #68C[C@@H]1OC(OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)[NH]C4=O)[C@H](O)[C@@H]2O)[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C4245.4Semi standard non polar33892256
GDP-L-fucose,3TMS,isomer #69C[C@@H]1OC(OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)[NH]C4=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C4234.0Semi standard non polar33892256
GDP-L-fucose,3TMS,isomer #7C[C@@H]1OC(OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)N([Si](C)(C)C)C4=O)[C@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@@H]1O4318.9Semi standard non polar33892256
GDP-L-fucose,3TMS,isomer #70C[C@@H]1OC(OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N[Si](C)(C)C)[NH]C4=O)[C@H](O)[C@@H]2O)[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C4271.1Semi standard non polar33892256
GDP-L-fucose,3TMS,isomer #71C[C@@H]1OC(OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)N([Si](C)(C)C)C4=O)[C@H](O)[C@@H]2O)[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C4279.0Semi standard non polar33892256
GDP-L-fucose,3TMS,isomer #72C[C@@H]1OC(OP(=O)(O[Si](C)(C)C)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)[NH]C4=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H]1O4273.3Semi standard non polar33892256
GDP-L-fucose,3TMS,isomer #73C[C@@H]1OC(OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N[Si](C)(C)C)[NH]C4=O)[C@H](O)[C@@H]2O)[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H]1O4318.6Semi standard non polar33892256
GDP-L-fucose,3TMS,isomer #74C[C@@H]1OC(OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)N([Si](C)(C)C)C4=O)[C@H](O)[C@@H]2O)[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H]1O4321.6Semi standard non polar33892256
GDP-L-fucose,3TMS,isomer #75C[C@@H]1OC(OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N[Si](C)(C)C)[NH]C4=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H]1O4309.5Semi standard non polar33892256
GDP-L-fucose,3TMS,isomer #76C[C@@H]1OC(OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)N([Si](C)(C)C)C4=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H]1O4312.3Semi standard non polar33892256
GDP-L-fucose,3TMS,isomer #77C[C@@H]1OC(OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N[Si](C)(C)C)N([Si](C)(C)C)C4=O)[C@H](O)[C@@H]2O)[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H]1O4379.6Semi standard non polar33892256
GDP-L-fucose,3TMS,isomer #78C[C@@H]1OC(OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]C4=O)[C@H](O)[C@@H]2O)[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H]1O4338.6Semi standard non polar33892256
GDP-L-fucose,3TMS,isomer #79C[C@@H]1OC(OP(=O)(O[Si](C)(C)C)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)[NH]C4=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@@H]1O[Si](C)(C)C4311.2Semi standard non polar33892256
GDP-L-fucose,3TMS,isomer #8C[C@@H]1OC(OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)[NH]C4=O)[C@H](O[Si](C)(C)C)[C@@H]2O)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H]1O4202.7Semi standard non polar33892256
GDP-L-fucose,3TMS,isomer #80C[C@@H]1OC(OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N[Si](C)(C)C)[NH]C4=O)[C@H](O)[C@@H]2O)[C@@H](O)[C@H](O)[C@@H]1O[Si](C)(C)C4346.1Semi standard non polar33892256
GDP-L-fucose,3TMS,isomer #81C[C@@H]1OC(OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)N([Si](C)(C)C)C4=O)[C@H](O)[C@@H]2O)[C@@H](O)[C@H](O)[C@@H]1O[Si](C)(C)C4346.7Semi standard non polar33892256
GDP-L-fucose,3TMS,isomer #82C[C@@H]1OC(OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N[Si](C)(C)C)[NH]C4=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@@H]1O[Si](C)(C)C4336.1Semi standard non polar33892256
GDP-L-fucose,3TMS,isomer #83C[C@@H]1OC(OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)N([Si](C)(C)C)C4=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@@H]1O[Si](C)(C)C4337.1Semi standard non polar33892256
GDP-L-fucose,3TMS,isomer #84C[C@@H]1OC(OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N[Si](C)(C)C)N([Si](C)(C)C)C4=O)[C@H](O)[C@@H]2O)[C@@H](O)[C@H](O)[C@@H]1O[Si](C)(C)C4406.7Semi standard non polar33892256
GDP-L-fucose,3TMS,isomer #85C[C@@H]1OC(OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]C4=O)[C@H](O)[C@@H]2O)[C@@H](O)[C@H](O)[C@@H]1O[Si](C)(C)C4367.1Semi standard non polar33892256
GDP-L-fucose,3TMS,isomer #86C[C@@H]1OC(OP(=O)(O[Si](C)(C)C)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N[Si](C)(C)C)[NH]C4=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@@H]1O4405.4Semi standard non polar33892256
GDP-L-fucose,3TMS,isomer #87C[C@@H]1OC(OP(=O)(O[Si](C)(C)C)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)N([Si](C)(C)C)C4=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@@H]1O4402.7Semi standard non polar33892256
GDP-L-fucose,3TMS,isomer #88C[C@@H]1OC(OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N[Si](C)(C)C)N([Si](C)(C)C)C4=O)[C@H](O)[C@@H]2O)[C@@H](O)[C@H](O)[C@@H]1O4472.9Semi standard non polar33892256
GDP-L-fucose,3TMS,isomer #89C[C@@H]1OC(OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]C4=O)[C@H](O)[C@@H]2O)[C@@H](O)[C@H](O)[C@@H]1O4441.2Semi standard non polar33892256
GDP-L-fucose,3TMS,isomer #9C[C@@H]1OC(OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)[NH]C4=O)[C@H](O[Si](C)(C)C)[C@@H]2O)[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H]1O[Si](C)(C)C4214.1Semi standard non polar33892256
GDP-L-fucose,3TMS,isomer #90C[C@@H]1OC(OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N[Si](C)(C)C)N([Si](C)(C)C)C4=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@@H]1O4461.5Semi standard non polar33892256
GDP-L-fucose,3TMS,isomer #91C[C@@H]1OC(OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]C4=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@@H]1O4430.9Semi standard non polar33892256
GDP-L-fucose,3TMS,isomer #92C[C@@H]1OC(OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N([Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)C4=O)[C@H](O)[C@@H]2O)[C@@H](O)[C@H](O)[C@@H]1O4515.6Semi standard non polar33892256
GDP-L-fucose,4TMS,isomer #1C[C@@H]1OC(OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)[NH]C4=O)[C@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H]1O4122.2Semi standard non polar33892256
GDP-L-fucose,4TMS,isomer #10C[C@@H]1OC(OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N[Si](C)(C)C)[NH]C4=O)[C@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H]1O4166.7Semi standard non polar33892256
GDP-L-fucose,4TMS,isomer #100C[C@@H]1OC(OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N[Si](C)(C)C)N([Si](C)(C)C)C4=O)[C@H](O)[C@@H]2O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@@H]1O4334.0Semi standard non polar33892256
GDP-L-fucose,4TMS,isomer #101C[C@@H]1OC(OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]C4=O)[C@H](O)[C@@H]2O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@@H]1O4303.3Semi standard non polar33892256
GDP-L-fucose,4TMS,isomer #102C[C@@H]1OC(OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N[Si](C)(C)C)N([Si](C)(C)C)C4=O)[C@H](O)[C@@H]2O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@@H]1O4330.3Semi standard non polar33892256
GDP-L-fucose,4TMS,isomer #103C[C@@H]1OC(OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]C4=O)[C@H](O)[C@@H]2O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@@H]1O4295.3Semi standard non polar33892256
GDP-L-fucose,4TMS,isomer #104C[C@@H]1OC(OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N([Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)C4=O)[C@H](O)[C@@H]2O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@@H]1O4367.3Semi standard non polar33892256
GDP-L-fucose,4TMS,isomer #105C[C@@H]1OC(OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)[NH]C4=O)[C@H](O)[C@@H]2O)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C4183.8Semi standard non polar33892256
GDP-L-fucose,4TMS,isomer #106C[C@@H]1OC(OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)[NH]C4=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C4170.9Semi standard non polar33892256
GDP-L-fucose,4TMS,isomer #107C[C@@H]1OC(OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N[Si](C)(C)C)[NH]C4=O)[C@H](O)[C@@H]2O)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C4211.4Semi standard non polar33892256
GDP-L-fucose,4TMS,isomer #108C[C@@H]1OC(OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)N([Si](C)(C)C)C4=O)[C@H](O)[C@@H]2O)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C4243.9Semi standard non polar33892256
GDP-L-fucose,4TMS,isomer #109C[C@@H]1OC(OP(=O)(O[Si](C)(C)C)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)[NH]C4=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H]1O4180.6Semi standard non polar33892256
GDP-L-fucose,4TMS,isomer #11C[C@@H]1OC(OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)N([Si](C)(C)C)C4=O)[C@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H]1O4202.2Semi standard non polar33892256
GDP-L-fucose,4TMS,isomer #110C[C@@H]1OC(OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N[Si](C)(C)C)[NH]C4=O)[C@H](O)[C@@H]2O)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H]1O4240.1Semi standard non polar33892256
GDP-L-fucose,4TMS,isomer #111C[C@@H]1OC(OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)N([Si](C)(C)C)C4=O)[C@H](O)[C@@H]2O)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H]1O4262.7Semi standard non polar33892256
GDP-L-fucose,4TMS,isomer #112C[C@@H]1OC(OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N[Si](C)(C)C)[NH]C4=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H]1O4225.3Semi standard non polar33892256
GDP-L-fucose,4TMS,isomer #113C[C@@H]1OC(OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)N([Si](C)(C)C)C4=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H]1O4252.2Semi standard non polar33892256
GDP-L-fucose,4TMS,isomer #114C[C@@H]1OC(OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N[Si](C)(C)C)N([Si](C)(C)C)C4=O)[C@H](O)[C@@H]2O)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H]1O4307.9Semi standard non polar33892256
GDP-L-fucose,4TMS,isomer #115C[C@@H]1OC(OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]C4=O)[C@H](O)[C@@H]2O)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H]1O4265.3Semi standard non polar33892256
GDP-L-fucose,4TMS,isomer #116C[C@@H]1OC(OP(=O)(O[Si](C)(C)C)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)[NH]C4=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H]1O[Si](C)(C)C4188.3Semi standard non polar33892256
GDP-L-fucose,4TMS,isomer #117C[C@@H]1OC(OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N[Si](C)(C)C)[NH]C4=O)[C@H](O)[C@@H]2O)[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H]1O[Si](C)(C)C4241.5Semi standard non polar33892256
GDP-L-fucose,4TMS,isomer #118C[C@@H]1OC(OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)N([Si](C)(C)C)C4=O)[C@H](O)[C@@H]2O)[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H]1O[Si](C)(C)C4274.7Semi standard non polar33892256
GDP-L-fucose,4TMS,isomer #119C[C@@H]1OC(OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N[Si](C)(C)C)[NH]C4=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H]1O[Si](C)(C)C4227.6Semi standard non polar33892256
GDP-L-fucose,4TMS,isomer #12C[C@@H]1OC(OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)[NH]C4=O)[C@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@@H]1O[Si](C)(C)C4141.2Semi standard non polar33892256
GDP-L-fucose,4TMS,isomer #120C[C@@H]1OC(OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)N([Si](C)(C)C)C4=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H]1O[Si](C)(C)C4263.7Semi standard non polar33892256
GDP-L-fucose,4TMS,isomer #121C[C@@H]1OC(OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N[Si](C)(C)C)N([Si](C)(C)C)C4=O)[C@H](O)[C@@H]2O)[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H]1O[Si](C)(C)C4315.6Semi standard non polar33892256
GDP-L-fucose,4TMS,isomer #122C[C@@H]1OC(OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]C4=O)[C@H](O)[C@@H]2O)[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H]1O[Si](C)(C)C4264.6Semi standard non polar33892256
GDP-L-fucose,4TMS,isomer #123C[C@@H]1OC(OP(=O)(O[Si](C)(C)C)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N[Si](C)(C)C)[NH]C4=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H]1O4288.2Semi standard non polar33892256
GDP-L-fucose,4TMS,isomer #124C[C@@H]1OC(OP(=O)(O[Si](C)(C)C)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)N([Si](C)(C)C)C4=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H]1O4310.1Semi standard non polar33892256
GDP-L-fucose,4TMS,isomer #125C[C@@H]1OC(OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N[Si](C)(C)C)N([Si](C)(C)C)C4=O)[C@H](O)[C@@H]2O)[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H]1O4367.5Semi standard non polar33892256
GDP-L-fucose,4TMS,isomer #126C[C@@H]1OC(OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]C4=O)[C@H](O)[C@@H]2O)[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H]1O4319.9Semi standard non polar33892256
GDP-L-fucose,4TMS,isomer #127C[C@@H]1OC(OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N[Si](C)(C)C)N([Si](C)(C)C)C4=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H]1O4360.0Semi standard non polar33892256
GDP-L-fucose,4TMS,isomer #128C[C@@H]1OC(OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]C4=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H]1O4309.1Semi standard non polar33892256
GDP-L-fucose,4TMS,isomer #129C[C@@H]1OC(OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N([Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)C4=O)[C@H](O)[C@@H]2O)[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H]1O4391.7Semi standard non polar33892256
GDP-L-fucose,4TMS,isomer #13C[C@@H]1OC(OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)[NH]C4=O)[C@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@@H]1O[Si](C)(C)C4130.4Semi standard non polar33892256
GDP-L-fucose,4TMS,isomer #130C[C@@H]1OC(OP(=O)(O[Si](C)(C)C)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)[NH]C4=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C4154.3Semi standard non polar33892256
GDP-L-fucose,4TMS,isomer #131C[C@@H]1OC(OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N[Si](C)(C)C)[NH]C4=O)[C@H](O)[C@@H]2O)[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C4212.9Semi standard non polar33892256
GDP-L-fucose,4TMS,isomer #132C[C@@H]1OC(OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)N([Si](C)(C)C)C4=O)[C@H](O)[C@@H]2O)[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C4245.6Semi standard non polar33892256
GDP-L-fucose,4TMS,isomer #133C[C@@H]1OC(OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N[Si](C)(C)C)[NH]C4=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C4198.2Semi standard non polar33892256
GDP-L-fucose,4TMS,isomer #134C[C@@H]1OC(OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)N([Si](C)(C)C)C4=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C4234.1Semi standard non polar33892256
GDP-L-fucose,4TMS,isomer #135C[C@@H]1OC(OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N[Si](C)(C)C)N([Si](C)(C)C)C4=O)[C@H](O)[C@@H]2O)[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C4278.0Semi standard non polar33892256
GDP-L-fucose,4TMS,isomer #136C[C@@H]1OC(OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]C4=O)[C@H](O)[C@@H]2O)[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C4240.2Semi standard non polar33892256
GDP-L-fucose,4TMS,isomer #137C[C@@H]1OC(OP(=O)(O[Si](C)(C)C)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N[Si](C)(C)C)[NH]C4=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H]1O4243.4Semi standard non polar33892256
GDP-L-fucose,4TMS,isomer #138C[C@@H]1OC(OP(=O)(O[Si](C)(C)C)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)N([Si](C)(C)C)C4=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H]1O4261.6Semi standard non polar33892256
GDP-L-fucose,4TMS,isomer #139C[C@@H]1OC(OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N[Si](C)(C)C)N([Si](C)(C)C)C4=O)[C@H](O)[C@@H]2O)[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H]1O4324.8Semi standard non polar33892256
GDP-L-fucose,4TMS,isomer #14C[C@@H]1OC(OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N[Si](C)(C)C)[NH]C4=O)[C@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@@H]1O[Si](C)(C)C4181.3Semi standard non polar33892256
GDP-L-fucose,4TMS,isomer #140C[C@@H]1OC(OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]C4=O)[C@H](O)[C@@H]2O)[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H]1O4277.8Semi standard non polar33892256
GDP-L-fucose,4TMS,isomer #141C[C@@H]1OC(OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N[Si](C)(C)C)N([Si](C)(C)C)C4=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H]1O4317.0Semi standard non polar33892256
GDP-L-fucose,4TMS,isomer #142C[C@@H]1OC(OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]C4=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H]1O4269.1Semi standard non polar33892256
GDP-L-fucose,4TMS,isomer #143C[C@@H]1OC(OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N([Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)C4=O)[C@H](O)[C@@H]2O)[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H]1O4342.0Semi standard non polar33892256
GDP-L-fucose,4TMS,isomer #144C[C@@H]1OC(OP(=O)(O[Si](C)(C)C)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N[Si](C)(C)C)[NH]C4=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@@H]1O[Si](C)(C)C4260.9Semi standard non polar33892256
GDP-L-fucose,4TMS,isomer #145C[C@@H]1OC(OP(=O)(O[Si](C)(C)C)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)N([Si](C)(C)C)C4=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@@H]1O[Si](C)(C)C4281.8Semi standard non polar33892256
GDP-L-fucose,4TMS,isomer #146C[C@@H]1OC(OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N[Si](C)(C)C)N([Si](C)(C)C)C4=O)[C@H](O)[C@@H]2O)[C@@H](O)[C@H](O)[C@@H]1O[Si](C)(C)C4342.8Semi standard non polar33892256
GDP-L-fucose,4TMS,isomer #147C[C@@H]1OC(OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]C4=O)[C@H](O)[C@@H]2O)[C@@H](O)[C@H](O)[C@@H]1O[Si](C)(C)C4294.6Semi standard non polar33892256
GDP-L-fucose,4TMS,isomer #148C[C@@H]1OC(OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N[Si](C)(C)C)N([Si](C)(C)C)C4=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@@H]1O[Si](C)(C)C4334.1Semi standard non polar33892256
GDP-L-fucose,4TMS,isomer #149C[C@@H]1OC(OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]C4=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@@H]1O[Si](C)(C)C4282.8Semi standard non polar33892256
GDP-L-fucose,4TMS,isomer #15C[C@@H]1OC(OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)N([Si](C)(C)C)C4=O)[C@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@@H]1O[Si](C)(C)C4214.7Semi standard non polar33892256
GDP-L-fucose,4TMS,isomer #150C[C@@H]1OC(OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N([Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)C4=O)[C@H](O)[C@@H]2O)[C@@H](O)[C@H](O)[C@@H]1O[Si](C)(C)C4362.5Semi standard non polar33892256
GDP-L-fucose,4TMS,isomer #151C[C@@H]1OC(OP(=O)(O[Si](C)(C)C)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N[Si](C)(C)C)N([Si](C)(C)C)C4=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@@H]1O4380.8Semi standard non polar33892256
GDP-L-fucose,4TMS,isomer #152C[C@@H]1OC(OP(=O)(O[Si](C)(C)C)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]C4=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@@H]1O4340.5Semi standard non polar33892256
GDP-L-fucose,4TMS,isomer #153C[C@@H]1OC(OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N([Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)C4=O)[C@H](O)[C@@H]2O)[C@@H](O)[C@H](O)[C@@H]1O4419.1Semi standard non polar33892256
GDP-L-fucose,4TMS,isomer #154C[C@@H]1OC(OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N([Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)C4=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@@H]1O4408.9Semi standard non polar33892256
GDP-L-fucose,4TMS,isomer #16C[C@@H]1OC(OP(=O)(O[Si](C)(C)C)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)[NH]C4=O)[C@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@@H]1O4171.7Semi standard non polar33892256
GDP-L-fucose,4TMS,isomer #17C[C@@H]1OC(OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N[Si](C)(C)C)[NH]C4=O)[C@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@@H]1O4235.5Semi standard non polar33892256
GDP-L-fucose,4TMS,isomer #18C[C@@H]1OC(OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)N([Si](C)(C)C)C4=O)[C@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@@H]1O4259.4Semi standard non polar33892256
GDP-L-fucose,4TMS,isomer #19C[C@@H]1OC(OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N[Si](C)(C)C)[NH]C4=O)[C@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@@H]1O4224.3Semi standard non polar33892256
GDP-L-fucose,4TMS,isomer #2C[C@@H]1OC(OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)[NH]C4=O)[C@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H]1O[Si](C)(C)C4125.7Semi standard non polar33892256
GDP-L-fucose,4TMS,isomer #20C[C@@H]1OC(OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)N([Si](C)(C)C)C4=O)[C@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@@H]1O4253.8Semi standard non polar33892256
GDP-L-fucose,4TMS,isomer #21C[C@@H]1OC(OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N[Si](C)(C)C)N([Si](C)(C)C)C4=O)[C@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@@H]1O4304.9Semi standard non polar33892256
GDP-L-fucose,4TMS,isomer #22C[C@@H]1OC(OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]C4=O)[C@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@@H]1O4265.1Semi standard non polar33892256
GDP-L-fucose,4TMS,isomer #23C[C@@H]1OC(OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)[NH]C4=O)[C@H](O[Si](C)(C)C)[C@@H]2O)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C4134.7Semi standard non polar33892256
GDP-L-fucose,4TMS,isomer #24C[C@@H]1OC(OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)[NH]C4=O)[C@H](O[Si](C)(C)C)[C@@H]2O)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H]1O4140.2Semi standard non polar33892256
GDP-L-fucose,4TMS,isomer #25C[C@@H]1OC(OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)[NH]C4=O)[C@H](O[Si](C)(C)C)[C@@H]2O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H]1O4127.7Semi standard non polar33892256
GDP-L-fucose,4TMS,isomer #26C[C@@H]1OC(OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N[Si](C)(C)C)[NH]C4=O)[C@H](O[Si](C)(C)C)[C@@H]2O)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H]1O4176.0Semi standard non polar33892256
GDP-L-fucose,4TMS,isomer #27C[C@@H]1OC(OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)N([Si](C)(C)C)C4=O)[C@H](O[Si](C)(C)C)[C@@H]2O)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H]1O4206.4Semi standard non polar33892256
GDP-L-fucose,4TMS,isomer #28C[C@@H]1OC(OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)[NH]C4=O)[C@H](O[Si](C)(C)C)[C@@H]2O)[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H]1O[Si](C)(C)C4148.3Semi standard non polar33892256
GDP-L-fucose,4TMS,isomer #29C[C@@H]1OC(OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)[NH]C4=O)[C@H](O[Si](C)(C)C)[C@@H]2O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H]1O[Si](C)(C)C4135.1Semi standard non polar33892256
GDP-L-fucose,4TMS,isomer #3C[C@@H]1OC(OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)[NH]C4=O)[C@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H]1O4168.2Semi standard non polar33892256
GDP-L-fucose,4TMS,isomer #30C[C@@H]1OC(OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N[Si](C)(C)C)[NH]C4=O)[C@H](O[Si](C)(C)C)[C@@H]2O)[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H]1O[Si](C)(C)C4177.4Semi standard non polar33892256
GDP-L-fucose,4TMS,isomer #31C[C@@H]1OC(OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)N([Si](C)(C)C)C4=O)[C@H](O[Si](C)(C)C)[C@@H]2O)[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H]1O[Si](C)(C)C4216.0Semi standard non polar33892256
GDP-L-fucose,4TMS,isomer #32C[C@@H]1OC(OP(=O)(O[Si](C)(C)C)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)[NH]C4=O)[C@H](O[Si](C)(C)C)[C@@H]2O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H]1O4180.3Semi standard non polar33892256
GDP-L-fucose,4TMS,isomer #33C[C@@H]1OC(OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N[Si](C)(C)C)[NH]C4=O)[C@H](O[Si](C)(C)C)[C@@H]2O)[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H]1O4236.3Semi standard non polar33892256
GDP-L-fucose,4TMS,isomer #34C[C@@H]1OC(OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)N([Si](C)(C)C)C4=O)[C@H](O[Si](C)(C)C)[C@@H]2O)[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H]1O4262.1Semi standard non polar33892256
GDP-L-fucose,4TMS,isomer #35C[C@@H]1OC(OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N[Si](C)(C)C)[NH]C4=O)[C@H](O[Si](C)(C)C)[C@@H]2O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H]1O4223.4Semi standard non polar33892256
GDP-L-fucose,4TMS,isomer #36C[C@@H]1OC(OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)N([Si](C)(C)C)C4=O)[C@H](O[Si](C)(C)C)[C@@H]2O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H]1O4252.1Semi standard non polar33892256
GDP-L-fucose,4TMS,isomer #37C[C@@H]1OC(OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N[Si](C)(C)C)N([Si](C)(C)C)C4=O)[C@H](O[Si](C)(C)C)[C@@H]2O)[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H]1O4315.7Semi standard non polar33892256
GDP-L-fucose,4TMS,isomer #38C[C@@H]1OC(OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]C4=O)[C@H](O[Si](C)(C)C)[C@@H]2O)[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H]1O4264.7Semi standard non polar33892256
GDP-L-fucose,4TMS,isomer #39C[C@@H]1OC(OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)[NH]C4=O)[C@H](O[Si](C)(C)C)[C@@H]2O)[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C4119.2Semi standard non polar33892256
GDP-L-fucose,4TMS,isomer #4C[C@@H]1OC(OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)[NH]C4=O)[C@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H]1O4157.5Semi standard non polar33892256
GDP-L-fucose,4TMS,isomer #40C[C@@H]1OC(OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)[NH]C4=O)[C@H](O[Si](C)(C)C)[C@@H]2O)O[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C4110.0Semi standard non polar33892256
GDP-L-fucose,4TMS,isomer #41C[C@@H]1OC(OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N[Si](C)(C)C)[NH]C4=O)[C@H](O[Si](C)(C)C)[C@@H]2O)[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C4156.7Semi standard non polar33892256
GDP-L-fucose,4TMS,isomer #42C[C@@H]1OC(OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)N([Si](C)(C)C)C4=O)[C@H](O[Si](C)(C)C)[C@@H]2O)[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C4190.3Semi standard non polar33892256
GDP-L-fucose,4TMS,isomer #43C[C@@H]1OC(OP(=O)(O[Si](C)(C)C)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)[NH]C4=O)[C@H](O[Si](C)(C)C)[C@@H]2O)O[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H]1O4127.7Semi standard non polar33892256
GDP-L-fucose,4TMS,isomer #44C[C@@H]1OC(OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N[Si](C)(C)C)[NH]C4=O)[C@H](O[Si](C)(C)C)[C@@H]2O)[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H]1O4197.6Semi standard non polar33892256
GDP-L-fucose,4TMS,isomer #45C[C@@H]1OC(OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)N([Si](C)(C)C)C4=O)[C@H](O[Si](C)(C)C)[C@@H]2O)[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H]1O4221.9Semi standard non polar33892256
GDP-L-fucose,4TMS,isomer #46C[C@@H]1OC(OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N[Si](C)(C)C)[NH]C4=O)[C@H](O[Si](C)(C)C)[C@@H]2O)O[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H]1O4186.6Semi standard non polar33892256
GDP-L-fucose,4TMS,isomer #47C[C@@H]1OC(OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)N([Si](C)(C)C)C4=O)[C@H](O[Si](C)(C)C)[C@@H]2O)O[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H]1O4212.0Semi standard non polar33892256
GDP-L-fucose,4TMS,isomer #48C[C@@H]1OC(OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N[Si](C)(C)C)N([Si](C)(C)C)C4=O)[C@H](O[Si](C)(C)C)[C@@H]2O)[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H]1O4271.4Semi standard non polar33892256
GDP-L-fucose,4TMS,isomer #49C[C@@H]1OC(OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]C4=O)[C@H](O[Si](C)(C)C)[C@@H]2O)[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H]1O4222.3Semi standard non polar33892256
GDP-L-fucose,4TMS,isomer #5C[C@@H]1OC(OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N[Si](C)(C)C)[NH]C4=O)[C@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H]1O4208.8Semi standard non polar33892256
GDP-L-fucose,4TMS,isomer #50C[C@@H]1OC(OP(=O)(O[Si](C)(C)C)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)[NH]C4=O)[C@H](O[Si](C)(C)C)[C@@H]2O)O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@@H]1O[Si](C)(C)C4150.9Semi standard non polar33892256
GDP-L-fucose,4TMS,isomer #51C[C@@H]1OC(OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N[Si](C)(C)C)[NH]C4=O)[C@H](O[Si](C)(C)C)[C@@H]2O)[C@@H](O)[C@H](O)[C@@H]1O[Si](C)(C)C4211.4Semi standard non polar33892256
GDP-L-fucose,4TMS,isomer #52C[C@@H]1OC(OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)N([Si](C)(C)C)C4=O)[C@H](O[Si](C)(C)C)[C@@H]2O)[C@@H](O)[C@H](O)[C@@H]1O[Si](C)(C)C4235.5Semi standard non polar33892256
GDP-L-fucose,4TMS,isomer #53C[C@@H]1OC(OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N[Si](C)(C)C)[NH]C4=O)[C@H](O[Si](C)(C)C)[C@@H]2O)O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@@H]1O[Si](C)(C)C4199.0Semi standard non polar33892256
GDP-L-fucose,4TMS,isomer #54C[C@@H]1OC(OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)N([Si](C)(C)C)C4=O)[C@H](O[Si](C)(C)C)[C@@H]2O)O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@@H]1O[Si](C)(C)C4224.4Semi standard non polar33892256
GDP-L-fucose,4TMS,isomer #55C[C@@H]1OC(OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N[Si](C)(C)C)N([Si](C)(C)C)C4=O)[C@H](O[Si](C)(C)C)[C@@H]2O)[C@@H](O)[C@H](O)[C@@H]1O[Si](C)(C)C4286.2Semi standard non polar33892256
GDP-L-fucose,4TMS,isomer #56C[C@@H]1OC(OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]C4=O)[C@H](O[Si](C)(C)C)[C@@H]2O)[C@@H](O)[C@H](O)[C@@H]1O[Si](C)(C)C4233.7Semi standard non polar33892256
GDP-L-fucose,4TMS,isomer #57C[C@@H]1OC(OP(=O)(O[Si](C)(C)C)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N[Si](C)(C)C)[NH]C4=O)[C@H](O[Si](C)(C)C)[C@@H]2O)O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@@H]1O4264.1Semi standard non polar33892256
GDP-L-fucose,4TMS,isomer #58C[C@@H]1OC(OP(=O)(O[Si](C)(C)C)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)N([Si](C)(C)C)C4=O)[C@H](O[Si](C)(C)C)[C@@H]2O)O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@@H]1O4273.0Semi standard non polar33892256
GDP-L-fucose,4TMS,isomer #59C[C@@H]1OC(OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N[Si](C)(C)C)N([Si](C)(C)C)C4=O)[C@H](O[Si](C)(C)C)[C@@H]2O)[C@@H](O)[C@H](O)[C@@H]1O4333.7Semi standard non polar33892256
GDP-L-fucose,4TMS,isomer #6C[C@@H]1OC(OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)N([Si](C)(C)C)C4=O)[C@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H]1O4242.2Semi standard non polar33892256
GDP-L-fucose,4TMS,isomer #60C[C@@H]1OC(OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]C4=O)[C@H](O[Si](C)(C)C)[C@@H]2O)[C@@H](O)[C@H](O)[C@@H]1O4296.4Semi standard non polar33892256
GDP-L-fucose,4TMS,isomer #61C[C@@H]1OC(OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N[Si](C)(C)C)N([Si](C)(C)C)C4=O)[C@H](O[Si](C)(C)C)[C@@H]2O)O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@@H]1O4328.1Semi standard non polar33892256
GDP-L-fucose,4TMS,isomer #62C[C@@H]1OC(OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]C4=O)[C@H](O[Si](C)(C)C)[C@@H]2O)O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@@H]1O4286.2Semi standard non polar33892256
GDP-L-fucose,4TMS,isomer #63C[C@@H]1OC(OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N([Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)C4=O)[C@H](O[Si](C)(C)C)[C@@H]2O)[C@@H](O)[C@H](O)[C@@H]1O4367.1Semi standard non polar33892256
GDP-L-fucose,4TMS,isomer #64C[C@@H]1OC(OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)[NH]C4=O)[C@H](O)[C@@H]2O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C4141.4Semi standard non polar33892256
GDP-L-fucose,4TMS,isomer #65C[C@@H]1OC(OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)[NH]C4=O)[C@H](O)[C@@H]2O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H]1O4148.9Semi standard non polar33892256
GDP-L-fucose,4TMS,isomer #66C[C@@H]1OC(OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)[NH]C4=O)[C@H](O)[C@@H]2O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H]1O4137.8Semi standard non polar33892256
GDP-L-fucose,4TMS,isomer #67C[C@@H]1OC(OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N[Si](C)(C)C)[NH]C4=O)[C@H](O)[C@@H]2O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H]1O4181.1Semi standard non polar33892256
GDP-L-fucose,4TMS,isomer #68C[C@@H]1OC(OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)N([Si](C)(C)C)C4=O)[C@H](O)[C@@H]2O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H]1O4219.6Semi standard non polar33892256
GDP-L-fucose,4TMS,isomer #69C[C@@H]1OC(OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)[NH]C4=O)[C@H](O)[C@@H]2O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H]1O[Si](C)(C)C4156.9Semi standard non polar33892256
GDP-L-fucose,4TMS,isomer #7C[C@@H]1OC(OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)[NH]C4=O)[C@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C4102.5Semi standard non polar33892256
GDP-L-fucose,4TMS,isomer #70C[C@@H]1OC(OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)[NH]C4=O)[C@H](O)[C@@H]2O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H]1O[Si](C)(C)C4145.0Semi standard non polar33892256
GDP-L-fucose,4TMS,isomer #71C[C@@H]1OC(OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N[Si](C)(C)C)[NH]C4=O)[C@H](O)[C@@H]2O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H]1O[Si](C)(C)C4182.3Semi standard non polar33892256
GDP-L-fucose,4TMS,isomer #72C[C@@H]1OC(OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)N([Si](C)(C)C)C4=O)[C@H](O)[C@@H]2O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H]1O[Si](C)(C)C4230.1Semi standard non polar33892256
GDP-L-fucose,4TMS,isomer #73C[C@@H]1OC(OP(=O)(O[Si](C)(C)C)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)[NH]C4=O)[C@H](O)[C@@H]2O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H]1O4190.6Semi standard non polar33892256
GDP-L-fucose,4TMS,isomer #74C[C@@H]1OC(OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N[Si](C)(C)C)[NH]C4=O)[C@H](O)[C@@H]2O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H]1O4241.8Semi standard non polar33892256
GDP-L-fucose,4TMS,isomer #75C[C@@H]1OC(OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)N([Si](C)(C)C)C4=O)[C@H](O)[C@@H]2O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H]1O4274.7Semi standard non polar33892256
GDP-L-fucose,4TMS,isomer #76C[C@@H]1OC(OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N[Si](C)(C)C)[NH]C4=O)[C@H](O)[C@@H]2O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H]1O4227.6Semi standard non polar33892256
GDP-L-fucose,4TMS,isomer #77C[C@@H]1OC(OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)N([Si](C)(C)C)C4=O)[C@H](O)[C@@H]2O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H]1O4265.5Semi standard non polar33892256
GDP-L-fucose,4TMS,isomer #78C[C@@H]1OC(OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N[Si](C)(C)C)N([Si](C)(C)C)C4=O)[C@H](O)[C@@H]2O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H]1O4317.4Semi standard non polar33892256
GDP-L-fucose,4TMS,isomer #79C[C@@H]1OC(OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]C4=O)[C@H](O)[C@@H]2O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H]1O4271.1Semi standard non polar33892256
GDP-L-fucose,4TMS,isomer #8C[C@@H]1OC(OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)[NH]C4=O)[C@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H]1O4116.3Semi standard non polar33892256
GDP-L-fucose,4TMS,isomer #80C[C@@H]1OC(OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)[NH]C4=O)[C@H](O)[C@@H]2O[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C4127.9Semi standard non polar33892256
GDP-L-fucose,4TMS,isomer #81C[C@@H]1OC(OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)[NH]C4=O)[C@H](O)[C@@H]2O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C4118.0Semi standard non polar33892256
GDP-L-fucose,4TMS,isomer #82C[C@@H]1OC(OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N[Si](C)(C)C)[NH]C4=O)[C@H](O)[C@@H]2O[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C4161.4Semi standard non polar33892256
GDP-L-fucose,4TMS,isomer #83C[C@@H]1OC(OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)N([Si](C)(C)C)C4=O)[C@H](O)[C@@H]2O[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C4204.0Semi standard non polar33892256
GDP-L-fucose,4TMS,isomer #84C[C@@H]1OC(OP(=O)(O[Si](C)(C)C)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)[NH]C4=O)[C@H](O)[C@@H]2O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H]1O4139.9Semi standard non polar33892256
GDP-L-fucose,4TMS,isomer #85C[C@@H]1OC(OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N[Si](C)(C)C)[NH]C4=O)[C@H](O)[C@@H]2O[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H]1O4201.7Semi standard non polar33892256
GDP-L-fucose,4TMS,isomer #86C[C@@H]1OC(OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)N([Si](C)(C)C)C4=O)[C@H](O)[C@@H]2O[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H]1O4237.9Semi standard non polar33892256
GDP-L-fucose,4TMS,isomer #87C[C@@H]1OC(OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N[Si](C)(C)C)[NH]C4=O)[C@H](O)[C@@H]2O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H]1O4190.2Semi standard non polar33892256
GDP-L-fucose,4TMS,isomer #88C[C@@H]1OC(OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)N([Si](C)(C)C)C4=O)[C@H](O)[C@@H]2O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H]1O4228.8Semi standard non polar33892256
GDP-L-fucose,4TMS,isomer #89C[C@@H]1OC(OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N[Si](C)(C)C)N([Si](C)(C)C)C4=O)[C@H](O)[C@@H]2O[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H]1O4275.2Semi standard non polar33892256
GDP-L-fucose,4TMS,isomer #9C[C@@H]1OC(OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)[NH]C4=O)[C@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H]1O4109.6Semi standard non polar33892256
GDP-L-fucose,4TMS,isomer #90C[C@@H]1OC(OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]C4=O)[C@H](O)[C@@H]2O[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H]1O4232.2Semi standard non polar33892256
GDP-L-fucose,4TMS,isomer #91C[C@@H]1OC(OP(=O)(O[Si](C)(C)C)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)[NH]C4=O)[C@H](O)[C@@H]2O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@@H]1O[Si](C)(C)C4163.3Semi standard non polar33892256
GDP-L-fucose,4TMS,isomer #92C[C@@H]1OC(OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N[Si](C)(C)C)[NH]C4=O)[C@H](O)[C@@H]2O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@@H]1O[Si](C)(C)C4217.8Semi standard non polar33892256
GDP-L-fucose,4TMS,isomer #93C[C@@H]1OC(OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)N([Si](C)(C)C)C4=O)[C@H](O)[C@@H]2O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@@H]1O[Si](C)(C)C4250.9Semi standard non polar33892256
GDP-L-fucose,4TMS,isomer #94C[C@@H]1OC(OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N[Si](C)(C)C)[NH]C4=O)[C@H](O)[C@@H]2O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@@H]1O[Si](C)(C)C4204.5Semi standard non polar33892256
GDP-L-fucose,4TMS,isomer #95C[C@@H]1OC(OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)N([Si](C)(C)C)C4=O)[C@H](O)[C@@H]2O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@@H]1O[Si](C)(C)C4240.0Semi standard non polar33892256
GDP-L-fucose,4TMS,isomer #96C[C@@H]1OC(OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N[Si](C)(C)C)N([Si](C)(C)C)C4=O)[C@H](O)[C@@H]2O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@@H]1O[Si](C)(C)C4289.8Semi standard non polar33892256
GDP-L-fucose,4TMS,isomer #97C[C@@H]1OC(OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]C4=O)[C@H](O)[C@@H]2O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@@H]1O[Si](C)(C)C4242.0Semi standard non polar33892256
GDP-L-fucose,4TMS,isomer #98C[C@@H]1OC(OP(=O)(O[Si](C)(C)C)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N[Si](C)(C)C)[NH]C4=O)[C@H](O)[C@@H]2O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@@H]1O4268.3Semi standard non polar33892256
GDP-L-fucose,4TMS,isomer #99C[C@@H]1OC(OP(=O)(O[Si](C)(C)C)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)N([Si](C)(C)C)C4=O)[C@H](O)[C@@H]2O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@@H]1O4287.7Semi standard non polar33892256
GDP-L-fucose,1TBDMS,isomer #1C[C@@H]1OC(OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)[NH]C4=O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]2O)[C@@H](O)[C@H](O)[C@@H]1O4758.0Semi standard non polar33892256
GDP-L-fucose,1TBDMS,isomer #2C[C@@H]1OC(OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)[NH]C4=O)[C@H](O)[C@@H]2O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O)[C@@H]1O4764.5Semi standard non polar33892256
GDP-L-fucose,1TBDMS,isomer #3C[C@@H]1OC(OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)[NH]C4=O)[C@H](O)[C@@H]2O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H]1O4738.4Semi standard non polar33892256
GDP-L-fucose,1TBDMS,isomer #4C[C@@H]1OC(OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)[NH]C4=O)[C@H](O)[C@@H]2O)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O4715.2Semi standard non polar33892256
GDP-L-fucose,1TBDMS,isomer #5C[C@@H]1OC(OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)[NH]C4=O)[C@H](O)[C@@H]2O)[C@@H](O)[C@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C4754.0Semi standard non polar33892256
GDP-L-fucose,1TBDMS,isomer #6C[C@@H]1OC(OP(=O)(O[Si](C)(C)C(C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)[NH]C4=O)[C@H](O)[C@@H]2O)[C@@H](O)[C@H](O)[C@@H]1O4815.8Semi standard non polar33892256
GDP-L-fucose,1TBDMS,isomer #7C[C@@H]1OC(OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)[NH]C4=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O)[C@@H]1O4804.3Semi standard non polar33892256
GDP-L-fucose,1TBDMS,isomer #8C[C@@H]1OC(OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N[Si](C)(C)C(C)(C)C)[NH]C4=O)[C@H](O)[C@@H]2O)[C@@H](O)[C@H](O)[C@@H]1O4760.0Semi standard non polar33892256
GDP-L-fucose,1TBDMS,isomer #9C[C@@H]1OC(OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)N([Si](C)(C)C(C)(C)C)C4=O)[C@H](O)[C@@H]2O)[C@@H](O)[C@H](O)[C@@H]1O4747.3Semi standard non polar33892256
GDP-L-fucose,2TBDMS,isomer #1C[C@@H]1OC(OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)[NH]C4=O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]2O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O)[C@@H]1O4724.9Semi standard non polar33892256
GDP-L-fucose,2TBDMS,isomer #10C[C@@H]1OC(OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)[NH]C4=O)[C@H](O)[C@@H]2O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O4674.5Semi standard non polar33892256
GDP-L-fucose,2TBDMS,isomer #11C[C@@H]1OC(OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)[NH]C4=O)[C@H](O)[C@@H]2O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C4703.4Semi standard non polar33892256
GDP-L-fucose,2TBDMS,isomer #12C[C@@H]1OC(OP(=O)(O[Si](C)(C)C(C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)[NH]C4=O)[C@H](O)[C@@H]2O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O)[C@@H]1O4766.3Semi standard non polar33892256
GDP-L-fucose,2TBDMS,isomer #13C[C@@H]1OC(OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)[NH]C4=O)[C@H](O)[C@@H]2O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O)[C@@H]1O4759.9Semi standard non polar33892256
GDP-L-fucose,2TBDMS,isomer #14C[C@@H]1OC(OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N[Si](C)(C)C(C)(C)C)[NH]C4=O)[C@H](O)[C@@H]2O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O)[C@@H]1O4741.0Semi standard non polar33892256
GDP-L-fucose,2TBDMS,isomer #15C[C@@H]1OC(OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)N([Si](C)(C)C(C)(C)C)C4=O)[C@H](O)[C@@H]2O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O)[C@@H]1O4765.7Semi standard non polar33892256
GDP-L-fucose,2TBDMS,isomer #16C[C@@H]1OC(OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)[NH]C4=O)[C@H](O)[C@@H]2O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O4680.1Semi standard non polar33892256
GDP-L-fucose,2TBDMS,isomer #17C[C@@H]1OC(OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)[NH]C4=O)[C@H](O)[C@@H]2O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C4687.0Semi standard non polar33892256
GDP-L-fucose,2TBDMS,isomer #18C[C@@H]1OC(OP(=O)(O[Si](C)(C)C(C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)[NH]C4=O)[C@H](O)[C@@H]2O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H]1O4758.1Semi standard non polar33892256
GDP-L-fucose,2TBDMS,isomer #19C[C@@H]1OC(OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)[NH]C4=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H]1O4751.2Semi standard non polar33892256
GDP-L-fucose,2TBDMS,isomer #2C[C@@H]1OC(OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)[NH]C4=O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]2O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H]1O4702.4Semi standard non polar33892256
GDP-L-fucose,2TBDMS,isomer #20C[C@@H]1OC(OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N[Si](C)(C)C(C)(C)C)[NH]C4=O)[C@H](O)[C@@H]2O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H]1O4739.7Semi standard non polar33892256
GDP-L-fucose,2TBDMS,isomer #21C[C@@H]1OC(OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)N([Si](C)(C)C(C)(C)C)C4=O)[C@H](O)[C@@H]2O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H]1O4766.4Semi standard non polar33892256
GDP-L-fucose,2TBDMS,isomer #22C[C@@H]1OC(OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)[NH]C4=O)[C@H](O)[C@@H]2O)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C4657.4Semi standard non polar33892256
GDP-L-fucose,2TBDMS,isomer #23C[C@@H]1OC(OP(=O)(O[Si](C)(C)C(C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)[NH]C4=O)[C@H](O)[C@@H]2O)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O4728.6Semi standard non polar33892256
GDP-L-fucose,2TBDMS,isomer #24C[C@@H]1OC(OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)[NH]C4=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O4721.2Semi standard non polar33892256
GDP-L-fucose,2TBDMS,isomer #25C[C@@H]1OC(OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N[Si](C)(C)C(C)(C)C)[NH]C4=O)[C@H](O)[C@@H]2O)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O4712.9Semi standard non polar33892256
GDP-L-fucose,2TBDMS,isomer #26C[C@@H]1OC(OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)N([Si](C)(C)C(C)(C)C)C4=O)[C@H](O)[C@@H]2O)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O4740.7Semi standard non polar33892256
GDP-L-fucose,2TBDMS,isomer #27C[C@@H]1OC(OP(=O)(O[Si](C)(C)C(C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)[NH]C4=O)[C@H](O)[C@@H]2O)[C@@H](O)[C@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C4758.2Semi standard non polar33892256
GDP-L-fucose,2TBDMS,isomer #28C[C@@H]1OC(OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)[NH]C4=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C4754.1Semi standard non polar33892256
GDP-L-fucose,2TBDMS,isomer #29C[C@@H]1OC(OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N[Si](C)(C)C(C)(C)C)[NH]C4=O)[C@H](O)[C@@H]2O)[C@@H](O)[C@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C4725.0Semi standard non polar33892256
GDP-L-fucose,2TBDMS,isomer #3C[C@@H]1OC(OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)[NH]C4=O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]2O)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O4675.2Semi standard non polar33892256
GDP-L-fucose,2TBDMS,isomer #30C[C@@H]1OC(OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)N([Si](C)(C)C(C)(C)C)C4=O)[C@H](O)[C@@H]2O)[C@@H](O)[C@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C4748.9Semi standard non polar33892256
GDP-L-fucose,2TBDMS,isomer #31C[C@@H]1OC(OP(=O)(O[Si](C)(C)C(C)(C)C)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)[NH]C4=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O)[C@@H]1O4813.7Semi standard non polar33892256
GDP-L-fucose,2TBDMS,isomer #32C[C@@H]1OC(OP(=O)(O[Si](C)(C)C(C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N[Si](C)(C)C(C)(C)C)[NH]C4=O)[C@H](O)[C@@H]2O)[C@@H](O)[C@H](O)[C@@H]1O4820.0Semi standard non polar33892256
GDP-L-fucose,2TBDMS,isomer #33C[C@@H]1OC(OP(=O)(O[Si](C)(C)C(C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)N([Si](C)(C)C(C)(C)C)C4=O)[C@H](O)[C@@H]2O)[C@@H](O)[C@H](O)[C@@H]1O4824.8Semi standard non polar33892256
GDP-L-fucose,2TBDMS,isomer #34C[C@@H]1OC(OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N[Si](C)(C)C(C)(C)C)[NH]C4=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O)[C@@H]1O4809.2Semi standard non polar33892256
GDP-L-fucose,2TBDMS,isomer #35C[C@@H]1OC(OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)N([Si](C)(C)C(C)(C)C)C4=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O)[C@@H]1O4813.0Semi standard non polar33892256
GDP-L-fucose,2TBDMS,isomer #36C[C@@H]1OC(OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)C4=O)[C@H](O)[C@@H]2O)[C@@H](O)[C@H](O)[C@@H]1O4860.8Semi standard non polar33892256
GDP-L-fucose,2TBDMS,isomer #37C[C@@H]1OC(OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[NH]C4=O)[C@H](O)[C@@H]2O)[C@@H](O)[C@H](O)[C@@H]1O4833.9Semi standard non polar33892256
GDP-L-fucose,2TBDMS,isomer #4C[C@@H]1OC(OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)[NH]C4=O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]2O)[C@@H](O)[C@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C4705.6Semi standard non polar33892256
GDP-L-fucose,2TBDMS,isomer #5C[C@@H]1OC(OP(=O)(O[Si](C)(C)C(C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)[NH]C4=O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]2O)[C@@H](O)[C@H](O)[C@@H]1O4768.0Semi standard non polar33892256
GDP-L-fucose,2TBDMS,isomer #6C[C@@H]1OC(OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)[NH]C4=O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]2O)O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O)[C@@H]1O4763.6Semi standard non polar33892256
GDP-L-fucose,2TBDMS,isomer #7C[C@@H]1OC(OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N[Si](C)(C)C(C)(C)C)[NH]C4=O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]2O)[C@@H](O)[C@H](O)[C@@H]1O4748.2Semi standard non polar33892256
GDP-L-fucose,2TBDMS,isomer #8C[C@@H]1OC(OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)N([Si](C)(C)C(C)(C)C)C4=O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]2O)[C@@H](O)[C@H](O)[C@@H]1O4770.8Semi standard non polar33892256
GDP-L-fucose,2TBDMS,isomer #9C[C@@H]1OC(OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N=C(N)[NH]C4=O)[C@H](O)[C@@H]2O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H]1O4699.7Semi standard non polar33892256
Spectra

GC-MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted GC-MSPredicted GC-MS Spectrum - GDP-L-fucose GC-MS (Non-derivatized) - 70eV, Positivesplash10-05bf-6985780000-f2b6a0fdececb1ffd4092017-09-01Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - GDP-L-fucose GC-MS (1 TMS) - 70eV, Positivesplash10-0007-6173159000-1cf7c64a7a19bbd73e282017-10-06Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - GDP-L-fucose GC-MS ("GDP-L-fucose,1TMS,#1" TMS) - 70eV, PositiveNot Available2021-10-14Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - GDP-L-fucose GC-MS (TMS_1_2) - 70eV, PositiveNot Available2021-10-15Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - GDP-L-fucose GC-MS (TMS_1_3) - 70eV, PositiveNot Available2021-10-15Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - GDP-L-fucose GC-MS (TMS_1_4) - 70eV, PositiveNot Available2021-10-15Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - GDP-L-fucose GC-MS (TMS_1_5) - 70eV, PositiveNot Available2021-10-15Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - GDP-L-fucose GC-MS (TMS_1_6) - 70eV, PositiveNot Available2021-10-15Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - GDP-L-fucose GC-MS (TMS_1_7) - 70eV, PositiveNot Available2021-10-15Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - GDP-L-fucose GC-MS (TMS_1_8) - 70eV, PositiveNot Available2021-10-15Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - GDP-L-fucose GC-MS (TMS_1_9) - 70eV, PositiveNot Available2021-10-15Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - GDP-L-fucose GC-MS (TMS_2_1) - 70eV, PositiveNot Available2021-10-15Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - GDP-L-fucose GC-MS (TMS_2_2) - 70eV, PositiveNot Available2021-10-15Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - GDP-L-fucose GC-MS (TMS_2_3) - 70eV, PositiveNot Available2021-10-15Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - GDP-L-fucose GC-MS (TMS_2_4) - 70eV, PositiveNot Available2021-10-15Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - GDP-L-fucose GC-MS (TMS_2_5) - 70eV, PositiveNot Available2021-10-15Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - GDP-L-fucose GC-MS (TMS_2_6) - 70eV, PositiveNot Available2021-10-15Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - GDP-L-fucose GC-MS (TMS_2_7) - 70eV, PositiveNot Available2021-10-15Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - GDP-L-fucose GC-MS (TMS_2_8) - 70eV, PositiveNot Available2021-10-15Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - GDP-L-fucose GC-MS (TMS_2_9) - 70eV, PositiveNot Available2021-10-15Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - GDP-L-fucose GC-MS (TMS_2_10) - 70eV, PositiveNot Available2021-10-15Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - GDP-L-fucose GC-MS (TMS_2_11) - 70eV, PositiveNot Available2021-10-15Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - GDP-L-fucose GC-MS (TMS_2_12) - 70eV, PositiveNot Available2021-10-15Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - GDP-L-fucose GC-MS (TMS_2_13) - 70eV, PositiveNot Available2021-10-15Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - GDP-L-fucose GC-MS (TMS_2_14) - 70eV, PositiveNot Available2021-10-15Wishart LabView Spectrum

MS/MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - GDP-L-fucose 10V, Positive-QTOFsplash10-0udi-0910420000-6f2823064a15be7fc9a82015-09-15Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - GDP-L-fucose 20V, Positive-QTOFsplash10-0udi-0910000000-866d48af83abebf463392015-09-15Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - GDP-L-fucose 40V, Positive-QTOFsplash10-0udi-1900000000-8b884fd821ce0574d9f12015-09-15Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - GDP-L-fucose 10V, Negative-QTOFsplash10-0ukl-2801490000-f519f8992a1d7307dde62015-09-15Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - GDP-L-fucose 20V, Negative-QTOFsplash10-0udi-1901000000-5004fbddcfb22c8ecd5f2015-09-15Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - GDP-L-fucose 40V, Negative-QTOFsplash10-0pdl-3900000000-4c564cfa5a166417a5fa2015-09-15Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - GDP-L-fucose 10V, Negative-QTOFsplash10-000i-0000090000-2f459a27134486d5a1ca2021-09-22Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - GDP-L-fucose 20V, Negative-QTOFsplash10-00c9-9401260000-e8773e96d7afecfae8152021-09-22Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - GDP-L-fucose 40V, Negative-QTOFsplash10-00di-1501900000-343d428ef047e49497952021-09-22Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - GDP-L-fucose 10V, Positive-QTOFsplash10-0006-0100090000-a6f771b381799c776be62021-09-23Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - GDP-L-fucose 20V, Positive-QTOFsplash10-0f6x-5922540000-c4c21e0fb882f03ef8632021-09-23Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - GDP-L-fucose 40V, Positive-QTOFsplash10-0f7x-9740000000-e90684222b98c6e2cd5a2021-09-23Wishart LabView Spectrum

NMR Spectra

Spectrum TypeDescriptionDeposition DateSourceView
Predicted 1D NMR13C NMR Spectrum (1D, 100 MHz, D2O, predicted)2021-09-29Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 100 MHz, D2O, predicted)2021-09-29Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 1000 MHz, D2O, predicted)2021-09-29Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 1000 MHz, D2O, predicted)2021-09-29Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 200 MHz, D2O, predicted)2021-09-29Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 200 MHz, D2O, predicted)2021-09-29Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 300 MHz, D2O, predicted)2021-09-29Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 300 MHz, D2O, predicted)2021-09-29Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 400 MHz, D2O, predicted)2021-09-29Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 400 MHz, D2O, predicted)2021-09-29Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 500 MHz, D2O, predicted)2021-09-29Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 500 MHz, D2O, predicted)2021-09-29Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 600 MHz, D2O, predicted)2021-09-29Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 600 MHz, D2O, predicted)2021-09-29Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 700 MHz, D2O, predicted)2021-09-29Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 700 MHz, D2O, predicted)2021-09-29Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 800 MHz, D2O, predicted)2021-09-29Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 800 MHz, D2O, predicted)2021-09-29Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 900 MHz, D2O, predicted)2021-09-29Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 900 MHz, D2O, predicted)2021-09-29Wishart LabView Spectrum
Biological Properties
Cellular Locations
  • Golgi apparatus
Biospecimen LocationsNot Available
Tissue Locations
  • Epidermis
  • Fibroblasts
  • Intestine
  • Kidney
  • Neuron
  • Placenta
  • Platelet
  • Prostate
  • Spleen
Pathways
Normal Concentrations
Not Available
Abnormal Concentrations
Not Available
Associated Disorders and Diseases
Disease ReferencesNone
Associated OMIM IDsNone
DrugBank IDNot Available
Phenol Explorer Compound IDNot Available
FooDB IDFDB030882
KNApSAcK IDC00007245
Chemspider ID388350
KEGG Compound IDC00325
BioCyc IDNot Available
BiGG ID34623
Wikipedia LinkNot Available
METLIN ID6001
PubChem Compound439211
PDB IDGFB
ChEBI ID17009
Food Biomarker OntologyNot Available
VMH IDGDPFUC
MarkerDB IDNot Available
Good Scents IDNot Available
References
Synthesis ReferenceYamamoto, Kenji; Maruyama, Takashi; Kumagai, Hidehiko; Tochikura, Tatsurokuro; Seno, Taiko; Yamaguchi, Hideo. Preparation of GDP-L-fucose by using microbial enzymes. Agricultural and Biological Chemistry (1984), 48(3), 823-4.
Material Safety Data Sheet (MSDS)Not Available
General References
  1. Qi H, Fournier A, Grenier J, Fillion C, Labrie Y, Labrie C: Isolation of the novel human guanine nucleotide exchange factor Src homology 3 domain-containing guanine nucleotide exchange factor (SGEF) and of C-terminal SGEF, an N-terminally truncated form of SGEF, the expression of which is regulated by androgen in prostate cancer cells. Endocrinology. 2003 May;144(5):1742-52. [PubMed:12697679 ]
  2. Quirk S, Seley KL: Substrate discrimination by the human GTP fucose pyrophosphorylase. Biochemistry. 2005 Aug 16;44(32):10854-63. [PubMed:16086588 ]
  3. Sawamura D, Abe R, Goto M, Akiyama M, Hemmi H, Akira S, Shimizu H: Direct injection of plasmid DNA into the skin induces dermatitis by activation of monocytes through toll-like receptor 9. J Gene Med. 2005 May;7(5):664-71. [PubMed:15655803 ]
  4. Sales ME, Sterin-Borda L, de Bracco MM, Rodriguez M, Narbaitz M, Borda E: IgA from HIV+ haemophilic patients triggers intracellular signals coupled to the cholinergic system of the intestine. Clin Exp Immunol. 1997 Nov;110(2):189-95. [PubMed:9367401 ]
  5. Palma AS, Morais VA, Coelho AV, Costa J: Effect of the manganese ion on human alpha3/4 fucosyltransferase III activity. Biometals. 2004 Feb;17(1):35-43. [PubMed:14977360 ]
  6. Yegorov YE, Kazimirchuk EV, Terekhov SM, Karachentsev DN, Shirokova EA, Khandazhinskaya AL, Meshcheryakova JA, Corey DR, Zelenin AV: Telomerase-dependent reactivation of DNA synthesis in macrophages implies alteration of telomeres. Cell Biol Int. 2002;26(12):1019-27. [PubMed:12468377 ]
  7. Coates SW Jr, Hogenauer C, Santa Ana CA, Rosenblatt RL, Emmett M, Fordtran JS: Inhibition of neutral sodium absorption by a prostaglandin analogue in patients with cystic fibrosis. Gastroenterology. 2004 Jul;127(1):65-72. [PubMed:15236173 ]
  8. Galiegue S, Mary S, Marchand J, Dussossoy D, Carriere D, Carayon P, Bouaboula M, Shire D, Le Fur G, Casellas P: Expression of central and peripheral cannabinoid receptors in human immune tissues and leukocyte subpopulations. Eur J Biochem. 1995 Aug 15;232(1):54-61. [PubMed:7556170 ]
  9. Anfossi G, Russo I, Massucco P, Mattiello L, Doronzo G, De Salve A, Trovati M: Impaired synthesis and action of antiaggregating cyclic nucleotides in platelets from obese subjects: possible role in platelet hyperactivation in obesity. Eur J Clin Invest. 2004 Jul;34(7):482-9. [PubMed:15255785 ]
  10. Rastaldi MP, Armelloni S, Berra S, Li M, Pesaresi M, Poczewski H, Langer B, Kerjaschki D, Henger A, Blattner SM, Kretzler M, Wanke R, D'Amico G: Glomerular podocytes possess the synaptic vesicle molecule Rab3A and its specific effector rabphilin-3a. Am J Pathol. 2003 Sep;163(3):889-99. [PubMed:12937130 ]
  11. Sibley CP, Hochberg A, Boime I: Bromo-adenosine stimulates choriogonadotropin production in JAr and cytotrophoblast cells: evidence for effects on two stages of differentiation. Mol Endocrinol. 1991 Apr;5(4):582-6. [PubMed:1922090 ]
  12. Rosenfeldt HM, Hobson JP, Milstien S, Spiegel S: The sphingosine-1-phosphate receptor EDG-1 is essential for platelet-derived growth factor-induced cell motility. Biochem Soc Trans. 2001 Nov;29(Pt 6):836-9. [PubMed:11709084 ]
  13. Huopaniemi L, Kolmer M, Niittymaki J, Pelto-Huikko M, Renkonen R: Inflammation-induced transcriptional regulation of Golgi transporters required for the synthesis of sulfo sLex glycan epitopes. Glycobiology. 2004 Dec;14(12):1285-94. Epub 2004 Jul 21. [PubMed:15269183 ]
  14. Noda K, Miyoshi E, Gu J, Gao CX, Nakahara S, Kitada T, Honke K, Suzuki K, Yoshihara H, Yoshikawa K, Kawano K, Tonetti M, Kasahara A, Hori M, Hayashi N, Taniguchi N: Relationship between elevated FX expression and increased production of GDP-L-fucose, a common donor substrate for fucosylation in human hepatocellular carcinoma and hepatoma cell lines. Cancer Res. 2003 Oct 1;63(19):6282-9. [PubMed:14559815 ]
  15. Jakob G, Mair J, Vorderwinkler KP, Judmaier G, Konig P, Zwierzina H, Pichler M, Puschendorf B: Clinical significance of urinary cyclic guanosine monophosphate in diagnosis of heart failure. Clin Chem. 1994 Jan;40(1):96-100. [PubMed:8287551 ]
  16. da Silva CD, Brunini TM, Reis PF, Moss MB, Santos SF, Roberts NB, Ellory JC, Mann GE, Mendes-Ribeiro AC: Effects of nutritional status on the L-arginine-nitric oxide pathway in platelets from hemodialysis patients. Kidney Int. 2005 Nov;68(5):2173-9. [PubMed:16221216 ]
  17. Andre M, Latado H, Felley-Bosco E: Inducible nitric oxide synthase-dependent stimulation of PKGI and phosphorylation of VASP in human embryonic kidney cells. Biochem Pharmacol. 2005 Feb 15;69(4):595-602. Epub 2004 Dec 22. [PubMed:15670578 ]
  18. Benitah SA, Frye M, Glogauer M, Watt FM: Stem cell depletion through epidermal deletion of Rac1. Science. 2005 Aug 5;309(5736):933-5. [PubMed:16081735 ]

Enzymes

General function:
Involved in fucose-1-phosphate guanylyltransferase acti
Specific function:
Catalyzes the formation of GDP-L-fucose from GTP and L-fucose-1-phosphate. Functions as a salvage pathway to reutilize L-fucose arising from the turnover of glycoproteins and glycolipids.
Gene Name:
FPGT
Uniprot ID:
O14772
Molecular weight:
37630.405
Reactions
Guanosine triphosphate + Fucose 1-phosphate → Pyrophosphate + GDP-L-fucosedetails
General function:
Involved in galactoside 2-alpha-L-fucosyltransferase activity
Specific function:
Creates a soluble precursor oligosaccharide FuC-alpha ((1,2)Galbeta-) called the H antigen which is an essential substrate for the final step in the soluble A and B antigen synthesis pathway. H and Se enzymes fucosylate the same acceptor substrates but exhibit different Km values.
Gene Name:
FUT2
Uniprot ID:
Q10981
Molecular weight:
39016.84
Reactions
GDP-L-fucose + beta-D-galactosyl-(1->3)-N-acetyl-beta-D-glucosaminyl-(1->3)-beta-D-galactosyl-(1->4)-beta-D-glucosyl-(1<->1)-ceramide → Guanosine diphosphate + alpha-L-fucosyl-(1->2)-beta-D-galactosyl-(1->3)-N-acetyl-beta-D-glucosaminyl-(1->3)-beta-D-galactosyl-(1->4)-beta-D-glucosyl-(1<->1)-ceramidedetails
General function:
Involved in galactoside 2-alpha-L-fucosyltransferase activity
Specific function:
Creates a soluble precursor oligosaccharide FuC-alpha ((1,2)Galbeta-) called the H antigen which is an essential substrate for the final step in the soluble A and B antigen synthesis pathway. H and Se enzymes fucosylate the same acceptor substrates but exhibit different Km values.
Gene Name:
FUT1
Uniprot ID:
P19526
Molecular weight:
41251.11
Reactions
GDP-L-fucose + beta-D-galactosyl-(1->3)-N-acetyl-beta-D-glucosaminyl-(1->3)-beta-D-galactosyl-(1->4)-beta-D-glucosyl-(1<->1)-ceramide → Guanosine diphosphate + alpha-L-fucosyl-(1->2)-beta-D-galactosyl-(1->3)-N-acetyl-beta-D-glucosaminyl-(1->3)-beta-D-galactosyl-(1->4)-beta-D-glucosyl-(1<->1)-ceramidedetails
General function:
Involved in catalytic activity
Specific function:
Two step NADP-dependent conversion of GDP-4-dehydro-6-deoxy-D-mannose to GDP-fucose, involving an epimerase and a reductase reaction.
Gene Name:
TSTA3
Uniprot ID:
Q13630
Molecular weight:
35892.46
Reactions
GDP-L-fucose + NADP → GDP-4-Dehydro-6-deoxy-D-mannose + NADPHdetails
GDP-L-fucose + NADP → GDP-4-Dehydro-6-deoxy-D-mannose + NADPH + Hydrogen Iondetails
General function:
Involved in fucosyltransferase activity
Specific function:
May catalyze alpha-1,3 glycosidic linkages involved in the expression of VIM-2, Lewis X/SSEA-1 and sialyl Lewis X antigens.
Gene Name:
FUT5
Uniprot ID:
Q11128
Molecular weight:
42988.655
Reactions
GDP-L-fucose + beta-D-galactosyl-(1->3)-N-acetyl-D-glucosaminyl-R → Guanosine diphosphate + beta-D-galactosyl-(1->3)-(alpha-L-fucosyl-(1->4))-N-acetyl-beta-D-glucosaminyl-Rdetails
General function:
Involved in fucosyltransferase activity
Specific function:
Transfers a fucose to lacto-N-neotetraose but not to either alpha2,3-sialyl lacto-N-neotetraose or lacto-N-tetraose. Can catalyze the last step in the biosynthesis of Lewis antigen, the addition of a fucose to precursor polysaccharides
Gene Name:
FUT9
Uniprot ID:
Q9Y231
Molecular weight:
42040.7
General function:
Involved in glycoprotein 6-alpha-L-fucosyltransferase activity
Specific function:
Catalyzes the addition of fucose in alpha 1-6 linkage to the first GlcNAc residue, next to the peptide chains in N-glycans.
Gene Name:
FUT8
Uniprot ID:
Q9BYC5
Molecular weight:
66515.32
Reactions
GDP-L-fucose + N(4)-(N-acetyl-beta-D-glucosaminyl-(1->2)-alpha-D-mannosyl-(1->3)-(N-acetyl-beta-D-glucosaminyl-(1->2)-alpha-D-mannosyl-(1->6))-beta-D-mannosyl-(1->4)-N-acetyl-beta-D-glucosaminyl-(1->4)-N-acetyl-beta-D-glucosaminyl)asparagine → Guanosine diphosphate + N(4)-(N-acetyl-beta-D-glucosaminyl-(1->2)-alpha-D-mannosyl-(1->3)-(N-acetyl-beta-D-glucosaminyl-(1->2)-alpha-D-mannosyl-(1->6))-beta-D-mannosyl-(1->4)-N-acetyl-beta-D-glucosaminyl-(1->4)-(alpha-L-fucosyl-(1->6))-N-acetyl-beta-D-glucosaminyl)asparaginedetails
General function:
Involved in fucosyltransferase activity
Specific function:
Enzyme involved in the biosynthesis of the E-Selectin ligand, sialyl-Lewis X. Catalyzes the transfer of fucose from GDP-beta-fucose to alpha-2,3 sialylated substrates.
Gene Name:
FUT6
Uniprot ID:
P51993
Molecular weight:
41859.42
Reactions
GDP-L-fucose + beta-D-galactosyl-(1->3)-N-acetyl-D-glucosaminyl-R → Guanosine diphosphate + beta-D-galactosyl-(1->3)-(alpha-L-fucosyl-(1->4))-N-acetyl-beta-D-glucosaminyl-Rdetails
General function:
Involved in fucosyltransferase activity
Specific function:
May catalyze alpha-1,3 glycosidic linkages involved in the expression of sialyl Lewis X antigens.
Gene Name:
FUT7
Uniprot ID:
Q11130
Molecular weight:
39238.495
Reactions
GDP-L-fucose + alpha-2,3-Neu-N-acetyl-1,4-beta-D-galactosyl-N-acetyl-D-glucosaminyl-R → Guanosine diphosphate + alpha-2,3-Neu-N-acetyl-1,4-beta-D-galactosyl-(alpha-1,3-L-fucosyl)-N-acetyl-D-glucosaminyl-Rdetails
General function:
Not Available
Specific function:
May catalyze alpha-1,3 and alpha-1,4 glycosidic linkages involved in the expression of Vim-2, Lewis A, Lewis B, sialyl Lewis X and Lewis X/SSEA-1 antigens. May be involved in blood group Lewis determination; Lewis-positive (Le(+)) individuals have an active enzyme while Lewis-negative (Le(-)) individuals have an inactive enzyme. Also acts on the corresponding 1,4-galactosyl derivative, forming 1,3-L-fucosyl links.
Gene Name:
FUT3
Uniprot ID:
P21217
Molecular weight:
42116.69
Reactions
GDP-L-fucose + beta-D-galactosyl-(1->3)-N-acetyl-D-glucosaminyl-R → Guanosine diphosphate + beta-D-galactosyl-(1->3)-(alpha-L-fucosyl-(1->4))-N-acetyl-beta-D-glucosaminyl-Rdetails