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Record Information
Version5.0
StatusExpected but not Quantified
Creation Date2009-04-06 16:21:00 UTC
Update Date2021-09-14 15:48:15 UTC
HMDB IDHMDB0012206
Secondary Accession Numbers
  • HMDB12206
Metabolite Identification
Common NameCMP-N-glycoloylneuraminate
DescriptionCMP-N-glycoloylneuraminate, also known as CMP-N-glycoloylneuraminic acid, belongs to the class of organic compounds known as glycosylamines. Glycosylamines are compounds consisting of an amine with a beta-N-glycosidic bond to a carbohydrate, thus forming a cyclic hemiaminal ether bond (alpha-amino ether). CMP-N-glycoloylneuraminate has been detected, but not quantified in, a few different foods, such as anatidaes (Anatidae), chickens (Gallus gallus), and domestic pigs (Sus scrofa domestica). This could make CMP-N-glycoloylneuraminate a potential biomarker for the consumption of these foods. Based on a literature review very few articles have been published on CMP-N-glycoloylneuraminate.
Structure
Data?1582753026
Synonyms
ValueSource
CMP-N-Glycoloylneuraminic acidGenerator
(2R,4S,5R,6R)-2-[({[(2R,3S,4R,5R)-5-(4-amino-2-oxo-1,2-dihydropyrimidin-1-yl)-3,4-dihydroxyoxolan-2-yl]methoxy}phosphinato)oxy]-4-hydroxy-5-(2-hydroxyacetamido)-6-[(1R,2R)-1,2,3-trihydroxypropyl]oxane-2-carboxylateHMDB
CMP-N-GlycolylneuraminateHMDB
CMP-N-Glycolylneuraminic acidHMDB
CMP-Neu5GCHMDB
CMP-NeungcHMDB
Cytidine monophosphate-N-glycoloylneuraminic acidHMDB
(2S,4S,6R)-6-[(1S,2S)-3-[({[(2R,3S,4R,5R)-3,4-dihydroxy-5-(2-hydroxy-4-imino-1,4-dihydropyrimidin-1-yl)oxolan-2-yl]methoxy}(hydroxy)phosphoryl)oxy]-1,2-dihydroxypropyl]-5-[(1,2-dihydroxyethylidene)amino]-2,4-dihydroxyoxane-2-carboxylateGenerator, HMDB
Chemical FormulaC20H31N4O17P
Average Molecular Weight630.4505
Monoisotopic Molecular Weight630.142182098
IUPAC Name(2S,4S,6R)-6-[(1S,2S)-3-[({[(2R,3S,4R,5R)-5-(4-amino-2-oxo-1,2-dihydropyrimidin-1-yl)-3,4-dihydroxyoxolan-2-yl]methoxy}(hydroxy)phosphoryl)oxy]-1,2-dihydroxypropyl]-2,4-dihydroxy-5-(2-hydroxyacetamido)oxane-2-carboxylic acid
Traditional Name(2S,4S,6R)-6-[(1S,2S)-3-({[(2R,3S,4R,5R)-5-(4-amino-2-oxopyrimidin-1-yl)-3,4-dihydroxyoxolan-2-yl]methoxy(hydroxy)phosphoryl}oxy)-1,2-dihydroxypropyl]-2,4-dihydroxy-5-(2-hydroxyacetamido)oxane-2-carboxylic acid
CAS Registry Number98300-80-2
SMILES
NC1=NC(=O)N(C=C1)[C@@H]1O[C@H](COP(O)(=O)OC[C@H](O)[C@H](O)[C@@H]2O[C@@](O)(C[C@H](O)C2NC(=O)CO)C(O)=O)[C@@H](O)[C@H]1O
InChI Identifier
InChI=1S/C20H31N4O17P/c21-10-1-2-24(19(34)22-10)17-15(31)14(30)9(40-17)6-39-42(36,37)38-5-8(27)13(29)16-12(23-11(28)4-25)7(26)3-20(35,41-16)18(32)33/h1-2,7-9,12-17,25-27,29-31,35H,3-6H2,(H,23,28)(H,32,33)(H,36,37)(H2,21,22,34)/t7-,8-,9+,12?,13-,14+,15+,16+,17+,20-/m0/s1
InChI KeyAOOQVSNKZOZOHI-LBTQWYOJSA-N
Chemical Taxonomy
Description Belongs to the class of organic compounds known as glycosylamines. Glycosylamines are compounds consisting of an amine with a beta-N-glycosidic bond to a carbohydrate, thus forming a cyclic hemiaminal ether bond (alpha-amino ether).
KingdomOrganic compounds
Super ClassOrganic oxygen compounds
ClassOrganooxygen compounds
Sub ClassCarbohydrates and carbohydrate conjugates
Direct ParentGlycosylamines
Alternative Parents
Substituents
  • Hexose monosaccharide
  • N-glycosyl compound
  • 6-alkylaminopurine
  • 6-aminopurine
  • Purine
  • Imidazopyrimidine
  • Aminopyrimidine
  • Imidolactam
  • Pyrimidine
  • Monosaccharide
  • Oxane
  • N-substituted imidazole
  • Heteroaromatic compound
  • Azole
  • Imidazole
  • Secondary alcohol
  • Polyol
  • Organoheterocyclic compound
  • Azacycle
  • Oxacycle
  • Primary alcohol
  • Hydrocarbon derivative
  • Organic nitrogen compound
  • Alcohol
  • Amine
  • Organonitrogen compound
  • Aromatic heteropolycyclic compound
Molecular FrameworkAromatic heteropolycyclic compounds
External DescriptorsNot Available
Ontology
Physiological effectNot Available
Disposition
ProcessNot Available
RoleNot Available
Physical Properties
StateSolid
Experimental Molecular Properties
PropertyValueReference
Melting PointNot AvailableNot Available
Boiling PointNot AvailableNot Available
Water SolubilityNot AvailableNot Available
LogPNot AvailableNot Available
Experimental Chromatographic PropertiesNot Available
Predicted Molecular Properties
PropertyValueSource
Water Solubility29.9 g/LALOGPS
logP-2.9ALOGPS
logP-6.4ChemAxon
logS-1.3ALOGPS
pKa (Strongest Acidic)1.84ChemAxon
pKa (Strongest Basic)-0.77ChemAxon
Physiological Charge-2ChemAxon
Hydrogen Acceptor Count17ChemAxon
Hydrogen Donor Count11ChemAxon
Polar Surface Area340.92 ŲChemAxon
Rotatable Bond Count12ChemAxon
Refractivity127.12 m³·mol⁻¹ChemAxon
Polarizability54.2 ųChemAxon
Number of Rings3ChemAxon
BioavailabilityNoChemAxon
Rule of FiveNoChemAxon
Ghose FilterNoChemAxon
Veber's RuleNoChemAxon
MDDR-like RuleYesChemAxon
Predicted Chromatographic Properties

Predicted Collision Cross Sections

PredictorAdduct TypeCCS Value (Å2)Reference
DeepCCS[M+H]+210.830932474
DeepCCS[M-H]-208.9730932474
DeepCCS[M-2H]-242.65230932474
DeepCCS[M+Na]+216.43630932474
AllCCS[M+H]+229.432859911
AllCCS[M+H-H2O]+228.432859911
AllCCS[M+NH4]+230.332859911
AllCCS[M+Na]+230.632859911
AllCCS[M-H]-227.632859911
AllCCS[M+Na-2H]-229.132859911
AllCCS[M+HCOO]-230.932859911

Predicted Kovats Retention Indices

Underivatized

MetaboliteSMILESKovats RI ValueColumn TypeReference
CMP-N-glycoloylneuraminateNC1=NC(=O)N(C=C1)[C@@H]1O[C@H](COP(O)(=O)OC[C@H](O)[C@H](O)[C@@H]2O[C@@](O)(C[C@H](O)C2NC(=O)CO)C(O)=O)[C@@H](O)[C@H]1O4865.7Standard polar33892256
CMP-N-glycoloylneuraminateNC1=NC(=O)N(C=C1)[C@@H]1O[C@H](COP(O)(=O)OC[C@H](O)[C@H](O)[C@@H]2O[C@@](O)(C[C@H](O)C2NC(=O)CO)C(O)=O)[C@@H](O)[C@H]1O3935.0Standard non polar33892256
CMP-N-glycoloylneuraminateNC1=NC(=O)N(C=C1)[C@@H]1O[C@H](COP(O)(=O)OC[C@H](O)[C@H](O)[C@@H]2O[C@@](O)(C[C@H](O)C2NC(=O)CO)C(O)=O)[C@@H](O)[C@H]1O5653.4Semi standard non polar33892256

Derivatized

Derivative Name / StructureSMILESKovats RI ValueColumn TypeReference
CMP-N-glycoloylneuraminate,1TMS,isomer #1C[Si](C)(C)O[C@@H](COP(=O)(O)OC[C@H]1O[C@@H](N2C=CC(N)=NC2=O)[C@H](O)[C@@H]1O)[C@H](O)[C@@H]1O[C@](O)(C(=O)O)C[C@H](O)C1NC(=O)CO5028.6Semi standard non polar33892256
CMP-N-glycoloylneuraminate,1TMS,isomer #10C[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O)OC[C@H](O)[C@H](O)[C@@H]3O[C@](O)(C(=O)O)C[C@H](O)C3NC(=O)CO)[C@@H](O)[C@H]2O)C=C15119.4Semi standard non polar33892256
CMP-N-glycoloylneuraminate,1TMS,isomer #11C[Si](C)(C)N(C(=O)CO)C1[C@@H](O)C[C@@](O)(C(=O)O)O[C@H]1[C@@H](O)[C@@H](O)COP(=O)(O)OC[C@H]1O[C@@H](N2C=CC(N)=NC2=O)[C@H](O)[C@@H]1O4951.7Semi standard non polar33892256
CMP-N-glycoloylneuraminate,1TMS,isomer #2C[Si](C)(C)O[C@@H]([C@@H](O)COP(=O)(O)OC[C@H]1O[C@@H](N2C=CC(N)=NC2=O)[C@H](O)[C@@H]1O)[C@@H]1O[C@](O)(C(=O)O)C[C@H](O)C1NC(=O)CO5029.4Semi standard non polar33892256
CMP-N-glycoloylneuraminate,1TMS,isomer #3C[Si](C)(C)O[C@@]1(C(=O)O)C[C@H](O)C(NC(=O)CO)[C@H]([C@@H](O)[C@@H](O)COP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O)O15003.0Semi standard non polar33892256
CMP-N-glycoloylneuraminate,1TMS,isomer #4C[Si](C)(C)O[C@H]1C[C@@](O)(C(=O)O)O[C@@H]([C@@H](O)[C@@H](O)COP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O)C1NC(=O)CO5010.6Semi standard non polar33892256
CMP-N-glycoloylneuraminate,1TMS,isomer #5C[Si](C)(C)OCC(=O)NC1[C@@H](O)C[C@@](O)(C(=O)O)O[C@H]1[C@@H](O)[C@@H](O)COP(=O)(O)OC[C@H]1O[C@@H](N2C=CC(N)=NC2=O)[C@H](O)[C@@H]1O4981.7Semi standard non polar33892256
CMP-N-glycoloylneuraminate,1TMS,isomer #6C[Si](C)(C)OC(=O)[C@]1(O)C[C@H](O)C(NC(=O)CO)[C@H]([C@@H](O)[C@@H](O)COP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O)O14940.4Semi standard non polar33892256
CMP-N-glycoloylneuraminate,1TMS,isomer #7C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)OC[C@H](O)[C@H](O)[C@@H]2O[C@](O)(C(=O)O)C[C@H](O)C2NC(=O)CO)O[C@@H](N2C=CC(N)=NC2=O)[C@@H]1O4985.8Semi standard non polar33892256
CMP-N-glycoloylneuraminate,1TMS,isomer #8C[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O)OC[C@H](O)[C@H](O)[C@@H]2O[C@](O)(C(=O)O)C[C@H](O)C2NC(=O)CO)O[C@H]1N1C=CC(N)=NC1=O4972.9Semi standard non polar33892256
CMP-N-glycoloylneuraminate,1TMS,isomer #9C[Si](C)(C)OP(=O)(OC[C@H](O)[C@H](O)[C@@H]1O[C@](O)(C(=O)O)C[C@H](O)C1NC(=O)CO)OC[C@H]1O[C@@H](N2C=CC(N)=NC2=O)[C@H](O)[C@@H]1O5076.4Semi standard non polar33892256
CMP-N-glycoloylneuraminate,2TMS,isomer #1C[Si](C)(C)O[C@@H](COP(=O)(O)OC[C@H]1O[C@@H](N2C=CC(N)=NC2=O)[C@H](O[Si](C)(C)C)[C@@H]1O)[C@H](O)[C@@H]1O[C@](O)(C(=O)O)C[C@H](O)C1NC(=O)CO4846.6Semi standard non polar33892256
CMP-N-glycoloylneuraminate,2TMS,isomer #10C[Si](C)(C)O[C@@H](COP(=O)(O)OC[C@H]1O[C@@H](N2C=CC(N)=NC2=O)[C@H](O)[C@@H]1O)[C@H](O)[C@@H]1O[C@](O)(C(=O)O)C[C@H](O)C1N(C(=O)CO)[Si](C)(C)C4822.8Semi standard non polar33892256
CMP-N-glycoloylneuraminate,2TMS,isomer #11C[Si](C)(C)O[C@@H]([C@@H](O)COP(=O)(O)OC[C@H]1O[C@@H](N2C=CC(N)=NC2=O)[C@H](O[Si](C)(C)C)[C@@H]1O)[C@@H]1O[C@](O)(C(=O)O)C[C@H](O)C1NC(=O)CO4846.6Semi standard non polar33892256
CMP-N-glycoloylneuraminate,2TMS,isomer #12C[Si](C)(C)O[C@@H]([C@@H](O)COP(=O)(O)OC[C@H]1O[C@@H](N2C=CC(N)=NC2=O)[C@H](O)[C@@H]1O[Si](C)(C)C)[C@@H]1O[C@](O)(C(=O)O)C[C@H](O)C1NC(=O)CO4862.6Semi standard non polar33892256
CMP-N-glycoloylneuraminate,2TMS,isomer #13C[Si](C)(C)O[C@@H]([C@@H](O)COP(=O)(O)OC[C@H]1O[C@@H](N2C=CC(N)=NC2=O)[C@H](O)[C@@H]1O)[C@@H]1O[C@](O[Si](C)(C)C)(C(=O)O)C[C@H](O)C1NC(=O)CO4858.9Semi standard non polar33892256
CMP-N-glycoloylneuraminate,2TMS,isomer #14C[Si](C)(C)OC(=O)[C@]1(O)C[C@H](O)C(NC(=O)CO)[C@H]([C@@H](O[Si](C)(C)C)[C@@H](O)COP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O)O14813.8Semi standard non polar33892256
CMP-N-glycoloylneuraminate,2TMS,isomer #15C[Si](C)(C)O[C@H]1C[C@@](O)(C(=O)O)O[C@@H]([C@@H](O[Si](C)(C)C)[C@@H](O)COP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O)C1NC(=O)CO4856.7Semi standard non polar33892256
CMP-N-glycoloylneuraminate,2TMS,isomer #16C[Si](C)(C)OCC(=O)NC1[C@@H](O)C[C@@](O)(C(=O)O)O[C@H]1[C@@H](O[Si](C)(C)C)[C@@H](O)COP(=O)(O)OC[C@H]1O[C@@H](N2C=CC(N)=NC2=O)[C@H](O)[C@@H]1O4845.7Semi standard non polar33892256
CMP-N-glycoloylneuraminate,2TMS,isomer #17C[Si](C)(C)O[C@@H]([C@@H](O)COP(=O)(OC[C@H]1O[C@@H](N2C=CC(N)=NC2=O)[C@H](O)[C@@H]1O)O[Si](C)(C)C)[C@@H]1O[C@](O)(C(=O)O)C[C@H](O)C1NC(=O)CO4926.4Semi standard non polar33892256
CMP-N-glycoloylneuraminate,2TMS,isomer #18C[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O)OC[C@H](O)[C@H](O[Si](C)(C)C)[C@@H]3O[C@](O)(C(=O)O)C[C@H](O)C3NC(=O)CO)[C@@H](O)[C@H]2O)C=C15027.0Semi standard non polar33892256
CMP-N-glycoloylneuraminate,2TMS,isomer #19C[Si](C)(C)O[C@@H]([C@@H](O)COP(=O)(O)OC[C@H]1O[C@@H](N2C=CC(N)=NC2=O)[C@H](O)[C@@H]1O)[C@@H]1O[C@](O)(C(=O)O)C[C@H](O)C1N(C(=O)CO)[Si](C)(C)C4819.8Semi standard non polar33892256
CMP-N-glycoloylneuraminate,2TMS,isomer #2C[Si](C)(C)O[C@@H](COP(=O)(O)OC[C@H]1O[C@@H](N2C=CC(N)=NC2=O)[C@H](O)[C@@H]1O[Si](C)(C)C)[C@H](O)[C@@H]1O[C@](O)(C(=O)O)C[C@H](O)C1NC(=O)CO4865.1Semi standard non polar33892256
CMP-N-glycoloylneuraminate,2TMS,isomer #20C[Si](C)(C)OC(=O)[C@]1(O[Si](C)(C)C)C[C@H](O)C(NC(=O)CO)[C@H]([C@@H](O)[C@@H](O)COP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O)O14780.1Semi standard non polar33892256
CMP-N-glycoloylneuraminate,2TMS,isomer #21C[Si](C)(C)O[C@H]1C[C@@](O[Si](C)(C)C)(C(=O)O)O[C@@H]([C@@H](O)[C@@H](O)COP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O)C1NC(=O)CO4856.7Semi standard non polar33892256
CMP-N-glycoloylneuraminate,2TMS,isomer #22C[Si](C)(C)OCC(=O)NC1[C@@H](O)C[C@@](O[Si](C)(C)C)(C(=O)O)O[C@H]1[C@@H](O)[C@@H](O)COP(=O)(O)OC[C@H]1O[C@@H](N2C=CC(N)=NC2=O)[C@H](O)[C@@H]1O4840.9Semi standard non polar33892256
CMP-N-glycoloylneuraminate,2TMS,isomer #23C[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O)OC[C@H](O)[C@H](O)[C@@H]2O[C@](O[Si](C)(C)C)(C(=O)O)C[C@H](O)C2NC(=O)CO)O[C@H]1N1C=CC(N)=NC1=O4826.5Semi standard non polar33892256
CMP-N-glycoloylneuraminate,2TMS,isomer #24C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)OC[C@H](O)[C@H](O)[C@@H]2O[C@](O[Si](C)(C)C)(C(=O)O)C[C@H](O)C2NC(=O)CO)O[C@@H](N2C=CC(N)=NC2=O)[C@@H]1O4843.4Semi standard non polar33892256
CMP-N-glycoloylneuraminate,2TMS,isomer #25C[Si](C)(C)O[C@@]1(C(=O)O)C[C@H](O)C(NC(=O)CO)[C@H]([C@@H](O)[C@@H](O)COP(=O)(OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)O14915.9Semi standard non polar33892256
CMP-N-glycoloylneuraminate,2TMS,isomer #26C[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O)OC[C@H](O)[C@H](O)[C@@H]3O[C@](O[Si](C)(C)C)(C(=O)O)C[C@H](O)C3NC(=O)CO)[C@@H](O)[C@H]2O)C=C14994.8Semi standard non polar33892256
CMP-N-glycoloylneuraminate,2TMS,isomer #27C[Si](C)(C)O[C@@]1(C(=O)O)C[C@H](O)C(N(C(=O)CO)[Si](C)(C)C)[C@H]([C@@H](O)[C@@H](O)COP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O)O14812.5Semi standard non polar33892256
CMP-N-glycoloylneuraminate,2TMS,isomer #28C[Si](C)(C)OC(=O)[C@]1(O)C[C@H](O[Si](C)(C)C)C(NC(=O)CO)[C@H]([C@@H](O)[C@@H](O)COP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O)O14776.7Semi standard non polar33892256
CMP-N-glycoloylneuraminate,2TMS,isomer #29C[Si](C)(C)O[C@H]1C[C@@](O)(C(=O)O)O[C@@H]([C@@H](O)[C@@H](O)COP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O[Si](C)(C)C)[C@@H]2O)C1NC(=O)CO4827.2Semi standard non polar33892256
CMP-N-glycoloylneuraminate,2TMS,isomer #3C[Si](C)(C)O[C@@H](COP(=O)(O)OC[C@H]1O[C@@H](N2C=CC(N)=NC2=O)[C@H](O)[C@@H]1O)[C@H](O[Si](C)(C)C)[C@@H]1O[C@](O)(C(=O)O)C[C@H](O)C1NC(=O)CO4901.3Semi standard non polar33892256
CMP-N-glycoloylneuraminate,2TMS,isomer #30C[Si](C)(C)O[C@H]1C[C@@](O)(C(=O)O)O[C@@H]([C@@H](O)[C@@H](O)COP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O[Si](C)(C)C)C1NC(=O)CO4846.2Semi standard non polar33892256
CMP-N-glycoloylneuraminate,2TMS,isomer #31C[Si](C)(C)OCC(=O)NC1[C@@H](O[Si](C)(C)C)C[C@@](O)(C(=O)O)O[C@H]1[C@@H](O)[C@@H](O)COP(=O)(O)OC[C@H]1O[C@@H](N2C=CC(N)=NC2=O)[C@H](O)[C@@H]1O4834.7Semi standard non polar33892256
CMP-N-glycoloylneuraminate,2TMS,isomer #32C[Si](C)(C)O[C@H]1C[C@@](O)(C(=O)O)O[C@@H]([C@@H](O)[C@@H](O)COP(=O)(OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)C1NC(=O)CO4903.9Semi standard non polar33892256
CMP-N-glycoloylneuraminate,2TMS,isomer #33C[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O)OC[C@H](O)[C@H](O)[C@@H]3O[C@](O)(C(=O)O)C[C@H](O[Si](C)(C)C)C3NC(=O)CO)[C@@H](O)[C@H]2O)C=C15005.8Semi standard non polar33892256
CMP-N-glycoloylneuraminate,2TMS,isomer #34C[Si](C)(C)O[C@H]1C[C@@](O)(C(=O)O)O[C@@H]([C@@H](O)[C@@H](O)COP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O)C1N(C(=O)CO)[Si](C)(C)C4836.8Semi standard non polar33892256
CMP-N-glycoloylneuraminate,2TMS,isomer #35C[Si](C)(C)OCC(=O)NC1[C@@H](O)C[C@@](O)(C(=O)O[Si](C)(C)C)O[C@H]1[C@@H](O)[C@@H](O)COP(=O)(O)OC[C@H]1O[C@@H](N2C=CC(N)=NC2=O)[C@H](O)[C@@H]1O4752.7Semi standard non polar33892256
CMP-N-glycoloylneuraminate,2TMS,isomer #36C[Si](C)(C)OCC(=O)NC1[C@@H](O)C[C@@](O)(C(=O)O)O[C@H]1[C@@H](O)[C@@H](O)COP(=O)(O)OC[C@H]1O[C@@H](N2C=CC(N)=NC2=O)[C@H](O[Si](C)(C)C)[C@@H]1O4787.9Semi standard non polar33892256
CMP-N-glycoloylneuraminate,2TMS,isomer #37C[Si](C)(C)OCC(=O)NC1[C@@H](O)C[C@@](O)(C(=O)O)O[C@H]1[C@@H](O)[C@@H](O)COP(=O)(O)OC[C@H]1O[C@@H](N2C=CC(N)=NC2=O)[C@H](O)[C@@H]1O[Si](C)(C)C4809.7Semi standard non polar33892256
CMP-N-glycoloylneuraminate,2TMS,isomer #38C[Si](C)(C)OCC(=O)NC1[C@@H](O)C[C@@](O)(C(=O)O)O[C@H]1[C@@H](O)[C@@H](O)COP(=O)(OC[C@H]1O[C@@H](N2C=CC(N)=NC2=O)[C@H](O)[C@@H]1O)O[Si](C)(C)C4884.1Semi standard non polar33892256
CMP-N-glycoloylneuraminate,2TMS,isomer #39C[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O)OC[C@H](O)[C@H](O)[C@@H]3O[C@](O)(C(=O)O)C[C@H](O)C3NC(=O)CO[Si](C)(C)C)[C@@H](O)[C@H]2O)C=C15002.0Semi standard non polar33892256
CMP-N-glycoloylneuraminate,2TMS,isomer #4C[Si](C)(C)O[C@@H](COP(=O)(O)OC[C@H]1O[C@@H](N2C=CC(N)=NC2=O)[C@H](O)[C@@H]1O)[C@H](O)[C@@H]1O[C@](O[Si](C)(C)C)(C(=O)O)C[C@H](O)C1NC(=O)CO4885.0Semi standard non polar33892256
CMP-N-glycoloylneuraminate,2TMS,isomer #40C[Si](C)(C)OCC(=O)N(C1[C@@H](O)C[C@@](O)(C(=O)O)O[C@H]1[C@@H](O)[C@@H](O)COP(=O)(O)OC[C@H]1O[C@@H](N2C=CC(N)=NC2=O)[C@H](O)[C@@H]1O)[Si](C)(C)C4837.5Semi standard non polar33892256
CMP-N-glycoloylneuraminate,2TMS,isomer #41C[Si](C)(C)OC(=O)[C@]1(O)C[C@H](O)C(NC(=O)CO)[C@H]([C@@H](O)[C@@H](O)COP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O[Si](C)(C)C)[C@@H]2O)O14756.2Semi standard non polar33892256
CMP-N-glycoloylneuraminate,2TMS,isomer #42C[Si](C)(C)OC(=O)[C@]1(O)C[C@H](O)C(NC(=O)CO)[C@H]([C@@H](O)[C@@H](O)COP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O[Si](C)(C)C)O14772.6Semi standard non polar33892256
CMP-N-glycoloylneuraminate,2TMS,isomer #43C[Si](C)(C)OC(=O)[C@]1(O)C[C@H](O)C(NC(=O)CO)[C@H]([C@@H](O)[C@@H](O)COP(=O)(OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)O14856.8Semi standard non polar33892256
CMP-N-glycoloylneuraminate,2TMS,isomer #44C[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O)OC[C@H](O)[C@H](O)[C@@H]3O[C@](O)(C(=O)O[Si](C)(C)C)C[C@H](O)C3NC(=O)CO)[C@@H](O)[C@H]2O)C=C14944.5Semi standard non polar33892256
CMP-N-glycoloylneuraminate,2TMS,isomer #45C[Si](C)(C)OC(=O)[C@]1(O)C[C@H](O)C(N(C(=O)CO)[Si](C)(C)C)[C@H]([C@@H](O)[C@@H](O)COP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O)O14737.6Semi standard non polar33892256
CMP-N-glycoloylneuraminate,2TMS,isomer #46C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)OC[C@H](O)[C@H](O)[C@@H]2O[C@](O)(C(=O)O)C[C@H](O)C2NC(=O)CO)O[C@@H](N2C=CC(N)=NC2=O)[C@@H]1O[Si](C)(C)C4815.6Semi standard non polar33892256
CMP-N-glycoloylneuraminate,2TMS,isomer #47C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(OC[C@H](O)[C@H](O)[C@@H]2O[C@](O)(C(=O)O)C[C@H](O)C2NC(=O)CO)O[Si](C)(C)C)O[C@@H](N2C=CC(N)=NC2=O)[C@@H]1O4887.1Semi standard non polar33892256
CMP-N-glycoloylneuraminate,2TMS,isomer #48C[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O)OC[C@H](O)[C@H](O)[C@@H]3O[C@](O)(C(=O)O)C[C@H](O)C3NC(=O)CO)[C@@H](O[Si](C)(C)C)[C@H]2O)C=C14987.6Semi standard non polar33892256
CMP-N-glycoloylneuraminate,2TMS,isomer #49C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)OC[C@H](O)[C@H](O)[C@@H]2O[C@](O)(C(=O)O)C[C@H](O)C2N(C(=O)CO)[Si](C)(C)C)O[C@@H](N2C=CC(N)=NC2=O)[C@@H]1O4783.4Semi standard non polar33892256
CMP-N-glycoloylneuraminate,2TMS,isomer #5C[Si](C)(C)OC(=O)[C@]1(O)C[C@H](O)C(NC(=O)CO)[C@H]([C@@H](O)[C@H](COP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)O14810.3Semi standard non polar33892256
CMP-N-glycoloylneuraminate,2TMS,isomer #50C[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(OC[C@H](O)[C@H](O)[C@@H]2O[C@](O)(C(=O)O)C[C@H](O)C2NC(=O)CO)O[Si](C)(C)C)O[C@H]1N1C=CC(N)=NC1=O4872.1Semi standard non polar33892256
CMP-N-glycoloylneuraminate,2TMS,isomer #51C[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O)OC[C@H](O)[C@H](O)[C@@H]3O[C@](O)(C(=O)O)C[C@H](O)C3NC(=O)CO)[C@@H](O)[C@H]2O[Si](C)(C)C)C=C14977.9Semi standard non polar33892256
CMP-N-glycoloylneuraminate,2TMS,isomer #52C[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O)OC[C@H](O)[C@H](O)[C@@H]2O[C@](O)(C(=O)O)C[C@H](O)C2N(C(=O)CO)[Si](C)(C)C)O[C@H]1N1C=CC(N)=NC1=O4774.0Semi standard non polar33892256
CMP-N-glycoloylneuraminate,2TMS,isomer #53C[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(OC[C@H](O)[C@H](O)[C@@H]3O[C@](O)(C(=O)O)C[C@H](O)C3NC(=O)CO)O[Si](C)(C)C)[C@@H](O)[C@H]2O)C=C15043.5Semi standard non polar33892256
CMP-N-glycoloylneuraminate,2TMS,isomer #54C[Si](C)(C)OP(=O)(OC[C@H](O)[C@H](O)[C@@H]1O[C@](O)(C(=O)O)C[C@H](O)C1N(C(=O)CO)[Si](C)(C)C)OC[C@H]1O[C@@H](N2C=CC(N)=NC2=O)[C@H](O)[C@@H]1O4843.0Semi standard non polar33892256
CMP-N-glycoloylneuraminate,2TMS,isomer #55C[Si](C)(C)N(C1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O)OC[C@H](O)[C@H](O)[C@@H]3O[C@](O)(C(=O)O)C[C@H](O)C3NC(=O)CO)[C@@H](O)[C@H]2O)C=C1)[Si](C)(C)C4915.6Semi standard non polar33892256
CMP-N-glycoloylneuraminate,2TMS,isomer #56C[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O)OC[C@H](O)[C@H](O)[C@@H]3O[C@](O)(C(=O)O)C[C@H](O)C3N(C(=O)CO)[Si](C)(C)C)[C@@H](O)[C@H]2O)C=C14985.2Semi standard non polar33892256
CMP-N-glycoloylneuraminate,2TMS,isomer #6C[Si](C)(C)O[C@H]1C[C@@](O)(C(=O)O)O[C@@H]([C@@H](O)[C@H](COP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)C1NC(=O)CO4889.8Semi standard non polar33892256
CMP-N-glycoloylneuraminate,2TMS,isomer #7C[Si](C)(C)OCC(=O)NC1[C@@H](O)C[C@@](O)(C(=O)O)O[C@H]1[C@@H](O)[C@H](COP(=O)(O)OC[C@H]1O[C@@H](N2C=CC(N)=NC2=O)[C@H](O)[C@@H]1O)O[Si](C)(C)C4842.6Semi standard non polar33892256
CMP-N-glycoloylneuraminate,2TMS,isomer #8C[Si](C)(C)O[C@@H](COP(=O)(OC[C@H]1O[C@@H](N2C=CC(N)=NC2=O)[C@H](O)[C@@H]1O)O[Si](C)(C)C)[C@H](O)[C@@H]1O[C@](O)(C(=O)O)C[C@H](O)C1NC(=O)CO4912.8Semi standard non polar33892256
CMP-N-glycoloylneuraminate,2TMS,isomer #9C[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O)OC[C@H](O[Si](C)(C)C)[C@H](O)[C@@H]3O[C@](O)(C(=O)O)C[C@H](O)C3NC(=O)CO)[C@@H](O)[C@H]2O)C=C15019.8Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #1C[Si](C)(C)O[C@@H](COP(=O)(O)OC[C@H]1O[C@@H](N2C=CC(N)=NC2=O)[C@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C)[C@H](O)[C@@H]1O[C@](O)(C(=O)O)C[C@H](O)C1NC(=O)CO4685.0Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #10C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)OC[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H]2O[C@](O)(C(=O)O)C[C@H](O)C2NC(=O)CO)O[C@@H](N2C=CC(N)=NC2=O)[C@@H]1O4722.4Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #100C[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O)OC[C@H](O)[C@H](O)[C@@H]3O[C@](O[Si](C)(C)C)(C(=O)O)C[C@H](O)C3NC(=O)CO[Si](C)(C)C)[C@@H](O)[C@H]2O)C=C14870.0Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #101C[Si](C)(C)OCC(=O)N(C1[C@@H](O)C[C@@](O[Si](C)(C)C)(C(=O)O)O[C@H]1[C@@H](O)[C@@H](O)COP(=O)(O)OC[C@H]1O[C@@H](N2C=CC(N)=NC2=O)[C@H](O)[C@@H]1O)[Si](C)(C)C4703.5Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #102C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)OC[C@H](O)[C@H](O)[C@@H]2O[C@](O[Si](C)(C)C)(C(=O)O)C[C@H](O)C2NC(=O)CO)O[C@@H](N2C=CC(N)=NC2=O)[C@@H]1O[Si](C)(C)C4675.0Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #103C[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(OC[C@H](O)[C@H](O)[C@@H]2O[C@](O[Si](C)(C)C)(C(=O)O)C[C@H](O)C2NC(=O)CO)O[Si](C)(C)C)O[C@H]1N1C=CC(N)=NC1=O4733.8Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #104C[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O)OC[C@H](O)[C@H](O)[C@@H]3O[C@](O[Si](C)(C)C)(C(=O)O)C[C@H](O)C3NC(=O)CO)[C@@H](O)[C@H]2O[Si](C)(C)C)C=C14842.9Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #105C[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O)OC[C@H](O)[C@H](O)[C@@H]2O[C@](O[Si](C)(C)C)(C(=O)O)C[C@H](O)C2N(C(=O)CO)[Si](C)(C)C)O[C@H]1N1C=CC(N)=NC1=O4653.0Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #106C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(OC[C@H](O)[C@H](O)[C@@H]2O[C@](O[Si](C)(C)C)(C(=O)O)C[C@H](O)C2NC(=O)CO)O[Si](C)(C)C)O[C@@H](N2C=CC(N)=NC2=O)[C@@H]1O4744.7Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #107C[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O)OC[C@H](O)[C@H](O)[C@@H]3O[C@](O[Si](C)(C)C)(C(=O)O)C[C@H](O)C3NC(=O)CO)[C@@H](O[Si](C)(C)C)[C@H]2O)C=C14854.5Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #108C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)OC[C@H](O)[C@H](O)[C@@H]2O[C@](O[Si](C)(C)C)(C(=O)O)C[C@H](O)C2N(C(=O)CO)[Si](C)(C)C)O[C@@H](N2C=CC(N)=NC2=O)[C@@H]1O4661.7Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #109C[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(OC[C@H](O)[C@H](O)[C@@H]3O[C@](O[Si](C)(C)C)(C(=O)O)C[C@H](O)C3NC(=O)CO)O[Si](C)(C)C)[C@@H](O)[C@H]2O)C=C14903.4Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #11C[Si](C)(C)O[C@@H](COP(=O)(O)OC[C@H]1O[C@@H](N2C=CC(N)=NC2=O)[C@H](O)[C@@H]1O[Si](C)(C)C)[C@H](O)[C@@H]1O[C@](O[Si](C)(C)C)(C(=O)O)C[C@H](O)C1NC(=O)CO4717.1Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #110C[Si](C)(C)O[C@@]1(C(=O)O)C[C@H](O)C(N(C(=O)CO)[Si](C)(C)C)[C@H]([C@@H](O)[C@@H](O)COP(=O)(OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)O14708.8Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #111C[Si](C)(C)O[C@@]1(C(=O)O)C[C@H](O)C(NC(=O)CO)[C@H]([C@@H](O)[C@@H](O)COP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N([Si](C)(C)C)[Si](C)(C)C)=NC3=O)[C@H](O)[C@@H]2O)O14769.9Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #112C[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O)OC[C@H](O)[C@H](O)[C@@H]3O[C@](O[Si](C)(C)C)(C(=O)O)C[C@H](O)C3N(C(=O)CO)[Si](C)(C)C)[C@@H](O)[C@H]2O)C=C14853.3Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #113C[Si](C)(C)OCC(=O)NC1[C@@H](O[Si](C)(C)C)C[C@@](O)(C(=O)O[Si](C)(C)C)O[C@H]1[C@@H](O)[C@@H](O)COP(=O)(O)OC[C@H]1O[C@@H](N2C=CC(N)=NC2=O)[C@H](O)[C@@H]1O4591.9Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #114C[Si](C)(C)OC(=O)[C@]1(O)C[C@H](O[Si](C)(C)C)C(NC(=O)CO)[C@H]([C@@H](O)[C@@H](O)COP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O[Si](C)(C)C)[C@@H]2O)O14602.8Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #115C[Si](C)(C)OC(=O)[C@]1(O)C[C@H](O[Si](C)(C)C)C(NC(=O)CO)[C@H]([C@@H](O)[C@@H](O)COP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O[Si](C)(C)C)O14618.9Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #116C[Si](C)(C)OC(=O)[C@]1(O)C[C@H](O[Si](C)(C)C)C(NC(=O)CO)[C@H]([C@@H](O)[C@@H](O)COP(=O)(OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)O14668.5Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #117C[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O)OC[C@H](O)[C@H](O)[C@@H]3O[C@](O)(C(=O)O[Si](C)(C)C)C[C@H](O[Si](C)(C)C)C3NC(=O)CO)[C@@H](O)[C@H]2O)C=C14785.1Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #118C[Si](C)(C)OC(=O)[C@]1(O)C[C@H](O[Si](C)(C)C)C(N(C(=O)CO)[Si](C)(C)C)[C@H]([C@@H](O)[C@@H](O)COP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O)O14617.2Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #119C[Si](C)(C)O[C@H]1C[C@@](O)(C(=O)O)O[C@@H]([C@@H](O)[C@@H](O)COP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)C1NC(=O)CO4672.7Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #12C[Si](C)(C)OC(=O)[C@]1(O)C[C@H](O)C(NC(=O)CO)[C@H]([C@@H](O)[C@H](COP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O[Si](C)(C)C)O[Si](C)(C)C)O14647.1Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #120C[Si](C)(C)OCC(=O)NC1[C@@H](O[Si](C)(C)C)C[C@@](O)(C(=O)O)O[C@H]1[C@@H](O)[C@@H](O)COP(=O)(O)OC[C@H]1O[C@@H](N2C=CC(N)=NC2=O)[C@H](O[Si](C)(C)C)[C@@H]1O4646.3Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #121C[Si](C)(C)O[C@H]1C[C@@](O)(C(=O)O)O[C@@H]([C@@H](O)[C@@H](O)COP(=O)(OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O[Si](C)(C)C)[C@@H]2O)O[Si](C)(C)C)C1NC(=O)CO4723.4Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #122C[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O)OC[C@H](O)[C@H](O)[C@@H]3O[C@](O)(C(=O)O)C[C@H](O[Si](C)(C)C)C3NC(=O)CO)[C@@H](O)[C@H]2O[Si](C)(C)C)C=C14839.5Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #123C[Si](C)(C)O[C@H]1C[C@@](O)(C(=O)O)O[C@@H]([C@@H](O)[C@@H](O)COP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O[Si](C)(C)C)[C@@H]2O)C1N(C(=O)CO)[Si](C)(C)C4660.8Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #124C[Si](C)(C)OCC(=O)NC1[C@@H](O[Si](C)(C)C)C[C@@](O)(C(=O)O)O[C@H]1[C@@H](O)[C@@H](O)COP(=O)(O)OC[C@H]1O[C@@H](N2C=CC(N)=NC2=O)[C@H](O)[C@@H]1O[Si](C)(C)C4664.2Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #125C[Si](C)(C)O[C@H]1C[C@@](O)(C(=O)O)O[C@@H]([C@@H](O)[C@@H](O)COP(=O)(OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O[Si](C)(C)C)O[Si](C)(C)C)C1NC(=O)CO4737.0Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #126C[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O)OC[C@H](O)[C@H](O)[C@@H]3O[C@](O)(C(=O)O)C[C@H](O[Si](C)(C)C)C3NC(=O)CO)[C@@H](O[Si](C)(C)C)[C@H]2O)C=C14853.1Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #127C[Si](C)(C)O[C@H]1C[C@@](O)(C(=O)O)O[C@@H]([C@@H](O)[C@@H](O)COP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O[Si](C)(C)C)C1N(C(=O)CO)[Si](C)(C)C4671.5Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #128C[Si](C)(C)OCC(=O)NC1[C@@H](O[Si](C)(C)C)C[C@@](O)(C(=O)O)O[C@H]1[C@@H](O)[C@@H](O)COP(=O)(OC[C@H]1O[C@@H](N2C=CC(N)=NC2=O)[C@H](O)[C@@H]1O)O[Si](C)(C)C4725.2Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #129C[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O)OC[C@H](O)[C@H](O)[C@@H]3O[C@](O)(C(=O)O)C[C@H](O[Si](C)(C)C)C3NC(=O)CO[Si](C)(C)C)[C@@H](O)[C@H]2O)C=C14864.8Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #13C[Si](C)(C)O[C@H]1C[C@@](O)(C(=O)O)O[C@@H]([C@@H](O)[C@H](COP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O[Si](C)(C)C)O[Si](C)(C)C)C1NC(=O)CO4710.0Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #130C[Si](C)(C)OCC(=O)N(C1[C@@H](O[Si](C)(C)C)C[C@@](O)(C(=O)O)O[C@H]1[C@@H](O)[C@@H](O)COP(=O)(O)OC[C@H]1O[C@@H](N2C=CC(N)=NC2=O)[C@H](O)[C@@H]1O)[Si](C)(C)C4725.0Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #131C[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(OC[C@H](O)[C@H](O)[C@@H]3O[C@](O)(C(=O)O)C[C@H](O[Si](C)(C)C)C3NC(=O)CO)O[Si](C)(C)C)[C@@H](O)[C@H]2O)C=C14894.6Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #132C[Si](C)(C)O[C@H]1C[C@@](O)(C(=O)O)O[C@@H]([C@@H](O)[C@@H](O)COP(=O)(OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)C1N(C(=O)CO)[Si](C)(C)C4723.2Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #133C[Si](C)(C)O[C@H]1C[C@@](O)(C(=O)O)O[C@@H]([C@@H](O)[C@@H](O)COP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N([Si](C)(C)C)[Si](C)(C)C)=NC3=O)[C@H](O)[C@@H]2O)C1NC(=O)CO4763.8Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #134C[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O)OC[C@H](O)[C@H](O)[C@@H]3O[C@](O)(C(=O)O)C[C@H](O[Si](C)(C)C)C3N(C(=O)CO)[Si](C)(C)C)[C@@H](O)[C@H]2O)C=C14879.1Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #135C[Si](C)(C)OCC(=O)NC1[C@@H](O)C[C@@](O)(C(=O)O[Si](C)(C)C)O[C@H]1[C@@H](O)[C@@H](O)COP(=O)(O)OC[C@H]1O[C@@H](N2C=CC(N)=NC2=O)[C@H](O[Si](C)(C)C)[C@@H]1O4587.6Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #136C[Si](C)(C)OCC(=O)NC1[C@@H](O)C[C@@](O)(C(=O)O[Si](C)(C)C)O[C@H]1[C@@H](O)[C@@H](O)COP(=O)(O)OC[C@H]1O[C@@H](N2C=CC(N)=NC2=O)[C@H](O)[C@@H]1O[Si](C)(C)C4603.0Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #137C[Si](C)(C)OCC(=O)NC1[C@@H](O)C[C@@](O)(C(=O)O[Si](C)(C)C)O[C@H]1[C@@H](O)[C@@H](O)COP(=O)(OC[C@H]1O[C@@H](N2C=CC(N)=NC2=O)[C@H](O)[C@@H]1O)O[Si](C)(C)C4653.1Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #138C[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O)OC[C@H](O)[C@H](O)[C@@H]3O[C@](O)(C(=O)O[Si](C)(C)C)C[C@H](O)C3NC(=O)CO[Si](C)(C)C)[C@@H](O)[C@H]2O)C=C14798.8Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #139C[Si](C)(C)OCC(=O)N(C1[C@@H](O)C[C@@](O)(C(=O)O[Si](C)(C)C)O[C@H]1[C@@H](O)[C@@H](O)COP(=O)(O)OC[C@H]1O[C@@H](N2C=CC(N)=NC2=O)[C@H](O)[C@@H]1O)[Si](C)(C)C4638.7Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #14C[Si](C)(C)OCC(=O)NC1[C@@H](O)C[C@@](O)(C(=O)O)O[C@H]1[C@@H](O)[C@H](COP(=O)(O)OC[C@H]1O[C@@H](N2C=CC(N)=NC2=O)[C@H](O)[C@@H]1O[Si](C)(C)C)O[Si](C)(C)C4669.4Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #140C[Si](C)(C)OCC(=O)NC1[C@@H](O)C[C@@](O)(C(=O)O)O[C@H]1[C@@H](O)[C@@H](O)COP(=O)(O)OC[C@H]1O[C@@H](N2C=CC(N)=NC2=O)[C@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C4633.8Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #141C[Si](C)(C)OCC(=O)NC1[C@@H](O)C[C@@](O)(C(=O)O)O[C@H]1[C@@H](O)[C@@H](O)COP(=O)(OC[C@H]1O[C@@H](N2C=CC(N)=NC2=O)[C@H](O[Si](C)(C)C)[C@@H]1O)O[Si](C)(C)C4691.6Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #142C[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O)OC[C@H](O)[C@H](O)[C@@H]3O[C@](O)(C(=O)O)C[C@H](O)C3NC(=O)CO[Si](C)(C)C)[C@@H](O)[C@H]2O[Si](C)(C)C)C=C14827.0Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #143C[Si](C)(C)OCC(=O)N(C1[C@@H](O)C[C@@](O)(C(=O)O)O[C@H]1[C@@H](O)[C@@H](O)COP(=O)(O)OC[C@H]1O[C@@H](N2C=CC(N)=NC2=O)[C@H](O[Si](C)(C)C)[C@@H]1O)[Si](C)(C)C4669.4Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #144C[Si](C)(C)OCC(=O)NC1[C@@H](O)C[C@@](O)(C(=O)O)O[C@H]1[C@@H](O)[C@@H](O)COP(=O)(OC[C@H]1O[C@@H](N2C=CC(N)=NC2=O)[C@H](O)[C@@H]1O[Si](C)(C)C)O[Si](C)(C)C4705.0Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #145C[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O)OC[C@H](O)[C@H](O)[C@@H]3O[C@](O)(C(=O)O)C[C@H](O)C3NC(=O)CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]2O)C=C14843.8Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #146C[Si](C)(C)OCC(=O)N(C1[C@@H](O)C[C@@](O)(C(=O)O)O[C@H]1[C@@H](O)[C@@H](O)COP(=O)(O)OC[C@H]1O[C@@H](N2C=CC(N)=NC2=O)[C@H](O)[C@@H]1O[Si](C)(C)C)[Si](C)(C)C4682.6Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #147C[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(OC[C@H](O)[C@H](O)[C@@H]3O[C@](O)(C(=O)O)C[C@H](O)C3NC(=O)CO[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O)[C@H]2O)C=C14897.7Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #148C[Si](C)(C)OCC(=O)N(C1[C@@H](O)C[C@@](O)(C(=O)O)O[C@H]1[C@@H](O)[C@@H](O)COP(=O)(OC[C@H]1O[C@@H](N2C=CC(N)=NC2=O)[C@H](O)[C@@H]1O)O[Si](C)(C)C)[Si](C)(C)C4742.2Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #149C[Si](C)(C)OCC(=O)NC1[C@@H](O)C[C@@](O)(C(=O)O)O[C@H]1[C@@H](O)[C@@H](O)COP(=O)(O)OC[C@H]1O[C@@H](N2C=CC(N([Si](C)(C)C)[Si](C)(C)C)=NC2=O)[C@H](O)[C@@H]1O4753.3Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #15C[Si](C)(C)O[C@@H](COP(=O)(OC[C@H]1O[C@@H](N2C=CC(N)=NC2=O)[C@H](O)[C@@H]1O[Si](C)(C)C)O[Si](C)(C)C)[C@H](O)[C@@H]1O[C@](O)(C(=O)O)C[C@H](O)C1NC(=O)CO4736.1Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #150C[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O)OC[C@H](O)[C@H](O)[C@@H]3O[C@](O)(C(=O)O)C[C@H](O)C3N(C(=O)CO[Si](C)(C)C)[Si](C)(C)C)[C@@H](O)[C@H]2O)C=C14881.0Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #151C[Si](C)(C)OC(=O)[C@]1(O)C[C@H](O)C(NC(=O)CO)[C@H]([C@@H](O)[C@@H](O)COP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)O14622.7Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #152C[Si](C)(C)OC(=O)[C@]1(O)C[C@H](O)C(NC(=O)CO)[C@H]([C@@H](O)[C@@H](O)COP(=O)(OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O[Si](C)(C)C)[C@@H]2O)O[Si](C)(C)C)O14669.8Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #153C[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O)OC[C@H](O)[C@H](O)[C@@H]3O[C@](O)(C(=O)O[Si](C)(C)C)C[C@H](O)C3NC(=O)CO)[C@@H](O)[C@H]2O[Si](C)(C)C)C=C14775.9Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #154C[Si](C)(C)OC(=O)[C@]1(O)C[C@H](O)C(N(C(=O)CO)[Si](C)(C)C)[C@H]([C@@H](O)[C@@H](O)COP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O[Si](C)(C)C)[C@@H]2O)O14594.1Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #155C[Si](C)(C)OC(=O)[C@]1(O)C[C@H](O)C(NC(=O)CO)[C@H]([C@@H](O)[C@@H](O)COP(=O)(OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O[Si](C)(C)C)O[Si](C)(C)C)O14681.6Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #156C[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O)OC[C@H](O)[C@H](O)[C@@H]3O[C@](O)(C(=O)O[Si](C)(C)C)C[C@H](O)C3NC(=O)CO)[C@@H](O[Si](C)(C)C)[C@H]2O)C=C14789.6Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #157C[Si](C)(C)OC(=O)[C@]1(O)C[C@H](O)C(N(C(=O)CO)[Si](C)(C)C)[C@H]([C@@H](O)[C@@H](O)COP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O[Si](C)(C)C)O14603.0Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #158C[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(OC[C@H](O)[C@H](O)[C@@H]3O[C@](O)(C(=O)O[Si](C)(C)C)C[C@H](O)C3NC(=O)CO)O[Si](C)(C)C)[C@@H](O)[C@H]2O)C=C14849.6Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #159C[Si](C)(C)OC(=O)[C@]1(O)C[C@H](O)C(N(C(=O)CO)[Si](C)(C)C)[C@H]([C@@H](O)[C@@H](O)COP(=O)(OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)O14656.1Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #16C[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O)OC[C@H](O[Si](C)(C)C)[C@H](O)[C@@H]3O[C@](O)(C(=O)O)C[C@H](O)C3NC(=O)CO)[C@@H](O[Si](C)(C)C)[C@H]2O)C=C14865.5Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #160C[Si](C)(C)OC(=O)[C@]1(O)C[C@H](O)C(NC(=O)CO)[C@H]([C@@H](O)[C@@H](O)COP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N([Si](C)(C)C)[Si](C)(C)C)=NC3=O)[C@H](O)[C@@H]2O)O14706.0Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #161C[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O)OC[C@H](O)[C@H](O)[C@@H]3O[C@](O)(C(=O)O[Si](C)(C)C)C[C@H](O)C3N(C(=O)CO)[Si](C)(C)C)[C@@H](O)[C@H]2O)C=C14793.2Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #162C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(OC[C@H](O)[C@H](O)[C@@H]2O[C@](O)(C(=O)O)C[C@H](O)C2NC(=O)CO)O[Si](C)(C)C)O[C@@H](N2C=CC(N)=NC2=O)[C@@H]1O[Si](C)(C)C4702.7Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #163C[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O)OC[C@H](O)[C@H](O)[C@@H]3O[C@](O)(C(=O)O)C[C@H](O)C3NC(=O)CO)[C@@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)C=C14835.1Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #164C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)OC[C@H](O)[C@H](O)[C@@H]2O[C@](O)(C(=O)O)C[C@H](O)C2N(C(=O)CO)[Si](C)(C)C)O[C@@H](N2C=CC(N)=NC2=O)[C@@H]1O[Si](C)(C)C4649.6Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #165C[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(OC[C@H](O)[C@H](O)[C@@H]3O[C@](O)(C(=O)O)C[C@H](O)C3NC(=O)CO)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]2O)C=C14880.2Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #166C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(OC[C@H](O)[C@H](O)[C@@H]2O[C@](O)(C(=O)O)C[C@H](O)C2N(C(=O)CO)[Si](C)(C)C)O[Si](C)(C)C)O[C@@H](N2C=CC(N)=NC2=O)[C@@H]1O4695.1Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #167C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)OC[C@H](O)[C@H](O)[C@@H]2O[C@](O)(C(=O)O)C[C@H](O)C2NC(=O)CO)O[C@@H](N2C=CC(N([Si](C)(C)C)[Si](C)(C)C)=NC2=O)[C@@H]1O4744.5Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #168C[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O)OC[C@H](O)[C@H](O)[C@@H]3O[C@](O)(C(=O)O)C[C@H](O)C3N(C(=O)CO)[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]2O)C=C14835.5Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #169C[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(OC[C@H](O)[C@H](O)[C@@H]3O[C@](O)(C(=O)O)C[C@H](O)C3NC(=O)CO)O[Si](C)(C)C)[C@@H](O)[C@H]2O[Si](C)(C)C)C=C14873.5Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #17C[Si](C)(C)O[C@@H](COP(=O)(O)OC[C@H]1O[C@@H](N2C=CC(N)=NC2=O)[C@H](O)[C@@H]1O[Si](C)(C)C)[C@H](O)[C@@H]1O[C@](O)(C(=O)O)C[C@H](O)C1N(C(=O)CO)[Si](C)(C)C4669.4Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #170C[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(OC[C@H](O)[C@H](O)[C@@H]2O[C@](O)(C(=O)O)C[C@H](O)C2N(C(=O)CO)[Si](C)(C)C)O[Si](C)(C)C)O[C@H]1N1C=CC(N)=NC1=O4686.5Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #171C[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O)OC[C@H](O)[C@H](O)[C@@H]2O[C@](O)(C(=O)O)C[C@H](O)C2NC(=O)CO)O[C@H]1N1C=CC(N([Si](C)(C)C)[Si](C)(C)C)=NC1=O4730.0Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #172C[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O)OC[C@H](O)[C@H](O)[C@@H]3O[C@](O)(C(=O)O)C[C@H](O)C3N(C(=O)CO)[Si](C)(C)C)[C@@H](O)[C@H]2O[Si](C)(C)C)C=C14828.9Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #173C[Si](C)(C)OP(=O)(OC[C@H](O)[C@H](O)[C@@H]1O[C@](O)(C(=O)O)C[C@H](O)C1NC(=O)CO)OC[C@H]1O[C@@H](N2C=CC(N([Si](C)(C)C)[Si](C)(C)C)=NC2=O)[C@H](O)[C@@H]1O4795.6Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #174C[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(OC[C@H](O)[C@H](O)[C@@H]3O[C@](O)(C(=O)O)C[C@H](O)C3N(C(=O)CO)[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O)[C@H]2O)C=C14878.2Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #175C[Si](C)(C)N(C(=O)CO)C1[C@@H](O)C[C@@](O)(C(=O)O)O[C@H]1[C@@H](O)[C@@H](O)COP(=O)(O)OC[C@H]1O[C@@H](N2C=CC(N([Si](C)(C)C)[Si](C)(C)C)=NC2=O)[C@H](O)[C@@H]1O4733.4Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #18C[Si](C)(C)O[C@@H](COP(=O)(O)OC[C@H]1O[C@@H](N2C=CC(N)=NC2=O)[C@H](O)[C@@H]1O)[C@H](O[Si](C)(C)C)[C@@H]1O[C@](O[Si](C)(C)C)(C(=O)O)C[C@H](O)C1NC(=O)CO4725.7Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #19C[Si](C)(C)OC(=O)[C@]1(O)C[C@H](O)C(NC(=O)CO)[C@H]([C@@H](O[Si](C)(C)C)[C@H](COP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)O14671.0Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #2C[Si](C)(C)O[C@@H](COP(=O)(O)OC[C@H]1O[C@@H](N2C=CC(N)=NC2=O)[C@H](O[Si](C)(C)C)[C@@H]1O)[C@H](O[Si](C)(C)C)[C@@H]1O[C@](O)(C(=O)O)C[C@H](O)C1NC(=O)CO4705.3Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #20C[Si](C)(C)O[C@H]1C[C@@](O)(C(=O)O)O[C@@H]([C@@H](O[Si](C)(C)C)[C@H](COP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)C1NC(=O)CO4717.5Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #21C[Si](C)(C)OCC(=O)NC1[C@@H](O)C[C@@](O)(C(=O)O)O[C@H]1[C@@H](O[Si](C)(C)C)[C@H](COP(=O)(O)OC[C@H]1O[C@@H](N2C=CC(N)=NC2=O)[C@H](O)[C@@H]1O)O[Si](C)(C)C4698.7Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #22C[Si](C)(C)O[C@@H](COP(=O)(OC[C@H]1O[C@@H](N2C=CC(N)=NC2=O)[C@H](O)[C@@H]1O)O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H]1O[C@](O)(C(=O)O)C[C@H](O)C1NC(=O)CO4756.0Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #23C[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O)OC[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H]3O[C@](O)(C(=O)O)C[C@H](O)C3NC(=O)CO)[C@@H](O)[C@H]2O)C=C14888.5Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #24C[Si](C)(C)O[C@@H](COP(=O)(O)OC[C@H]1O[C@@H](N2C=CC(N)=NC2=O)[C@H](O)[C@@H]1O)[C@H](O[Si](C)(C)C)[C@@H]1O[C@](O)(C(=O)O)C[C@H](O)C1N(C(=O)CO)[Si](C)(C)C4701.2Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #25C[Si](C)(C)OC(=O)[C@]1(O[Si](C)(C)C)C[C@H](O)C(NC(=O)CO)[C@H]([C@@H](O)[C@H](COP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)O14653.8Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #26C[Si](C)(C)O[C@H]1C[C@@](O[Si](C)(C)C)(C(=O)O)O[C@@H]([C@@H](O)[C@H](COP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)C1NC(=O)CO4731.2Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #27C[Si](C)(C)OCC(=O)NC1[C@@H](O)C[C@@](O[Si](C)(C)C)(C(=O)O)O[C@H]1[C@@H](O)[C@H](COP(=O)(O)OC[C@H]1O[C@@H](N2C=CC(N)=NC2=O)[C@H](O)[C@@H]1O)O[Si](C)(C)C4705.9Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #28C[Si](C)(C)O[C@@H](COP(=O)(OC[C@H]1O[C@@H](N2C=CC(N)=NC2=O)[C@H](O)[C@@H]1O)O[Si](C)(C)C)[C@H](O)[C@@H]1O[C@](O[Si](C)(C)C)(C(=O)O)C[C@H](O)C1NC(=O)CO4767.8Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #29C[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O)OC[C@H](O[Si](C)(C)C)[C@H](O)[C@@H]3O[C@](O[Si](C)(C)C)(C(=O)O)C[C@H](O)C3NC(=O)CO)[C@@H](O)[C@H]2O)C=C14887.6Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #3C[Si](C)(C)O[C@@H](COP(=O)(O)OC[C@H]1O[C@@H](N2C=CC(N)=NC2=O)[C@H](O[Si](C)(C)C)[C@@H]1O)[C@H](O)[C@@H]1O[C@](O[Si](C)(C)C)(C(=O)O)C[C@H](O)C1NC(=O)CO4700.8Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #30C[Si](C)(C)O[C@@H](COP(=O)(O)OC[C@H]1O[C@@H](N2C=CC(N)=NC2=O)[C@H](O)[C@@H]1O)[C@H](O)[C@@H]1O[C@](O[Si](C)(C)C)(C(=O)O)C[C@H](O)C1N(C(=O)CO)[Si](C)(C)C4691.6Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #31C[Si](C)(C)OC(=O)[C@]1(O)C[C@H](O[Si](C)(C)C)C(NC(=O)CO)[C@H]([C@@H](O)[C@H](COP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)O14638.2Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #32C[Si](C)(C)OCC(=O)NC1[C@@H](O)C[C@@](O)(C(=O)O[Si](C)(C)C)O[C@H]1[C@@H](O)[C@H](COP(=O)(O)OC[C@H]1O[C@@H](N2C=CC(N)=NC2=O)[C@H](O)[C@@H]1O)O[Si](C)(C)C4610.2Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #33C[Si](C)(C)OC(=O)[C@]1(O)C[C@H](O)C(NC(=O)CO)[C@H]([C@@H](O)[C@H](COP(=O)(OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)O[Si](C)(C)C)O14683.0Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #34C[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O)OC[C@H](O[Si](C)(C)C)[C@H](O)[C@@H]3O[C@](O)(C(=O)O[Si](C)(C)C)C[C@H](O)C3NC(=O)CO)[C@@H](O)[C@H]2O)C=C14819.6Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #35C[Si](C)(C)OC(=O)[C@]1(O)C[C@H](O)C(N(C(=O)CO)[Si](C)(C)C)[C@H]([C@@H](O)[C@H](COP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)O14628.6Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #36C[Si](C)(C)OCC(=O)NC1[C@@H](O[Si](C)(C)C)C[C@@](O)(C(=O)O)O[C@H]1[C@@H](O)[C@H](COP(=O)(O)OC[C@H]1O[C@@H](N2C=CC(N)=NC2=O)[C@H](O)[C@@H]1O)O[Si](C)(C)C4696.0Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #37C[Si](C)(C)O[C@H]1C[C@@](O)(C(=O)O)O[C@@H]([C@@H](O)[C@H](COP(=O)(OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)O[Si](C)(C)C)C1NC(=O)CO4763.7Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #38C[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O)OC[C@H](O[Si](C)(C)C)[C@H](O)[C@@H]3O[C@](O)(C(=O)O)C[C@H](O[Si](C)(C)C)C3NC(=O)CO)[C@@H](O)[C@H]2O)C=C14880.3Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #39C[Si](C)(C)O[C@H]1C[C@@](O)(C(=O)O)O[C@@H]([C@@H](O)[C@H](COP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)C1N(C(=O)CO)[Si](C)(C)C4701.0Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #4C[Si](C)(C)OC(=O)[C@]1(O)C[C@H](O)C(NC(=O)CO)[C@H]([C@@H](O)[C@H](COP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O[Si](C)(C)C)[C@@H]2O)O[Si](C)(C)C)O14631.1Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #40C[Si](C)(C)OCC(=O)NC1[C@@H](O)C[C@@](O)(C(=O)O)O[C@H]1[C@@H](O)[C@H](COP(=O)(OC[C@H]1O[C@@H](N2C=CC(N)=NC2=O)[C@H](O)[C@@H]1O)O[Si](C)(C)C)O[Si](C)(C)C4715.1Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #41C[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O)OC[C@H](O[Si](C)(C)C)[C@H](O)[C@@H]3O[C@](O)(C(=O)O)C[C@H](O)C3NC(=O)CO[Si](C)(C)C)[C@@H](O)[C@H]2O)C=C14870.1Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #42C[Si](C)(C)OCC(=O)N(C1[C@@H](O)C[C@@](O)(C(=O)O)O[C@H]1[C@@H](O)[C@H](COP(=O)(O)OC[C@H]1O[C@@H](N2C=CC(N)=NC2=O)[C@H](O)[C@@H]1O)O[Si](C)(C)C)[Si](C)(C)C4704.3Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #43C[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(OC[C@H](O[Si](C)(C)C)[C@H](O)[C@@H]3O[C@](O)(C(=O)O)C[C@H](O)C3NC(=O)CO)O[Si](C)(C)C)[C@@H](O)[C@H]2O)C=C14902.0Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #44C[Si](C)(C)O[C@@H](COP(=O)(OC[C@H]1O[C@@H](N2C=CC(N)=NC2=O)[C@H](O)[C@@H]1O)O[Si](C)(C)C)[C@H](O)[C@@H]1O[C@](O)(C(=O)O)C[C@H](O)C1N(C(=O)CO)[Si](C)(C)C4711.2Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #45C[Si](C)(C)O[C@@H](COP(=O)(O)OC[C@H]1O[C@@H](N2C=CC(N([Si](C)(C)C)[Si](C)(C)C)=NC2=O)[C@H](O)[C@@H]1O)[C@H](O)[C@@H]1O[C@](O)(C(=O)O)C[C@H](O)C1NC(=O)CO4783.4Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #46C[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O)OC[C@H](O[Si](C)(C)C)[C@H](O)[C@@H]3O[C@](O)(C(=O)O)C[C@H](O)C3N(C(=O)CO)[Si](C)(C)C)[C@@H](O)[C@H]2O)C=C14865.5Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #47C[Si](C)(C)O[C@@H]([C@@H](O)COP(=O)(O)OC[C@H]1O[C@@H](N2C=CC(N)=NC2=O)[C@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C)[C@@H]1O[C@](O)(C(=O)O)C[C@H](O)C1NC(=O)CO4698.8Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #48C[Si](C)(C)O[C@@H]([C@@H](O)COP(=O)(O)OC[C@H]1O[C@@H](N2C=CC(N)=NC2=O)[C@H](O[Si](C)(C)C)[C@@H]1O)[C@@H]1O[C@](O[Si](C)(C)C)(C(=O)O)C[C@H](O)C1NC(=O)CO4685.5Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #49C[Si](C)(C)OC(=O)[C@]1(O)C[C@H](O)C(NC(=O)CO)[C@H]([C@@H](O[Si](C)(C)C)[C@@H](O)COP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O[Si](C)(C)C)[C@@H]2O)O14647.3Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #5C[Si](C)(C)O[C@H]1C[C@@](O)(C(=O)O)O[C@@H]([C@@H](O)[C@H](COP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O[Si](C)(C)C)[C@@H]2O)O[Si](C)(C)C)C1NC(=O)CO4691.6Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #50C[Si](C)(C)O[C@H]1C[C@@](O)(C(=O)O)O[C@@H]([C@@H](O[Si](C)(C)C)[C@@H](O)COP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O[Si](C)(C)C)[C@@H]2O)C1NC(=O)CO4672.8Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #51C[Si](C)(C)OCC(=O)NC1[C@@H](O)C[C@@](O)(C(=O)O)O[C@H]1[C@@H](O[Si](C)(C)C)[C@@H](O)COP(=O)(O)OC[C@H]1O[C@@H](N2C=CC(N)=NC2=O)[C@H](O[Si](C)(C)C)[C@@H]1O4662.3Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #52C[Si](C)(C)O[C@@H]([C@@H](O)COP(=O)(OC[C@H]1O[C@@H](N2C=CC(N)=NC2=O)[C@H](O[Si](C)(C)C)[C@@H]1O)O[Si](C)(C)C)[C@@H]1O[C@](O)(C(=O)O)C[C@H](O)C1NC(=O)CO4744.9Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #53C[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O)OC[C@H](O)[C@H](O[Si](C)(C)C)[C@@H]3O[C@](O)(C(=O)O)C[C@H](O)C3NC(=O)CO)[C@@H](O)[C@H]2O[Si](C)(C)C)C=C14856.9Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #54C[Si](C)(C)O[C@@H]([C@@H](O)COP(=O)(O)OC[C@H]1O[C@@H](N2C=CC(N)=NC2=O)[C@H](O[Si](C)(C)C)[C@@H]1O)[C@@H]1O[C@](O)(C(=O)O)C[C@H](O)C1N(C(=O)CO)[Si](C)(C)C4664.9Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #55C[Si](C)(C)O[C@@H]([C@@H](O)COP(=O)(O)OC[C@H]1O[C@@H](N2C=CC(N)=NC2=O)[C@H](O)[C@@H]1O[Si](C)(C)C)[C@@H]1O[C@](O[Si](C)(C)C)(C(=O)O)C[C@H](O)C1NC(=O)CO4699.8Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #56C[Si](C)(C)OC(=O)[C@]1(O)C[C@H](O)C(NC(=O)CO)[C@H]([C@@H](O[Si](C)(C)C)[C@@H](O)COP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O[Si](C)(C)C)O14663.2Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #57C[Si](C)(C)O[C@H]1C[C@@](O)(C(=O)O)O[C@@H]([C@@H](O[Si](C)(C)C)[C@@H](O)COP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O[Si](C)(C)C)C1NC(=O)CO4687.6Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #58C[Si](C)(C)OCC(=O)NC1[C@@H](O)C[C@@](O)(C(=O)O)O[C@H]1[C@@H](O[Si](C)(C)C)[C@@H](O)COP(=O)(O)OC[C@H]1O[C@@H](N2C=CC(N)=NC2=O)[C@H](O)[C@@H]1O[Si](C)(C)C4680.1Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #59C[Si](C)(C)O[C@@H]([C@@H](O)COP(=O)(OC[C@H]1O[C@@H](N2C=CC(N)=NC2=O)[C@H](O)[C@@H]1O[Si](C)(C)C)O[Si](C)(C)C)[C@@H]1O[C@](O)(C(=O)O)C[C@H](O)C1NC(=O)CO4755.9Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #6C[Si](C)(C)OCC(=O)NC1[C@@H](O)C[C@@](O)(C(=O)O)O[C@H]1[C@@H](O)[C@H](COP(=O)(O)OC[C@H]1O[C@@H](N2C=CC(N)=NC2=O)[C@H](O[Si](C)(C)C)[C@@H]1O)O[Si](C)(C)C4649.6Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #60C[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O)OC[C@H](O)[C@H](O[Si](C)(C)C)[C@@H]3O[C@](O)(C(=O)O)C[C@H](O)C3NC(=O)CO)[C@@H](O[Si](C)(C)C)[C@H]2O)C=C14869.1Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #61C[Si](C)(C)O[C@@H]([C@@H](O)COP(=O)(O)OC[C@H]1O[C@@H](N2C=CC(N)=NC2=O)[C@H](O)[C@@H]1O[Si](C)(C)C)[C@@H]1O[C@](O)(C(=O)O)C[C@H](O)C1N(C(=O)CO)[Si](C)(C)C4675.7Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #62C[Si](C)(C)OC(=O)[C@]1(O[Si](C)(C)C)C[C@H](O)C(NC(=O)CO)[C@H]([C@@H](O[Si](C)(C)C)[C@@H](O)COP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O)O14635.4Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #63C[Si](C)(C)O[C@H]1C[C@@](O[Si](C)(C)C)(C(=O)O)O[C@@H]([C@@H](O[Si](C)(C)C)[C@@H](O)COP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O)C1NC(=O)CO4682.1Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #64C[Si](C)(C)OCC(=O)NC1[C@@H](O)C[C@@](O[Si](C)(C)C)(C(=O)O)O[C@H]1[C@@H](O[Si](C)(C)C)[C@@H](O)COP(=O)(O)OC[C@H]1O[C@@H](N2C=CC(N)=NC2=O)[C@H](O)[C@@H]1O4685.0Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #65C[Si](C)(C)O[C@@H]([C@@H](O)COP(=O)(OC[C@H]1O[C@@H](N2C=CC(N)=NC2=O)[C@H](O)[C@@H]1O)O[Si](C)(C)C)[C@@H]1O[C@](O[Si](C)(C)C)(C(=O)O)C[C@H](O)C1NC(=O)CO4748.5Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #66C[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O)OC[C@H](O)[C@H](O[Si](C)(C)C)[C@@H]3O[C@](O[Si](C)(C)C)(C(=O)O)C[C@H](O)C3NC(=O)CO)[C@@H](O)[C@H]2O)C=C14868.0Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #67C[Si](C)(C)O[C@@H]([C@@H](O)COP(=O)(O)OC[C@H]1O[C@@H](N2C=CC(N)=NC2=O)[C@H](O)[C@@H]1O)[C@@H]1O[C@](O[Si](C)(C)C)(C(=O)O)C[C@H](O)C1N(C(=O)CO)[Si](C)(C)C4684.4Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #68C[Si](C)(C)OC(=O)[C@]1(O)C[C@H](O[Si](C)(C)C)C(NC(=O)CO)[C@H]([C@@H](O[Si](C)(C)C)[C@@H](O)COP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O)O14633.0Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #69C[Si](C)(C)OCC(=O)NC1[C@@H](O)C[C@@](O)(C(=O)O[Si](C)(C)C)O[C@H]1[C@@H](O[Si](C)(C)C)[C@@H](O)COP(=O)(O)OC[C@H]1O[C@@H](N2C=CC(N)=NC2=O)[C@H](O)[C@@H]1O4628.7Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #7C[Si](C)(C)O[C@@H](COP(=O)(OC[C@H]1O[C@@H](N2C=CC(N)=NC2=O)[C@H](O[Si](C)(C)C)[C@@H]1O)O[Si](C)(C)C)[C@H](O)[C@@H]1O[C@](O)(C(=O)O)C[C@H](O)C1NC(=O)CO4723.8Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #70C[Si](C)(C)OC(=O)[C@]1(O)C[C@H](O)C(NC(=O)CO)[C@H]([C@@H](O[Si](C)(C)C)[C@@H](O)COP(=O)(OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)O14707.5Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #71C[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O)OC[C@H](O)[C@H](O[Si](C)(C)C)[C@@H]3O[C@](O)(C(=O)O[Si](C)(C)C)C[C@H](O)C3NC(=O)CO)[C@@H](O)[C@H]2O)C=C14826.4Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #72C[Si](C)(C)OC(=O)[C@]1(O)C[C@H](O)C(N(C(=O)CO)[Si](C)(C)C)[C@H]([C@@H](O[Si](C)(C)C)[C@@H](O)COP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O)O14636.8Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #73C[Si](C)(C)OCC(=O)NC1[C@@H](O[Si](C)(C)C)C[C@@](O)(C(=O)O)O[C@H]1[C@@H](O[Si](C)(C)C)[C@@H](O)COP(=O)(O)OC[C@H]1O[C@@H](N2C=CC(N)=NC2=O)[C@H](O)[C@@H]1O4667.0Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #74C[Si](C)(C)O[C@H]1C[C@@](O)(C(=O)O)O[C@@H]([C@@H](O[Si](C)(C)C)[C@@H](O)COP(=O)(OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)C1NC(=O)CO4738.9Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #75C[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O)OC[C@H](O)[C@H](O[Si](C)(C)C)[C@@H]3O[C@](O)(C(=O)O)C[C@H](O[Si](C)(C)C)C3NC(=O)CO)[C@@H](O)[C@H]2O)C=C14850.1Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #76C[Si](C)(C)O[C@H]1C[C@@](O)(C(=O)O)O[C@@H]([C@@H](O[Si](C)(C)C)[C@@H](O)COP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O)C1N(C(=O)CO)[Si](C)(C)C4701.8Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #77C[Si](C)(C)OCC(=O)NC1[C@@H](O)C[C@@](O)(C(=O)O)O[C@H]1[C@@H](O[Si](C)(C)C)[C@@H](O)COP(=O)(OC[C@H]1O[C@@H](N2C=CC(N)=NC2=O)[C@H](O)[C@@H]1O)O[Si](C)(C)C4732.1Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #78C[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O)OC[C@H](O)[C@H](O[Si](C)(C)C)[C@@H]3O[C@](O)(C(=O)O)C[C@H](O)C3NC(=O)CO[Si](C)(C)C)[C@@H](O)[C@H]2O)C=C14875.5Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #79C[Si](C)(C)OCC(=O)N(C1[C@@H](O)C[C@@](O)(C(=O)O)O[C@H]1[C@@H](O[Si](C)(C)C)[C@@H](O)COP(=O)(O)OC[C@H]1O[C@@H](N2C=CC(N)=NC2=O)[C@H](O)[C@@H]1O)[Si](C)(C)C4711.6Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #8C[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O)OC[C@H](O[Si](C)(C)C)[C@H](O)[C@@H]3O[C@](O)(C(=O)O)C[C@H](O)C3NC(=O)CO)[C@@H](O)[C@H]2O[Si](C)(C)C)C=C14852.6Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #80C[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(OC[C@H](O)[C@H](O[Si](C)(C)C)[C@@H]3O[C@](O)(C(=O)O)C[C@H](O)C3NC(=O)CO)O[Si](C)(C)C)[C@@H](O)[C@H]2O)C=C14914.3Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #81C[Si](C)(C)O[C@@H]([C@@H](O)COP(=O)(OC[C@H]1O[C@@H](N2C=CC(N)=NC2=O)[C@H](O)[C@@H]1O)O[Si](C)(C)C)[C@@H]1O[C@](O)(C(=O)O)C[C@H](O)C1N(C(=O)CO)[Si](C)(C)C4723.7Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #82C[Si](C)(C)O[C@@H]([C@@H](O)COP(=O)(O)OC[C@H]1O[C@@H](N2C=CC(N([Si](C)(C)C)[Si](C)(C)C)=NC2=O)[C@H](O)[C@@H]1O)[C@@H]1O[C@](O)(C(=O)O)C[C@H](O)C1NC(=O)CO4781.6Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #83C[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O)OC[C@H](O)[C@H](O[Si](C)(C)C)[C@@H]3O[C@](O)(C(=O)O)C[C@H](O)C3N(C(=O)CO)[Si](C)(C)C)[C@@H](O)[C@H]2O)C=C14870.7Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #84C[Si](C)(C)OC(=O)[C@]1(O[Si](C)(C)C)C[C@H](O[Si](C)(C)C)C(NC(=O)CO)[C@H]([C@@H](O)[C@@H](O)COP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O)O14627.5Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #85C[Si](C)(C)OCC(=O)NC1[C@@H](O)C[C@@](O[Si](C)(C)C)(C(=O)O[Si](C)(C)C)O[C@H]1[C@@H](O)[C@@H](O)COP(=O)(O)OC[C@H]1O[C@@H](N2C=CC(N)=NC2=O)[C@H](O)[C@@H]1O4615.8Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #86C[Si](C)(C)OC(=O)[C@]1(O[Si](C)(C)C)C[C@H](O)C(NC(=O)CO)[C@H]([C@@H](O)[C@@H](O)COP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O[Si](C)(C)C)[C@@H]2O)O14615.7Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #87C[Si](C)(C)OC(=O)[C@]1(O[Si](C)(C)C)C[C@H](O)C(NC(=O)CO)[C@H]([C@@H](O)[C@@H](O)COP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O[Si](C)(C)C)O14630.6Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #88C[Si](C)(C)OC(=O)[C@]1(O[Si](C)(C)C)C[C@H](O)C(NC(=O)CO)[C@H]([C@@H](O)[C@@H](O)COP(=O)(OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)O14685.6Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #89C[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O)OC[C@H](O)[C@H](O)[C@@H]3O[C@](O[Si](C)(C)C)(C(=O)O[Si](C)(C)C)C[C@H](O)C3NC(=O)CO)[C@@H](O)[C@H]2O)C=C14800.6Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #9C[Si](C)(C)O[C@@H](COP(=O)(O)OC[C@H]1O[C@@H](N2C=CC(N)=NC2=O)[C@H](O[Si](C)(C)C)[C@@H]1O)[C@H](O)[C@@H]1O[C@](O)(C(=O)O)C[C@H](O)C1N(C(=O)CO)[Si](C)(C)C4658.9Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #90C[Si](C)(C)OC(=O)[C@]1(O[Si](C)(C)C)C[C@H](O)C(N(C(=O)CO)[Si](C)(C)C)[C@H]([C@@H](O)[C@@H](O)COP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O)O14621.5Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #91C[Si](C)(C)O[C@H]1C[C@@](O[Si](C)(C)C)(C(=O)O)O[C@@H]([C@@H](O)[C@@H](O)COP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O[Si](C)(C)C)[C@@H]2O)C1NC(=O)CO4665.8Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #92C[Si](C)(C)O[C@H]1C[C@@](O[Si](C)(C)C)(C(=O)O)O[C@@H]([C@@H](O)[C@@H](O)COP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O[Si](C)(C)C)C1NC(=O)CO4683.8Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #93C[Si](C)(C)OCC(=O)NC1[C@@H](O[Si](C)(C)C)C[C@@](O[Si](C)(C)C)(C(=O)O)O[C@H]1[C@@H](O)[C@@H](O)COP(=O)(O)OC[C@H]1O[C@@H](N2C=CC(N)=NC2=O)[C@H](O)[C@@H]1O4679.0Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #94C[Si](C)(C)O[C@H]1C[C@@](O[Si](C)(C)C)(C(=O)O)O[C@@H]([C@@H](O)[C@@H](O)COP(=O)(OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)C1NC(=O)CO4750.7Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #95C[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O)OC[C@H](O)[C@H](O)[C@@H]3O[C@](O[Si](C)(C)C)(C(=O)O)C[C@H](O[Si](C)(C)C)C3NC(=O)CO)[C@@H](O)[C@H]2O)C=C14852.8Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #96C[Si](C)(C)O[C@H]1C[C@@](O[Si](C)(C)C)(C(=O)O)O[C@@H]([C@@H](O)[C@@H](O)COP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O)C1N(C(=O)CO)[Si](C)(C)C4691.7Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #97C[Si](C)(C)OCC(=O)NC1[C@@H](O)C[C@@](O[Si](C)(C)C)(C(=O)O)O[C@H]1[C@@H](O)[C@@H](O)COP(=O)(O)OC[C@H]1O[C@@H](N2C=CC(N)=NC2=O)[C@H](O[Si](C)(C)C)[C@@H]1O4656.2Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #98C[Si](C)(C)OCC(=O)NC1[C@@H](O)C[C@@](O[Si](C)(C)C)(C(=O)O)O[C@H]1[C@@H](O)[C@@H](O)COP(=O)(O)OC[C@H]1O[C@@H](N2C=CC(N)=NC2=O)[C@H](O)[C@@H]1O[Si](C)(C)C4673.7Semi standard non polar33892256
CMP-N-glycoloylneuraminate,3TMS,isomer #99C[Si](C)(C)OCC(=O)NC1[C@@H](O)C[C@@](O[Si](C)(C)C)(C(=O)O)O[C@H]1[C@@H](O)[C@@H](O)COP(=O)(OC[C@H]1O[C@@H](N2C=CC(N)=NC2=O)[C@H](O)[C@@H]1O)O[Si](C)(C)C4734.1Semi standard non polar33892256
CMP-N-glycoloylneuraminate,1TBDMS,isomer #1CC(C)(C)[Si](C)(C)O[C@@H](COP(=O)(O)OC[C@H]1O[C@@H](N2C=CC(N)=NC2=O)[C@H](O)[C@@H]1O)[C@H](O)[C@@H]1O[C@](O)(C(=O)O)C[C@H](O)C1NC(=O)CO5194.5Semi standard non polar33892256
CMP-N-glycoloylneuraminate,1TBDMS,isomer #10CC(C)(C)[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O)OC[C@H](O)[C@H](O)[C@@H]3O[C@](O)(C(=O)O)C[C@H](O)C3NC(=O)CO)[C@@H](O)[C@H]2O)C=C15283.5Semi standard non polar33892256
CMP-N-glycoloylneuraminate,1TBDMS,isomer #11CC(C)(C)[Si](C)(C)N(C(=O)CO)C1[C@@H](O)C[C@@](O)(C(=O)O)O[C@H]1[C@@H](O)[C@@H](O)COP(=O)(O)OC[C@H]1O[C@@H](N2C=CC(N)=NC2=O)[C@H](O)[C@@H]1O5188.0Semi standard non polar33892256
CMP-N-glycoloylneuraminate,1TBDMS,isomer #2CC(C)(C)[Si](C)(C)O[C@@H]([C@@H](O)COP(=O)(O)OC[C@H]1O[C@@H](N2C=CC(N)=NC2=O)[C@H](O)[C@@H]1O)[C@@H]1O[C@](O)(C(=O)O)C[C@H](O)C1NC(=O)CO5197.9Semi standard non polar33892256
CMP-N-glycoloylneuraminate,1TBDMS,isomer #3CC(C)(C)[Si](C)(C)O[C@@]1(C(=O)O)C[C@H](O)C(NC(=O)CO)[C@H]([C@@H](O)[C@@H](O)COP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O)O15207.0Semi standard non polar33892256
CMP-N-glycoloylneuraminate,1TBDMS,isomer #4CC(C)(C)[Si](C)(C)O[C@H]1C[C@@](O)(C(=O)O)O[C@@H]([C@@H](O)[C@@H](O)COP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O)C1NC(=O)CO5167.4Semi standard non polar33892256
CMP-N-glycoloylneuraminate,1TBDMS,isomer #5CC(C)(C)[Si](C)(C)OCC(=O)NC1[C@@H](O)C[C@@](O)(C(=O)O)O[C@H]1[C@@H](O)[C@@H](O)COP(=O)(O)OC[C@H]1O[C@@H](N2C=CC(N)=NC2=O)[C@H](O)[C@@H]1O5161.4Semi standard non polar33892256
CMP-N-glycoloylneuraminate,1TBDMS,isomer #6CC(C)(C)[Si](C)(C)OC(=O)[C@]1(O)C[C@H](O)C(NC(=O)CO)[C@H]([C@@H](O)[C@@H](O)COP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O)O15156.3Semi standard non polar33892256
CMP-N-glycoloylneuraminate,1TBDMS,isomer #7CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)OC[C@H](O)[C@H](O)[C@@H]2O[C@](O)(C(=O)O)C[C@H](O)C2NC(=O)CO)O[C@@H](N2C=CC(N)=NC2=O)[C@@H]1O5162.7Semi standard non polar33892256
CMP-N-glycoloylneuraminate,1TBDMS,isomer #8CC(C)(C)[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O)OC[C@H](O)[C@H](O)[C@@H]2O[C@](O)(C(=O)O)C[C@H](O)C2NC(=O)CO)O[C@H]1N1C=CC(N)=NC1=O5150.1Semi standard non polar33892256
CMP-N-glycoloylneuraminate,1TBDMS,isomer #9CC(C)(C)[Si](C)(C)OP(=O)(OC[C@H](O)[C@H](O)[C@@H]1O[C@](O)(C(=O)O)C[C@H](O)C1NC(=O)CO)OC[C@H]1O[C@@H](N2C=CC(N)=NC2=O)[C@H](O)[C@@H]1O5287.1Semi standard non polar33892256
CMP-N-glycoloylneuraminate,2TBDMS,isomer #1CC(C)(C)[Si](C)(C)O[C@@H](COP(=O)(O)OC[C@H]1O[C@@H](N2C=CC(N)=NC2=O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O)[C@H](O)[C@@H]1O[C@](O)(C(=O)O)C[C@H](O)C1NC(=O)CO5157.6Semi standard non polar33892256
CMP-N-glycoloylneuraminate,2TBDMS,isomer #10CC(C)(C)[Si](C)(C)O[C@@H](COP(=O)(O)OC[C@H]1O[C@@H](N2C=CC(N)=NC2=O)[C@H](O)[C@@H]1O)[C@H](O)[C@@H]1O[C@](O)(C(=O)O)C[C@H](O)C1N(C(=O)CO)[Si](C)(C)C(C)(C)C5187.4Semi standard non polar33892256
CMP-N-glycoloylneuraminate,2TBDMS,isomer #11CC(C)(C)[Si](C)(C)O[C@@H]([C@@H](O)COP(=O)(O)OC[C@H]1O[C@@H](N2C=CC(N)=NC2=O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O)[C@@H]1O[C@](O)(C(=O)O)C[C@H](O)C1NC(=O)CO5174.6Semi standard non polar33892256
CMP-N-glycoloylneuraminate,2TBDMS,isomer #12CC(C)(C)[Si](C)(C)O[C@@H]([C@@H](O)COP(=O)(O)OC[C@H]1O[C@@H](N2C=CC(N)=NC2=O)[C@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C)[C@@H]1O[C@](O)(C(=O)O)C[C@H](O)C1NC(=O)CO5182.5Semi standard non polar33892256
CMP-N-glycoloylneuraminate,2TBDMS,isomer #13CC(C)(C)[Si](C)(C)O[C@@H]([C@@H](O)COP(=O)(O)OC[C@H]1O[C@@H](N2C=CC(N)=NC2=O)[C@H](O)[C@@H]1O)[C@@H]1O[C@](O[Si](C)(C)C(C)(C)C)(C(=O)O)C[C@H](O)C1NC(=O)CO5194.8Semi standard non polar33892256
CMP-N-glycoloylneuraminate,2TBDMS,isomer #14CC(C)(C)[Si](C)(C)OC(=O)[C@]1(O)C[C@H](O)C(NC(=O)CO)[C@H]([C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)COP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O)O15188.7Semi standard non polar33892256
CMP-N-glycoloylneuraminate,2TBDMS,isomer #15CC(C)(C)[Si](C)(C)O[C@H]1C[C@@](O)(C(=O)O)O[C@@H]([C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)COP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O)C1NC(=O)CO5163.6Semi standard non polar33892256
CMP-N-glycoloylneuraminate,2TBDMS,isomer #16CC(C)(C)[Si](C)(C)OCC(=O)NC1[C@@H](O)C[C@@](O)(C(=O)O)O[C@H]1[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)COP(=O)(O)OC[C@H]1O[C@@H](N2C=CC(N)=NC2=O)[C@H](O)[C@@H]1O5175.8Semi standard non polar33892256
CMP-N-glycoloylneuraminate,2TBDMS,isomer #17CC(C)(C)[Si](C)(C)O[C@@H]([C@@H](O)COP(=O)(OC[C@H]1O[C@@H](N2C=CC(N)=NC2=O)[C@H](O)[C@@H]1O)O[Si](C)(C)C(C)(C)C)[C@@H]1O[C@](O)(C(=O)O)C[C@H](O)C1NC(=O)CO5272.5Semi standard non polar33892256
CMP-N-glycoloylneuraminate,2TBDMS,isomer #18CC(C)(C)[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O)OC[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]3O[C@](O)(C(=O)O)C[C@H](O)C3NC(=O)CO)[C@@H](O)[C@H]2O)C=C15322.5Semi standard non polar33892256
CMP-N-glycoloylneuraminate,2TBDMS,isomer #19CC(C)(C)[Si](C)(C)O[C@@H]([C@@H](O)COP(=O)(O)OC[C@H]1O[C@@H](N2C=CC(N)=NC2=O)[C@H](O)[C@@H]1O)[C@@H]1O[C@](O)(C(=O)O)C[C@H](O)C1N(C(=O)CO)[Si](C)(C)C(C)(C)C5193.5Semi standard non polar33892256
CMP-N-glycoloylneuraminate,2TBDMS,isomer #2CC(C)(C)[Si](C)(C)O[C@@H](COP(=O)(O)OC[C@H]1O[C@@H](N2C=CC(N)=NC2=O)[C@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H]1O[C@](O)(C(=O)O)C[C@H](O)C1NC(=O)CO5166.5Semi standard non polar33892256
CMP-N-glycoloylneuraminate,2TBDMS,isomer #20CC(C)(C)[Si](C)(C)OC(=O)[C@]1(O[Si](C)(C)C(C)(C)C)C[C@H](O)C(NC(=O)CO)[C@H]([C@@H](O)[C@@H](O)COP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O)O15176.8Semi standard non polar33892256
CMP-N-glycoloylneuraminate,2TBDMS,isomer #21CC(C)(C)[Si](C)(C)O[C@H]1C[C@@](O[Si](C)(C)C(C)(C)C)(C(=O)O)O[C@@H]([C@@H](O)[C@@H](O)COP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O)C1NC(=O)CO5167.6Semi standard non polar33892256
CMP-N-glycoloylneuraminate,2TBDMS,isomer #22CC(C)(C)[Si](C)(C)OCC(=O)NC1[C@@H](O)C[C@@](O[Si](C)(C)C(C)(C)C)(C(=O)O)O[C@H]1[C@@H](O)[C@@H](O)COP(=O)(O)OC[C@H]1O[C@@H](N2C=CC(N)=NC2=O)[C@H](O)[C@@H]1O5181.0Semi standard non polar33892256
CMP-N-glycoloylneuraminate,2TBDMS,isomer #23CC(C)(C)[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O)OC[C@H](O)[C@H](O)[C@@H]2O[C@](O[Si](C)(C)C(C)(C)C)(C(=O)O)C[C@H](O)C2NC(=O)CO)O[C@H]1N1C=CC(N)=NC1=O5170.1Semi standard non polar33892256
CMP-N-glycoloylneuraminate,2TBDMS,isomer #24CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)OC[C@H](O)[C@H](O)[C@@H]2O[C@](O[Si](C)(C)C(C)(C)C)(C(=O)O)C[C@H](O)C2NC(=O)CO)O[C@@H](N2C=CC(N)=NC2=O)[C@@H]1O5177.7Semi standard non polar33892256
CMP-N-glycoloylneuraminate,2TBDMS,isomer #25CC(C)(C)[Si](C)(C)O[C@@]1(C(=O)O)C[C@H](O)C(NC(=O)CO)[C@H]([C@@H](O)[C@@H](O)COP(=O)(OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C(C)(C)C)O15285.7Semi standard non polar33892256
CMP-N-glycoloylneuraminate,2TBDMS,isomer #26CC(C)(C)[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O)OC[C@H](O)[C@H](O)[C@@H]3O[C@](O[Si](C)(C)C(C)(C)C)(C(=O)O)C[C@H](O)C3NC(=O)CO)[C@@H](O)[C@H]2O)C=C15329.2Semi standard non polar33892256
CMP-N-glycoloylneuraminate,2TBDMS,isomer #27CC(C)(C)[Si](C)(C)O[C@@]1(C(=O)O)C[C@H](O)C(N(C(=O)CO)[Si](C)(C)C(C)(C)C)[C@H]([C@@H](O)[C@@H](O)COP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O)O15202.1Semi standard non polar33892256
CMP-N-glycoloylneuraminate,2TBDMS,isomer #28CC(C)(C)[Si](C)(C)OC(=O)[C@]1(O)C[C@H](O[Si](C)(C)C(C)(C)C)C(NC(=O)CO)[C@H]([C@@H](O)[C@@H](O)COP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O)O15149.0Semi standard non polar33892256
CMP-N-glycoloylneuraminate,2TBDMS,isomer #29CC(C)(C)[Si](C)(C)O[C@H]1C[C@@](O)(C(=O)O)O[C@@H]([C@@H](O)[C@@H](O)COP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]2O)C1NC(=O)CO5148.0Semi standard non polar33892256
CMP-N-glycoloylneuraminate,2TBDMS,isomer #3CC(C)(C)[Si](C)(C)O[C@@H](COP(=O)(O)OC[C@H]1O[C@@H](N2C=CC(N)=NC2=O)[C@H](O)[C@@H]1O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[C@](O)(C(=O)O)C[C@H](O)C1NC(=O)CO5200.0Semi standard non polar33892256
CMP-N-glycoloylneuraminate,2TBDMS,isomer #30CC(C)(C)[Si](C)(C)O[C@H]1C[C@@](O)(C(=O)O)O[C@@H]([C@@H](O)[C@@H](O)COP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O[Si](C)(C)C(C)(C)C)C1NC(=O)CO5154.0Semi standard non polar33892256
CMP-N-glycoloylneuraminate,2TBDMS,isomer #31CC(C)(C)[Si](C)(C)OCC(=O)NC1[C@@H](O[Si](C)(C)C(C)(C)C)C[C@@](O)(C(=O)O)O[C@H]1[C@@H](O)[C@@H](O)COP(=O)(O)OC[C@H]1O[C@@H](N2C=CC(N)=NC2=O)[C@H](O)[C@@H]1O5150.9Semi standard non polar33892256
CMP-N-glycoloylneuraminate,2TBDMS,isomer #32CC(C)(C)[Si](C)(C)O[C@H]1C[C@@](O)(C(=O)O)O[C@@H]([C@@H](O)[C@@H](O)COP(=O)(OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C(C)(C)C)C1NC(=O)CO5247.6Semi standard non polar33892256
CMP-N-glycoloylneuraminate,2TBDMS,isomer #33CC(C)(C)[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O)OC[C@H](O)[C@H](O)[C@@H]3O[C@](O)(C(=O)O)C[C@H](O[Si](C)(C)C(C)(C)C)C3NC(=O)CO)[C@@H](O)[C@H]2O)C=C15298.6Semi standard non polar33892256
CMP-N-glycoloylneuraminate,2TBDMS,isomer #34CC(C)(C)[Si](C)(C)O[C@H]1C[C@@](O)(C(=O)O)O[C@@H]([C@@H](O)[C@@H](O)COP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O)C1N(C(=O)CO)[Si](C)(C)C(C)(C)C5185.6Semi standard non polar33892256
CMP-N-glycoloylneuraminate,2TBDMS,isomer #35CC(C)(C)[Si](C)(C)OCC(=O)NC1[C@@H](O)C[C@@](O)(C(=O)O[Si](C)(C)C(C)(C)C)O[C@H]1[C@@H](O)[C@@H](O)COP(=O)(O)OC[C@H]1O[C@@H](N2C=CC(N)=NC2=O)[C@H](O)[C@@H]1O5146.7Semi standard non polar33892256
CMP-N-glycoloylneuraminate,2TBDMS,isomer #36CC(C)(C)[Si](C)(C)OCC(=O)NC1[C@@H](O)C[C@@](O)(C(=O)O)O[C@H]1[C@@H](O)[C@@H](O)COP(=O)(O)OC[C@H]1O[C@@H](N2C=CC(N)=NC2=O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O5136.4Semi standard non polar33892256
CMP-N-glycoloylneuraminate,2TBDMS,isomer #37CC(C)(C)[Si](C)(C)OCC(=O)NC1[C@@H](O)C[C@@](O)(C(=O)O)O[C@H]1[C@@H](O)[C@@H](O)COP(=O)(O)OC[C@H]1O[C@@H](N2C=CC(N)=NC2=O)[C@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C5146.7Semi standard non polar33892256
CMP-N-glycoloylneuraminate,2TBDMS,isomer #38CC(C)(C)[Si](C)(C)OCC(=O)NC1[C@@H](O)C[C@@](O)(C(=O)O)O[C@H]1[C@@H](O)[C@@H](O)COP(=O)(OC[C@H]1O[C@@H](N2C=CC(N)=NC2=O)[C@H](O)[C@@H]1O)O[Si](C)(C)C(C)(C)C5244.6Semi standard non polar33892256
CMP-N-glycoloylneuraminate,2TBDMS,isomer #39CC(C)(C)[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O)OC[C@H](O)[C@H](O)[C@@H]3O[C@](O)(C(=O)O)C[C@H](O)C3NC(=O)CO[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]2O)C=C15313.3Semi standard non polar33892256
CMP-N-glycoloylneuraminate,2TBDMS,isomer #4CC(C)(C)[Si](C)(C)O[C@@H](COP(=O)(O)OC[C@H]1O[C@@H](N2C=CC(N)=NC2=O)[C@H](O)[C@@H]1O)[C@H](O)[C@@H]1O[C@](O[Si](C)(C)C(C)(C)C)(C(=O)O)C[C@H](O)C1NC(=O)CO5205.0Semi standard non polar33892256
CMP-N-glycoloylneuraminate,2TBDMS,isomer #40CC(C)(C)[Si](C)(C)OCC(=O)N(C1[C@@H](O)C[C@@](O)(C(=O)O)O[C@H]1[C@@H](O)[C@@H](O)COP(=O)(O)OC[C@H]1O[C@@H](N2C=CC(N)=NC2=O)[C@H](O)[C@@H]1O)[Si](C)(C)C(C)(C)C5223.3Semi standard non polar33892256
CMP-N-glycoloylneuraminate,2TBDMS,isomer #41CC(C)(C)[Si](C)(C)OC(=O)[C@]1(O)C[C@H](O)C(NC(=O)CO)[C@H]([C@@H](O)[C@@H](O)COP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]2O)O15141.9Semi standard non polar33892256
CMP-N-glycoloylneuraminate,2TBDMS,isomer #42CC(C)(C)[Si](C)(C)OC(=O)[C@]1(O)C[C@H](O)C(NC(=O)CO)[C@H]([C@@H](O)[C@@H](O)COP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O[Si](C)(C)C(C)(C)C)O15150.1Semi standard non polar33892256
CMP-N-glycoloylneuraminate,2TBDMS,isomer #43CC(C)(C)[Si](C)(C)OC(=O)[C@]1(O)C[C@H](O)C(NC(=O)CO)[C@H]([C@@H](O)[C@@H](O)COP(=O)(OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C(C)(C)C)O15252.8Semi standard non polar33892256
CMP-N-glycoloylneuraminate,2TBDMS,isomer #44CC(C)(C)[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O)OC[C@H](O)[C@H](O)[C@@H]3O[C@](O)(C(=O)O[Si](C)(C)C(C)(C)C)C[C@H](O)C3NC(=O)CO)[C@@H](O)[C@H]2O)C=C15296.6Semi standard non polar33892256
CMP-N-glycoloylneuraminate,2TBDMS,isomer #45CC(C)(C)[Si](C)(C)OC(=O)[C@]1(O)C[C@H](O)C(N(C(=O)CO)[Si](C)(C)C(C)(C)C)[C@H]([C@@H](O)[C@@H](O)COP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O)O15165.7Semi standard non polar33892256
CMP-N-glycoloylneuraminate,2TBDMS,isomer #46CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)OC[C@H](O)[C@H](O)[C@@H]2O[C@](O)(C(=O)O)C[C@H](O)C2NC(=O)CO)O[C@@H](N2C=CC(N)=NC2=O)[C@@H]1O[Si](C)(C)C(C)(C)C5143.1Semi standard non polar33892256
CMP-N-glycoloylneuraminate,2TBDMS,isomer #47CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(OC[C@H](O)[C@H](O)[C@@H]2O[C@](O)(C(=O)O)C[C@H](O)C2NC(=O)CO)O[Si](C)(C)C(C)(C)C)O[C@@H](N2C=CC(N)=NC2=O)[C@@H]1O5245.9Semi standard non polar33892256
CMP-N-glycoloylneuraminate,2TBDMS,isomer #48CC(C)(C)[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O)OC[C@H](O)[C@H](O)[C@@H]3O[C@](O)(C(=O)O)C[C@H](O)C3NC(=O)CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)C=C15290.2Semi standard non polar33892256
CMP-N-glycoloylneuraminate,2TBDMS,isomer #49CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)OC[C@H](O)[C@H](O)[C@@H]2O[C@](O)(C(=O)O)C[C@H](O)C2N(C(=O)CO)[Si](C)(C)C(C)(C)C)O[C@@H](N2C=CC(N)=NC2=O)[C@@H]1O5168.7Semi standard non polar33892256
CMP-N-glycoloylneuraminate,2TBDMS,isomer #5CC(C)(C)[Si](C)(C)OC(=O)[C@]1(O)C[C@H](O)C(NC(=O)CO)[C@H]([C@@H](O)[C@H](COP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C(C)(C)C)O15171.1Semi standard non polar33892256
CMP-N-glycoloylneuraminate,2TBDMS,isomer #50CC(C)(C)[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(OC[C@H](O)[C@H](O)[C@@H]2O[C@](O)(C(=O)O)C[C@H](O)C2NC(=O)CO)O[Si](C)(C)C(C)(C)C)O[C@H]1N1C=CC(N)=NC1=O5239.2Semi standard non polar33892256
CMP-N-glycoloylneuraminate,2TBDMS,isomer #51CC(C)(C)[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O)OC[C@H](O)[C@H](O)[C@@H]3O[C@](O)(C(=O)O)C[C@H](O)C3NC(=O)CO)[C@@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)C=C15281.9Semi standard non polar33892256
CMP-N-glycoloylneuraminate,2TBDMS,isomer #52CC(C)(C)[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O)OC[C@H](O)[C@H](O)[C@@H]2O[C@](O)(C(=O)O)C[C@H](O)C2N(C(=O)CO)[Si](C)(C)C(C)(C)C)O[C@H]1N1C=CC(N)=NC1=O5162.5Semi standard non polar33892256
CMP-N-glycoloylneuraminate,2TBDMS,isomer #53CC(C)(C)[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(OC[C@H](O)[C@H](O)[C@@H]3O[C@](O)(C(=O)O)C[C@H](O)C3NC(=O)CO)O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]2O)C=C15410.2Semi standard non polar33892256
CMP-N-glycoloylneuraminate,2TBDMS,isomer #54CC(C)(C)[Si](C)(C)OP(=O)(OC[C@H](O)[C@H](O)[C@@H]1O[C@](O)(C(=O)O)C[C@H](O)C1N(C(=O)CO)[Si](C)(C)C(C)(C)C)OC[C@H]1O[C@@H](N2C=CC(N)=NC2=O)[C@H](O)[C@@H]1O5265.2Semi standard non polar33892256
CMP-N-glycoloylneuraminate,2TBDMS,isomer #55CC(C)(C)[Si](C)(C)N(C1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O)OC[C@H](O)[C@H](O)[C@@H]3O[C@](O)(C(=O)O)C[C@H](O)C3NC(=O)CO)[C@@H](O)[C@H]2O)C=C1)[Si](C)(C)C(C)(C)C5225.6Semi standard non polar33892256
CMP-N-glycoloylneuraminate,2TBDMS,isomer #56CC(C)(C)[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O)OC[C@H](O)[C@H](O)[C@@H]3O[C@](O)(C(=O)O)C[C@H](O)C3N(C(=O)CO)[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]2O)C=C15341.5Semi standard non polar33892256
CMP-N-glycoloylneuraminate,2TBDMS,isomer #6CC(C)(C)[Si](C)(C)O[C@H]1C[C@@](O)(C(=O)O)O[C@@H]([C@@H](O)[C@H](COP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C(C)(C)C)C1NC(=O)CO5173.4Semi standard non polar33892256
CMP-N-glycoloylneuraminate,2TBDMS,isomer #7CC(C)(C)[Si](C)(C)OCC(=O)NC1[C@@H](O)C[C@@](O)(C(=O)O)O[C@H]1[C@@H](O)[C@H](COP(=O)(O)OC[C@H]1O[C@@H](N2C=CC(N)=NC2=O)[C@H](O)[C@@H]1O)O[Si](C)(C)C(C)(C)C5159.1Semi standard non polar33892256
CMP-N-glycoloylneuraminate,2TBDMS,isomer #8CC(C)(C)[Si](C)(C)O[C@@H](COP(=O)(OC[C@H]1O[C@@H](N2C=CC(N)=NC2=O)[C@H](O)[C@@H]1O)O[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H]1O[C@](O)(C(=O)O)C[C@H](O)C1NC(=O)CO5254.8Semi standard non polar33892256
CMP-N-glycoloylneuraminate,2TBDMS,isomer #9CC(C)(C)[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O)OC[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H]3O[C@](O)(C(=O)O)C[C@H](O)C3NC(=O)CO)[C@@H](O)[C@H]2O)C=C15311.8Semi standard non polar33892256
Spectra

GC-MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted GC-MSPredicted GC-MS Spectrum - CMP-N-glycoloylneuraminate GC-MS (Non-derivatized) - 70eV, Positivesplash10-03y0-2339634000-dfbf60ceffde2a26e4452017-09-01Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - CMP-N-glycoloylneuraminate GC-MS (TMS_1_1) - 70eV, PositiveNot Available2021-10-17Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - CMP-N-glycoloylneuraminate GC-MS (TMS_1_2) - 70eV, PositiveNot Available2021-10-17Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - CMP-N-glycoloylneuraminate GC-MS (TMS_1_3) - 70eV, PositiveNot Available2021-10-17Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - CMP-N-glycoloylneuraminate GC-MS (TMS_1_4) - 70eV, PositiveNot Available2021-10-17Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - CMP-N-glycoloylneuraminate GC-MS (TMS_1_5) - 70eV, PositiveNot Available2021-10-17Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - CMP-N-glycoloylneuraminate GC-MS (TMS_1_6) - 70eV, PositiveNot Available2021-10-17Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - CMP-N-glycoloylneuraminate GC-MS (TMS_1_7) - 70eV, PositiveNot Available2021-10-17Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - CMP-N-glycoloylneuraminate GC-MS (TMS_1_8) - 70eV, PositiveNot Available2021-10-17Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - CMP-N-glycoloylneuraminate GC-MS (TMS_1_9) - 70eV, PositiveNot Available2021-10-17Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - CMP-N-glycoloylneuraminate GC-MS (TMS_1_10) - 70eV, PositiveNot Available2021-10-17Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - CMP-N-glycoloylneuraminate GC-MS (TMS_1_11) - 70eV, PositiveNot Available2021-10-17Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - CMP-N-glycoloylneuraminate GC-MS (TMS_2_1) - 70eV, PositiveNot Available2021-10-17Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - CMP-N-glycoloylneuraminate GC-MS (TMS_2_2) - 70eV, PositiveNot Available2021-10-17Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - CMP-N-glycoloylneuraminate GC-MS (TMS_2_3) - 70eV, PositiveNot Available2021-10-17Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - CMP-N-glycoloylneuraminate GC-MS (TMS_2_4) - 70eV, PositiveNot Available2021-10-17Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - CMP-N-glycoloylneuraminate GC-MS (TMS_2_5) - 70eV, PositiveNot Available2021-10-17Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - CMP-N-glycoloylneuraminate GC-MS (TMS_2_6) - 70eV, PositiveNot Available2021-10-17Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - CMP-N-glycoloylneuraminate GC-MS (TMS_2_7) - 70eV, PositiveNot Available2021-10-17Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - CMP-N-glycoloylneuraminate GC-MS (TMS_2_8) - 70eV, PositiveNot Available2021-10-17Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - CMP-N-glycoloylneuraminate GC-MS (TMS_2_9) - 70eV, PositiveNot Available2021-10-17Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - CMP-N-glycoloylneuraminate GC-MS (TMS_2_10) - 70eV, PositiveNot Available2021-10-17Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - CMP-N-glycoloylneuraminate GC-MS (TMS_2_11) - 70eV, PositiveNot Available2021-10-17Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - CMP-N-glycoloylneuraminate GC-MS (TMS_2_12) - 70eV, PositiveNot Available2021-10-17Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - CMP-N-glycoloylneuraminate GC-MS (TMS_2_13) - 70eV, PositiveNot Available2021-10-17Wishart LabView Spectrum

MS/MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - CMP-N-glycoloylneuraminate 10V, Positive-QTOFsplash10-03di-0910002000-d4f1e52062015dc10b7f2017-09-01Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - CMP-N-glycoloylneuraminate 20V, Positive-QTOFsplash10-03di-2910000000-2d4cb8ba80ae2d1461662017-09-01Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - CMP-N-glycoloylneuraminate 40V, Positive-QTOFsplash10-03di-3930000000-8a1620c372f90002ef9b2017-09-01Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - CMP-N-glycoloylneuraminate 10V, Negative-QTOFsplash10-03dj-0943723000-7d8efafe708e2fdb94252017-09-01Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - CMP-N-glycoloylneuraminate 20V, Negative-QTOFsplash10-000i-9212000000-ad5d3dc896e26dbec3da2017-09-01Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - CMP-N-glycoloylneuraminate 40V, Negative-QTOFsplash10-01t9-9301000000-aa2110890252b1fb83882017-09-01Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - CMP-N-glycoloylneuraminate 10V, Negative-QTOFsplash10-004i-0001019000-a1f6a1653050af73187c2021-09-22Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - CMP-N-glycoloylneuraminate 20V, Negative-QTOFsplash10-01ta-9103362000-1b08ef836093e179cd762021-09-22Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - CMP-N-glycoloylneuraminate 40V, Negative-QTOFsplash10-002u-9701210000-f0cd86fffb2fb17d84fd2021-09-22Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - CMP-N-glycoloylneuraminate 10V, Positive-QTOFsplash10-03di-0900005000-3f1af9de1ed9e36d01b02021-09-23Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - CMP-N-glycoloylneuraminate 20V, Positive-QTOFsplash10-03di-1934141000-dfc8227cb9856499e7782021-09-23Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - CMP-N-glycoloylneuraminate 40V, Positive-QTOFsplash10-03di-2914200000-29d4f10326bd60eb9f972021-09-23Wishart LabView Spectrum

NMR Spectra

Spectrum TypeDescriptionDeposition DateSourceView
Predicted 1D NMR13C NMR Spectrum (1D, 100 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 100 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 1000 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 1000 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 200 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 200 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 300 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 300 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 400 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 400 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 500 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 500 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 600 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 600 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 700 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 700 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 800 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 800 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 900 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 900 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Biological Properties
Cellular LocationsNot Available
Biospecimen LocationsNot Available
Tissue LocationsNot Available
Pathways
Normal Concentrations
Not Available
Abnormal Concentrations
Not Available
Associated Disorders and Diseases
Disease ReferencesNone
Associated OMIM IDsNone
DrugBank IDNot Available
Phenol Explorer Compound IDNot Available
FooDB IDFDB028851
KNApSAcK IDNot Available
Chemspider ID35032415
KEGG Compound IDC03691
BioCyc IDCPD-262
BiGG IDNot Available
Wikipedia LinkNot Available
METLIN IDNot Available
PubChem Compound53481387
PDB IDNot Available
ChEBI ID18098
Food Biomarker OntologyNot Available
VMH IDHC01162
MarkerDB IDNot Available
Good Scents IDNot Available
References
Synthesis ReferenceNot Available
Material Safety Data Sheet (MSDS)Not Available
General ReferencesNot Available

Enzymes

General function:
Involved in lipopolysaccharide biosynthetic process
Specific function:
Catalyzes the activation of N-acetylneuraminic acid (NeuNAc) to cytidine 5'-monophosphate N-acetylneuraminic acid (CMP-NeuNAc), a substrate required for the addition of sialic acid. Has some activity toward NeuNAc, N-glycolylneuraminic acid (Neu5Gc) or 2-keto-3-deoxy-D-glycero-D-galacto-nononic acid (KDN).
Gene Name:
CMAS
Uniprot ID:
Q8NFW8
Molecular weight:
48378.835
Reactions
Cytidine triphosphate + N-Glycolylneuraminic acid → Pyrophosphate + CMP-N-glycoloylneuraminatedetails