Hmdb loader
Record Information
Version5.0
StatusExpected but not Quantified
Creation Date2009-07-25 00:20:02 UTC
Update Date2021-09-14 15:46:02 UTC
HMDB IDHMDB0013112
Secondary Accession Numbers
  • HMDB13112
Metabolite Identification
Common NameUDP-N-acetyl-D-mannosamine
DescriptionUDP-N-acetyl-D-mannosamine is involved in teichoic acid (poly-glycerol) biosynthesis pathway and enterobacterial common antigen biosynthesis pathway. It serves as both enzymatic reactants and products in those two pathways. In teichoic acid (poly-glycerol) biosynthesis pathway, UDP-N-acetyl-mannosamine is synthesized from UDP-N-acetyl-glocasamine by UDP-N-acetylglucosamine 2-epimerase, encoded by the mnaA gene.
Structure
Data?1582753089
Synonyms
ValueSource
Uridine diphosphate N-acetylgalactosamineHMDB
Uridine-diphosphate-N-acetylgalactosamineHMDB
Uridine-diphosphate-N-acetylglucosamineHMDB
Diphosphate N-acetylgalactosamine, uridineMeSH, HMDB
UDP AcetylgalactosamineMeSH, HMDB
Acetylgalactosamine, UDPMeSH, HMDB
Uridine diphosphate N acetylgalactosamineMeSH, HMDB
N-Acetylgalactosamine, uridine diphosphateMeSH, HMDB
Chemical FormulaC17H27N3O17P2
Average Molecular Weight607.3537
Monoisotopic Molecular Weight607.081569477
IUPAC Name[({[(2S,3R,4S,5S)-5-(2,4-dioxo-1,2,3,4-tetrahydropyrimidin-1-yl)-3,4-dihydroxyoxolan-2-yl]methoxy}(hydroxy)phosphoryl)oxy]({[(3R,4S,5R,6S)-3-acetamido-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy})phosphinic acid
Traditional Name{[(2S,3R,4S,5S)-5-(2,4-dioxo-3H-pyrimidin-1-yl)-3,4-dihydroxyoxolan-2-yl]methoxy(hydroxy)phosphoryl}oxy([(3R,4S,5R,6S)-3-acetamido-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy)phosphinic acid
CAS Registry NumberNot Available
SMILES
CC(=O)N[C@@H]1[C@H](O)[C@@H](O)[C@H](CO)OC1OP(O)(=O)OP(O)(=O)OC[C@@H]1O[C@@H]([C@@H](O)[C@H]1O)N1C=CC(=O)NC1=O
InChI Identifier
InChI=1S/C17H27N3O17P2/c1-6(22)18-10-13(26)11(24)7(4-21)35-16(10)36-39(31,32)37-38(29,30)33-5-8-12(25)14(27)15(34-8)20-3-2-9(23)19-17(20)28/h2-3,7-8,10-16,21,24-27H,4-5H2,1H3,(H,18,22)(H,29,30)(H,31,32)(H,19,23,28)/t7-,8-,10+,11-,12-,13-,14-,15-,16?/m0/s1
InChI KeyLFTYTUAZOPRMMI-IUPDHGCPSA-N
Chemical Taxonomy
Description Belongs to the class of organic compounds known as pyrimidine nucleotide sugars. These are pyrimidine nucleotides bound to a saccharide derivative through the terminal phosphate group.
KingdomOrganic compounds
Super ClassNucleosides, nucleotides, and analogues
ClassPyrimidine nucleotides
Sub ClassPyrimidine nucleotide sugars
Direct ParentPyrimidine nucleotide sugars
Alternative Parents
Substituents
  • Pyrimidine nucleotide sugar
  • Pyrimidine ribonucleoside diphosphate
  • Pentose phosphate
  • Pentose-5-phosphate
  • N-acyl-alpha-hexosamine
  • Glycosyl compound
  • N-glycosyl compound
  • Monosaccharide phosphate
  • Organic pyrophosphate
  • Pyrimidone
  • Monoalkyl phosphate
  • Hydropyrimidine
  • Monosaccharide
  • Organic phosphoric acid derivative
  • Oxane
  • Phosphoric acid ester
  • Pyrimidine
  • Alkyl phosphate
  • Vinylogous amide
  • Acetamide
  • Tetrahydrofuran
  • Heteroaromatic compound
  • Urea
  • Secondary carboxylic acid amide
  • Secondary alcohol
  • Carboxamide group
  • Lactam
  • Azacycle
  • Carboxylic acid derivative
  • Oxacycle
  • Organoheterocyclic compound
  • Organopnictogen compound
  • Organooxygen compound
  • Alcohol
  • Primary alcohol
  • Organic nitrogen compound
  • Organic oxygen compound
  • Organic oxide
  • Carbonyl group
  • Hydrocarbon derivative
  • Organonitrogen compound
  • Aromatic heteromonocyclic compound
Molecular FrameworkAromatic heteromonocyclic compounds
External DescriptorsNot Available
Ontology
Physiological effectNot Available
Disposition
Process
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 Solubility11.4 g/LALOGPS
logP-1.4ALOGPS
logP-5.3ChemAxon
logS-1.7ALOGPS
pKa (Strongest Acidic)1.74ChemAxon
pKa (Strongest Basic)-3.5ChemAxon
Physiological Charge-2ChemAxon
Hydrogen Acceptor Count14ChemAxon
Hydrogen Donor Count9ChemAxon
Polar Surface Area300.41 ŲChemAxon
Rotatable Bond Count10ChemAxon
Refractivity117.56 m³·mol⁻¹ChemAxon
Polarizability51.15 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]+191.86430932474
DeepCCS[M-H]-190.21130932474
DeepCCS[M-2H]-224.24530932474
DeepCCS[M+Na]+198.76230932474
AllCCS[M+H]+220.832859911
AllCCS[M+H-H2O]+219.632859911
AllCCS[M+NH4]+221.832859911
AllCCS[M+Na]+222.132859911
AllCCS[M-H]-217.432859911
AllCCS[M+Na-2H]-218.832859911
AllCCS[M+HCOO]-220.632859911

Predicted Kovats Retention Indices

Underivatized

MetaboliteSMILESKovats RI ValueColumn TypeReference
UDP-N-acetyl-D-mannosamineCC(=O)N[C@@H]1[C@H](O)[C@@H](O)[C@H](CO)OC1OP(O)(=O)OP(O)(=O)OC[C@@H]1O[C@@H]([C@@H](O)[C@H]1O)N1C=CC(=O)NC1=O5079.8Standard polar33892256
UDP-N-acetyl-D-mannosamineCC(=O)N[C@@H]1[C@H](O)[C@@H](O)[C@H](CO)OC1OP(O)(=O)OP(O)(=O)OC[C@@H]1O[C@@H]([C@@H](O)[C@H]1O)N1C=CC(=O)NC1=O3390.6Standard non polar33892256
UDP-N-acetyl-D-mannosamineCC(=O)N[C@@H]1[C@H](O)[C@@H](O)[C@H](CO)OC1OP(O)(=O)OP(O)(=O)OC[C@@H]1O[C@@H]([C@@H](O)[C@H]1O)N1C=CC(=O)NC1=O5122.7Semi standard non polar33892256

Derivatized

Derivative Name / StructureSMILESKovats RI ValueColumn TypeReference
UDP-N-acetyl-D-mannosamine,1TMS,isomer #1CC(=O)N[C@H]1C(OP(=O)(O)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O)[C@H]2O)O[C@@H](CO)[C@H](O)[C@H]1O[Si](C)(C)C4430.0Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,1TMS,isomer #2CC(=O)N[C@H]1C(OP(=O)(O)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O)[C@H]2O)O[C@@H](CO)[C@H](O[Si](C)(C)C)[C@H]1O4449.3Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,1TMS,isomer #3CC(=O)N[C@H]1C(OP(=O)(O)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O)[C@H]2O)O[C@@H](CO[Si](C)(C)C)[C@H](O)[C@H]1O4405.2Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,1TMS,isomer #4CC(=O)N[C@H]1C(OP(=O)(O)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O[Si](C)(C)C)[C@H]2O)O[C@@H](CO)[C@H](O)[C@H]1O4430.5Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,1TMS,isomer #5CC(=O)N[C@H]1C(OP(=O)(O)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O)[C@H]2O[Si](C)(C)C)O[C@@H](CO)[C@H](O)[C@H]1O4440.9Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,1TMS,isomer #6CC(=O)N[C@H]1C(OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O)[C@H]2O)O[C@@H](CO)[C@H](O)[C@H]1O4519.1Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,1TMS,isomer #7CC(=O)N[C@H]1C(OP(=O)(O)OP(=O)(OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O)[C@H]2O)O[Si](C)(C)C)O[C@@H](CO)[C@H](O)[C@H]1O4507.7Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,1TMS,isomer #8CC(=O)N([C@H]1C(OP(=O)(O)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O)[C@H]2O)O[C@@H](CO)[C@H](O)[C@H]1O)[Si](C)(C)C4487.3Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,1TMS,isomer #9CC(=O)N[C@H]1C(OP(=O)(O)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)N([Si](C)(C)C)C3=O)[C@@H](O)[C@H]2O)O[C@@H](CO)[C@H](O)[C@H]1O4540.8Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,2TMS,isomer #1CC(=O)N[C@H]1C(OP(=O)(O)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O[Si](C)(C)C)[C@H]2O)O[C@@H](CO)[C@H](O)[C@H]1O[Si](C)(C)C4245.8Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,2TMS,isomer #10CC(=O)N[C@H]1C(OP(=O)(O)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O)[C@H]2O[Si](C)(C)C)O[C@@H](CO)[C@H](O[Si](C)(C)C)[C@H]1O4279.2Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,2TMS,isomer #11CC(=O)N[C@H]1C(OP(=O)(O)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O)[C@H]2O)O[C@@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O4290.7Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,2TMS,isomer #12CC(=O)N[C@H]1C(OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O)[C@H]2O)O[C@@H](CO)[C@H](O[Si](C)(C)C)[C@H]1O4356.6Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,2TMS,isomer #13CC(=O)N[C@H]1C(OP(=O)(O)OP(=O)(OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O)[C@H]2O)O[Si](C)(C)C)O[C@@H](CO)[C@H](O[Si](C)(C)C)[C@H]1O4346.8Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,2TMS,isomer #14CC(=O)N([C@H]1C(OP(=O)(O)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O)[C@H]2O)O[C@@H](CO)[C@H](O[Si](C)(C)C)[C@H]1O)[Si](C)(C)C4320.6Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,2TMS,isomer #15CC(=O)N[C@H]1C(OP(=O)(O)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)N([Si](C)(C)C)C3=O)[C@@H](O)[C@H]2O)O[C@@H](CO)[C@H](O[Si](C)(C)C)[C@H]1O4435.5Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,2TMS,isomer #16CC(=O)N[C@H]1C(OP(=O)(O)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O[Si](C)(C)C)[C@H]2O)O[C@@H](CO[Si](C)(C)C)[C@H](O)[C@H]1O4242.1Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,2TMS,isomer #17CC(=O)N[C@H]1C(OP(=O)(O)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O)[C@H]2O[Si](C)(C)C)O[C@@H](CO[Si](C)(C)C)[C@H](O)[C@H]1O4255.0Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,2TMS,isomer #18CC(=O)N[C@H]1C(OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O)[C@H]2O)O[C@@H](CO[Si](C)(C)C)[C@H](O)[C@H]1O4327.3Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,2TMS,isomer #19CC(=O)N[C@H]1C(OP(=O)(O)OP(=O)(OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O)[C@H]2O)O[Si](C)(C)C)O[C@@H](CO[Si](C)(C)C)[C@H](O)[C@H]1O4315.6Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,2TMS,isomer #2CC(=O)N[C@H]1C(OP(=O)(O)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O)[C@H]2O[Si](C)(C)C)O[C@@H](CO)[C@H](O)[C@H]1O[Si](C)(C)C4258.3Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,2TMS,isomer #20CC(=O)N([C@H]1C(OP(=O)(O)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O)[C@H]2O)O[C@@H](CO[Si](C)(C)C)[C@H](O)[C@H]1O)[Si](C)(C)C4320.8Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,2TMS,isomer #21CC(=O)N[C@H]1C(OP(=O)(O)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)N([Si](C)(C)C)C3=O)[C@@H](O)[C@H]2O)O[C@@H](CO[Si](C)(C)C)[C@H](O)[C@H]1O4409.2Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,2TMS,isomer #22CC(=O)N[C@H]1C(OP(=O)(O)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)O[C@@H](CO)[C@H](O)[C@H]1O4283.6Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,2TMS,isomer #23CC(=O)N[C@H]1C(OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O[Si](C)(C)C)[C@H]2O)O[C@@H](CO)[C@H](O)[C@H]1O4327.2Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,2TMS,isomer #24CC(=O)N[C@H]1C(OP(=O)(O)OP(=O)(OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O[Si](C)(C)C)[C@H]2O)O[Si](C)(C)C)O[C@@H](CO)[C@H](O)[C@H]1O4319.3Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,2TMS,isomer #25CC(=O)N([C@H]1C(OP(=O)(O)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O[Si](C)(C)C)[C@H]2O)O[C@@H](CO)[C@H](O)[C@H]1O)[Si](C)(C)C4307.4Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,2TMS,isomer #26CC(=O)N[C@H]1C(OP(=O)(O)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)N([Si](C)(C)C)C3=O)[C@@H](O[Si](C)(C)C)[C@H]2O)O[C@@H](CO)[C@H](O)[C@H]1O4415.5Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,2TMS,isomer #27CC(=O)N[C@H]1C(OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O)[C@H]2O[Si](C)(C)C)O[C@@H](CO)[C@H](O)[C@H]1O4340.3Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,2TMS,isomer #28CC(=O)N[C@H]1C(OP(=O)(O)OP(=O)(OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O)[C@H]2O[Si](C)(C)C)O[Si](C)(C)C)O[C@@H](CO)[C@H](O)[C@H]1O4333.4Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,2TMS,isomer #29CC(=O)N([C@H]1C(OP(=O)(O)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O)[C@H]2O[Si](C)(C)C)O[C@@H](CO)[C@H](O)[C@H]1O)[Si](C)(C)C4311.4Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,2TMS,isomer #3CC(=O)N[C@H]1C(OP(=O)(O)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O)[C@H]2O)O[C@@H](CO[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C4261.1Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,2TMS,isomer #30CC(=O)N[C@H]1C(OP(=O)(O)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)N([Si](C)(C)C)C3=O)[C@@H](O)[C@H]2O[Si](C)(C)C)O[C@@H](CO)[C@H](O)[C@H]1O4423.8Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,2TMS,isomer #31CC(=O)N[C@H]1C(OP(=O)(O[Si](C)(C)C)OP(=O)(OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O)[C@H]2O)O[Si](C)(C)C)O[C@@H](CO)[C@H](O)[C@H]1O4404.4Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,2TMS,isomer #32CC(=O)N([C@H]1C(OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O)[C@H]2O)O[C@@H](CO)[C@H](O)[C@H]1O)[Si](C)(C)C4385.3Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,2TMS,isomer #33CC(=O)N[C@H]1C(OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)N([Si](C)(C)C)C3=O)[C@@H](O)[C@H]2O)O[C@@H](CO)[C@H](O)[C@H]1O4482.3Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,2TMS,isomer #34CC(=O)N([C@H]1C(OP(=O)(O)OP(=O)(OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O)[C@H]2O)O[Si](C)(C)C)O[C@@H](CO)[C@H](O)[C@H]1O)[Si](C)(C)C4380.7Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,2TMS,isomer #35CC(=O)N[C@H]1C(OP(=O)(O)OP(=O)(OC[C@@H]2O[C@H](N3C=CC(=O)N([Si](C)(C)C)C3=O)[C@@H](O)[C@H]2O)O[Si](C)(C)C)O[C@@H](CO)[C@H](O)[C@H]1O4469.9Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,2TMS,isomer #36CC(=O)N([C@H]1C(OP(=O)(O)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)N([Si](C)(C)C)C3=O)[C@@H](O)[C@H]2O)O[C@@H](CO)[C@H](O)[C@H]1O)[Si](C)(C)C4468.2Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,2TMS,isomer #4CC(=O)N[C@H]1C(OP(=O)(O)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O)[C@H]2O)O[C@@H](CO)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C4283.5Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,2TMS,isomer #5CC(=O)N[C@H]1C(OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O)[C@H]2O)O[C@@H](CO)[C@H](O)[C@H]1O[Si](C)(C)C4338.7Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,2TMS,isomer #6CC(=O)N[C@H]1C(OP(=O)(O)OP(=O)(OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O)[C@H]2O)O[Si](C)(C)C)O[C@@H](CO)[C@H](O)[C@H]1O[Si](C)(C)C4330.0Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,2TMS,isomer #7CC(=O)N([C@H]1C(OP(=O)(O)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O)[C@H]2O)O[C@@H](CO)[C@H](O)[C@H]1O[Si](C)(C)C)[Si](C)(C)C4309.7Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,2TMS,isomer #8CC(=O)N[C@H]1C(OP(=O)(O)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)N([Si](C)(C)C)C3=O)[C@@H](O)[C@H]2O)O[C@@H](CO)[C@H](O)[C@H]1O[Si](C)(C)C4422.7Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,2TMS,isomer #9CC(=O)N[C@H]1C(OP(=O)(O)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O[Si](C)(C)C)[C@H]2O)O[C@@H](CO)[C@H](O[Si](C)(C)C)[C@H]1O4265.1Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,3TMS,isomer #1CC(=O)N[C@H]1C(OP(=O)(O)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)O[C@@H](CO)[C@H](O)[C@H]1O[Si](C)(C)C4169.9Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,3TMS,isomer #10CC(=O)N[C@H]1C(OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O)[C@H]2O[Si](C)(C)C)O[C@@H](CO)[C@H](O)[C@H]1O[Si](C)(C)C4214.4Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,3TMS,isomer #11CC(=O)N[C@H]1C(OP(=O)(O)OP(=O)(OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O)[C@H]2O[Si](C)(C)C)O[Si](C)(C)C)O[C@@H](CO)[C@H](O)[C@H]1O[Si](C)(C)C4209.5Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,3TMS,isomer #12CC(=O)N([C@H]1C(OP(=O)(O)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O)[C@H]2O[Si](C)(C)C)O[C@@H](CO)[C@H](O)[C@H]1O[Si](C)(C)C)[Si](C)(C)C4168.6Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,3TMS,isomer #13CC(=O)N[C@H]1C(OP(=O)(O)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)N([Si](C)(C)C)C3=O)[C@@H](O)[C@H]2O[Si](C)(C)C)O[C@@H](CO)[C@H](O)[C@H]1O[Si](C)(C)C4285.4Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,3TMS,isomer #14CC(=O)N[C@H]1C(OP(=O)(O)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O)[C@H]2O)O[C@@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C4184.3Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,3TMS,isomer #15CC(=O)N[C@H]1C(OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O)[C@H]2O)O[C@@H](CO[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C4206.9Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,3TMS,isomer #16CC(=O)N[C@H]1C(OP(=O)(O)OP(=O)(OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O)[C@H]2O)O[Si](C)(C)C)O[C@@H](CO[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C4199.0Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,3TMS,isomer #17CC(=O)N([C@H]1C(OP(=O)(O)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O)[C@H]2O)O[C@@H](CO[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C)[Si](C)(C)C4183.8Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,3TMS,isomer #18CC(=O)N[C@H]1C(OP(=O)(O)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)N([Si](C)(C)C)C3=O)[C@@H](O)[C@H]2O)O[C@@H](CO[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C4291.1Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,3TMS,isomer #19CC(=O)N[C@H]1C(OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O)[C@H]2O)O[C@@H](CO)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C4223.4Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,3TMS,isomer #2CC(=O)N[C@H]1C(OP(=O)(O)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O[Si](C)(C)C)[C@H]2O)O[C@@H](CO[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C4148.8Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,3TMS,isomer #20CC(=O)N[C@H]1C(OP(=O)(O)OP(=O)(OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O)[C@H]2O)O[Si](C)(C)C)O[C@@H](CO)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C4216.5Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,3TMS,isomer #21CC(=O)N([C@H]1C(OP(=O)(O)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O)[C@H]2O)O[C@@H](CO)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C)[Si](C)(C)C4203.1Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,3TMS,isomer #22CC(=O)N[C@H]1C(OP(=O)(O)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)N([Si](C)(C)C)C3=O)[C@@H](O)[C@H]2O)O[C@@H](CO)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C4311.2Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,3TMS,isomer #23CC(=O)N[C@H]1C(OP(=O)(O[Si](C)(C)C)OP(=O)(OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O)[C@H]2O)O[Si](C)(C)C)O[C@@H](CO)[C@H](O)[C@H]1O[Si](C)(C)C4261.1Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,3TMS,isomer #24CC(=O)N([C@H]1C(OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O)[C@H]2O)O[C@@H](CO)[C@H](O)[C@H]1O[Si](C)(C)C)[Si](C)(C)C4219.7Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,3TMS,isomer #25CC(=O)N[C@H]1C(OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)N([Si](C)(C)C)C3=O)[C@@H](O)[C@H]2O)O[C@@H](CO)[C@H](O)[C@H]1O[Si](C)(C)C4344.0Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,3TMS,isomer #26CC(=O)N([C@H]1C(OP(=O)(O)OP(=O)(OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O)[C@H]2O)O[Si](C)(C)C)O[C@@H](CO)[C@H](O)[C@H]1O[Si](C)(C)C)[Si](C)(C)C4221.0Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,3TMS,isomer #27CC(=O)N[C@H]1C(OP(=O)(O)OP(=O)(OC[C@@H]2O[C@H](N3C=CC(=O)N([Si](C)(C)C)C3=O)[C@@H](O)[C@H]2O)O[Si](C)(C)C)O[C@@H](CO)[C@H](O)[C@H]1O[Si](C)(C)C4342.7Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,3TMS,isomer #28CC(=O)N([C@H]1C(OP(=O)(O)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)N([Si](C)(C)C)C3=O)[C@@H](O)[C@H]2O)O[C@@H](CO)[C@H](O)[C@H]1O[Si](C)(C)C)[Si](C)(C)C4331.7Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,3TMS,isomer #29CC(=O)N[C@H]1C(OP(=O)(O)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)O[C@@H](CO)[C@H](O[Si](C)(C)C)[C@H]1O4174.2Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,3TMS,isomer #3CC(=O)N[C@H]1C(OP(=O)(O)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O[Si](C)(C)C)[C@H]2O)O[C@@H](CO)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C4166.3Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,3TMS,isomer #30CC(=O)N[C@H]1C(OP(=O)(O)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O[Si](C)(C)C)[C@H]2O)O[C@@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O4154.5Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,3TMS,isomer #31CC(=O)N[C@H]1C(OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O[Si](C)(C)C)[C@H]2O)O[C@@H](CO)[C@H](O[Si](C)(C)C)[C@H]1O4210.3Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,3TMS,isomer #32CC(=O)N[C@H]1C(OP(=O)(O)OP(=O)(OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O[Si](C)(C)C)[C@H]2O)O[Si](C)(C)C)O[C@@H](CO)[C@H](O[Si](C)(C)C)[C@H]1O4204.3Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,3TMS,isomer #33CC(=O)N([C@H]1C(OP(=O)(O)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O[Si](C)(C)C)[C@H]2O)O[C@@H](CO)[C@H](O[Si](C)(C)C)[C@H]1O)[Si](C)(C)C4165.1Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,3TMS,isomer #34CC(=O)N[C@H]1C(OP(=O)(O)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)N([Si](C)(C)C)C3=O)[C@@H](O[Si](C)(C)C)[C@H]2O)O[C@@H](CO)[C@H](O[Si](C)(C)C)[C@H]1O4290.5Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,3TMS,isomer #35CC(=O)N[C@H]1C(OP(=O)(O)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O)[C@H]2O[Si](C)(C)C)O[C@@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O4162.5Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,3TMS,isomer #36CC(=O)N[C@H]1C(OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O)[C@H]2O[Si](C)(C)C)O[C@@H](CO)[C@H](O[Si](C)(C)C)[C@H]1O4218.3Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,3TMS,isomer #37CC(=O)N[C@H]1C(OP(=O)(O)OP(=O)(OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O)[C@H]2O[Si](C)(C)C)O[Si](C)(C)C)O[C@@H](CO)[C@H](O[Si](C)(C)C)[C@H]1O4212.3Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,3TMS,isomer #38CC(=O)N([C@H]1C(OP(=O)(O)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O)[C@H]2O[Si](C)(C)C)O[C@@H](CO)[C@H](O[Si](C)(C)C)[C@H]1O)[Si](C)(C)C4169.7Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,3TMS,isomer #39CC(=O)N[C@H]1C(OP(=O)(O)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)N([Si](C)(C)C)C3=O)[C@@H](O)[C@H]2O[Si](C)(C)C)O[C@@H](CO)[C@H](O[Si](C)(C)C)[C@H]1O4301.0Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,3TMS,isomer #4CC(=O)N[C@H]1C(OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O[Si](C)(C)C)[C@H]2O)O[C@@H](CO)[C@H](O)[C@H]1O[Si](C)(C)C4205.7Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,3TMS,isomer #40CC(=O)N[C@H]1C(OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O)[C@H]2O)O[C@@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O4216.1Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,3TMS,isomer #41CC(=O)N[C@H]1C(OP(=O)(O)OP(=O)(OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O)[C@H]2O)O[Si](C)(C)C)O[C@@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O4210.6Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,3TMS,isomer #42CC(=O)N([C@H]1C(OP(=O)(O)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O)[C@H]2O)O[C@@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O)[Si](C)(C)C4200.6Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,3TMS,isomer #43CC(=O)N[C@H]1C(OP(=O)(O)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)N([Si](C)(C)C)C3=O)[C@@H](O)[C@H]2O)O[C@@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O4310.9Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,3TMS,isomer #44CC(=O)N[C@H]1C(OP(=O)(O[Si](C)(C)C)OP(=O)(OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O)[C@H]2O)O[Si](C)(C)C)O[C@@H](CO)[C@H](O[Si](C)(C)C)[C@H]1O4261.1Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,3TMS,isomer #45CC(=O)N([C@H]1C(OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O)[C@H]2O)O[C@@H](CO)[C@H](O[Si](C)(C)C)[C@H]1O)[Si](C)(C)C4222.3Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,3TMS,isomer #46CC(=O)N[C@H]1C(OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)N([Si](C)(C)C)C3=O)[C@@H](O)[C@H]2O)O[C@@H](CO)[C@H](O[Si](C)(C)C)[C@H]1O4353.7Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,3TMS,isomer #47CC(=O)N([C@H]1C(OP(=O)(O)OP(=O)(OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O)[C@H]2O)O[Si](C)(C)C)O[C@@H](CO)[C@H](O[Si](C)(C)C)[C@H]1O)[Si](C)(C)C4224.9Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,3TMS,isomer #48CC(=O)N[C@H]1C(OP(=O)(O)OP(=O)(OC[C@@H]2O[C@H](N3C=CC(=O)N([Si](C)(C)C)C3=O)[C@@H](O)[C@H]2O)O[Si](C)(C)C)O[C@@H](CO)[C@H](O[Si](C)(C)C)[C@H]1O4351.6Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,3TMS,isomer #49CC(=O)N([C@H]1C(OP(=O)(O)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)N([Si](C)(C)C)C3=O)[C@@H](O)[C@H]2O)O[C@@H](CO)[C@H](O[Si](C)(C)C)[C@H]1O)[Si](C)(C)C4340.4Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,3TMS,isomer #5CC(=O)N[C@H]1C(OP(=O)(O)OP(=O)(OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O[Si](C)(C)C)[C@H]2O)O[Si](C)(C)C)O[C@@H](CO)[C@H](O)[C@H]1O[Si](C)(C)C4200.9Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,3TMS,isomer #50CC(=O)N[C@H]1C(OP(=O)(O)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)O[C@@H](CO[Si](C)(C)C)[C@H](O)[C@H]1O4141.5Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,3TMS,isomer #51CC(=O)N[C@H]1C(OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O[Si](C)(C)C)[C@H]2O)O[C@@H](CO[Si](C)(C)C)[C@H](O)[C@H]1O4176.8Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,3TMS,isomer #52CC(=O)N[C@H]1C(OP(=O)(O)OP(=O)(OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O[Si](C)(C)C)[C@H]2O)O[Si](C)(C)C)O[C@@H](CO[Si](C)(C)C)[C@H](O)[C@H]1O4169.3Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,3TMS,isomer #53CC(=O)N([C@H]1C(OP(=O)(O)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O[Si](C)(C)C)[C@H]2O)O[C@@H](CO[Si](C)(C)C)[C@H](O)[C@H]1O)[Si](C)(C)C4165.4Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,3TMS,isomer #54CC(=O)N[C@H]1C(OP(=O)(O)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)N([Si](C)(C)C)C3=O)[C@@H](O[Si](C)(C)C)[C@H]2O)O[C@@H](CO[Si](C)(C)C)[C@H](O)[C@H]1O4266.1Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,3TMS,isomer #55CC(=O)N[C@H]1C(OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O)[C@H]2O[Si](C)(C)C)O[C@@H](CO[Si](C)(C)C)[C@H](O)[C@H]1O4184.2Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,3TMS,isomer #56CC(=O)N[C@H]1C(OP(=O)(O)OP(=O)(OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O)[C@H]2O[Si](C)(C)C)O[Si](C)(C)C)O[C@@H](CO[Si](C)(C)C)[C@H](O)[C@H]1O4176.4Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,3TMS,isomer #57CC(=O)N([C@H]1C(OP(=O)(O)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O)[C@H]2O[Si](C)(C)C)O[C@@H](CO[Si](C)(C)C)[C@H](O)[C@H]1O)[Si](C)(C)C4172.0Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,3TMS,isomer #58CC(=O)N[C@H]1C(OP(=O)(O)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)N([Si](C)(C)C)C3=O)[C@@H](O)[C@H]2O[Si](C)(C)C)O[C@@H](CO[Si](C)(C)C)[C@H](O)[C@H]1O4275.3Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,3TMS,isomer #59CC(=O)N[C@H]1C(OP(=O)(O[Si](C)(C)C)OP(=O)(OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O)[C@H]2O)O[Si](C)(C)C)O[C@@H](CO[Si](C)(C)C)[C@H](O)[C@H]1O4228.5Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,3TMS,isomer #6CC(=O)N([C@H]1C(OP(=O)(O)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O[Si](C)(C)C)[C@H]2O)O[C@@H](CO)[C@H](O)[C@H]1O[Si](C)(C)C)[Si](C)(C)C4161.8Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,3TMS,isomer #60CC(=O)N([C@H]1C(OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O)[C@H]2O)O[C@@H](CO[Si](C)(C)C)[C@H](O)[C@H]1O)[Si](C)(C)C4221.0Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,3TMS,isomer #61CC(=O)N[C@H]1C(OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)N([Si](C)(C)C)C3=O)[C@@H](O)[C@H]2O)O[C@@H](CO[Si](C)(C)C)[C@H](O)[C@H]1O4334.0Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,3TMS,isomer #62CC(=O)N([C@H]1C(OP(=O)(O)OP(=O)(OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O)[C@H]2O)O[Si](C)(C)C)O[C@@H](CO[Si](C)(C)C)[C@H](O)[C@H]1O)[Si](C)(C)C4221.4Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,3TMS,isomer #63CC(=O)N[C@H]1C(OP(=O)(O)OP(=O)(OC[C@@H]2O[C@H](N3C=CC(=O)N([Si](C)(C)C)C3=O)[C@@H](O)[C@H]2O)O[Si](C)(C)C)O[C@@H](CO[Si](C)(C)C)[C@H](O)[C@H]1O4328.3Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,3TMS,isomer #64CC(=O)N([C@H]1C(OP(=O)(O)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)N([Si](C)(C)C)C3=O)[C@@H](O)[C@H]2O)O[C@@H](CO[Si](C)(C)C)[C@H](O)[C@H]1O)[Si](C)(C)C4337.5Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,3TMS,isomer #65CC(=O)N[C@H]1C(OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)O[C@@H](CO)[C@H](O)[C@H]1O4209.1Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,3TMS,isomer #66CC(=O)N[C@H]1C(OP(=O)(O)OP(=O)(OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)O[Si](C)(C)C)O[C@@H](CO)[C@H](O)[C@H]1O4201.5Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,3TMS,isomer #67CC(=O)N([C@H]1C(OP(=O)(O)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)O[C@@H](CO)[C@H](O)[C@H]1O)[Si](C)(C)C4189.7Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,3TMS,isomer #68CC(=O)N[C@H]1C(OP(=O)(O)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)N([Si](C)(C)C)C3=O)[C@@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)O[C@@H](CO)[C@H](O)[C@H]1O4301.0Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,3TMS,isomer #69CC(=O)N[C@H]1C(OP(=O)(O[Si](C)(C)C)OP(=O)(OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O[Si](C)(C)C)[C@H]2O)O[Si](C)(C)C)O[C@@H](CO)[C@H](O)[C@H]1O4243.3Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,3TMS,isomer #7CC(=O)N[C@H]1C(OP(=O)(O)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)N([Si](C)(C)C)C3=O)[C@@H](O[Si](C)(C)C)[C@H]2O)O[C@@H](CO)[C@H](O)[C@H]1O[Si](C)(C)C4276.2Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,3TMS,isomer #70CC(=O)N([C@H]1C(OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O[Si](C)(C)C)[C@H]2O)O[C@@H](CO)[C@H](O)[C@H]1O)[Si](C)(C)C4205.5Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,3TMS,isomer #71CC(=O)N[C@H]1C(OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)N([Si](C)(C)C)C3=O)[C@@H](O[Si](C)(C)C)[C@H]2O)O[C@@H](CO)[C@H](O)[C@H]1O4328.2Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,3TMS,isomer #72CC(=O)N([C@H]1C(OP(=O)(O)OP(=O)(OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O[Si](C)(C)C)[C@H]2O)O[Si](C)(C)C)O[C@@H](CO)[C@H](O)[C@H]1O)[Si](C)(C)C4208.5Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,3TMS,isomer #73CC(=O)N[C@H]1C(OP(=O)(O)OP(=O)(OC[C@@H]2O[C@H](N3C=CC(=O)N([Si](C)(C)C)C3=O)[C@@H](O[Si](C)(C)C)[C@H]2O)O[Si](C)(C)C)O[C@@H](CO)[C@H](O)[C@H]1O4328.2Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,3TMS,isomer #74CC(=O)N([C@H]1C(OP(=O)(O)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)N([Si](C)(C)C)C3=O)[C@@H](O[Si](C)(C)C)[C@H]2O)O[C@@H](CO)[C@H](O)[C@H]1O)[Si](C)(C)C4316.6Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,3TMS,isomer #75CC(=O)N[C@H]1C(OP(=O)(O[Si](C)(C)C)OP(=O)(OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O)[C@H]2O[Si](C)(C)C)O[Si](C)(C)C)O[C@@H](CO)[C@H](O)[C@H]1O4251.3Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,3TMS,isomer #76CC(=O)N([C@H]1C(OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O)[C@H]2O[Si](C)(C)C)O[C@@H](CO)[C@H](O)[C@H]1O)[Si](C)(C)C4211.5Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,3TMS,isomer #77CC(=O)N[C@H]1C(OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)N([Si](C)(C)C)C3=O)[C@@H](O)[C@H]2O[Si](C)(C)C)O[C@@H](CO)[C@H](O)[C@H]1O4336.8Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,3TMS,isomer #78CC(=O)N([C@H]1C(OP(=O)(O)OP(=O)(OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O)[C@H]2O[Si](C)(C)C)O[Si](C)(C)C)O[C@@H](CO)[C@H](O)[C@H]1O)[Si](C)(C)C4215.0Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,3TMS,isomer #79CC(=O)N[C@H]1C(OP(=O)(O)OP(=O)(OC[C@@H]2O[C@H](N3C=CC(=O)N([Si](C)(C)C)C3=O)[C@@H](O)[C@H]2O[Si](C)(C)C)O[Si](C)(C)C)O[C@@H](CO)[C@H](O)[C@H]1O4337.2Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,3TMS,isomer #8CC(=O)N[C@H]1C(OP(=O)(O)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O)[C@H]2O[Si](C)(C)C)O[C@@H](CO[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C4157.3Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,3TMS,isomer #80CC(=O)N([C@H]1C(OP(=O)(O)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)N([Si](C)(C)C)C3=O)[C@@H](O)[C@H]2O[Si](C)(C)C)O[C@@H](CO)[C@H](O)[C@H]1O)[Si](C)(C)C4321.8Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,3TMS,isomer #81CC(=O)N([C@H]1C(OP(=O)(O[Si](C)(C)C)OP(=O)(OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O)[C@H]2O)O[Si](C)(C)C)O[C@@H](CO)[C@H](O)[C@H]1O)[Si](C)(C)C4258.2Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,3TMS,isomer #82CC(=O)N[C@H]1C(OP(=O)(O[Si](C)(C)C)OP(=O)(OC[C@@H]2O[C@H](N3C=CC(=O)N([Si](C)(C)C)C3=O)[C@@H](O)[C@H]2O)O[Si](C)(C)C)O[C@@H](CO)[C@H](O)[C@H]1O4390.0Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,3TMS,isomer #83CC(=O)N([C@H]1C(OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)N([Si](C)(C)C)C3=O)[C@@H](O)[C@H]2O)O[C@@H](CO)[C@H](O)[C@H]1O)[Si](C)(C)C4377.4Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,3TMS,isomer #84CC(=O)N([C@H]1C(OP(=O)(O)OP(=O)(OC[C@@H]2O[C@H](N3C=CC(=O)N([Si](C)(C)C)C3=O)[C@@H](O)[C@H]2O)O[Si](C)(C)C)O[C@@H](CO)[C@H](O)[C@H]1O)[Si](C)(C)C4378.8Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,3TMS,isomer #9CC(=O)N[C@H]1C(OP(=O)(O)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O)[C@H]2O[Si](C)(C)C)O[C@@H](CO)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C4175.3Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,4TMS,isomer #1CC(=O)N[C@H]1C(OP(=O)(O)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)O[C@@H](CO[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C4116.7Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,4TMS,isomer #10CC(=O)N([C@H]1C(OP(=O)(O)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O[Si](C)(C)C)[C@H]2O)O[C@@H](CO[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C)[Si](C)(C)C4106.1Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,4TMS,isomer #100CC(=O)N[C@H]1C(OP(=O)(O)OP(=O)(OC[C@@H]2O[C@H](N3C=CC(=O)N([Si](C)(C)C)C3=O)[C@@H](O[Si](C)(C)C)[C@H]2O)O[Si](C)(C)C)O[C@@H](CO[Si](C)(C)C)[C@H](O)[C@H]1O4220.2Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,4TMS,isomer #101CC(=O)N([C@H]1C(OP(=O)(O)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)N([Si](C)(C)C)C3=O)[C@@H](O[Si](C)(C)C)[C@H]2O)O[C@@H](CO[Si](C)(C)C)[C@H](O)[C@H]1O)[Si](C)(C)C4222.9Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,4TMS,isomer #102CC(=O)N[C@H]1C(OP(=O)(O[Si](C)(C)C)OP(=O)(OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O)[C@H]2O[Si](C)(C)C)O[Si](C)(C)C)O[C@@H](CO[Si](C)(C)C)[C@H](O)[C@H]1O4152.8Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,4TMS,isomer #103CC(=O)N([C@H]1C(OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O)[C@H]2O[Si](C)(C)C)O[C@@H](CO[Si](C)(C)C)[C@H](O)[C@H]1O)[Si](C)(C)C4136.2Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,4TMS,isomer #104CC(=O)N[C@H]1C(OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)N([Si](C)(C)C)C3=O)[C@@H](O)[C@H]2O[Si](C)(C)C)O[C@@H](CO[Si](C)(C)C)[C@H](O)[C@H]1O4231.6Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,4TMS,isomer #105CC(=O)N([C@H]1C(OP(=O)(O)OP(=O)(OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O)[C@H]2O[Si](C)(C)C)O[Si](C)(C)C)O[C@@H](CO[Si](C)(C)C)[C@H](O)[C@H]1O)[Si](C)(C)C4135.8Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,4TMS,isomer #106CC(=O)N[C@H]1C(OP(=O)(O)OP(=O)(OC[C@@H]2O[C@H](N3C=CC(=O)N([Si](C)(C)C)C3=O)[C@@H](O)[C@H]2O[Si](C)(C)C)O[Si](C)(C)C)O[C@@H](CO[Si](C)(C)C)[C@H](O)[C@H]1O4230.6Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,4TMS,isomer #107CC(=O)N([C@H]1C(OP(=O)(O)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)N([Si](C)(C)C)C3=O)[C@@H](O)[C@H]2O[Si](C)(C)C)O[C@@H](CO[Si](C)(C)C)[C@H](O)[C@H]1O)[Si](C)(C)C4233.3Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,4TMS,isomer #108CC(=O)N([C@H]1C(OP(=O)(O[Si](C)(C)C)OP(=O)(OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O)[C@H]2O)O[Si](C)(C)C)O[C@@H](CO[Si](C)(C)C)[C@H](O)[C@H]1O)[Si](C)(C)C4154.0Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,4TMS,isomer #109CC(=O)N[C@H]1C(OP(=O)(O[Si](C)(C)C)OP(=O)(OC[C@@H]2O[C@H](N3C=CC(=O)N([Si](C)(C)C)C3=O)[C@@H](O)[C@H]2O)O[Si](C)(C)C)O[C@@H](CO[Si](C)(C)C)[C@H](O)[C@H]1O4265.5Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,4TMS,isomer #11CC(=O)N[C@H]1C(OP(=O)(O)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)N([Si](C)(C)C)C3=O)[C@@H](O[Si](C)(C)C)[C@H]2O)O[C@@H](CO[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C4218.0Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,4TMS,isomer #110CC(=O)N([C@H]1C(OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)N([Si](C)(C)C)C3=O)[C@@H](O)[C@H]2O)O[C@@H](CO[Si](C)(C)C)[C@H](O)[C@H]1O)[Si](C)(C)C4265.3Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,4TMS,isomer #111CC(=O)N([C@H]1C(OP(=O)(O)OP(=O)(OC[C@@H]2O[C@H](N3C=CC(=O)N([Si](C)(C)C)C3=O)[C@@H](O)[C@H]2O)O[Si](C)(C)C)O[C@@H](CO[Si](C)(C)C)[C@H](O)[C@H]1O)[Si](C)(C)C4267.4Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,4TMS,isomer #112CC(=O)N[C@H]1C(OP(=O)(O[Si](C)(C)C)OP(=O)(OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)O[Si](C)(C)C)O[C@@H](CO)[C@H](O)[C@H]1O4168.7Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,4TMS,isomer #113CC(=O)N([C@H]1C(OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)O[C@@H](CO)[C@H](O)[C@H]1O)[Si](C)(C)C4146.4Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,4TMS,isomer #114CC(=O)N[C@H]1C(OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)N([Si](C)(C)C)C3=O)[C@@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)O[C@@H](CO)[C@H](O)[C@H]1O4254.3Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,4TMS,isomer #115CC(=O)N([C@H]1C(OP(=O)(O)OP(=O)(OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)O[Si](C)(C)C)O[C@@H](CO)[C@H](O)[C@H]1O)[Si](C)(C)C4144.8Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,4TMS,isomer #116CC(=O)N[C@H]1C(OP(=O)(O)OP(=O)(OC[C@@H]2O[C@H](N3C=CC(=O)N([Si](C)(C)C)C3=O)[C@@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)O[Si](C)(C)C)O[C@@H](CO)[C@H](O)[C@H]1O4251.6Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,4TMS,isomer #117CC(=O)N([C@H]1C(OP(=O)(O)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)N([Si](C)(C)C)C3=O)[C@@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)O[C@@H](CO)[C@H](O)[C@H]1O)[Si](C)(C)C4242.9Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,4TMS,isomer #118CC(=O)N([C@H]1C(OP(=O)(O[Si](C)(C)C)OP(=O)(OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O[Si](C)(C)C)[C@H]2O)O[Si](C)(C)C)O[C@@H](CO)[C@H](O)[C@H]1O)[Si](C)(C)C4155.7Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,4TMS,isomer #119CC(=O)N[C@H]1C(OP(=O)(O[Si](C)(C)C)OP(=O)(OC[C@@H]2O[C@H](N3C=CC(=O)N([Si](C)(C)C)C3=O)[C@@H](O[Si](C)(C)C)[C@H]2O)O[Si](C)(C)C)O[C@@H](CO)[C@H](O)[C@H]1O4271.5Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,4TMS,isomer #12CC(=O)N[C@H]1C(OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O[Si](C)(C)C)[C@H]2O)O[C@@H](CO)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C4163.5Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,4TMS,isomer #120CC(=O)N([C@H]1C(OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)N([Si](C)(C)C)C3=O)[C@@H](O[Si](C)(C)C)[C@H]2O)O[C@@H](CO)[C@H](O)[C@H]1O)[Si](C)(C)C4252.0Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,4TMS,isomer #121CC(=O)N([C@H]1C(OP(=O)(O)OP(=O)(OC[C@@H]2O[C@H](N3C=CC(=O)N([Si](C)(C)C)C3=O)[C@@H](O[Si](C)(C)C)[C@H]2O)O[Si](C)(C)C)O[C@@H](CO)[C@H](O)[C@H]1O)[Si](C)(C)C4253.9Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,4TMS,isomer #122CC(=O)N([C@H]1C(OP(=O)(O[Si](C)(C)C)OP(=O)(OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O)[C@H]2O[Si](C)(C)C)O[Si](C)(C)C)O[C@@H](CO)[C@H](O)[C@H]1O)[Si](C)(C)C4171.0Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,4TMS,isomer #123CC(=O)N[C@H]1C(OP(=O)(O[Si](C)(C)C)OP(=O)(OC[C@@H]2O[C@H](N3C=CC(=O)N([Si](C)(C)C)C3=O)[C@@H](O)[C@H]2O[Si](C)(C)C)O[Si](C)(C)C)O[C@@H](CO)[C@H](O)[C@H]1O4280.5Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,4TMS,isomer #124CC(=O)N([C@H]1C(OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)N([Si](C)(C)C)C3=O)[C@@H](O)[C@H]2O[Si](C)(C)C)O[C@@H](CO)[C@H](O)[C@H]1O)[Si](C)(C)C4261.8Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,4TMS,isomer #125CC(=O)N([C@H]1C(OP(=O)(O)OP(=O)(OC[C@@H]2O[C@H](N3C=CC(=O)N([Si](C)(C)C)C3=O)[C@@H](O)[C@H]2O[Si](C)(C)C)O[Si](C)(C)C)O[C@@H](CO)[C@H](O)[C@H]1O)[Si](C)(C)C4264.6Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,4TMS,isomer #126CC(=O)N([C@H]1C(OP(=O)(O[Si](C)(C)C)OP(=O)(OC[C@@H]2O[C@H](N3C=CC(=O)N([Si](C)(C)C)C3=O)[C@@H](O)[C@H]2O)O[Si](C)(C)C)O[C@@H](CO)[C@H](O)[C@H]1O)[Si](C)(C)C4293.4Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,4TMS,isomer #13CC(=O)N[C@H]1C(OP(=O)(O)OP(=O)(OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O[Si](C)(C)C)[C@H]2O)O[Si](C)(C)C)O[C@@H](CO)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C4153.3Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,4TMS,isomer #14CC(=O)N([C@H]1C(OP(=O)(O)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O[Si](C)(C)C)[C@H]2O)O[C@@H](CO)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C)[Si](C)(C)C4126.6Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,4TMS,isomer #15CC(=O)N[C@H]1C(OP(=O)(O)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)N([Si](C)(C)C)C3=O)[C@@H](O[Si](C)(C)C)[C@H]2O)O[C@@H](CO)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C4235.4Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,4TMS,isomer #16CC(=O)N[C@H]1C(OP(=O)(O[Si](C)(C)C)OP(=O)(OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O[Si](C)(C)C)[C@H]2O)O[Si](C)(C)C)O[C@@H](CO)[C@H](O)[C@H]1O[Si](C)(C)C4200.8Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,4TMS,isomer #17CC(=O)N([C@H]1C(OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O[Si](C)(C)C)[C@H]2O)O[C@@H](CO)[C@H](O)[C@H]1O[Si](C)(C)C)[Si](C)(C)C4149.2Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,4TMS,isomer #18CC(=O)N[C@H]1C(OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)N([Si](C)(C)C)C3=O)[C@@H](O[Si](C)(C)C)[C@H]2O)O[C@@H](CO)[C@H](O)[C@H]1O[Si](C)(C)C4261.5Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,4TMS,isomer #19CC(=O)N([C@H]1C(OP(=O)(O)OP(=O)(OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O[Si](C)(C)C)[C@H]2O)O[Si](C)(C)C)O[C@@H](CO)[C@H](O)[C@H]1O[Si](C)(C)C)[Si](C)(C)C4143.1Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,4TMS,isomer #2CC(=O)N[C@H]1C(OP(=O)(O)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)O[C@@H](CO)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C4123.8Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,4TMS,isomer #20CC(=O)N[C@H]1C(OP(=O)(O)OP(=O)(OC[C@@H]2O[C@H](N3C=CC(=O)N([Si](C)(C)C)C3=O)[C@@H](O[Si](C)(C)C)[C@H]2O)O[Si](C)(C)C)O[C@@H](CO)[C@H](O)[C@H]1O[Si](C)(C)C4260.4Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,4TMS,isomer #21CC(=O)N([C@H]1C(OP(=O)(O)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)N([Si](C)(C)C)C3=O)[C@@H](O[Si](C)(C)C)[C@H]2O)O[C@@H](CO)[C@H](O)[C@H]1O[Si](C)(C)C)[Si](C)(C)C4229.7Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,4TMS,isomer #22CC(=O)N[C@H]1C(OP(=O)(O)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O)[C@H]2O[Si](C)(C)C)O[C@@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C4128.0Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,4TMS,isomer #23CC(=O)N[C@H]1C(OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O)[C@H]2O[Si](C)(C)C)O[C@@H](CO[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C4164.2Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,4TMS,isomer #24CC(=O)N[C@H]1C(OP(=O)(O)OP(=O)(OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O)[C@H]2O[Si](C)(C)C)O[Si](C)(C)C)O[C@@H](CO[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C4155.3Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,4TMS,isomer #25CC(=O)N([C@H]1C(OP(=O)(O)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O)[C@H]2O[Si](C)(C)C)O[C@@H](CO[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C)[Si](C)(C)C4115.0Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,4TMS,isomer #26CC(=O)N[C@H]1C(OP(=O)(O)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)N([Si](C)(C)C)C3=O)[C@@H](O)[C@H]2O[Si](C)(C)C)O[C@@H](CO[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C4229.7Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,4TMS,isomer #27CC(=O)N[C@H]1C(OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O)[C@H]2O[Si](C)(C)C)O[C@@H](CO)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C4170.4Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,4TMS,isomer #28CC(=O)N[C@H]1C(OP(=O)(O)OP(=O)(OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O)[C@H]2O[Si](C)(C)C)O[Si](C)(C)C)O[C@@H](CO)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C4160.8Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,4TMS,isomer #29CC(=O)N([C@H]1C(OP(=O)(O)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O)[C@H]2O[Si](C)(C)C)O[C@@H](CO)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C)[Si](C)(C)C4133.3Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,4TMS,isomer #3CC(=O)N[C@H]1C(OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)O[C@@H](CO)[C@H](O)[C@H]1O[Si](C)(C)C4169.2Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,4TMS,isomer #30CC(=O)N[C@H]1C(OP(=O)(O)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)N([Si](C)(C)C)C3=O)[C@@H](O)[C@H]2O[Si](C)(C)C)O[C@@H](CO)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C4246.8Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,4TMS,isomer #31CC(=O)N[C@H]1C(OP(=O)(O[Si](C)(C)C)OP(=O)(OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O)[C@H]2O[Si](C)(C)C)O[Si](C)(C)C)O[C@@H](CO)[C@H](O)[C@H]1O[Si](C)(C)C4209.6Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,4TMS,isomer #32CC(=O)N([C@H]1C(OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O)[C@H]2O[Si](C)(C)C)O[C@@H](CO)[C@H](O)[C@H]1O[Si](C)(C)C)[Si](C)(C)C4161.3Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,4TMS,isomer #33CC(=O)N[C@H]1C(OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)N([Si](C)(C)C)C3=O)[C@@H](O)[C@H]2O[Si](C)(C)C)O[C@@H](CO)[C@H](O)[C@H]1O[Si](C)(C)C4272.3Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,4TMS,isomer #34CC(=O)N([C@H]1C(OP(=O)(O)OP(=O)(OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O)[C@H]2O[Si](C)(C)C)O[Si](C)(C)C)O[C@@H](CO)[C@H](O)[C@H]1O[Si](C)(C)C)[Si](C)(C)C4157.0Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,4TMS,isomer #35CC(=O)N[C@H]1C(OP(=O)(O)OP(=O)(OC[C@@H]2O[C@H](N3C=CC(=O)N([Si](C)(C)C)C3=O)[C@@H](O)[C@H]2O[Si](C)(C)C)O[Si](C)(C)C)O[C@@H](CO)[C@H](O)[C@H]1O[Si](C)(C)C4272.5Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,4TMS,isomer #36CC(=O)N([C@H]1C(OP(=O)(O)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)N([Si](C)(C)C)C3=O)[C@@H](O)[C@H]2O[Si](C)(C)C)O[C@@H](CO)[C@H](O)[C@H]1O[Si](C)(C)C)[Si](C)(C)C4241.4Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,4TMS,isomer #37CC(=O)N[C@H]1C(OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O)[C@H]2O)O[C@@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C4163.2Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,4TMS,isomer #38CC(=O)N[C@H]1C(OP(=O)(O)OP(=O)(OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O)[C@H]2O)O[Si](C)(C)C)O[C@@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C4152.3Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,4TMS,isomer #39CC(=O)N([C@H]1C(OP(=O)(O)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O)[C@H]2O)O[C@@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C)[Si](C)(C)C4148.1Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,4TMS,isomer #4CC(=O)N[C@H]1C(OP(=O)(O)OP(=O)(OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)O[Si](C)(C)C)O[C@@H](CO)[C@H](O)[C@H]1O[Si](C)(C)C4160.8Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,4TMS,isomer #40CC(=O)N[C@H]1C(OP(=O)(O)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)N([Si](C)(C)C)C3=O)[C@@H](O)[C@H]2O)O[C@@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C4251.8Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,4TMS,isomer #41CC(=O)N[C@H]1C(OP(=O)(O[Si](C)(C)C)OP(=O)(OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O)[C@H]2O)O[Si](C)(C)C)O[C@@H](CO[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C4176.6Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,4TMS,isomer #42CC(=O)N([C@H]1C(OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O)[C@H]2O)O[C@@H](CO[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C)[Si](C)(C)C4151.0Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,4TMS,isomer #43CC(=O)N[C@H]1C(OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)N([Si](C)(C)C)C3=O)[C@@H](O)[C@H]2O)O[C@@H](CO[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C4259.5Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,4TMS,isomer #44CC(=O)N([C@H]1C(OP(=O)(O)OP(=O)(OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O)[C@H]2O)O[Si](C)(C)C)O[C@@H](CO[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C)[Si](C)(C)C4145.1Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,4TMS,isomer #45CC(=O)N[C@H]1C(OP(=O)(O)OP(=O)(OC[C@@H]2O[C@H](N3C=CC(=O)N([Si](C)(C)C)C3=O)[C@@H](O)[C@H]2O)O[Si](C)(C)C)O[C@@H](CO[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C4258.3Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,4TMS,isomer #46CC(=O)N([C@H]1C(OP(=O)(O)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)N([Si](C)(C)C)C3=O)[C@@H](O)[C@H]2O)O[C@@H](CO[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C)[Si](C)(C)C4247.6Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,4TMS,isomer #47CC(=O)N[C@H]1C(OP(=O)(O[Si](C)(C)C)OP(=O)(OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O)[C@H]2O)O[Si](C)(C)C)O[C@@H](CO)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C4185.6Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,4TMS,isomer #48CC(=O)N([C@H]1C(OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O)[C@H]2O)O[C@@H](CO)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C)[Si](C)(C)C4175.4Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,4TMS,isomer #49CC(=O)N[C@H]1C(OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)N([Si](C)(C)C)C3=O)[C@@H](O)[C@H]2O)O[C@@H](CO)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C4275.6Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,4TMS,isomer #5CC(=O)N([C@H]1C(OP(=O)(O)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)O[C@@H](CO)[C@H](O)[C@H]1O[Si](C)(C)C)[Si](C)(C)C4121.0Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,4TMS,isomer #50CC(=O)N([C@H]1C(OP(=O)(O)OP(=O)(OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O)[C@H]2O)O[Si](C)(C)C)O[C@@H](CO)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C)[Si](C)(C)C4166.9Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,4TMS,isomer #51CC(=O)N[C@H]1C(OP(=O)(O)OP(=O)(OC[C@@H]2O[C@H](N3C=CC(=O)N([Si](C)(C)C)C3=O)[C@@H](O)[C@H]2O)O[Si](C)(C)C)O[C@@H](CO)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C4274.0Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,4TMS,isomer #52CC(=O)N([C@H]1C(OP(=O)(O)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)N([Si](C)(C)C)C3=O)[C@@H](O)[C@H]2O)O[C@@H](CO)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C)[Si](C)(C)C4268.7Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,4TMS,isomer #53CC(=O)N([C@H]1C(OP(=O)(O[Si](C)(C)C)OP(=O)(OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O)[C@H]2O)O[Si](C)(C)C)O[C@@H](CO)[C@H](O)[C@H]1O[Si](C)(C)C)[Si](C)(C)C4192.1Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,4TMS,isomer #54CC(=O)N[C@H]1C(OP(=O)(O[Si](C)(C)C)OP(=O)(OC[C@@H]2O[C@H](N3C=CC(=O)N([Si](C)(C)C)C3=O)[C@@H](O)[C@H]2O)O[Si](C)(C)C)O[C@@H](CO)[C@H](O)[C@H]1O[Si](C)(C)C4300.2Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,4TMS,isomer #55CC(=O)N([C@H]1C(OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)N([Si](C)(C)C)C3=O)[C@@H](O)[C@H]2O)O[C@@H](CO)[C@H](O)[C@H]1O[Si](C)(C)C)[Si](C)(C)C4280.9Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,4TMS,isomer #56CC(=O)N([C@H]1C(OP(=O)(O)OP(=O)(OC[C@@H]2O[C@H](N3C=CC(=O)N([Si](C)(C)C)C3=O)[C@@H](O)[C@H]2O)O[Si](C)(C)C)O[C@@H](CO)[C@H](O)[C@H]1O[Si](C)(C)C)[Si](C)(C)C4280.2Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,4TMS,isomer #57CC(=O)N[C@H]1C(OP(=O)(O)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)O[C@@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O4108.6Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,4TMS,isomer #58CC(=O)N[C@H]1C(OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)O[C@@H](CO)[C@H](O[Si](C)(C)C)[C@H]1O4156.7Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,4TMS,isomer #59CC(=O)N[C@H]1C(OP(=O)(O)OP(=O)(OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)O[Si](C)(C)C)O[C@@H](CO)[C@H](O[Si](C)(C)C)[C@H]1O4148.2Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,4TMS,isomer #6CC(=O)N[C@H]1C(OP(=O)(O)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)N([Si](C)(C)C)C3=O)[C@@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)O[C@@H](CO)[C@H](O)[C@H]1O[Si](C)(C)C4244.2Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,4TMS,isomer #60CC(=O)N([C@H]1C(OP(=O)(O)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)O[C@@H](CO)[C@H](O[Si](C)(C)C)[C@H]1O)[Si](C)(C)C4120.7Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,4TMS,isomer #61CC(=O)N[C@H]1C(OP(=O)(O)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)N([Si](C)(C)C)C3=O)[C@@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)O[C@@H](CO)[C@H](O[Si](C)(C)C)[C@H]1O4242.3Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,4TMS,isomer #62CC(=O)N[C@H]1C(OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O[Si](C)(C)C)[C@H]2O)O[C@@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O4150.5Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,4TMS,isomer #63CC(=O)N[C@H]1C(OP(=O)(O)OP(=O)(OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O[Si](C)(C)C)[C@H]2O)O[Si](C)(C)C)O[C@@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O4137.9Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,4TMS,isomer #64CC(=O)N([C@H]1C(OP(=O)(O)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O[Si](C)(C)C)[C@H]2O)O[C@@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O)[Si](C)(C)C4112.2Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,4TMS,isomer #65CC(=O)N[C@H]1C(OP(=O)(O)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)N([Si](C)(C)C)C3=O)[C@@H](O[Si](C)(C)C)[C@H]2O)O[C@@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O4216.9Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,4TMS,isomer #66CC(=O)N[C@H]1C(OP(=O)(O[Si](C)(C)C)OP(=O)(OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O[Si](C)(C)C)[C@H]2O)O[Si](C)(C)C)O[C@@H](CO)[C@H](O[Si](C)(C)C)[C@H]1O4187.9Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,4TMS,isomer #67CC(=O)N([C@H]1C(OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O[Si](C)(C)C)[C@H]2O)O[C@@H](CO)[C@H](O[Si](C)(C)C)[C@H]1O)[Si](C)(C)C4144.2Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,4TMS,isomer #68CC(=O)N[C@H]1C(OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)N([Si](C)(C)C)C3=O)[C@@H](O[Si](C)(C)C)[C@H]2O)O[C@@H](CO)[C@H](O[Si](C)(C)C)[C@H]1O4256.8Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,4TMS,isomer #69CC(=O)N([C@H]1C(OP(=O)(O)OP(=O)(OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O[Si](C)(C)C)[C@H]2O)O[Si](C)(C)C)O[C@@H](CO)[C@H](O[Si](C)(C)C)[C@H]1O)[Si](C)(C)C4142.4Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,4TMS,isomer #7CC(=O)N[C@H]1C(OP(=O)(O)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O[Si](C)(C)C)[C@H]2O)O[C@@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C4124.1Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,4TMS,isomer #70CC(=O)N[C@H]1C(OP(=O)(O)OP(=O)(OC[C@@H]2O[C@H](N3C=CC(=O)N([Si](C)(C)C)C3=O)[C@@H](O[Si](C)(C)C)[C@H]2O)O[Si](C)(C)C)O[C@@H](CO)[C@H](O[Si](C)(C)C)[C@H]1O4257.3Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,4TMS,isomer #71CC(=O)N([C@H]1C(OP(=O)(O)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)N([Si](C)(C)C)C3=O)[C@@H](O[Si](C)(C)C)[C@H]2O)O[C@@H](CO)[C@H](O[Si](C)(C)C)[C@H]1O)[Si](C)(C)C4230.7Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,4TMS,isomer #72CC(=O)N[C@H]1C(OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O)[C@H]2O[Si](C)(C)C)O[C@@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O4156.3Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,4TMS,isomer #73CC(=O)N[C@H]1C(OP(=O)(O)OP(=O)(OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O)[C@H]2O[Si](C)(C)C)O[Si](C)(C)C)O[C@@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O4147.2Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,4TMS,isomer #74CC(=O)N([C@H]1C(OP(=O)(O)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O)[C@H]2O[Si](C)(C)C)O[C@@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O)[Si](C)(C)C4122.1Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,4TMS,isomer #75CC(=O)N[C@H]1C(OP(=O)(O)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)N([Si](C)(C)C)C3=O)[C@@H](O)[C@H]2O[Si](C)(C)C)O[C@@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O4227.6Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,4TMS,isomer #76CC(=O)N[C@H]1C(OP(=O)(O[Si](C)(C)C)OP(=O)(OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O)[C@H]2O[Si](C)(C)C)O[Si](C)(C)C)O[C@@H](CO)[C@H](O[Si](C)(C)C)[C@H]1O4198.6Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,4TMS,isomer #77CC(=O)N([C@H]1C(OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O)[C@H]2O[Si](C)(C)C)O[C@@H](CO)[C@H](O[Si](C)(C)C)[C@H]1O)[Si](C)(C)C4157.1Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,4TMS,isomer #78CC(=O)N[C@H]1C(OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)N([Si](C)(C)C)C3=O)[C@@H](O)[C@H]2O[Si](C)(C)C)O[C@@H](CO)[C@H](O[Si](C)(C)C)[C@H]1O4268.4Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,4TMS,isomer #79CC(=O)N([C@H]1C(OP(=O)(O)OP(=O)(OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O)[C@H]2O[Si](C)(C)C)O[Si](C)(C)C)O[C@@H](CO)[C@H](O[Si](C)(C)C)[C@H]1O)[Si](C)(C)C4155.7Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,4TMS,isomer #8CC(=O)N[C@H]1C(OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O[Si](C)(C)C)[C@H]2O)O[C@@H](CO[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C4158.9Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,4TMS,isomer #80CC(=O)N[C@H]1C(OP(=O)(O)OP(=O)(OC[C@@H]2O[C@H](N3C=CC(=O)N([Si](C)(C)C)C3=O)[C@@H](O)[C@H]2O[Si](C)(C)C)O[Si](C)(C)C)O[C@@H](CO)[C@H](O[Si](C)(C)C)[C@H]1O4269.2Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,4TMS,isomer #81CC(=O)N([C@H]1C(OP(=O)(O)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)N([Si](C)(C)C)C3=O)[C@@H](O)[C@H]2O[Si](C)(C)C)O[C@@H](CO)[C@H](O[Si](C)(C)C)[C@H]1O)[Si](C)(C)C4240.1Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,4TMS,isomer #82CC(=O)N[C@H]1C(OP(=O)(O[Si](C)(C)C)OP(=O)(OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O)[C@H]2O)O[Si](C)(C)C)O[C@@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O4175.6Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,4TMS,isomer #83CC(=O)N([C@H]1C(OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O)[C@H]2O)O[C@@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O)[Si](C)(C)C4156.4Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,4TMS,isomer #84CC(=O)N[C@H]1C(OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)N([Si](C)(C)C)C3=O)[C@@H](O)[C@H]2O)O[C@@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O4262.5Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,4TMS,isomer #85CC(=O)N([C@H]1C(OP(=O)(O)OP(=O)(OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O)[C@H]2O)O[Si](C)(C)C)O[C@@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O)[Si](C)(C)C4153.9Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,4TMS,isomer #86CC(=O)N[C@H]1C(OP(=O)(O)OP(=O)(OC[C@@H]2O[C@H](N3C=CC(=O)N([Si](C)(C)C)C3=O)[C@@H](O)[C@H]2O)O[Si](C)(C)C)O[C@@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O4261.2Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,4TMS,isomer #87CC(=O)N([C@H]1C(OP(=O)(O)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)N([Si](C)(C)C)C3=O)[C@@H](O)[C@H]2O)O[C@@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O)[Si](C)(C)C4258.3Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,4TMS,isomer #88CC(=O)N([C@H]1C(OP(=O)(O[Si](C)(C)C)OP(=O)(OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O)[C@H]2O)O[Si](C)(C)C)O[C@@H](CO)[C@H](O[Si](C)(C)C)[C@H]1O)[Si](C)(C)C4179.7Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,4TMS,isomer #89CC(=O)N[C@H]1C(OP(=O)(O[Si](C)(C)C)OP(=O)(OC[C@@H]2O[C@H](N3C=CC(=O)N([Si](C)(C)C)C3=O)[C@@H](O)[C@H]2O)O[Si](C)(C)C)O[C@@H](CO)[C@H](O[Si](C)(C)C)[C@H]1O4296.5Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,4TMS,isomer #9CC(=O)N[C@H]1C(OP(=O)(O)OP(=O)(OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O[Si](C)(C)C)[C@H]2O)O[Si](C)(C)C)O[C@@H](CO[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C4147.4Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,4TMS,isomer #90CC(=O)N([C@H]1C(OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)N([Si](C)(C)C)C3=O)[C@@H](O)[C@H]2O)O[C@@H](CO)[C@H](O[Si](C)(C)C)[C@H]1O)[Si](C)(C)C4278.5Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,4TMS,isomer #91CC(=O)N([C@H]1C(OP(=O)(O)OP(=O)(OC[C@@H]2O[C@H](N3C=CC(=O)N([Si](C)(C)C)C3=O)[C@@H](O)[C@H]2O)O[Si](C)(C)C)O[C@@H](CO)[C@H](O[Si](C)(C)C)[C@H]1O)[Si](C)(C)C4281.2Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,4TMS,isomer #92CC(=O)N[C@H]1C(OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)O[C@@H](CO[Si](C)(C)C)[C@H](O)[C@H]1O4118.6Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,4TMS,isomer #93CC(=O)N[C@H]1C(OP(=O)(O)OP(=O)(OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)O[Si](C)(C)C)O[C@@H](CO[Si](C)(C)C)[C@H](O)[C@H]1O4112.4Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,4TMS,isomer #94CC(=O)N([C@H]1C(OP(=O)(O)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)O[C@@H](CO[Si](C)(C)C)[C@H](O)[C@H]1O)[Si](C)(C)C4110.8Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,4TMS,isomer #95CC(=O)N[C@H]1C(OP(=O)(O)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)N([Si](C)(C)C)C3=O)[C@@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)O[C@@H](CO[Si](C)(C)C)[C@H](O)[C@H]1O4209.1Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,4TMS,isomer #96CC(=O)N[C@H]1C(OP(=O)(O[Si](C)(C)C)OP(=O)(OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O[Si](C)(C)C)[C@H]2O)O[Si](C)(C)C)O[C@@H](CO[Si](C)(C)C)[C@H](O)[C@H]1O4143.0Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,4TMS,isomer #97CC(=O)N([C@H]1C(OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O[Si](C)(C)C)[C@H]2O)O[C@@H](CO[Si](C)(C)C)[C@H](O)[C@H]1O)[Si](C)(C)C4121.7Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,4TMS,isomer #98CC(=O)N[C@H]1C(OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)N([Si](C)(C)C)C3=O)[C@@H](O[Si](C)(C)C)[C@H]2O)O[C@@H](CO[Si](C)(C)C)[C@H](O)[C@H]1O4221.8Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,4TMS,isomer #99CC(=O)N([C@H]1C(OP(=O)(O)OP(=O)(OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O[Si](C)(C)C)[C@H]2O)O[Si](C)(C)C)O[C@@H](CO[Si](C)(C)C)[C@H](O)[C@H]1O)[Si](C)(C)C4121.7Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,1TBDMS,isomer #1CC(=O)N[C@H]1C(OP(=O)(O)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O)[C@H]2O)O[C@@H](CO)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C4618.9Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,1TBDMS,isomer #2CC(=O)N[C@H]1C(OP(=O)(O)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O)[C@H]2O)O[C@@H](CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O4629.9Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,1TBDMS,isomer #3CC(=O)N[C@H]1C(OP(=O)(O)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O)[C@H]2O)O[C@@H](CO[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O4599.1Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,1TBDMS,isomer #4CC(=O)N[C@H]1C(OP(=O)(O)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)O[C@@H](CO)[C@H](O)[C@H]1O4622.1Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,1TBDMS,isomer #5CC(=O)N[C@H]1C(OP(=O)(O)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)O[C@@H](CO)[C@H](O)[C@H]1O4630.2Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,1TBDMS,isomer #6CC(=O)N[C@H]1C(OP(=O)(O[Si](C)(C)C(C)(C)C)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O)[C@H]2O)O[C@@H](CO)[C@H](O)[C@H]1O4710.9Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,1TBDMS,isomer #7CC(=O)N[C@H]1C(OP(=O)(O)OP(=O)(OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O)[C@H]2O)O[Si](C)(C)C(C)(C)C)O[C@@H](CO)[C@H](O)[C@H]1O4694.6Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,1TBDMS,isomer #8CC(=O)N([C@H]1C(OP(=O)(O)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O)[C@H]2O)O[C@@H](CO)[C@H](O)[C@H]1O)[Si](C)(C)C(C)(C)C4676.5Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,1TBDMS,isomer #9CC(=O)N[C@H]1C(OP(=O)(O)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)N([Si](C)(C)C(C)(C)C)C3=O)[C@@H](O)[C@H]2O)O[C@@H](CO)[C@H](O)[C@H]1O4738.3Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,2TBDMS,isomer #1CC(=O)N[C@H]1C(OP(=O)(O)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)O[C@@H](CO)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C4648.4Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,2TBDMS,isomer #10CC(=O)N[C@H]1C(OP(=O)(O)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)O[C@@H](CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O4651.6Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,2TBDMS,isomer #11CC(=O)N[C@H]1C(OP(=O)(O)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O)[C@H]2O)O[C@@H](CO[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O4648.6Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,2TBDMS,isomer #12CC(=O)N[C@H]1C(OP(=O)(O[Si](C)(C)C(C)(C)C)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O)[C@H]2O)O[C@@H](CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O4718.6Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,2TBDMS,isomer #13CC(=O)N[C@H]1C(OP(=O)(O)OP(=O)(OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O)[C@H]2O)O[Si](C)(C)C(C)(C)C)O[C@@H](CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O4704.4Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,2TBDMS,isomer #14CC(=O)N([C@H]1C(OP(=O)(O)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O)[C@H]2O)O[C@@H](CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O)[Si](C)(C)C(C)(C)C4675.8Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,2TBDMS,isomer #15CC(=O)N[C@H]1C(OP(=O)(O)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)N([Si](C)(C)C(C)(C)C)C3=O)[C@@H](O)[C@H]2O)O[C@@H](CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O4776.4Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,2TBDMS,isomer #16CC(=O)N[C@H]1C(OP(=O)(O)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)O[C@@H](CO[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O4636.6Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,2TBDMS,isomer #17CC(=O)N[C@H]1C(OP(=O)(O)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)O[C@@H](CO[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O4640.0Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,2TBDMS,isomer #18CC(=O)N[C@H]1C(OP(=O)(O[Si](C)(C)C(C)(C)C)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O)[C@H]2O)O[C@@H](CO[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O4704.7Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,2TBDMS,isomer #19CC(=O)N[C@H]1C(OP(=O)(O)OP(=O)(OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O)[C@H]2O)O[Si](C)(C)C(C)(C)C)O[C@@H](CO[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O4691.5Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,2TBDMS,isomer #2CC(=O)N[C@H]1C(OP(=O)(O)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)O[C@@H](CO)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C4649.5Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,2TBDMS,isomer #20CC(=O)N([C@H]1C(OP(=O)(O)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O)[C@H]2O)O[C@@H](CO[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O)[Si](C)(C)C(C)(C)C4671.4Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,2TBDMS,isomer #21CC(=O)N[C@H]1C(OP(=O)(O)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)N([Si](C)(C)C(C)(C)C)C3=O)[C@@H](O)[C@H]2O)O[C@@H](CO[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O4756.1Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,2TBDMS,isomer #22CC(=O)N[C@H]1C(OP(=O)(O)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]2O[Si](C)(C)C(C)(C)C)O[C@@H](CO)[C@H](O)[C@H]1O4667.4Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,2TBDMS,isomer #23CC(=O)N[C@H]1C(OP(=O)(O[Si](C)(C)C(C)(C)C)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)O[C@@H](CO)[C@H](O)[C@H]1O4720.0Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,2TBDMS,isomer #24CC(=O)N[C@H]1C(OP(=O)(O)OP(=O)(OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)O[Si](C)(C)C(C)(C)C)O[C@@H](CO)[C@H](O)[C@H]1O4706.6Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,2TBDMS,isomer #25CC(=O)N([C@H]1C(OP(=O)(O)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)O[C@@H](CO)[C@H](O)[C@H]1O)[Si](C)(C)C(C)(C)C4679.8Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,2TBDMS,isomer #26CC(=O)N[C@H]1C(OP(=O)(O)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)N([Si](C)(C)C(C)(C)C)C3=O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)O[C@@H](CO)[C@H](O)[C@H]1O4769.2Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,2TBDMS,isomer #27CC(=O)N[C@H]1C(OP(=O)(O[Si](C)(C)C(C)(C)C)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)O[C@@H](CO)[C@H](O)[C@H]1O4723.2Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,2TBDMS,isomer #28CC(=O)N[C@H]1C(OP(=O)(O)OP(=O)(OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)O[C@@H](CO)[C@H](O)[C@H]1O4710.1Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,2TBDMS,isomer #29CC(=O)N([C@H]1C(OP(=O)(O)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)O[C@@H](CO)[C@H](O)[C@H]1O)[Si](C)(C)C(C)(C)C4677.7Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,2TBDMS,isomer #3CC(=O)N[C@H]1C(OP(=O)(O)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O)[C@H]2O)O[C@@H](CO[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C4644.8Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,2TBDMS,isomer #30CC(=O)N[C@H]1C(OP(=O)(O)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)N([Si](C)(C)C(C)(C)C)C3=O)[C@@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)O[C@@H](CO)[C@H](O)[C@H]1O4770.5Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,2TBDMS,isomer #31CC(=O)N[C@H]1C(OP(=O)(O[Si](C)(C)C(C)(C)C)OP(=O)(OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O)[C@H]2O)O[Si](C)(C)C(C)(C)C)O[C@@H](CO)[C@H](O)[C@H]1O4782.4Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,2TBDMS,isomer #32CC(=O)N([C@H]1C(OP(=O)(O[Si](C)(C)C(C)(C)C)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O)[C@H]2O)O[C@@H](CO)[C@H](O)[C@H]1O)[Si](C)(C)C(C)(C)C4726.6Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,2TBDMS,isomer #33CC(=O)N[C@H]1C(OP(=O)(O[Si](C)(C)C(C)(C)C)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)N([Si](C)(C)C(C)(C)C)C3=O)[C@@H](O)[C@H]2O)O[C@@H](CO)[C@H](O)[C@H]1O4835.0Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,2TBDMS,isomer #34CC(=O)N([C@H]1C(OP(=O)(O)OP(=O)(OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O)[C@H]2O)O[Si](C)(C)C(C)(C)C)O[C@@H](CO)[C@H](O)[C@H]1O)[Si](C)(C)C(C)(C)C4718.7Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,2TBDMS,isomer #35CC(=O)N[C@H]1C(OP(=O)(O)OP(=O)(OC[C@@H]2O[C@H](N3C=CC(=O)N([Si](C)(C)C(C)(C)C)C3=O)[C@@H](O)[C@H]2O)O[Si](C)(C)C(C)(C)C)O[C@@H](CO)[C@H](O)[C@H]1O4821.5Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,2TBDMS,isomer #36CC(=O)N([C@H]1C(OP(=O)(O)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)N([Si](C)(C)C(C)(C)C)C3=O)[C@@H](O)[C@H]2O)O[C@@H](CO)[C@H](O)[C@H]1O)[Si](C)(C)C(C)(C)C4800.4Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,2TBDMS,isomer #4CC(=O)N[C@H]1C(OP(=O)(O)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O)[C@H]2O)O[C@@H](CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)C4639.8Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,2TBDMS,isomer #5CC(=O)N[C@H]1C(OP(=O)(O[Si](C)(C)C(C)(C)C)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O)[C@H]2O)O[C@@H](CO)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C4721.0Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,2TBDMS,isomer #6CC(=O)N[C@H]1C(OP(=O)(O)OP(=O)(OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O)[C@H]2O)O[Si](C)(C)C(C)(C)C)O[C@@H](CO)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C4704.9Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,2TBDMS,isomer #7CC(=O)N([C@H]1C(OP(=O)(O)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O)[C@H]2O)O[C@@H](CO)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C4681.1Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,2TBDMS,isomer #8CC(=O)N[C@H]1C(OP(=O)(O)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)N([Si](C)(C)C(C)(C)C)C3=O)[C@@H](O)[C@H]2O)O[C@@H](CO)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C4774.6Semi standard non polar33892256
UDP-N-acetyl-D-mannosamine,2TBDMS,isomer #9CC(=O)N[C@H]1C(OP(=O)(O)OP(=O)(O)OC[C@@H]2O[C@H](N3C=CC(=O)[NH]C3=O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)O[C@@H](CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O4649.9Semi standard non polar33892256
Spectra

GC-MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted GC-MSPredicted GC-MS Spectrum - UDP-N-acetyl-D-mannosamine GC-MS (Non-derivatized) - 70eV, Positivesplash10-0f96-5924660000-c11cc7fa21a050c0f3732017-09-01Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - UDP-N-acetyl-D-mannosamine GC-MS (1 TMS) - 70eV, Positivesplash10-0h03-7952838000-56b15bfcc0138d466a262017-10-06Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - UDP-N-acetyl-D-mannosamine GC-MS (TMS_1_2) - 70eV, PositiveNot Available2021-10-16Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - UDP-N-acetyl-D-mannosamine GC-MS (TMS_1_3) - 70eV, PositiveNot Available2021-10-16Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - UDP-N-acetyl-D-mannosamine GC-MS (TMS_1_4) - 70eV, PositiveNot Available2021-10-16Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - UDP-N-acetyl-D-mannosamine GC-MS (TMS_1_5) - 70eV, PositiveNot Available2021-10-16Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - UDP-N-acetyl-D-mannosamine GC-MS (TMS_1_6) - 70eV, PositiveNot Available2021-10-16Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - UDP-N-acetyl-D-mannosamine GC-MS (TMS_1_7) - 70eV, PositiveNot Available2021-10-16Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - UDP-N-acetyl-D-mannosamine GC-MS (TMS_1_8) - 70eV, PositiveNot Available2021-10-16Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - UDP-N-acetyl-D-mannosamine GC-MS (TMS_1_9) - 70eV, PositiveNot Available2021-10-16Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - UDP-N-acetyl-D-mannosamine GC-MS (TMS_2_1) - 70eV, PositiveNot Available2021-10-16Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - UDP-N-acetyl-D-mannosamine GC-MS (TMS_2_2) - 70eV, PositiveNot Available2021-10-16Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - UDP-N-acetyl-D-mannosamine GC-MS (TMS_2_3) - 70eV, PositiveNot Available2021-10-16Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - UDP-N-acetyl-D-mannosamine GC-MS (TMS_2_4) - 70eV, PositiveNot Available2021-10-16Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - UDP-N-acetyl-D-mannosamine GC-MS (TMS_2_5) - 70eV, PositiveNot Available2021-10-16Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - UDP-N-acetyl-D-mannosamine GC-MS (TMS_2_6) - 70eV, PositiveNot Available2021-10-16Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - UDP-N-acetyl-D-mannosamine GC-MS (TMS_2_7) - 70eV, PositiveNot Available2021-10-16Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - UDP-N-acetyl-D-mannosamine GC-MS (TMS_2_8) - 70eV, PositiveNot Available2021-10-16Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - UDP-N-acetyl-D-mannosamine GC-MS (TMS_2_9) - 70eV, PositiveNot Available2021-10-16Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - UDP-N-acetyl-D-mannosamine GC-MS (TMS_2_10) - 70eV, PositiveNot Available2021-10-16Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - UDP-N-acetyl-D-mannosamine GC-MS (TMS_2_11) - 70eV, PositiveNot Available2021-10-16Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - UDP-N-acetyl-D-mannosamine GC-MS (TMS_2_12) - 70eV, PositiveNot Available2021-10-16Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - UDP-N-acetyl-D-mannosamine GC-MS (TMS_2_13) - 70eV, PositiveNot Available2021-10-16Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - UDP-N-acetyl-D-mannosamine GC-MS (TMS_2_14) - 70eV, PositiveNot Available2021-10-16Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - UDP-N-acetyl-D-mannosamine GC-MS (TMS_2_15) - 70eV, PositiveNot Available2021-10-16Wishart LabView Spectrum

MS/MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - UDP-N-acetyl-D-mannosamine 10V, Positive-QTOFsplash10-03di-0910020000-4282200321d0bfe459432017-09-01Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - UDP-N-acetyl-D-mannosamine 20V, Positive-QTOFsplash10-03di-3921000000-6076288d599ab33134792017-09-01Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - UDP-N-acetyl-D-mannosamine 40V, Positive-QTOFsplash10-03di-5910000000-14d31d6720f9ec5396752017-09-01Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - UDP-N-acetyl-D-mannosamine 10V, Negative-QTOFsplash10-06ri-9502331000-138ea2dd91899208164e2017-09-01Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - UDP-N-acetyl-D-mannosamine 20V, Negative-QTOFsplash10-03dl-9504010000-0424c67ad101c9f6be362017-09-01Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - UDP-N-acetyl-D-mannosamine 40V, Negative-QTOFsplash10-06r6-5901000000-dce542e7a9e33e0e747c2017-09-01Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - UDP-N-acetyl-D-mannosamine 10V, Negative-QTOFsplash10-0a4i-0000029000-6a481f04b19fa31778892021-09-22Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - UDP-N-acetyl-D-mannosamine 20V, Negative-QTOFsplash10-0a6s-5100192000-07c7ec84c4bab85e334a2021-09-22Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - UDP-N-acetyl-D-mannosamine 40V, Negative-QTOFsplash10-053u-4719110000-3a1b07828c441361af2f2021-09-22Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - UDP-N-acetyl-D-mannosamine 10V, Positive-QTOFsplash10-00mk-0000982000-8e4f05f581cea906b6bb2021-09-23Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - UDP-N-acetyl-D-mannosamine 20V, Positive-QTOFsplash10-0hi2-0213591000-da4a947496986866c59e2021-09-23Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - UDP-N-acetyl-D-mannosamine 40V, Positive-QTOFsplash10-0a4j-6980020000-82befaa44d12d4c3c15d2021-09-23Wishart LabView Spectrum

NMR Spectra

Spectrum TypeDescriptionDeposition DateSourceView
Predicted 1D NMR13C NMR Spectrum (1D, 100 MHz, D2O, predicted)2021-09-16Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 100 MHz, D2O, predicted)2021-09-16Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 200 MHz, D2O, predicted)2021-09-16Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 200 MHz, D2O, predicted)2021-09-16Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 300 MHz, D2O, predicted)2021-09-16Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 300 MHz, D2O, predicted)2021-09-16Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 400 MHz, D2O, predicted)2021-09-16Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 400 MHz, D2O, predicted)2021-09-16Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 500 MHz, D2O, predicted)2021-09-16Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 500 MHz, D2O, predicted)2021-09-16Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 600 MHz, D2O, predicted)2021-09-16Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 600 MHz, D2O, predicted)2021-09-16Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 700 MHz, D2O, predicted)2021-09-16Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 700 MHz, D2O, predicted)2021-09-16Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 800 MHz, D2O, predicted)2021-09-16Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 800 MHz, D2O, predicted)2021-09-16Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 900 MHz, D2O, predicted)2021-09-16Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 900 MHz, D2O, predicted)2021-09-16Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 1000 MHz, D2O, predicted)2021-09-16Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 1000 MHz, D2O, predicted)2021-09-16Wishart 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 IDFDB029289
KNApSAcK IDC00019345
Chemspider ID35032576
KEGG Compound IDC01170
BioCyc IDNot Available
BiGG IDNot Available
Wikipedia LinkNot Available
METLIN IDNot Available
PubChem Compound53481607
PDB IDNot Available
ChEBI ID16287
Food Biomarker OntologyNot Available
VMH IDUACMAM
MarkerDB IDNot Available
Good Scents IDNot Available
References
Synthesis ReferenceNot Available
Material Safety Data Sheet (MSDS)Not Available
General ReferencesNot Available