Hmdb loader
Record Information
Version5.0
StatusExpected but not Quantified
Creation Date2009-04-06 16:22:38 UTC
Update Date2021-09-14 15:38:59 UTC
HMDB IDHMDB0012303
Secondary Accession Numbers
  • HMDB12303
Metabolite Identification
Common NameUDP-L-arabinose
DescriptionUDP-sugars, activated forms of monosaccharides, are synthesized through de novo and salvage pathways and serve as substrates for the synthesis of polysaccharides, glycolipids, and glycoproteins in higher plants. The enzyme catalyzed the formation of UDP-Glc, UDP-Gal, UDP-glucuronic acid, UDP-l-arabinose, and UDP-xylose from respective monosaccharide 1-phosphates in the presence of UTP as a co-substrate, indicating that the enzyme has broad substrate specificity toward monosaccharide 1-phosphates.
Structure
Data?1586896621
Synonyms
ValueSource
UDP-beta-L-ArabinoseChEBI
UDP-beta-L-ArapChEBI
Uridine 5'-diphospho-beta-L-arabinopyranoseChEBI
UDP-b-L-ArabinoseGenerator
UDP-Β-L-arabinoseGenerator
UDP-b-L-ArapGenerator
UDP-Β-L-arapGenerator
Uridine 5'-diphospho-b-L-arabinopyranoseGenerator
Uridine 5'-diphospho-β-L-arabinopyranoseGenerator
UDP-b-L-ArabinopyranoseGenerator
UDP-β-L-arabinopyranoseGenerator
UDP-L-arabinoseHMDB
UDP-arabinoseHMDB
UDP-beta-L-arabinopyranoseHMDB
Uridine 5'-(trihydrogen diphosphate) mono-L-arabinopyranosyl esterHMDB
Uridine 5'-(trihydrogen pyrophosphate) mono-L-arabinopyranosyl esterHMDB
Uridine 5'-(trihydrogen pyrophosphate) mono-L-arabinosyl esterHMDB
Uridine 5'-diphosphate arabinosideHMDB
Uridine 5'-pyrophosphate, beta-L-arabinosyl esterHMDB
Uridine 5'-pyrophosphate, β-L-arabinosyl esterHMDB
Uridine 5’-(trihydrogen diphosphate) mono-L-arabinopyranosyl esterHMDB
Uridine 5’-(trihydrogen pyrophosphate) mono-L-arabinopyranosyl esterHMDB
Uridine 5’-(trihydrogen pyrophosphate) mono-L-arabinosyl esterHMDB
Uridine 5’-diphosphate arabinosideHMDB
Uridine 5’-pyrophosphate, β-L-arabinosyl esterHMDB
Uridine diphosphate arabinoseHMDB
Uridine diphospho-beta-L-arabinopyranoseHMDB
Uridine diphospho-β-L-arabinopyranoseHMDB
Uridine diphosphoarabinoseHMDB
Chemical FormulaC14H22N2O16P2
Average Molecular Weight536.2758
Monoisotopic Molecular Weight536.04445569
IUPAC Name{[(2R,3S,4R,5R)-3,4-dihydroxy-5-(4-hydroxy-2-oxo-1,2-dihydropyrimidin-1-yl)oxolan-2-yl]methoxy}({[hydroxy({[(2R,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxy})phosphoryl]oxy})phosphinic acid
Traditional Name[(2R,3S,4R,5R)-3,4-dihydroxy-5-(4-hydroxy-2-oxopyrimidin-1-yl)oxolan-2-yl]methoxy([hydroxy([(2R,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxy)phosphoryl]oxy)phosphinic acid
CAS Registry Number15839-78-8
SMILES
O[C@@H]1[C@@H](COP(O)(=O)OP(O)(=O)O[C@H]2OC[C@H](O)[C@H](O)[C@H]2O)O[C@H]([C@@H]1O)N1C=CC(=O)NC1=O
InChI Identifier
InChI=1S/C14H22N2O16P2/c17-5-3-28-13(11(22)8(5)19)31-34(26,27)32-33(24,25)29-4-6-9(20)10(21)12(30-6)16-2-1-7(18)15-14(16)23/h1-2,5-6,8-13,17,19-22H,3-4H2,(H,24,25)(H,26,27)(H,15,18,23)/t5-,6+,8-,9+,10+,11+,12+,13+/m0/s1
InChI KeyDQQDLYVHOTZLOR-IAZOVDBXSA-N
Chemical Taxonomy
Description Belongs to the class of organic compounds known as pyrimidine ribonucleoside diphosphates. These are pyrimidine ribonucleotides with diphosphate group linked to the ribose moiety.
KingdomOrganic compounds
Super ClassNucleosides, nucleotides, and analogues
ClassPyrimidine nucleotides
Sub ClassPyrimidine ribonucleotides
Direct ParentPyrimidine ribonucleoside diphosphates
Alternative Parents
Substituents
  • Pyrimidine ribonucleoside diphosphate
  • Pentose phosphate
  • Pentose-5-phosphate
  • 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
  • Heteroaromatic compound
  • Tetrahydrofuran
  • Lactam
  • Urea
  • Secondary alcohol
  • Oxacycle
  • Polyol
  • Organoheterocyclic compound
  • Azacycle
  • Alcohol
  • Organic nitrogen compound
  • Organic oxide
  • Organonitrogen compound
  • Organooxygen compound
  • Organic oxygen compound
  • Organopnictogen compound
  • Hydrocarbon derivative
  • Aromatic heteromonocyclic compound
Molecular FrameworkAromatic heteromonocyclic compounds
External Descriptors
Ontology
Physiological effectNot Available
Disposition
Source
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 Solubility13.6 g/LALOGPS
logP-1.2ALOGPS
logP-4ChemAxon
logS-1.4ALOGPS
pKa (Strongest Acidic)1.73ChemAxon
pKa (Strongest Basic)-3.5ChemAxon
Physiological Charge-2ChemAxon
Hydrogen Acceptor Count14ChemAxon
Hydrogen Donor Count8ChemAxon
Polar Surface Area274.8 ŲChemAxon
Rotatable Bond Count8ChemAxon
Refractivity100.82 m³·mol⁻¹ChemAxon
Polarizability43.61 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
DarkChem[M+H]+214.85331661259
DarkChem[M-H]-204.19631661259
DeepCCS[M+H]+197.32330932474
DeepCCS[M-H]-195.49830932474
DeepCCS[M-2H]-228.73430932474
DeepCCS[M+Na]+202.92930932474
AllCCS[M+H]+208.332859911
AllCCS[M+H-H2O]+206.632859911
AllCCS[M+NH4]+209.832859911
AllCCS[M+Na]+210.232859911
AllCCS[M-H]-200.632859911
AllCCS[M+Na-2H]-201.332859911
AllCCS[M+HCOO]-202.332859911

Predicted Kovats Retention Indices

Underivatized

MetaboliteSMILESKovats RI ValueColumn TypeReference
UDP-L-arabinoseO[C@@H]1[C@@H](COP(O)(=O)OP(O)(=O)O[C@H]2OC[C@H](O)[C@H](O)[C@H]2O)O[C@H]([C@@H]1O)N1C=CC(=O)NC1=O4576.3Standard polar33892256
UDP-L-arabinoseO[C@@H]1[C@@H](COP(O)(=O)OP(O)(=O)O[C@H]2OC[C@H](O)[C@H](O)[C@H]2O)O[C@H]([C@@H]1O)N1C=CC(=O)NC1=O3106.5Standard non polar33892256
UDP-L-arabinoseO[C@@H]1[C@@H](COP(O)(=O)OP(O)(=O)O[C@H]2OC[C@H](O)[C@H](O)[C@H]2O)O[C@H]([C@@H]1O)N1C=CC(=O)NC1=O4539.5Semi standard non polar33892256

Derivatized

Derivative Name / StructureSMILESKovats RI ValueColumn TypeReference
UDP-L-arabinose,1TMS,isomer #1C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]2OC[C@H](O)[C@H](O)[C@H]2O)O[C@@H](N2C=CC(=O)[NH]C2=O)[C@@H]1O4037.7Semi standard non polar33892256
UDP-L-arabinose,1TMS,isomer #2C[Si](C)(C)O[C@H]1CO[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(=O)[NH]C3=O)[C@H](O)[C@@H]2O)[C@H](O)[C@H]1O4039.5Semi standard non polar33892256
UDP-L-arabinose,1TMS,isomer #3C[Si](C)(C)O[C@H]1[C@@H](O)CO[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(=O)[NH]C3=O)[C@H](O)[C@@H]2O)[C@@H]1O3992.4Semi standard non polar33892256
UDP-L-arabinose,1TMS,isomer #4C[Si](C)(C)O[C@@H]1[C@@H](O)[C@@H](O)CO[C@@H]1OP(=O)(O)OP(=O)(O)OC[C@H]1O[C@@H](N2C=CC(=O)[NH]C2=O)[C@H](O)[C@@H]1O4015.4Semi standard non polar33892256
UDP-L-arabinose,1TMS,isomer #5C[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]2OC[C@H](O)[C@H](O)[C@H]2O)O[C@H]1N1C=CC(=O)[NH]C1=O4029.9Semi standard non polar33892256
UDP-L-arabinose,1TMS,isomer #6C[Si](C)(C)OP(=O)(OC[C@H]1O[C@@H](N2C=CC(=O)[NH]C2=O)[C@H](O)[C@@H]1O)OP(=O)(O)O[C@H]1OC[C@H](O)[C@H](O)[C@H]1O4123.1Semi standard non polar33892256
UDP-L-arabinose,1TMS,isomer #7C[Si](C)(C)OP(=O)(O[C@H]1OC[C@H](O)[C@H](O)[C@H]1O)OP(=O)(O)OC[C@H]1O[C@@H](N2C=CC(=O)[NH]C2=O)[C@H](O)[C@@H]1O4133.9Semi standard non polar33892256
UDP-L-arabinose,1TMS,isomer #8C[Si](C)(C)N1C(=O)C=CN([C@@H]2O[C@H](COP(=O)(O)OP(=O)(O)O[C@H]3OC[C@H](O)[C@H](O)[C@H]3O)[C@@H](O)[C@H]2O)C1=O4138.2Semi standard non polar33892256
UDP-L-arabinose,2TMS,isomer #1C[Si](C)(C)O[C@H]1CO[C@H](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@H](O)[C@H]1O3900.5Semi standard non polar33892256
UDP-L-arabinose,2TMS,isomer #10C[Si](C)(C)O[C@H]1CO[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(=O)[NH]C3=O)[C@H](O)[C@@H]2O)[C@H](O)[C@H]1O[Si](C)(C)C3872.8Semi standard non polar33892256
UDP-L-arabinose,2TMS,isomer #11C[Si](C)(C)O[C@H]1CO[C@H](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)[C@H](O)[C@H]1O3991.5Semi standard non polar33892256
UDP-L-arabinose,2TMS,isomer #12C[Si](C)(C)O[C@H]1CO[C@H](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@H](O)[C@H]1O3984.2Semi standard non polar33892256
UDP-L-arabinose,2TMS,isomer #13C[Si](C)(C)O[C@H]1CO[C@H](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)[C@H](O)[C@H]1O4068.1Semi standard non polar33892256
UDP-L-arabinose,2TMS,isomer #14C[Si](C)(C)O[C@H]1[C@@H](O)CO[C@H](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)[C@@H]1O3846.2Semi standard non polar33892256
UDP-L-arabinose,2TMS,isomer #15C[Si](C)(C)O[C@H]1[C@@H](O)CO[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(=O)[NH]C3=O)[C@H](O)[C@@H]2O)[C@@H]1O[Si](C)(C)C3874.6Semi standard non polar33892256
UDP-L-arabinose,2TMS,isomer #16C[Si](C)(C)O[C@H]1[C@@H](O)CO[C@H](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)[C@@H]1O3935.3Semi standard non polar33892256
UDP-L-arabinose,2TMS,isomer #17C[Si](C)(C)O[C@H]1[C@@H](O)CO[C@H](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@@H]1O3929.5Semi standard non polar33892256
UDP-L-arabinose,2TMS,isomer #18C[Si](C)(C)O[C@H]1[C@@H](O)CO[C@H](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)[C@@H]1O4010.7Semi standard non polar33892256
UDP-L-arabinose,2TMS,isomer #19C[Si](C)(C)O[C@@H]1[C@@H](O)[C@@H](O)CO[C@@H]1OP(=O)(O)OP(=O)(O)OC[C@H]1O[C@@H](N2C=CC(=O)[NH]C2=O)[C@H](O[Si](C)(C)C)[C@@H]1O3869.6Semi standard non polar33892256
UDP-L-arabinose,2TMS,isomer #2C[Si](C)(C)O[C@H]1[C@@H](O)CO[C@H](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@@H]1O3855.6Semi standard non polar33892256
UDP-L-arabinose,2TMS,isomer #20C[Si](C)(C)O[C@@H]1[C@@H](O)[C@@H](O)CO[C@@H]1OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]1O[C@@H](N2C=CC(=O)[NH]C2=O)[C@H](O)[C@@H]1O3960.5Semi standard non polar33892256
UDP-L-arabinose,2TMS,isomer #21C[Si](C)(C)O[C@@H]1[C@@H](O)[C@@H](O)CO[C@@H]1OP(=O)(O)OP(=O)(OC[C@H]1O[C@@H](N2C=CC(=O)[NH]C2=O)[C@H](O)[C@@H]1O)O[Si](C)(C)C3951.6Semi standard non polar33892256
UDP-L-arabinose,2TMS,isomer #22C[Si](C)(C)O[C@@H]1[C@@H](O)[C@@H](O)CO[C@@H]1OP(=O)(O)OP(=O)(O)OC[C@H]1O[C@@H](N2C=CC(=O)N([Si](C)(C)C)C2=O)[C@H](O)[C@@H]1O4034.0Semi standard non polar33892256
UDP-L-arabinose,2TMS,isomer #23C[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O)O[C@H]2OC[C@H](O)[C@H](O)[C@H]2O)O[C@H]1N1C=CC(=O)[NH]C1=O3959.0Semi standard non polar33892256
UDP-L-arabinose,2TMS,isomer #24C[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O[C@H]2OC[C@H](O)[C@H](O)[C@H]2O)O[Si](C)(C)C)O[C@H]1N1C=CC(=O)[NH]C1=O3969.8Semi standard non polar33892256
UDP-L-arabinose,2TMS,isomer #25C[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]2OC[C@H](O)[C@H](O)[C@H]2O)O[C@H]1N1C=CC(=O)N([Si](C)(C)C)C1=O4044.3Semi standard non polar33892256
UDP-L-arabinose,2TMS,isomer #26C[Si](C)(C)OP(=O)(OC[C@H]1O[C@@H](N2C=CC(=O)[NH]C2=O)[C@H](O)[C@@H]1O)OP(=O)(O[C@H]1OC[C@H](O)[C@H](O)[C@H]1O)O[Si](C)(C)C4056.0Semi standard non polar33892256
UDP-L-arabinose,2TMS,isomer #27C[Si](C)(C)OP(=O)(OC[C@H]1O[C@@H](N2C=CC(=O)N([Si](C)(C)C)C2=O)[C@H](O)[C@@H]1O)OP(=O)(O)O[C@H]1OC[C@H](O)[C@H](O)[C@H]1O4109.5Semi standard non polar33892256
UDP-L-arabinose,2TMS,isomer #28C[Si](C)(C)OP(=O)(O[C@H]1OC[C@H](O)[C@H](O)[C@H]1O)OP(=O)(O)OC[C@H]1O[C@@H](N2C=CC(=O)N([Si](C)(C)C)C2=O)[C@H](O)[C@@H]1O4123.2Semi standard non polar33892256
UDP-L-arabinose,2TMS,isomer #3C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]2OC[C@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)O[C@@H](N2C=CC(=O)[NH]C2=O)[C@@H]1O3877.4Semi standard non polar33892256
UDP-L-arabinose,2TMS,isomer #4C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]2OC[C@H](O)[C@H](O)[C@H]2O)O[C@@H](N2C=CC(=O)[NH]C2=O)[C@@H]1O[Si](C)(C)C3905.7Semi standard non polar33892256
UDP-L-arabinose,2TMS,isomer #5C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O)O[C@H]2OC[C@H](O)[C@H](O)[C@H]2O)O[C@@H](N2C=CC(=O)[NH]C2=O)[C@@H]1O3972.2Semi standard non polar33892256
UDP-L-arabinose,2TMS,isomer #6C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)OP(=O)(O[C@H]2OC[C@H](O)[C@H](O)[C@H]2O)O[Si](C)(C)C)O[C@@H](N2C=CC(=O)[NH]C2=O)[C@@H]1O3980.1Semi standard non polar33892256
UDP-L-arabinose,2TMS,isomer #7C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]2OC[C@H](O)[C@H](O)[C@H]2O)O[C@@H](N2C=CC(=O)N([Si](C)(C)C)C2=O)[C@@H]1O4049.1Semi standard non polar33892256
UDP-L-arabinose,2TMS,isomer #8C[Si](C)(C)O[C@H]1CO[C@H](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)[C@H](O)[C@H]1O3889.2Semi standard non polar33892256
UDP-L-arabinose,2TMS,isomer #9C[Si](C)(C)O[C@H]1CO[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(=O)[NH]C3=O)[C@H](O)[C@@H]2O)[C@H](O[Si](C)(C)C)[C@H]1O3881.8Semi standard non polar33892256
UDP-L-arabinose,3TMS,isomer #1C[Si](C)(C)O[C@H]1CO[C@H](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)[C@H](O)[C@H]1O3777.3Semi standard non polar33892256
UDP-L-arabinose,3TMS,isomer #10C[Si](C)(C)O[C@H]1[C@@H](O)CO[C@H](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)[C@@H]1O3804.8Semi standard non polar33892256
UDP-L-arabinose,3TMS,isomer #11C[Si](C)(C)O[C@H]1[C@@H](O)CO[C@H](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)[C@@H]1O3889.8Semi standard non polar33892256
UDP-L-arabinose,3TMS,isomer #12C[Si](C)(C)O[C@@H]1[C@@H](O)[C@@H](O)CO[C@@H]1OP(=O)(O)OP(=O)(O)OC[C@H]1O[C@@H](N2C=CC(=O)[NH]C2=O)[C@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C3768.3Semi standard non polar33892256
UDP-L-arabinose,3TMS,isomer #13C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O)O[C@H]2OC[C@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)O[C@@H](N2C=CC(=O)[NH]C2=O)[C@@H]1O3814.4Semi standard non polar33892256
UDP-L-arabinose,3TMS,isomer #14C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)OP(=O)(O[C@H]2OC[C@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)O[Si](C)(C)C)O[C@@H](N2C=CC(=O)[NH]C2=O)[C@@H]1O3820.9Semi standard non polar33892256
UDP-L-arabinose,3TMS,isomer #15C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]2OC[C@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)O[C@@H](N2C=CC(=O)N([Si](C)(C)C)C2=O)[C@@H]1O3899.2Semi standard non polar33892256
UDP-L-arabinose,3TMS,isomer #16C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O)O[C@H]2OC[C@H](O)[C@H](O)[C@H]2O)O[C@@H](N2C=CC(=O)[NH]C2=O)[C@@H]1O[Si](C)(C)C3839.1Semi standard non polar33892256
UDP-L-arabinose,3TMS,isomer #17C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)OP(=O)(O[C@H]2OC[C@H](O)[C@H](O)[C@H]2O)O[Si](C)(C)C)O[C@@H](N2C=CC(=O)[NH]C2=O)[C@@H]1O[Si](C)(C)C3849.2Semi standard non polar33892256
UDP-L-arabinose,3TMS,isomer #18C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]2OC[C@H](O)[C@H](O)[C@H]2O)O[C@@H](N2C=CC(=O)N([Si](C)(C)C)C2=O)[C@@H]1O[Si](C)(C)C3931.4Semi standard non polar33892256
UDP-L-arabinose,3TMS,isomer #19C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O[C@H]2OC[C@H](O)[C@H](O)[C@H]2O)O[Si](C)(C)C)O[C@@H](N2C=CC(=O)[NH]C2=O)[C@@H]1O3888.8Semi standard non polar33892256
UDP-L-arabinose,3TMS,isomer #2C[Si](C)(C)O[C@H]1CO[C@H](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@H](O[Si](C)(C)C)[C@H]1O3759.0Semi standard non polar33892256
UDP-L-arabinose,3TMS,isomer #20C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O)O[C@H]2OC[C@H](O)[C@H](O)[C@H]2O)O[C@@H](N2C=CC(=O)N([Si](C)(C)C)C2=O)[C@@H]1O3981.6Semi standard non polar33892256
UDP-L-arabinose,3TMS,isomer #21C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)OP(=O)(O[C@H]2OC[C@H](O)[C@H](O)[C@H]2O)O[Si](C)(C)C)O[C@@H](N2C=CC(=O)N([Si](C)(C)C)C2=O)[C@@H]1O3981.7Semi standard non polar33892256
UDP-L-arabinose,3TMS,isomer #22C[Si](C)(C)O[C@H]1CO[C@H](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)[C@H](O[Si](C)(C)C)[C@H]1O3751.3Semi standard non polar33892256
UDP-L-arabinose,3TMS,isomer #23C[Si](C)(C)O[C@H]1CO[C@H](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)[C@H](O)[C@H]1O[Si](C)(C)C3742.8Semi standard non polar33892256
UDP-L-arabinose,3TMS,isomer #24C[Si](C)(C)O[C@H]1CO[C@H](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)[C@H](O)[C@H]1O3830.0Semi standard non polar33892256
UDP-L-arabinose,3TMS,isomer #25C[Si](C)(C)O[C@H]1CO[C@H](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)[C@H](O)[C@H]1O3825.4Semi standard non polar33892256
UDP-L-arabinose,3TMS,isomer #26C[Si](C)(C)O[C@H]1CO[C@H](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)[C@H](O)[C@H]1O3925.7Semi standard non polar33892256
UDP-L-arabinose,3TMS,isomer #27C[Si](C)(C)O[C@H]1CO[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(=O)[NH]C3=O)[C@H](O)[C@@H]2O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C3787.0Semi standard non polar33892256
UDP-L-arabinose,3TMS,isomer #28C[Si](C)(C)O[C@H]1CO[C@H](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)[C@H](O[Si](C)(C)C)[C@H]1O3820.1Semi standard non polar33892256
UDP-L-arabinose,3TMS,isomer #29C[Si](C)(C)O[C@H]1CO[C@H](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@H](O[Si](C)(C)C)[C@H]1O3816.0Semi standard non polar33892256
UDP-L-arabinose,3TMS,isomer #3C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]2OC[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O)O[C@@H](N2C=CC(=O)[NH]C2=O)[C@@H]1O3749.9Semi standard non polar33892256
UDP-L-arabinose,3TMS,isomer #30C[Si](C)(C)O[C@H]1CO[C@H](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)[C@H](O[Si](C)(C)C)[C@H]1O3912.1Semi standard non polar33892256
UDP-L-arabinose,3TMS,isomer #31C[Si](C)(C)O[C@H]1CO[C@H](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)[C@H](O)[C@H]1O[Si](C)(C)C3815.5Semi standard non polar33892256
UDP-L-arabinose,3TMS,isomer #32C[Si](C)(C)O[C@H]1CO[C@H](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@H](O)[C@H]1O[Si](C)(C)C3805.4Semi standard non polar33892256
UDP-L-arabinose,3TMS,isomer #33C[Si](C)(C)O[C@H]1CO[C@H](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)[C@H](O)[C@H]1O[Si](C)(C)C3912.3Semi standard non polar33892256
UDP-L-arabinose,3TMS,isomer #34C[Si](C)(C)O[C@H]1CO[C@H](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)[C@H](O)[C@H]1O3894.9Semi standard non polar33892256
UDP-L-arabinose,3TMS,isomer #35C[Si](C)(C)O[C@H]1CO[C@H](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)[C@H](O)[C@H]1O4006.9Semi standard non polar33892256
UDP-L-arabinose,3TMS,isomer #36C[Si](C)(C)O[C@H]1CO[C@H](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)[C@H](O)[C@H]1O4006.3Semi standard non polar33892256
UDP-L-arabinose,3TMS,isomer #37C[Si](C)(C)O[C@H]1[C@@H](O)CO[C@H](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)[C@@H]1O[Si](C)(C)C3757.9Semi standard non polar33892256
UDP-L-arabinose,3TMS,isomer #38C[Si](C)(C)O[C@H]1[C@@H](O)CO[C@H](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)[C@@H]1O3807.3Semi standard non polar33892256
UDP-L-arabinose,3TMS,isomer #39C[Si](C)(C)O[C@H]1[C@@H](O)CO[C@H](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)[C@@H]1O3797.9Semi standard non polar33892256
UDP-L-arabinose,3TMS,isomer #4C[Si](C)(C)O[C@H]1CO[C@H](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)[C@H](O)[C@H]1O3834.4Semi standard non polar33892256
UDP-L-arabinose,3TMS,isomer #40C[Si](C)(C)O[C@H]1[C@@H](O)CO[C@H](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)[C@@H]1O3882.9Semi standard non polar33892256
UDP-L-arabinose,3TMS,isomer #41C[Si](C)(C)O[C@H]1[C@@H](O)CO[C@H](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)[C@@H]1O[Si](C)(C)C3827.6Semi standard non polar33892256
UDP-L-arabinose,3TMS,isomer #42C[Si](C)(C)O[C@H]1[C@@H](O)CO[C@H](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@@H]1O[Si](C)(C)C3816.9Semi standard non polar33892256
UDP-L-arabinose,3TMS,isomer #43C[Si](C)(C)O[C@H]1[C@@H](O)CO[C@H](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)[C@@H]1O[Si](C)(C)C3901.5Semi standard non polar33892256
UDP-L-arabinose,3TMS,isomer #44C[Si](C)(C)O[C@H]1[C@@H](O)CO[C@H](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)[C@@H]1O3860.9Semi standard non polar33892256
UDP-L-arabinose,3TMS,isomer #45C[Si](C)(C)O[C@H]1[C@@H](O)CO[C@H](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)[C@@H]1O3951.8Semi standard non polar33892256
UDP-L-arabinose,3TMS,isomer #46C[Si](C)(C)O[C@H]1[C@@H](O)CO[C@H](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)[C@@H]1O3945.0Semi standard non polar33892256
UDP-L-arabinose,3TMS,isomer #47C[Si](C)(C)O[C@@H]1[C@@H](O)[C@@H](O)CO[C@@H]1OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]1O[C@@H](N2C=CC(=O)[NH]C2=O)[C@H](O[Si](C)(C)C)[C@@H]1O3817.8Semi standard non polar33892256
UDP-L-arabinose,3TMS,isomer #48C[Si](C)(C)O[C@@H]1[C@@H](O)[C@@H](O)CO[C@@H]1OP(=O)(O)OP(=O)(OC[C@H]1O[C@@H](N2C=CC(=O)[NH]C2=O)[C@H](O[Si](C)(C)C)[C@@H]1O)O[Si](C)(C)C3811.0Semi standard non polar33892256
UDP-L-arabinose,3TMS,isomer #49C[Si](C)(C)O[C@@H]1[C@@H](O)[C@@H](O)CO[C@@H]1OP(=O)(O)OP(=O)(O)OC[C@H]1O[C@@H](N2C=CC(=O)N([Si](C)(C)C)C2=O)[C@H](O[Si](C)(C)C)[C@@H]1O3892.4Semi standard non polar33892256
UDP-L-arabinose,3TMS,isomer #5C[Si](C)(C)O[C@H]1CO[C@H](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)[C@H](O)[C@H]1O3830.7Semi standard non polar33892256
UDP-L-arabinose,3TMS,isomer #50C[Si](C)(C)O[C@@H]1[C@@H](O)[C@@H](O)CO[C@@H]1OP(=O)(O[Si](C)(C)C)OP(=O)(OC[C@H]1O[C@@H](N2C=CC(=O)[NH]C2=O)[C@H](O)[C@@H]1O)O[Si](C)(C)C3868.9Semi standard non polar33892256
UDP-L-arabinose,3TMS,isomer #51C[Si](C)(C)O[C@@H]1[C@@H](O)[C@@H](O)CO[C@@H]1OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]1O[C@@H](N2C=CC(=O)N([Si](C)(C)C)C2=O)[C@H](O)[C@@H]1O3967.7Semi standard non polar33892256
UDP-L-arabinose,3TMS,isomer #52C[Si](C)(C)O[C@@H]1[C@@H](O)[C@@H](O)CO[C@@H]1OP(=O)(O)OP(=O)(OC[C@H]1O[C@@H](N2C=CC(=O)N([Si](C)(C)C)C2=O)[C@H](O)[C@@H]1O)O[Si](C)(C)C3962.4Semi standard non polar33892256
UDP-L-arabinose,3TMS,isomer #53C[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O[C@H]2OC[C@H](O)[C@H](O)[C@H]2O)O[Si](C)(C)C)O[C@H]1N1C=CC(=O)[NH]C1=O3887.1Semi standard non polar33892256
UDP-L-arabinose,3TMS,isomer #54C[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O)O[C@H]2OC[C@H](O)[C@H](O)[C@H]2O)O[C@H]1N1C=CC(=O)N([Si](C)(C)C)C1=O3972.4Semi standard non polar33892256
UDP-L-arabinose,3TMS,isomer #55C[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O[C@H]2OC[C@H](O)[C@H](O)[C@H]2O)O[Si](C)(C)C)O[C@H]1N1C=CC(=O)N([Si](C)(C)C)C1=O3976.5Semi standard non polar33892256
UDP-L-arabinose,3TMS,isomer #56C[Si](C)(C)OP(=O)(OC[C@H]1O[C@@H](N2C=CC(=O)N([Si](C)(C)C)C2=O)[C@H](O)[C@@H]1O)OP(=O)(O[C@H]1OC[C@H](O)[C@H](O)[C@H]1O)O[Si](C)(C)C4035.2Semi standard non polar33892256
UDP-L-arabinose,3TMS,isomer #6C[Si](C)(C)O[C@H]1CO[C@H](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)[C@H](O)[C@H]1O3933.4Semi standard non polar33892256
UDP-L-arabinose,3TMS,isomer #7C[Si](C)(C)O[C@H]1[C@@H](O)CO[C@H](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)[C@@H]1O3754.9Semi standard non polar33892256
UDP-L-arabinose,3TMS,isomer #8C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]2OC[C@H](O)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)O[C@@H](N2C=CC(=O)[NH]C2=O)[C@@H]1O3764.3Semi standard non polar33892256
UDP-L-arabinose,3TMS,isomer #9C[Si](C)(C)O[C@H]1[C@@H](O)CO[C@H](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)[C@@H]1O3814.5Semi standard non polar33892256
UDP-L-arabinose,4TMS,isomer #1C[Si](C)(C)O[C@H]1CO[C@H](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)[C@H](O[Si](C)(C)C)[C@H]1O3713.1Semi standard non polar33892256
UDP-L-arabinose,4TMS,isomer #10C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O)O[C@H]2OC[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O)O[C@@H](N2C=CC(=O)[NH]C2=O)[C@@H]1O3754.8Semi standard non polar33892256
UDP-L-arabinose,4TMS,isomer #11C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)OP(=O)(O[C@H]2OC[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O)O[Si](C)(C)C)O[C@@H](N2C=CC(=O)[NH]C2=O)[C@@H]1O3769.0Semi standard non polar33892256
UDP-L-arabinose,4TMS,isomer #12C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]2OC[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O)O[C@@H](N2C=CC(=O)N([Si](C)(C)C)C2=O)[C@@H]1O3830.4Semi standard non polar33892256
UDP-L-arabinose,4TMS,isomer #13C[Si](C)(C)O[C@H]1CO[C@H](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)[C@H](O)[C@H]1O3825.4Semi standard non polar33892256
UDP-L-arabinose,4TMS,isomer #14C[Si](C)(C)O[C@H]1CO[C@H](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)[C@H](O)[C@H]1O3889.1Semi standard non polar33892256
UDP-L-arabinose,4TMS,isomer #15C[Si](C)(C)O[C@H]1CO[C@H](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)[C@H](O)[C@H]1O3892.6Semi standard non polar33892256
UDP-L-arabinose,4TMS,isomer #16C[Si](C)(C)O[C@H]1[C@@H](O)CO[C@H](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)[C@@H]1O[Si](C)(C)C3714.5Semi standard non polar33892256
UDP-L-arabinose,4TMS,isomer #17C[Si](C)(C)O[C@H]1[C@@H](O)CO[C@H](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)[C@@H]1O3766.5Semi standard non polar33892256
UDP-L-arabinose,4TMS,isomer #18C[Si](C)(C)O[C@H]1[C@@H](O)CO[C@H](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)[C@@H]1O3752.6Semi standard non polar33892256
UDP-L-arabinose,4TMS,isomer #19C[Si](C)(C)O[C@H]1[C@@H](O)CO[C@H](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)[C@@H]1O3838.4Semi standard non polar33892256
UDP-L-arabinose,4TMS,isomer #2C[Si](C)(C)O[C@H]1CO[C@H](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)[C@H](O)[C@H]1O[Si](C)(C)C3710.6Semi standard non polar33892256
UDP-L-arabinose,4TMS,isomer #20C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O)O[C@H]2OC[C@H](O)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)O[C@@H](N2C=CC(=O)[NH]C2=O)[C@@H]1O3761.2Semi standard non polar33892256
UDP-L-arabinose,4TMS,isomer #21C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)OP(=O)(O[C@H]2OC[C@H](O)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)O[Si](C)(C)C)O[C@@H](N2C=CC(=O)[NH]C2=O)[C@@H]1O3775.0Semi standard non polar33892256
UDP-L-arabinose,4TMS,isomer #22C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]2OC[C@H](O)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)O[C@@H](N2C=CC(=O)N([Si](C)(C)C)C2=O)[C@@H]1O3839.8Semi standard non polar33892256
UDP-L-arabinose,4TMS,isomer #23C[Si](C)(C)O[C@H]1[C@@H](O)CO[C@H](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)[C@@H]1O3817.0Semi standard non polar33892256
UDP-L-arabinose,4TMS,isomer #24C[Si](C)(C)O[C@H]1[C@@H](O)CO[C@H](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)[C@@H]1O3877.9Semi standard non polar33892256
UDP-L-arabinose,4TMS,isomer #25C[Si](C)(C)O[C@H]1[C@@H](O)CO[C@H](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)[C@@H]1O3877.4Semi standard non polar33892256
UDP-L-arabinose,4TMS,isomer #26C[Si](C)(C)O[C@@H]1[C@@H](O)[C@@H](O)CO[C@@H]1OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]1O[C@@H](N2C=CC(=O)[NH]C2=O)[C@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C3758.8Semi standard non polar33892256
UDP-L-arabinose,4TMS,isomer #27C[Si](C)(C)O[C@@H]1[C@@H](O)[C@@H](O)CO[C@@H]1OP(=O)(O)OP(=O)(OC[C@H]1O[C@@H](N2C=CC(=O)[NH]C2=O)[C@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C)O[Si](C)(C)C3750.4Semi standard non polar33892256
UDP-L-arabinose,4TMS,isomer #28C[Si](C)(C)O[C@@H]1[C@@H](O)[C@@H](O)CO[C@@H]1OP(=O)(O)OP(=O)(O)OC[C@H]1O[C@@H](N2C=CC(=O)N([Si](C)(C)C)C2=O)[C@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C3835.7Semi standard non polar33892256
UDP-L-arabinose,4TMS,isomer #29C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O[C@H]2OC[C@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)O[Si](C)(C)C)O[C@@H](N2C=CC(=O)[NH]C2=O)[C@@H]1O3809.8Semi standard non polar33892256
UDP-L-arabinose,4TMS,isomer #3C[Si](C)(C)O[C@H]1CO[C@H](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)[C@H](O)[C@H]1O3773.8Semi standard non polar33892256
UDP-L-arabinose,4TMS,isomer #30C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O)O[C@H]2OC[C@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)O[C@@H](N2C=CC(=O)N([Si](C)(C)C)C2=O)[C@@H]1O3869.8Semi standard non polar33892256
UDP-L-arabinose,4TMS,isomer #31C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)OP(=O)(O[C@H]2OC[C@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)O[Si](C)(C)C)O[C@@H](N2C=CC(=O)N([Si](C)(C)C)C2=O)[C@@H]1O3867.8Semi standard non polar33892256
UDP-L-arabinose,4TMS,isomer #32C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O[C@H]2OC[C@H](O)[C@H](O)[C@H]2O)O[Si](C)(C)C)O[C@@H](N2C=CC(=O)[NH]C2=O)[C@@H]1O[Si](C)(C)C3820.9Semi standard non polar33892256
UDP-L-arabinose,4TMS,isomer #33C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O)O[C@H]2OC[C@H](O)[C@H](O)[C@H]2O)O[C@@H](N2C=CC(=O)N([Si](C)(C)C)C2=O)[C@@H]1O[Si](C)(C)C3893.8Semi standard non polar33892256
UDP-L-arabinose,4TMS,isomer #34C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)OP(=O)(O[C@H]2OC[C@H](O)[C@H](O)[C@H]2O)O[Si](C)(C)C)O[C@@H](N2C=CC(=O)N([Si](C)(C)C)C2=O)[C@@H]1O[Si](C)(C)C3890.3Semi standard non polar33892256
UDP-L-arabinose,4TMS,isomer #35C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O[C@H]2OC[C@H](O)[C@H](O)[C@H]2O)O[Si](C)(C)C)O[C@@H](N2C=CC(=O)N([Si](C)(C)C)C2=O)[C@@H]1O3925.9Semi standard non polar33892256
UDP-L-arabinose,4TMS,isomer #36C[Si](C)(C)O[C@H]1CO[C@H](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)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C3719.9Semi standard non polar33892256
UDP-L-arabinose,4TMS,isomer #37C[Si](C)(C)O[C@H]1CO[C@H](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)[C@H](O[Si](C)(C)C)[C@H]1O3758.9Semi standard non polar33892256
UDP-L-arabinose,4TMS,isomer #38C[Si](C)(C)O[C@H]1CO[C@H](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)[C@H](O[Si](C)(C)C)[C@H]1O3750.5Semi standard non polar33892256
UDP-L-arabinose,4TMS,isomer #39C[Si](C)(C)O[C@H]1CO[C@H](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)[C@H](O[Si](C)(C)C)[C@H]1O3825.9Semi standard non polar33892256
UDP-L-arabinose,4TMS,isomer #4C[Si](C)(C)O[C@H]1CO[C@H](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)[C@H](O)[C@H]1O3765.8Semi standard non polar33892256
UDP-L-arabinose,4TMS,isomer #40C[Si](C)(C)O[C@H]1CO[C@H](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)[C@H](O)[C@H]1O[Si](C)(C)C3759.1Semi standard non polar33892256
UDP-L-arabinose,4TMS,isomer #41C[Si](C)(C)O[C@H]1CO[C@H](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)[C@H](O)[C@H]1O[Si](C)(C)C3745.1Semi standard non polar33892256
UDP-L-arabinose,4TMS,isomer #42C[Si](C)(C)O[C@H]1CO[C@H](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)[C@H](O)[C@H]1O[Si](C)(C)C3823.7Semi standard non polar33892256
UDP-L-arabinose,4TMS,isomer #43C[Si](C)(C)O[C@H]1CO[C@H](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)[C@H](O)[C@H]1O3822.2Semi standard non polar33892256
UDP-L-arabinose,4TMS,isomer #44C[Si](C)(C)O[C@H]1CO[C@H](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)[C@H](O)[C@H]1O3885.5Semi standard non polar33892256
UDP-L-arabinose,4TMS,isomer #45C[Si](C)(C)O[C@H]1CO[C@H](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)[C@H](O)[C@H]1O3888.7Semi standard non polar33892256
UDP-L-arabinose,4TMS,isomer #46C[Si](C)(C)O[C@H]1CO[C@H](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)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C3787.9Semi standard non polar33892256
UDP-L-arabinose,4TMS,isomer #47C[Si](C)(C)O[C@H]1CO[C@H](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@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C3776.1Semi standard non polar33892256
UDP-L-arabinose,4TMS,isomer #48C[Si](C)(C)O[C@H]1CO[C@H](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)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C3862.4Semi standard non polar33892256
UDP-L-arabinose,4TMS,isomer #49C[Si](C)(C)O[C@H]1CO[C@H](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)[C@H](O[Si](C)(C)C)[C@H]1O3818.2Semi standard non polar33892256
UDP-L-arabinose,4TMS,isomer #5C[Si](C)(C)O[C@H]1CO[C@H](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)[C@H](O)[C@H]1O3852.9Semi standard non polar33892256
UDP-L-arabinose,4TMS,isomer #50C[Si](C)(C)O[C@H]1CO[C@H](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)[C@H](O[Si](C)(C)C)[C@H]1O3877.3Semi standard non polar33892256
UDP-L-arabinose,4TMS,isomer #51C[Si](C)(C)O[C@H]1CO[C@H](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)[C@H](O[Si](C)(C)C)[C@H]1O3877.6Semi standard non polar33892256
UDP-L-arabinose,4TMS,isomer #52C[Si](C)(C)O[C@H]1CO[C@H](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)[C@H](O)[C@H]1O[Si](C)(C)C3817.0Semi standard non polar33892256
UDP-L-arabinose,4TMS,isomer #53C[Si](C)(C)O[C@H]1CO[C@H](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)[C@H](O)[C@H]1O[Si](C)(C)C3878.5Semi standard non polar33892256
UDP-L-arabinose,4TMS,isomer #54C[Si](C)(C)O[C@H]1CO[C@H](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)[C@H](O)[C@H]1O[Si](C)(C)C3873.9Semi standard non polar33892256
UDP-L-arabinose,4TMS,isomer #55C[Si](C)(C)O[C@H]1CO[C@H](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)[C@H](O)[C@H]1O3935.4Semi standard non polar33892256
UDP-L-arabinose,4TMS,isomer #56C[Si](C)(C)O[C@H]1[C@@H](O)CO[C@H](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)[C@@H]1O[Si](C)(C)C3768.1Semi standard non polar33892256
UDP-L-arabinose,4TMS,isomer #57C[Si](C)(C)O[C@H]1[C@@H](O)CO[C@H](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)[C@@H]1O[Si](C)(C)C3754.4Semi standard non polar33892256
UDP-L-arabinose,4TMS,isomer #58C[Si](C)(C)O[C@H]1[C@@H](O)CO[C@H](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)[C@@H]1O[Si](C)(C)C3832.5Semi standard non polar33892256
UDP-L-arabinose,4TMS,isomer #59C[Si](C)(C)O[C@H]1[C@@H](O)CO[C@H](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)[C@@H]1O3811.4Semi standard non polar33892256
UDP-L-arabinose,4TMS,isomer #6C[Si](C)(C)O[C@H]1CO[C@H](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@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C3727.5Semi standard non polar33892256
UDP-L-arabinose,4TMS,isomer #60C[Si](C)(C)O[C@H]1[C@@H](O)CO[C@H](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)[C@@H]1O3871.9Semi standard non polar33892256
UDP-L-arabinose,4TMS,isomer #61C[Si](C)(C)O[C@H]1[C@@H](O)CO[C@H](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)[C@@H]1O3870.5Semi standard non polar33892256
UDP-L-arabinose,4TMS,isomer #62C[Si](C)(C)O[C@H]1[C@@H](O)CO[C@H](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)[C@@H]1O[Si](C)(C)C3817.9Semi standard non polar33892256
UDP-L-arabinose,4TMS,isomer #63C[Si](C)(C)O[C@H]1[C@@H](O)CO[C@H](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)[C@@H]1O[Si](C)(C)C3879.7Semi standard non polar33892256
UDP-L-arabinose,4TMS,isomer #64C[Si](C)(C)O[C@H]1[C@@H](O)CO[C@H](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)[C@@H]1O[Si](C)(C)C3877.5Semi standard non polar33892256
UDP-L-arabinose,4TMS,isomer #65C[Si](C)(C)O[C@H]1[C@@H](O)CO[C@H](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)[C@@H]1O3918.5Semi standard non polar33892256
UDP-L-arabinose,4TMS,isomer #66C[Si](C)(C)O[C@@H]1[C@@H](O)[C@@H](O)CO[C@@H]1OP(=O)(O[Si](C)(C)C)OP(=O)(OC[C@H]1O[C@@H](N2C=CC(=O)[NH]C2=O)[C@H](O[Si](C)(C)C)[C@@H]1O)O[Si](C)(C)C3805.8Semi standard non polar33892256
UDP-L-arabinose,4TMS,isomer #67C[Si](C)(C)O[C@@H]1[C@@H](O)[C@@H](O)CO[C@@H]1OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]1O[C@@H](N2C=CC(=O)N([Si](C)(C)C)C2=O)[C@H](O[Si](C)(C)C)[C@@H]1O3865.0Semi standard non polar33892256
UDP-L-arabinose,4TMS,isomer #68C[Si](C)(C)O[C@@H]1[C@@H](O)[C@@H](O)CO[C@@H]1OP(=O)(O)OP(=O)(OC[C@H]1O[C@@H](N2C=CC(=O)N([Si](C)(C)C)C2=O)[C@H](O[Si](C)(C)C)[C@@H]1O)O[Si](C)(C)C3865.8Semi standard non polar33892256
UDP-L-arabinose,4TMS,isomer #69C[Si](C)(C)O[C@@H]1[C@@H](O)[C@@H](O)CO[C@@H]1OP(=O)(O[Si](C)(C)C)OP(=O)(OC[C@H]1O[C@@H](N2C=CC(=O)N([Si](C)(C)C)C2=O)[C@H](O)[C@@H]1O)O[Si](C)(C)C3913.8Semi standard non polar33892256
UDP-L-arabinose,4TMS,isomer #7C[Si](C)(C)O[C@H]1CO[C@H](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)[C@H](O[Si](C)(C)C)[C@H]1O3767.7Semi standard non polar33892256
UDP-L-arabinose,4TMS,isomer #70C[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O[C@H]2OC[C@H](O)[C@H](O)[C@H]2O)O[Si](C)(C)C)O[C@H]1N1C=CC(=O)N([Si](C)(C)C)C1=O3923.9Semi standard non polar33892256
UDP-L-arabinose,4TMS,isomer #8C[Si](C)(C)O[C@H]1CO[C@H](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)[C@H](O[Si](C)(C)C)[C@H]1O3759.2Semi standard non polar33892256
UDP-L-arabinose,4TMS,isomer #9C[Si](C)(C)O[C@H]1CO[C@H](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)[C@H](O[Si](C)(C)C)[C@H]1O3831.8Semi standard non polar33892256
UDP-L-arabinose,5TMS,isomer #1C[Si](C)(C)O[C@H]1CO[C@H](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)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C3711.6Semi standard non polar33892256
UDP-L-arabinose,5TMS,isomer #10C[Si](C)(C)O[C@H]1CO[C@H](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)[C@H](O)[C@H]1O3870.9Semi standard non polar33892256
UDP-L-arabinose,5TMS,isomer #11C[Si](C)(C)O[C@H]1CO[C@H](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)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C3759.4Semi standard non polar33892256
UDP-L-arabinose,5TMS,isomer #12C[Si](C)(C)O[C@H]1CO[C@H](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)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C3747.9Semi standard non polar33892256
UDP-L-arabinose,5TMS,isomer #13C[Si](C)(C)O[C@H]1CO[C@H](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)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C3846.3Semi standard non polar33892256
UDP-L-arabinose,5TMS,isomer #14C[Si](C)(C)O[C@H]1CO[C@H](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)[C@H](O[Si](C)(C)C)[C@H]1O3781.6Semi standard non polar33892256
UDP-L-arabinose,5TMS,isomer #15C[Si](C)(C)O[C@H]1CO[C@H](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)[C@H](O[Si](C)(C)C)[C@H]1O3867.5Semi standard non polar33892256
UDP-L-arabinose,5TMS,isomer #16C[Si](C)(C)O[C@H]1CO[C@H](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)[C@H](O[Si](C)(C)C)[C@H]1O3865.7Semi standard non polar33892256
UDP-L-arabinose,5TMS,isomer #17C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O[C@H]2OC[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O)O[Si](C)(C)C)O[C@@H](N2C=CC(=O)[NH]C2=O)[C@@H]1O3790.1Semi standard non polar33892256
UDP-L-arabinose,5TMS,isomer #18C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O)O[C@H]2OC[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O)O[C@@H](N2C=CC(=O)N([Si](C)(C)C)C2=O)[C@@H]1O3869.6Semi standard non polar33892256
UDP-L-arabinose,5TMS,isomer #19C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)OP(=O)(O[C@H]2OC[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O)O[Si](C)(C)C)O[C@@H](N2C=CC(=O)N([Si](C)(C)C)C2=O)[C@@H]1O3875.8Semi standard non polar33892256
UDP-L-arabinose,5TMS,isomer #2C[Si](C)(C)O[C@H]1CO[C@H](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)[C@H](O[Si](C)(C)C)[C@H]1O3739.4Semi standard non polar33892256
UDP-L-arabinose,5TMS,isomer #20C[Si](C)(C)O[C@H]1CO[C@H](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)[C@H](O)[C@H]1O3909.9Semi standard non polar33892256
UDP-L-arabinose,5TMS,isomer #21C[Si](C)(C)O[C@H]1[C@@H](O)CO[C@H](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)[C@@H]1O[Si](C)(C)C3743.3Semi standard non polar33892256
UDP-L-arabinose,5TMS,isomer #22C[Si](C)(C)O[C@H]1[C@@H](O)CO[C@H](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)[C@@H]1O[Si](C)(C)C3733.0Semi standard non polar33892256
UDP-L-arabinose,5TMS,isomer #23C[Si](C)(C)O[C@H]1[C@@H](O)CO[C@H](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)[C@@H]1O[Si](C)(C)C3832.3Semi standard non polar33892256
UDP-L-arabinose,5TMS,isomer #24C[Si](C)(C)O[C@H]1[C@@H](O)CO[C@H](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)[C@@H]1O3774.5Semi standard non polar33892256
UDP-L-arabinose,5TMS,isomer #25C[Si](C)(C)O[C@H]1[C@@H](O)CO[C@H](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)[C@@H]1O3871.4Semi standard non polar33892256
UDP-L-arabinose,5TMS,isomer #26C[Si](C)(C)O[C@H]1[C@@H](O)CO[C@H](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)[C@@H]1O3864.6Semi standard non polar33892256
UDP-L-arabinose,5TMS,isomer #27C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O[C@H]2OC[C@H](O)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)O[Si](C)(C)C)O[C@@H](N2C=CC(=O)[NH]C2=O)[C@@H]1O3784.4Semi standard non polar33892256
UDP-L-arabinose,5TMS,isomer #28C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O)O[C@H]2OC[C@H](O)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)O[C@@H](N2C=CC(=O)N([Si](C)(C)C)C2=O)[C@@H]1O3871.2Semi standard non polar33892256
UDP-L-arabinose,5TMS,isomer #29C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)OP(=O)(O[C@H]2OC[C@H](O)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)O[Si](C)(C)C)O[C@@H](N2C=CC(=O)N([Si](C)(C)C)C2=O)[C@@H]1O3875.9Semi standard non polar33892256
UDP-L-arabinose,5TMS,isomer #3C[Si](C)(C)O[C@H]1CO[C@H](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)[C@H](O[Si](C)(C)C)[C@H]1O3730.6Semi standard non polar33892256
UDP-L-arabinose,5TMS,isomer #30C[Si](C)(C)O[C@H]1[C@@H](O)CO[C@H](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)[C@@H]1O3911.5Semi standard non polar33892256
UDP-L-arabinose,5TMS,isomer #31C[Si](C)(C)O[C@@H]1[C@@H](O)[C@@H](O)CO[C@@H]1OP(=O)(O[Si](C)(C)C)OP(=O)(OC[C@H]1O[C@@H](N2C=CC(=O)[NH]C2=O)[C@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C)O[Si](C)(C)C3749.9Semi standard non polar33892256
UDP-L-arabinose,5TMS,isomer #32C[Si](C)(C)O[C@@H]1[C@@H](O)[C@@H](O)CO[C@@H]1OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]1O[C@@H](N2C=CC(=O)N([Si](C)(C)C)C2=O)[C@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C3852.3Semi standard non polar33892256
UDP-L-arabinose,5TMS,isomer #33C[Si](C)(C)O[C@@H]1[C@@H](O)[C@@H](O)CO[C@@H]1OP(=O)(O)OP(=O)(OC[C@H]1O[C@@H](N2C=CC(=O)N([Si](C)(C)C)C2=O)[C@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C)O[Si](C)(C)C3848.1Semi standard non polar33892256
UDP-L-arabinose,5TMS,isomer #34C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O[C@H]2OC[C@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)O[Si](C)(C)C)O[C@@H](N2C=CC(=O)N([Si](C)(C)C)C2=O)[C@@H]1O3892.1Semi standard non polar33892256
UDP-L-arabinose,5TMS,isomer #35C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O[C@H]2OC[C@H](O)[C@H](O)[C@H]2O)O[Si](C)(C)C)O[C@@H](N2C=CC(=O)N([Si](C)(C)C)C2=O)[C@@H]1O[Si](C)(C)C3898.9Semi standard non polar33892256
UDP-L-arabinose,5TMS,isomer #36C[Si](C)(C)O[C@H]1CO[C@H](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)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C3752.5Semi standard non polar33892256
UDP-L-arabinose,5TMS,isomer #37C[Si](C)(C)O[C@H]1CO[C@H](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)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C3739.2Semi standard non polar33892256
UDP-L-arabinose,5TMS,isomer #38C[Si](C)(C)O[C@H]1CO[C@H](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)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C3835.3Semi standard non polar33892256
UDP-L-arabinose,5TMS,isomer #39C[Si](C)(C)O[C@H]1CO[C@H](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)[C@H](O[Si](C)(C)C)[C@H]1O3770.9Semi standard non polar33892256
UDP-L-arabinose,5TMS,isomer #4C[Si](C)(C)O[C@H]1CO[C@H](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)[C@H](O[Si](C)(C)C)[C@H]1O3829.7Semi standard non polar33892256
UDP-L-arabinose,5TMS,isomer #40C[Si](C)(C)O[C@H]1CO[C@H](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)[C@H](O[Si](C)(C)C)[C@H]1O3854.6Semi standard non polar33892256
UDP-L-arabinose,5TMS,isomer #41C[Si](C)(C)O[C@H]1CO[C@H](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)[C@H](O[Si](C)(C)C)[C@H]1O3854.4Semi standard non polar33892256
UDP-L-arabinose,5TMS,isomer #42C[Si](C)(C)O[C@H]1CO[C@H](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)[C@H](O)[C@H]1O[Si](C)(C)C3777.0Semi standard non polar33892256
UDP-L-arabinose,5TMS,isomer #43C[Si](C)(C)O[C@H]1CO[C@H](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)[C@H](O)[C@H]1O[Si](C)(C)C3862.4Semi standard non polar33892256
UDP-L-arabinose,5TMS,isomer #44C[Si](C)(C)O[C@H]1CO[C@H](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)[C@H](O)[C@H]1O[Si](C)(C)C3856.3Semi standard non polar33892256
UDP-L-arabinose,5TMS,isomer #45C[Si](C)(C)O[C@H]1CO[C@H](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)[C@H](O)[C@H]1O3900.9Semi standard non polar33892256
UDP-L-arabinose,5TMS,isomer #46C[Si](C)(C)O[C@H]1CO[C@H](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)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C3778.6Semi standard non polar33892256
UDP-L-arabinose,5TMS,isomer #47C[Si](C)(C)O[C@H]1CO[C@H](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)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C3883.3Semi standard non polar33892256
UDP-L-arabinose,5TMS,isomer #48C[Si](C)(C)O[C@H]1CO[C@H](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)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C3878.1Semi standard non polar33892256
UDP-L-arabinose,5TMS,isomer #49C[Si](C)(C)O[C@H]1CO[C@H](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)[C@H](O[Si](C)(C)C)[C@H]1O3899.5Semi standard non polar33892256
UDP-L-arabinose,5TMS,isomer #5C[Si](C)(C)O[C@H]1CO[C@H](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)[C@H](O)[C@H]1O[Si](C)(C)C3749.3Semi standard non polar33892256
UDP-L-arabinose,5TMS,isomer #50C[Si](C)(C)O[C@H]1CO[C@H](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)[C@H](O)[C@H]1O[Si](C)(C)C3902.2Semi standard non polar33892256
UDP-L-arabinose,5TMS,isomer #51C[Si](C)(C)O[C@H]1[C@@H](O)CO[C@H](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)[C@@H]1O[Si](C)(C)C3775.8Semi standard non polar33892256
UDP-L-arabinose,5TMS,isomer #52C[Si](C)(C)O[C@H]1[C@@H](O)CO[C@H](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)[C@@H]1O[Si](C)(C)C3864.9Semi standard non polar33892256
UDP-L-arabinose,5TMS,isomer #53C[Si](C)(C)O[C@H]1[C@@H](O)CO[C@H](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)[C@@H]1O[Si](C)(C)C3859.8Semi standard non polar33892256
UDP-L-arabinose,5TMS,isomer #54C[Si](C)(C)O[C@H]1[C@@H](O)CO[C@H](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)[C@@H]1O3899.3Semi standard non polar33892256
UDP-L-arabinose,5TMS,isomer #55C[Si](C)(C)O[C@H]1[C@@H](O)CO[C@H](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)[C@@H]1O[Si](C)(C)C3900.2Semi standard non polar33892256
UDP-L-arabinose,5TMS,isomer #56C[Si](C)(C)O[C@@H]1[C@@H](O)[C@@H](O)CO[C@@H]1OP(=O)(O[Si](C)(C)C)OP(=O)(OC[C@H]1O[C@@H](N2C=CC(=O)N([Si](C)(C)C)C2=O)[C@H](O[Si](C)(C)C)[C@@H]1O)O[Si](C)(C)C3883.1Semi standard non polar33892256
UDP-L-arabinose,5TMS,isomer #6C[Si](C)(C)O[C@H]1CO[C@H](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)[C@H](O)[C@H]1O[Si](C)(C)C3735.1Semi standard non polar33892256
UDP-L-arabinose,5TMS,isomer #7C[Si](C)(C)O[C@H]1CO[C@H](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)[C@H](O)[C@H]1O[Si](C)(C)C3833.5Semi standard non polar33892256
UDP-L-arabinose,5TMS,isomer #8C[Si](C)(C)O[C@H]1CO[C@H](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)[C@H](O)[C@H]1O3771.8Semi standard non polar33892256
UDP-L-arabinose,5TMS,isomer #9C[Si](C)(C)O[C@H]1CO[C@H](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)[C@H](O)[C@H]1O3871.7Semi standard non polar33892256
UDP-L-arabinose,1TBDMS,isomer #1CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]2OC[C@H](O)[C@H](O)[C@H]2O)O[C@@H](N2C=CC(=O)[NH]C2=O)[C@@H]1O4252.3Semi standard non polar33892256
UDP-L-arabinose,1TBDMS,isomer #2CC(C)(C)[Si](C)(C)O[C@H]1CO[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(=O)[NH]C3=O)[C@H](O)[C@@H]2O)[C@H](O)[C@H]1O4231.3Semi standard non polar33892256
UDP-L-arabinose,1TBDMS,isomer #3CC(C)(C)[Si](C)(C)O[C@H]1[C@@H](O)CO[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(=O)[NH]C3=O)[C@H](O)[C@@H]2O)[C@@H]1O4201.5Semi standard non polar33892256
UDP-L-arabinose,1TBDMS,isomer #4CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](O)[C@@H](O)CO[C@@H]1OP(=O)(O)OP(=O)(O)OC[C@H]1O[C@@H](N2C=CC(=O)[NH]C2=O)[C@H](O)[C@@H]1O4215.1Semi standard non polar33892256
UDP-L-arabinose,1TBDMS,isomer #5CC(C)(C)[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]2OC[C@H](O)[C@H](O)[C@H]2O)O[C@H]1N1C=CC(=O)[NH]C1=O4250.3Semi standard non polar33892256
UDP-L-arabinose,1TBDMS,isomer #6CC(C)(C)[Si](C)(C)OP(=O)(OC[C@H]1O[C@@H](N2C=CC(=O)[NH]C2=O)[C@H](O)[C@@H]1O)OP(=O)(O)O[C@H]1OC[C@H](O)[C@H](O)[C@H]1O4325.3Semi standard non polar33892256
UDP-L-arabinose,1TBDMS,isomer #7CC(C)(C)[Si](C)(C)OP(=O)(O[C@H]1OC[C@H](O)[C@H](O)[C@H]1O)OP(=O)(O)OC[C@H]1O[C@@H](N2C=CC(=O)[NH]C2=O)[C@H](O)[C@@H]1O4339.2Semi standard non polar33892256
UDP-L-arabinose,1TBDMS,isomer #8CC(C)(C)[Si](C)(C)N1C(=O)C=CN([C@@H]2O[C@H](COP(=O)(O)OP(=O)(O)O[C@H]3OC[C@H](O)[C@H](O)[C@H]3O)[C@@H](O)[C@H]2O)C1=O4366.3Semi standard non polar33892256
UDP-L-arabinose,2TBDMS,isomer #1CC(C)(C)[Si](C)(C)O[C@H]1CO[C@H](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)[C@H](O)[C@H]1O4303.8Semi standard non polar33892256
UDP-L-arabinose,2TBDMS,isomer #10CC(C)(C)[Si](C)(C)O[C@H]1CO[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(=O)[NH]C3=O)[C@H](O)[C@@H]2O)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C4248.7Semi standard non polar33892256
UDP-L-arabinose,2TBDMS,isomer #11CC(C)(C)[Si](C)(C)O[C@H]1CO[C@H](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)[C@H](O)[C@H]1O4360.3Semi standard non polar33892256
UDP-L-arabinose,2TBDMS,isomer #12CC(C)(C)[Si](C)(C)O[C@H]1CO[C@H](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)[C@H](O)[C@H]1O4354.3Semi standard non polar33892256
UDP-L-arabinose,2TBDMS,isomer #13CC(C)(C)[Si](C)(C)O[C@H]1CO[C@H](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)[C@H](O)[C@H]1O4431.5Semi standard non polar33892256
UDP-L-arabinose,2TBDMS,isomer #14CC(C)(C)[Si](C)(C)O[C@H]1[C@@H](O)CO[C@H](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)[C@@H]1O4260.1Semi standard non polar33892256
UDP-L-arabinose,2TBDMS,isomer #15CC(C)(C)[Si](C)(C)O[C@H]1[C@@H](O)CO[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(=O)[NH]C3=O)[C@H](O)[C@@H]2O)[C@@H]1O[Si](C)(C)C(C)(C)C4266.7Semi standard non polar33892256
UDP-L-arabinose,2TBDMS,isomer #16CC(C)(C)[Si](C)(C)O[C@H]1[C@@H](O)CO[C@H](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)[C@@H]1O4330.8Semi standard non polar33892256
UDP-L-arabinose,2TBDMS,isomer #17CC(C)(C)[Si](C)(C)O[C@H]1[C@@H](O)CO[C@H](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)[C@@H]1O4314.2Semi standard non polar33892256
UDP-L-arabinose,2TBDMS,isomer #18CC(C)(C)[Si](C)(C)O[C@H]1[C@@H](O)CO[C@H](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)[C@@H]1O4387.8Semi standard non polar33892256
UDP-L-arabinose,2TBDMS,isomer #19CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](O)[C@@H](O)CO[C@@H]1OP(=O)(O)OP(=O)(O)OC[C@H]1O[C@@H](N2C=CC(=O)[NH]C2=O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O4271.3Semi standard non polar33892256
UDP-L-arabinose,2TBDMS,isomer #2CC(C)(C)[Si](C)(C)O[C@H]1[C@@H](O)CO[C@H](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)[C@@H]1O4269.2Semi standard non polar33892256
UDP-L-arabinose,2TBDMS,isomer #20CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](O)[C@@H](O)CO[C@@H]1OP(=O)(O[Si](C)(C)C(C)(C)C)OP(=O)(O)OC[C@H]1O[C@@H](N2C=CC(=O)[NH]C2=O)[C@H](O)[C@@H]1O4334.0Semi standard non polar33892256
UDP-L-arabinose,2TBDMS,isomer #21CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](O)[C@@H](O)CO[C@@H]1OP(=O)(O)OP(=O)(OC[C@H]1O[C@@H](N2C=CC(=O)[NH]C2=O)[C@H](O)[C@@H]1O)O[Si](C)(C)C(C)(C)C4320.2Semi standard non polar33892256
UDP-L-arabinose,2TBDMS,isomer #22CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](O)[C@@H](O)CO[C@@H]1OP(=O)(O)OP(=O)(O)OC[C@H]1O[C@@H](N2C=CC(=O)N([Si](C)(C)C(C)(C)C)C2=O)[C@H](O)[C@@H]1O4399.4Semi standard non polar33892256
UDP-L-arabinose,2TBDMS,isomer #23CC(C)(C)[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C(C)(C)C)OP(=O)(O)O[C@H]2OC[C@H](O)[C@H](O)[C@H]2O)O[C@H]1N1C=CC(=O)[NH]C1=O4362.9Semi standard non polar33892256
UDP-L-arabinose,2TBDMS,isomer #24CC(C)(C)[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O[C@H]2OC[C@H](O)[C@H](O)[C@H]2O)O[Si](C)(C)C(C)(C)C)O[C@H]1N1C=CC(=O)[NH]C1=O4369.6Semi standard non polar33892256
UDP-L-arabinose,2TBDMS,isomer #25CC(C)(C)[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]2OC[C@H](O)[C@H](O)[C@H]2O)O[C@H]1N1C=CC(=O)N([Si](C)(C)C(C)(C)C)C1=O4434.6Semi standard non polar33892256
UDP-L-arabinose,2TBDMS,isomer #26CC(C)(C)[Si](C)(C)OP(=O)(OC[C@H]1O[C@@H](N2C=CC(=O)[NH]C2=O)[C@H](O)[C@@H]1O)OP(=O)(O[C@H]1OC[C@H](O)[C@H](O)[C@H]1O)O[Si](C)(C)C(C)(C)C4422.3Semi standard non polar33892256
UDP-L-arabinose,2TBDMS,isomer #27CC(C)(C)[Si](C)(C)OP(=O)(OC[C@H]1O[C@@H](N2C=CC(=O)N([Si](C)(C)C(C)(C)C)C2=O)[C@H](O)[C@@H]1O)OP(=O)(O)O[C@H]1OC[C@H](O)[C@H](O)[C@H]1O4484.4Semi standard non polar33892256
UDP-L-arabinose,2TBDMS,isomer #28CC(C)(C)[Si](C)(C)OP(=O)(O[C@H]1OC[C@H](O)[C@H](O)[C@H]1O)OP(=O)(O)OC[C@H]1O[C@@H](N2C=CC(=O)N([Si](C)(C)C(C)(C)C)C2=O)[C@H](O)[C@@H]1O4492.6Semi standard non polar33892256
UDP-L-arabinose,2TBDMS,isomer #3CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]2OC[C@H](O)[C@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)O[C@@H](N2C=CC(=O)[NH]C2=O)[C@@H]1O4276.4Semi standard non polar33892256
UDP-L-arabinose,2TBDMS,isomer #4CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]2OC[C@H](O)[C@H](O)[C@H]2O)O[C@@H](N2C=CC(=O)[NH]C2=O)[C@@H]1O[Si](C)(C)C(C)(C)C4316.1Semi standard non polar33892256
UDP-L-arabinose,2TBDMS,isomer #5CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C(C)(C)C)OP(=O)(O)O[C@H]2OC[C@H](O)[C@H](O)[C@H]2O)O[C@@H](N2C=CC(=O)[NH]C2=O)[C@@H]1O4365.3Semi standard non polar33892256
UDP-L-arabinose,2TBDMS,isomer #6CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)OP(=O)(O[C@H]2OC[C@H](O)[C@H](O)[C@H]2O)O[Si](C)(C)C(C)(C)C)O[C@@H](N2C=CC(=O)[NH]C2=O)[C@@H]1O4372.6Semi standard non polar33892256
UDP-L-arabinose,2TBDMS,isomer #7CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]2OC[C@H](O)[C@H](O)[C@H]2O)O[C@@H](N2C=CC(=O)N([Si](C)(C)C(C)(C)C)C2=O)[C@@H]1O4434.3Semi standard non polar33892256
UDP-L-arabinose,2TBDMS,isomer #8CC(C)(C)[Si](C)(C)O[C@H]1CO[C@H](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)[C@H](O)[C@H]1O4296.8Semi standard non polar33892256
UDP-L-arabinose,2TBDMS,isomer #9CC(C)(C)[Si](C)(C)O[C@H]1CO[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(=O)[NH]C3=O)[C@H](O)[C@@H]2O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O4259.5Semi standard non polar33892256
UDP-L-arabinose,3TBDMS,isomer #1CC(C)(C)[Si](C)(C)O[C@H]1CO[C@H](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)[C@H](O)[C@H]1O4407.5Semi standard non polar33892256
UDP-L-arabinose,3TBDMS,isomer #10CC(C)(C)[Si](C)(C)O[C@H]1[C@@H](O)CO[C@H](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)[C@@H]1O4423.6Semi standard non polar33892256
UDP-L-arabinose,3TBDMS,isomer #11CC(C)(C)[Si](C)(C)O[C@H]1[C@@H](O)CO[C@H](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)[C@@H]1O4493.0Semi standard non polar33892256
UDP-L-arabinose,3TBDMS,isomer #12CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](O)[C@@H](O)CO[C@@H]1OP(=O)(O)OP(=O)(O)OC[C@H]1O[C@@H](N2C=CC(=O)[NH]C2=O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C4377.0Semi standard non polar33892256
UDP-L-arabinose,3TBDMS,isomer #13CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C(C)(C)C)OP(=O)(O)O[C@H]2OC[C@H](O)[C@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)O[C@@H](N2C=CC(=O)[NH]C2=O)[C@@H]1O4414.4Semi standard non polar33892256
UDP-L-arabinose,3TBDMS,isomer #14CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)OP(=O)(O[C@H]2OC[C@H](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](N2C=CC(=O)[NH]C2=O)[C@@H]1O4424.5Semi standard non polar33892256
UDP-L-arabinose,3TBDMS,isomer #15CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]2OC[C@H](O)[C@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)O[C@@H](N2C=CC(=O)N([Si](C)(C)C(C)(C)C)C2=O)[C@@H]1O4492.4Semi standard non polar33892256
UDP-L-arabinose,3TBDMS,isomer #16CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C(C)(C)C)OP(=O)(O)O[C@H]2OC[C@H](O)[C@H](O)[C@H]2O)O[C@@H](N2C=CC(=O)[NH]C2=O)[C@@H]1O[Si](C)(C)C(C)(C)C4455.8Semi standard non polar33892256
UDP-L-arabinose,3TBDMS,isomer #17CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)OP(=O)(O[C@H]2OC[C@H](O)[C@H](O)[C@H]2O)O[Si](C)(C)C(C)(C)C)O[C@@H](N2C=CC(=O)[NH]C2=O)[C@@H]1O[Si](C)(C)C(C)(C)C4458.4Semi standard non polar33892256
UDP-L-arabinose,3TBDMS,isomer #18CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]2OC[C@H](O)[C@H](O)[C@H]2O)O[C@@H](N2C=CC(=O)N([Si](C)(C)C(C)(C)C)C2=O)[C@@H]1O[Si](C)(C)C(C)(C)C4533.1Semi standard non polar33892256
UDP-L-arabinose,3TBDMS,isomer #19CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C(C)(C)C)OP(=O)(O[C@H]2OC[C@H](O)[C@H](O)[C@H]2O)O[Si](C)(C)C(C)(C)C)O[C@@H](N2C=CC(=O)[NH]C2=O)[C@@H]1O4491.8Semi standard non polar33892256
UDP-L-arabinose,3TBDMS,isomer #2CC(C)(C)[Si](C)(C)O[C@H]1CO[C@H](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)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O4379.3Semi standard non polar33892256
UDP-L-arabinose,3TBDMS,isomer #20CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C(C)(C)C)OP(=O)(O)O[C@H]2OC[C@H](O)[C@H](O)[C@H]2O)O[C@@H](N2C=CC(=O)N([Si](C)(C)C(C)(C)C)C2=O)[C@@H]1O4557.5Semi standard non polar33892256
UDP-L-arabinose,3TBDMS,isomer #21CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)OP(=O)(O[C@H]2OC[C@H](O)[C@H](O)[C@H]2O)O[Si](C)(C)C(C)(C)C)O[C@@H](N2C=CC(=O)N([Si](C)(C)C(C)(C)C)C2=O)[C@@H]1O4558.7Semi standard non polar33892256
UDP-L-arabinose,3TBDMS,isomer #22CC(C)(C)[Si](C)(C)O[C@H]1CO[C@H](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)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O4379.4Semi standard non polar33892256
UDP-L-arabinose,3TBDMS,isomer #23CC(C)(C)[Si](C)(C)O[C@H]1CO[C@H](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)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C4372.3Semi standard non polar33892256
UDP-L-arabinose,3TBDMS,isomer #24CC(C)(C)[Si](C)(C)O[C@H]1CO[C@H](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)[C@H](O)[C@H]1O4446.8Semi standard non polar33892256
UDP-L-arabinose,3TBDMS,isomer #25CC(C)(C)[Si](C)(C)O[C@H]1CO[C@H](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)[C@H](O)[C@H]1O4442.1Semi standard non polar33892256
UDP-L-arabinose,3TBDMS,isomer #26CC(C)(C)[Si](C)(C)O[C@H]1CO[C@H](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)[C@H](O)[C@H]1O4523.4Semi standard non polar33892256
UDP-L-arabinose,3TBDMS,isomer #27CC(C)(C)[Si](C)(C)O[C@H]1CO[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(=O)[NH]C3=O)[C@H](O)[C@@H]2O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)C4371.6Semi standard non polar33892256
UDP-L-arabinose,3TBDMS,isomer #28CC(C)(C)[Si](C)(C)O[C@H]1CO[C@H](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)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O4418.1Semi standard non polar33892256
UDP-L-arabinose,3TBDMS,isomer #29CC(C)(C)[Si](C)(C)O[C@H]1CO[C@H](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)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O4410.2Semi standard non polar33892256
UDP-L-arabinose,3TBDMS,isomer #3CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]2OC[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)O[C@@H](N2C=CC(=O)[NH]C2=O)[C@@H]1O4373.7Semi standard non polar33892256
UDP-L-arabinose,3TBDMS,isomer #30CC(C)(C)[Si](C)(C)O[C@H]1CO[C@H](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)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O4480.2Semi standard non polar33892256
UDP-L-arabinose,3TBDMS,isomer #31CC(C)(C)[Si](C)(C)O[C@H]1CO[C@H](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)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C4412.8Semi standard non polar33892256
UDP-L-arabinose,3TBDMS,isomer #32CC(C)(C)[Si](C)(C)O[C@H]1CO[C@H](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)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C4395.9Semi standard non polar33892256
UDP-L-arabinose,3TBDMS,isomer #33CC(C)(C)[Si](C)(C)O[C@H]1CO[C@H](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)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C4468.8Semi standard non polar33892256
UDP-L-arabinose,3TBDMS,isomer #34CC(C)(C)[Si](C)(C)O[C@H]1CO[C@H](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)[C@H](O)[C@H]1O4478.4Semi standard non polar33892256
UDP-L-arabinose,3TBDMS,isomer #35CC(C)(C)[Si](C)(C)O[C@H]1CO[C@H](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)[C@H](O)[C@H]1O4544.9Semi standard non polar33892256
UDP-L-arabinose,3TBDMS,isomer #36CC(C)(C)[Si](C)(C)O[C@H]1CO[C@H](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)[C@H](O)[C@H]1O4545.7Semi standard non polar33892256
UDP-L-arabinose,3TBDMS,isomer #37CC(C)(C)[Si](C)(C)O[C@H]1[C@@H](O)CO[C@H](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)[C@@H]1O[Si](C)(C)C(C)(C)C4388.2Semi standard non polar33892256
UDP-L-arabinose,3TBDMS,isomer #38CC(C)(C)[Si](C)(C)O[C@H]1[C@@H](O)CO[C@H](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)[C@@H]1O4437.0Semi standard non polar33892256
UDP-L-arabinose,3TBDMS,isomer #39CC(C)(C)[Si](C)(C)O[C@H]1[C@@H](O)CO[C@H](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)[C@@H]1O4421.9Semi standard non polar33892256
UDP-L-arabinose,3TBDMS,isomer #4CC(C)(C)[Si](C)(C)O[C@H]1CO[C@H](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)[C@H](O)[C@H]1O4446.4Semi standard non polar33892256
UDP-L-arabinose,3TBDMS,isomer #40CC(C)(C)[Si](C)(C)O[C@H]1[C@@H](O)CO[C@H](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)[C@@H]1O4496.5Semi standard non polar33892256
UDP-L-arabinose,3TBDMS,isomer #41CC(C)(C)[Si](C)(C)O[C@H]1[C@@H](O)CO[C@H](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)[C@@H]1O[Si](C)(C)C(C)(C)C4430.8Semi standard non polar33892256
UDP-L-arabinose,3TBDMS,isomer #42CC(C)(C)[Si](C)(C)O[C@H]1[C@@H](O)CO[C@H](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)[C@@H]1O[Si](C)(C)C(C)(C)C4416.1Semi standard non polar33892256
UDP-L-arabinose,3TBDMS,isomer #43CC(C)(C)[Si](C)(C)O[C@H]1[C@@H](O)CO[C@H](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)[C@@H]1O[Si](C)(C)C(C)(C)C4479.8Semi standard non polar33892256
UDP-L-arabinose,3TBDMS,isomer #44CC(C)(C)[Si](C)(C)O[C@H]1[C@@H](O)CO[C@H](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)[C@@H]1O4462.7Semi standard non polar33892256
UDP-L-arabinose,3TBDMS,isomer #45CC(C)(C)[Si](C)(C)O[C@H]1[C@@H](O)CO[C@H](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)[C@@H]1O4526.8Semi standard non polar33892256
UDP-L-arabinose,3TBDMS,isomer #46CC(C)(C)[Si](C)(C)O[C@H]1[C@@H](O)CO[C@H](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)[C@@H]1O4513.8Semi standard non polar33892256
UDP-L-arabinose,3TBDMS,isomer #47CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](O)[C@@H](O)CO[C@@H]1OP(=O)(O[Si](C)(C)C(C)(C)C)OP(=O)(O)OC[C@H]1O[C@@H](N2C=CC(=O)[NH]C2=O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O4427.6Semi standard non polar33892256
UDP-L-arabinose,3TBDMS,isomer #48CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](O)[C@@H](O)CO[C@@H]1OP(=O)(O)OP(=O)(OC[C@H]1O[C@@H](N2C=CC(=O)[NH]C2=O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O)O[Si](C)(C)C(C)(C)C4416.2Semi standard non polar33892256
UDP-L-arabinose,3TBDMS,isomer #49CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](O)[C@@H](O)CO[C@@H]1OP(=O)(O)OP(=O)(O)OC[C@H]1O[C@@H](N2C=CC(=O)N([Si](C)(C)C(C)(C)C)C2=O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O4496.3Semi standard non polar33892256
UDP-L-arabinose,3TBDMS,isomer #5CC(C)(C)[Si](C)(C)O[C@H]1CO[C@H](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)[C@H](O)[C@H]1O4441.8Semi standard non polar33892256
UDP-L-arabinose,3TBDMS,isomer #50CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](O)[C@@H](O)CO[C@@H]1OP(=O)(O[Si](C)(C)C(C)(C)C)OP(=O)(OC[C@H]1O[C@@H](N2C=CC(=O)[NH]C2=O)[C@H](O)[C@@H]1O)O[Si](C)(C)C(C)(C)C4459.2Semi standard non polar33892256
UDP-L-arabinose,3TBDMS,isomer #51CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](O)[C@@H](O)CO[C@@H]1OP(=O)(O[Si](C)(C)C(C)(C)C)OP(=O)(O)OC[C@H]1O[C@@H](N2C=CC(=O)N([Si](C)(C)C(C)(C)C)C2=O)[C@H](O)[C@@H]1O4523.0Semi standard non polar33892256
UDP-L-arabinose,3TBDMS,isomer #52CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](O)[C@@H](O)CO[C@@H]1OP(=O)(O)OP(=O)(OC[C@H]1O[C@@H](N2C=CC(=O)N([Si](C)(C)C(C)(C)C)C2=O)[C@H](O)[C@@H]1O)O[Si](C)(C)C(C)(C)C4515.7Semi standard non polar33892256
UDP-L-arabinose,3TBDMS,isomer #53CC(C)(C)[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C(C)(C)C)OP(=O)(O[C@H]2OC[C@H](O)[C@H](O)[C@H]2O)O[Si](C)(C)C(C)(C)C)O[C@H]1N1C=CC(=O)[NH]C1=O4492.7Semi standard non polar33892256
UDP-L-arabinose,3TBDMS,isomer #54CC(C)(C)[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C(C)(C)C)OP(=O)(O)O[C@H]2OC[C@H](O)[C@H](O)[C@H]2O)O[C@H]1N1C=CC(=O)N([Si](C)(C)C(C)(C)C)C1=O4561.0Semi standard non polar33892256
UDP-L-arabinose,3TBDMS,isomer #55CC(C)(C)[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O[C@H]2OC[C@H](O)[C@H](O)[C@H]2O)O[Si](C)(C)C(C)(C)C)O[C@H]1N1C=CC(=O)N([Si](C)(C)C(C)(C)C)C1=O4561.2Semi standard non polar33892256
UDP-L-arabinose,3TBDMS,isomer #56CC(C)(C)[Si](C)(C)OP(=O)(OC[C@H]1O[C@@H](N2C=CC(=O)N([Si](C)(C)C(C)(C)C)C2=O)[C@H](O)[C@@H]1O)OP(=O)(O[C@H]1OC[C@H](O)[C@H](O)[C@H]1O)O[Si](C)(C)C(C)(C)C4576.8Semi standard non polar33892256
UDP-L-arabinose,3TBDMS,isomer #6CC(C)(C)[Si](C)(C)O[C@H]1CO[C@H](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)[C@H](O)[C@H]1O4519.2Semi standard non polar33892256
UDP-L-arabinose,3TBDMS,isomer #7CC(C)(C)[Si](C)(C)O[C@H]1[C@@H](O)CO[C@H](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)[C@@H]1O4396.4Semi standard non polar33892256
UDP-L-arabinose,3TBDMS,isomer #8CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]2OC[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O[Si](C)(C)C(C)(C)C)O[C@@H](N2C=CC(=O)[NH]C2=O)[C@@H]1O4389.0Semi standard non polar33892256
UDP-L-arabinose,3TBDMS,isomer #9CC(C)(C)[Si](C)(C)O[C@H]1[C@@H](O)CO[C@H](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)[C@@H]1O4439.5Semi standard non polar33892256
Spectra

GC-MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted GC-MSPredicted GC-MS Spectrum - UDP-L-arabinose GC-MS (Non-derivatized) - 70eV, Positivesplash10-016r-4936760000-00f37a38fe624376e23d2017-09-01Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - UDP-L-arabinose GC-MS (2 TMS) - 70eV, Positivesplash10-0300-4642229000-26e6ed2c6eb4497585c22017-10-06Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - UDP-L-arabinose GC-MS (TMS_1_1) - 70eV, PositiveNot Available2021-10-13Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - UDP-L-arabinose GC-MS (TMS_1_2) - 70eV, PositiveNot Available2021-10-13Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - UDP-L-arabinose GC-MS (TMS_1_3) - 70eV, PositiveNot Available2021-10-13Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - UDP-L-arabinose GC-MS (TMS_1_4) - 70eV, PositiveNot Available2021-10-13Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - UDP-L-arabinose GC-MS (TMS_1_5) - 70eV, PositiveNot Available2021-10-13Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - UDP-L-arabinose GC-MS (TMS_1_6) - 70eV, PositiveNot Available2021-10-13Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - UDP-L-arabinose GC-MS (TMS_1_7) - 70eV, PositiveNot Available2021-10-13Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - UDP-L-arabinose GC-MS (TMS_1_8) - 70eV, PositiveNot Available2021-10-13Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - UDP-L-arabinose GC-MS (TMS_2_2) - 70eV, PositiveNot Available2021-10-13Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - UDP-L-arabinose GC-MS (TMS_2_3) - 70eV, PositiveNot Available2021-10-13Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - UDP-L-arabinose GC-MS (TMS_2_4) - 70eV, PositiveNot Available2021-10-13Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - UDP-L-arabinose GC-MS (TMS_2_5) - 70eV, PositiveNot Available2021-10-13Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - UDP-L-arabinose GC-MS (TMS_2_6) - 70eV, PositiveNot Available2021-10-13Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - UDP-L-arabinose GC-MS (TMS_2_7) - 70eV, PositiveNot Available2021-10-13Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - UDP-L-arabinose GC-MS (TMS_2_8) - 70eV, PositiveNot Available2021-10-13Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - UDP-L-arabinose GC-MS (TMS_2_9) - 70eV, PositiveNot Available2021-10-13Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - UDP-L-arabinose GC-MS (TMS_2_10) - 70eV, PositiveNot Available2021-10-13Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - UDP-L-arabinose GC-MS (TMS_2_11) - 70eV, PositiveNot Available2021-10-13Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - UDP-L-arabinose GC-MS (TMS_2_12) - 70eV, PositiveNot Available2021-10-13Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - UDP-L-arabinose GC-MS (TMS_2_13) - 70eV, PositiveNot Available2021-10-13Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - UDP-L-arabinose GC-MS (TMS_2_14) - 70eV, PositiveNot Available2021-10-13Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - UDP-L-arabinose GC-MS (TMS_2_15) - 70eV, PositiveNot Available2021-10-13Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - UDP-L-arabinose GC-MS (TMS_2_16) - 70eV, PositiveNot Available2021-10-13Wishart LabView Spectrum

MS/MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - UDP-L-arabinose 10V, Positive-QTOFsplash10-03di-0901110000-8ae0db777cff3d445c4c2017-09-01Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - UDP-L-arabinose 20V, Positive-QTOFsplash10-03di-4910000000-67006286cf564f62ff422017-09-01Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - UDP-L-arabinose 40V, Positive-QTOFsplash10-03di-5900000000-da262c67a1973399a7552017-09-01Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - UDP-L-arabinose 10V, Negative-QTOFsplash10-000f-8713790000-946e0081f7ad1a09d3d62017-09-01Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - UDP-L-arabinose 20V, Negative-QTOFsplash10-01ox-9622010000-7089747eea74980128f42017-09-01Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - UDP-L-arabinose 40V, Negative-QTOFsplash10-06tf-4900000000-53eebd3beb66a7fd8d3f2017-09-01Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - UDP-L-arabinose 10V, Negative-QTOFsplash10-000i-0001090000-5cb9330b784831a318c02021-09-21Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - UDP-L-arabinose 20V, Negative-QTOFsplash10-0btc-5913210000-b3ea7476b5c2e48ecb1f2021-09-21Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - UDP-L-arabinose 40V, Negative-QTOFsplash10-0a4l-4956200000-d7160be3d1a922677c832021-09-21Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - UDP-L-arabinose 10V, Positive-QTOFsplash10-03dr-1800690000-ee1b02fe5fb340e69a4b2021-09-25Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - UDP-L-arabinose 20V, Positive-QTOFsplash10-03di-4961210000-998fdbdb53c26f8dfaa22021-09-25Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - UDP-L-arabinose 40V, Positive-QTOFsplash10-03ea-5921000000-c5798a971977016536d72021-09-25Wishart LabView Spectrum

NMR Spectra

Spectrum TypeDescriptionDeposition DateSourceView
Predicted 1D NMR1H NMR Spectrum (1D, 100 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 100 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, 1000 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, 200 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, 300 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, 400 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, 500 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, 600 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, 700 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, 800 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 900 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C 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 IDFDB028926
KNApSAcK IDNot Available
Chemspider ID559145
KEGG Compound IDC00935
BioCyc IDCPD-12513
BiGG IDNot Available
Wikipedia LinkNot Available
METLIN IDNot Available
PubChem Compound644105
PDB IDNot Available
ChEBI ID61455
Food Biomarker OntologyNot Available
VMH IDNot Available
MarkerDB IDNot Available
Good Scents IDNot Available
References
Synthesis ReferenceNot Available
Material Safety Data Sheet (MSDS)Not Available
General ReferencesNot Available