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Record Information
Version5.0
StatusExpected but not Quantified
Creation Date2012-09-12 00:13:45 UTC
Update Date2022-03-07 02:55:58 UTC
HMDB IDHMDB0038881
Secondary Accession Numbers
  • HMDB38881
Metabolite Identification
Common Name2-O-b-D-Xylopyranosyl-L-arabinose
Description2-O-b-D-Xylopyranosyl-L-arabinose belongs to the class of organic compounds known as o-glycosyl compounds. These are glycoside in which a sugar group is bonded through one carbon to another group via a O-glycosidic bond. 2-O-b-D-Xylopyranosyl-L-arabinose has been detected, but not quantified in, breakfast cereal and cereals and cereal products. This could make 2-O-b-D-xylopyranosyl-L-arabinose a potential biomarker for the consumption of these foods. Based on a literature review very few articles have been published on 2-O-b-D-Xylopyranosyl-L-arabinose.
Structure
Data?1563863274
SynonymsNot Available
Chemical FormulaC10H18O9
Average Molecular Weight282.2445
Monoisotopic Molecular Weight282.095082174
IUPAC Name(2S,3R,4S,5R)-2-{[(3R,4S,5S)-2,4,5-trihydroxyoxan-3-yl]oxy}oxane-3,4,5-triol
Traditional Name(2S,3R,4S,5R)-2-{[(3R,4S,5S)-2,4,5-trihydroxyoxan-3-yl]oxy}oxane-3,4,5-triol
CAS Registry NumberNot Available
SMILES
O[C@@H]1CO[C@@H](O[C@H]2C(O)OC[C@H](O)[C@@H]2O)[C@H](O)[C@H]1O
InChI Identifier
InChI=1S/C10H18O9/c11-3-2-18-10(7(15)5(3)13)19-8-6(14)4(12)1-17-9(8)16/h3-16H,1-2H2/t3-,4+,5+,6+,7-,8-,9?,10+/m1/s1
InChI KeyHBIRURHHLFDSPS-BIDIDBDVSA-N
Chemical Taxonomy
Description Belongs to the class of organic compounds known as o-glycosyl compounds. These are glycoside in which a sugar group is bonded through one carbon to another group via a O-glycosidic bond.
KingdomOrganic compounds
Super ClassOrganic oxygen compounds
ClassOrganooxygen compounds
Sub ClassCarbohydrates and carbohydrate conjugates
Direct ParentO-glycosyl compounds
Alternative Parents
Substituents
  • O-glycosyl compound
  • Disaccharide
  • Oxane
  • Secondary alcohol
  • Hemiacetal
  • Oxacycle
  • Organoheterocyclic compound
  • Polyol
  • Acetal
  • Hydrocarbon derivative
  • Alcohol
  • Aliphatic heteromonocyclic compound
Molecular FrameworkAliphatic heteromonocyclic compounds
External DescriptorsNot Available
Ontology
Physiological effectNot Available
Disposition
ProcessNot Available
Role
Physical Properties
StateSolid
Experimental Molecular Properties
PropertyValueReference
Melting Point98 - 99 °CNot Available
Boiling PointNot AvailableNot Available
Water SolubilityNot AvailableNot Available
LogPNot AvailableNot Available
Experimental Chromatographic PropertiesNot Available
Predicted Molecular Properties
PropertyValueSource
Water Solubility613 g/LALOGPS
logP-3ALOGPS
logP-3.4ChemAxon
logS0.34ALOGPS
pKa (Strongest Acidic)11.28ChemAxon
pKa (Strongest Basic)-3.5ChemAxon
Physiological Charge0ChemAxon
Hydrogen Acceptor Count9ChemAxon
Hydrogen Donor Count6ChemAxon
Polar Surface Area149.07 ŲChemAxon
Rotatable Bond Count2ChemAxon
Refractivity56.41 m³·mol⁻¹ChemAxon
Polarizability25.47 ųChemAxon
Number of Rings2ChemAxon
BioavailabilityYesChemAxon
Rule of FiveNoChemAxon
Ghose FilterNoChemAxon
Veber's RuleNoChemAxon
MDDR-like RuleNoChemAxon
Predicted Chromatographic Properties

Predicted Collision Cross Sections

PredictorAdduct TypeCCS Value (Å2)Reference
DarkChem[M+H]+162.75631661259
DarkChem[M-H]-159.31531661259
DeepCCS[M+H]+163.37530932474
DeepCCS[M-H]-160.9830932474
DeepCCS[M-2H]-195.5830932474
DeepCCS[M+Na]+170.01930932474
AllCCS[M+H]+165.332859911
AllCCS[M+H-H2O]+161.832859911
AllCCS[M+NH4]+168.632859911
AllCCS[M+Na]+169.532859911
AllCCS[M-H]-160.532859911
AllCCS[M+Na-2H]-160.332859911
AllCCS[M+HCOO]-160.132859911

Predicted Kovats Retention Indices

Underivatized

MetaboliteSMILESKovats RI ValueColumn TypeReference
2-O-b-D-Xylopyranosyl-L-arabinoseO[C@@H]1CO[C@@H](O[C@H]2C(O)OC[C@H](O)[C@@H]2O)[C@H](O)[C@H]1O2843.9Standard polar33892256
2-O-b-D-Xylopyranosyl-L-arabinoseO[C@@H]1CO[C@@H](O[C@H]2C(O)OC[C@H](O)[C@@H]2O)[C@H](O)[C@H]1O2647.6Standard non polar33892256
2-O-b-D-Xylopyranosyl-L-arabinoseO[C@@H]1CO[C@@H](O[C@H]2C(O)OC[C@H](O)[C@@H]2O)[C@H](O)[C@H]1O2415.5Semi standard non polar33892256

Derivatized

Derivative Name / StructureSMILESKovats RI ValueColumn TypeReference
2-O-b-D-Xylopyranosyl-L-arabinose,1TMS,isomer #1C[Si](C)(C)O[C@@H]1CO[C@@H](O[C@H]2C(O)OC[C@H](O)[C@@H]2O)[C@H](O)[C@H]1O2375.5Semi standard non polar33892256
2-O-b-D-Xylopyranosyl-L-arabinose,1TMS,isomer #2C[Si](C)(C)OC1OC[C@H](O)[C@H](O)[C@H]1O[C@@H]1OC[C@@H](O)[C@H](O)[C@H]1O2345.5Semi standard non polar33892256
2-O-b-D-Xylopyranosyl-L-arabinose,1TMS,isomer #3C[Si](C)(C)O[C@H]1COC(O)[C@H](O[C@@H]2OC[C@@H](O)[C@H](O)[C@H]2O)[C@H]1O2349.4Semi standard non polar33892256
2-O-b-D-Xylopyranosyl-L-arabinose,1TMS,isomer #4C[Si](C)(C)O[C@H]1[C@@H](O)COC(O)[C@@H]1O[C@@H]1OC[C@@H](O)[C@H](O)[C@H]1O2341.8Semi standard non polar33892256
2-O-b-D-Xylopyranosyl-L-arabinose,1TMS,isomer #5C[Si](C)(C)O[C@H]1[C@H](O[C@H]2C(O)OC[C@H](O)[C@@H]2O)OC[C@@H](O)[C@@H]1O2362.3Semi standard non polar33892256
2-O-b-D-Xylopyranosyl-L-arabinose,1TMS,isomer #6C[Si](C)(C)O[C@H]1[C@H](O)CO[C@@H](O[C@H]2C(O)OC[C@H](O)[C@@H]2O)[C@@H]1O2360.8Semi standard non polar33892256
2-O-b-D-Xylopyranosyl-L-arabinose,2TMS,isomer #1C[Si](C)(C)OC1OC[C@H](O)[C@H](O)[C@H]1O[C@@H]1OC[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]1O2389.0Semi standard non polar33892256
2-O-b-D-Xylopyranosyl-L-arabinose,2TMS,isomer #10C[Si](C)(C)O[C@H]1[C@H](O)CO[C@@H](O[C@H]2C(O)OC[C@H](O[Si](C)(C)C)[C@@H]2O)[C@@H]1O2369.3Semi standard non polar33892256
2-O-b-D-Xylopyranosyl-L-arabinose,2TMS,isomer #11C[Si](C)(C)O[C@H]1COC(O)[C@H](O[C@@H]2OC[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)[C@H]1O2377.1Semi standard non polar33892256
2-O-b-D-Xylopyranosyl-L-arabinose,2TMS,isomer #12C[Si](C)(C)O[C@H]1COC(O)[C@H](O[C@@H]2OC[C@@H](O)[C@H](O)[C@H]2O)[C@H]1O[Si](C)(C)C2347.6Semi standard non polar33892256
2-O-b-D-Xylopyranosyl-L-arabinose,2TMS,isomer #13C[Si](C)(C)O[C@H]1[C@@H](O)COC(O)[C@@H]1O[C@@H]1OC[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]1O2354.1Semi standard non polar33892256
2-O-b-D-Xylopyranosyl-L-arabinose,2TMS,isomer #14C[Si](C)(C)O[C@H]1[C@@H](O)COC(O)[C@@H]1O[C@@H]1OC[C@@H](O)[C@H](O)[C@H]1O[Si](C)(C)C2365.4Semi standard non polar33892256
2-O-b-D-Xylopyranosyl-L-arabinose,2TMS,isomer #15C[Si](C)(C)O[C@H]1[C@H](O)CO[C@@H](O[C@H]2C(O)OC[C@H](O)[C@@H]2O)[C@@H]1O[Si](C)(C)C2362.3Semi standard non polar33892256
2-O-b-D-Xylopyranosyl-L-arabinose,2TMS,isomer #2C[Si](C)(C)O[C@H]1COC(O)[C@H](O[C@@H]2OC[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)[C@H]1O2389.4Semi standard non polar33892256
2-O-b-D-Xylopyranosyl-L-arabinose,2TMS,isomer #3C[Si](C)(C)O[C@H]1[C@@H](O)COC(O)[C@@H]1O[C@@H]1OC[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]1O2370.5Semi standard non polar33892256
2-O-b-D-Xylopyranosyl-L-arabinose,2TMS,isomer #4C[Si](C)(C)O[C@@H]1CO[C@@H](O[C@H]2C(O)OC[C@H](O)[C@@H]2O)[C@H](O[Si](C)(C)C)[C@H]1O2373.2Semi standard non polar33892256
2-O-b-D-Xylopyranosyl-L-arabinose,2TMS,isomer #5C[Si](C)(C)O[C@@H]1CO[C@@H](O[C@H]2C(O)OC[C@H](O)[C@@H]2O)[C@H](O)[C@H]1O[Si](C)(C)C2374.0Semi standard non polar33892256
2-O-b-D-Xylopyranosyl-L-arabinose,2TMS,isomer #6C[Si](C)(C)OC1OC[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[C@@H]1OC[C@@H](O)[C@H](O)[C@H]1O2356.6Semi standard non polar33892256
2-O-b-D-Xylopyranosyl-L-arabinose,2TMS,isomer #7C[Si](C)(C)OC1OC[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[C@@H]1OC[C@@H](O)[C@H](O)[C@H]1O2356.0Semi standard non polar33892256
2-O-b-D-Xylopyranosyl-L-arabinose,2TMS,isomer #8C[Si](C)(C)OC1OC[C@H](O)[C@H](O)[C@H]1O[C@@H]1OC[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]1O2362.0Semi standard non polar33892256
2-O-b-D-Xylopyranosyl-L-arabinose,2TMS,isomer #9C[Si](C)(C)OC1OC[C@H](O)[C@H](O)[C@H]1O[C@@H]1OC[C@@H](O)[C@H](O)[C@H]1O[Si](C)(C)C2374.4Semi standard non polar33892256
2-O-b-D-Xylopyranosyl-L-arabinose,3TMS,isomer #1C[Si](C)(C)OC1OC[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[C@@H]1OC[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]1O2332.2Semi standard non polar33892256
2-O-b-D-Xylopyranosyl-L-arabinose,3TMS,isomer #10C[Si](C)(C)O[C@H]1[C@H](O[Si](C)(C)C)CO[C@@H](O[C@H]2C(O)OC[C@H](O)[C@@H]2O)[C@@H]1O[Si](C)(C)C2312.7Semi standard non polar33892256
2-O-b-D-Xylopyranosyl-L-arabinose,3TMS,isomer #11C[Si](C)(C)OC1OC[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[C@@H]1OC[C@@H](O)[C@H](O)[C@H]1O2267.7Semi standard non polar33892256
2-O-b-D-Xylopyranosyl-L-arabinose,3TMS,isomer #12C[Si](C)(C)OC1OC[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[C@@H]1OC[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]1O2329.5Semi standard non polar33892256
2-O-b-D-Xylopyranosyl-L-arabinose,3TMS,isomer #13C[Si](C)(C)OC1OC[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[C@@H]1OC[C@@H](O)[C@H](O)[C@H]1O[Si](C)(C)C2320.0Semi standard non polar33892256
2-O-b-D-Xylopyranosyl-L-arabinose,3TMS,isomer #14C[Si](C)(C)OC1OC[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[C@@H]1OC[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]1O2338.7Semi standard non polar33892256
2-O-b-D-Xylopyranosyl-L-arabinose,3TMS,isomer #15C[Si](C)(C)OC1OC[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[C@@H]1OC[C@@H](O)[C@H](O)[C@H]1O[Si](C)(C)C2326.3Semi standard non polar33892256
2-O-b-D-Xylopyranosyl-L-arabinose,3TMS,isomer #16C[Si](C)(C)OC1OC[C@H](O)[C@H](O)[C@H]1O[C@@H]1OC[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C2329.4Semi standard non polar33892256
2-O-b-D-Xylopyranosyl-L-arabinose,3TMS,isomer #17C[Si](C)(C)O[C@H]1[C@H](O)CO[C@@H](O[C@H]2C(O)OC[C@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)[C@@H]1O2339.7Semi standard non polar33892256
2-O-b-D-Xylopyranosyl-L-arabinose,3TMS,isomer #18C[Si](C)(C)O[C@H]1[C@H](O)CO[C@@H](O[C@H]2C(O)OC[C@H](O[Si](C)(C)C)[C@@H]2O)[C@@H]1O[Si](C)(C)C2340.9Semi standard non polar33892256
2-O-b-D-Xylopyranosyl-L-arabinose,3TMS,isomer #19C[Si](C)(C)O[C@H]1COC(O)[C@H](O[C@@H]2OC[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)[C@H]1O[Si](C)(C)C2329.4Semi standard non polar33892256
2-O-b-D-Xylopyranosyl-L-arabinose,3TMS,isomer #2C[Si](C)(C)OC1OC[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[C@@H]1OC[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]1O2334.7Semi standard non polar33892256
2-O-b-D-Xylopyranosyl-L-arabinose,3TMS,isomer #20C[Si](C)(C)O[C@H]1[C@@H](O)COC(O)[C@@H]1O[C@@H]1OC[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C2334.9Semi standard non polar33892256
2-O-b-D-Xylopyranosyl-L-arabinose,3TMS,isomer #3C[Si](C)(C)OC1OC[C@H](O)[C@H](O)[C@H]1O[C@@H]1OC[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O2326.2Semi standard non polar33892256
2-O-b-D-Xylopyranosyl-L-arabinose,3TMS,isomer #4C[Si](C)(C)OC1OC[C@H](O)[C@H](O)[C@H]1O[C@@H]1OC[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C2348.3Semi standard non polar33892256
2-O-b-D-Xylopyranosyl-L-arabinose,3TMS,isomer #5C[Si](C)(C)O[C@H]1COC(O)[C@H](O[C@@H]2OC[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O)[C@H]1O2334.6Semi standard non polar33892256
2-O-b-D-Xylopyranosyl-L-arabinose,3TMS,isomer #6C[Si](C)(C)O[C@H]1COC(O)[C@H](O[C@@H]2OC[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O[Si](C)(C)C)[C@H]1O2351.1Semi standard non polar33892256
2-O-b-D-Xylopyranosyl-L-arabinose,3TMS,isomer #7C[Si](C)(C)O[C@H]1COC(O)[C@H](O[C@@H]2OC[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)[C@H]1O[Si](C)(C)C2330.7Semi standard non polar33892256
2-O-b-D-Xylopyranosyl-L-arabinose,3TMS,isomer #8C[Si](C)(C)O[C@H]1[C@@H](O)COC(O)[C@@H]1O[C@@H]1OC[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O2331.0Semi standard non polar33892256
2-O-b-D-Xylopyranosyl-L-arabinose,3TMS,isomer #9C[Si](C)(C)O[C@H]1[C@@H](O)COC(O)[C@@H]1O[C@@H]1OC[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C2339.0Semi standard non polar33892256
2-O-b-D-Xylopyranosyl-L-arabinose,4TMS,isomer #1C[Si](C)(C)OC1OC[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[C@@H]1OC[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]1O2288.9Semi standard non polar33892256
2-O-b-D-Xylopyranosyl-L-arabinose,4TMS,isomer #10C[Si](C)(C)O[C@H]1[C@@H](O)COC(O)[C@@H]1O[C@@H]1OC[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C2316.7Semi standard non polar33892256
2-O-b-D-Xylopyranosyl-L-arabinose,4TMS,isomer #11C[Si](C)(C)OC1OC[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[C@@H]1OC[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]1O2316.5Semi standard non polar33892256
2-O-b-D-Xylopyranosyl-L-arabinose,4TMS,isomer #12C[Si](C)(C)OC1OC[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[C@@H]1OC[C@@H](O)[C@H](O)[C@H]1O[Si](C)(C)C2262.3Semi standard non polar33892256
2-O-b-D-Xylopyranosyl-L-arabinose,4TMS,isomer #13C[Si](C)(C)OC1OC[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[C@@H]1OC[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C2312.0Semi standard non polar33892256
2-O-b-D-Xylopyranosyl-L-arabinose,4TMS,isomer #14C[Si](C)(C)OC1OC[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[C@@H]1OC[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C2336.8Semi standard non polar33892256
2-O-b-D-Xylopyranosyl-L-arabinose,4TMS,isomer #15C[Si](C)(C)O[C@H]1[C@H](O)CO[C@@H](O[C@H]2C(O)OC[C@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C2332.4Semi standard non polar33892256
2-O-b-D-Xylopyranosyl-L-arabinose,4TMS,isomer #2C[Si](C)(C)OC1OC[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[C@@H]1OC[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O2319.3Semi standard non polar33892256
2-O-b-D-Xylopyranosyl-L-arabinose,4TMS,isomer #3C[Si](C)(C)OC1OC[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[C@@H]1OC[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C2326.2Semi standard non polar33892256
2-O-b-D-Xylopyranosyl-L-arabinose,4TMS,isomer #4C[Si](C)(C)OC1OC[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[C@@H]1OC[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O2352.6Semi standard non polar33892256
2-O-b-D-Xylopyranosyl-L-arabinose,4TMS,isomer #5C[Si](C)(C)OC1OC[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[C@@H]1OC[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C2324.6Semi standard non polar33892256
2-O-b-D-Xylopyranosyl-L-arabinose,4TMS,isomer #6C[Si](C)(C)OC1OC[C@H](O)[C@H](O)[C@H]1O[C@@H]1OC[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C2284.4Semi standard non polar33892256
2-O-b-D-Xylopyranosyl-L-arabinose,4TMS,isomer #7C[Si](C)(C)O[C@H]1[C@H](O[Si](C)(C)C)CO[C@@H](O[C@H]2C(O)OC[C@H](O[Si](C)(C)C)[C@@H]2O)[C@@H]1O[Si](C)(C)C2309.9Semi standard non polar33892256
2-O-b-D-Xylopyranosyl-L-arabinose,4TMS,isomer #8C[Si](C)(C)O[C@H]1COC(O)[C@H](O[C@@H]2OC[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O)[C@H]1O[Si](C)(C)C2338.9Semi standard non polar33892256
2-O-b-D-Xylopyranosyl-L-arabinose,4TMS,isomer #9C[Si](C)(C)O[C@H]1COC(O)[C@H](O[C@@H]2OC[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O[Si](C)(C)C)[C@H]1O[Si](C)(C)C2330.8Semi standard non polar33892256
2-O-b-D-Xylopyranosyl-L-arabinose,5TMS,isomer #1C[Si](C)(C)OC1OC[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[C@@H]1OC[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O2333.8Semi standard non polar33892256
2-O-b-D-Xylopyranosyl-L-arabinose,5TMS,isomer #2C[Si](C)(C)OC1OC[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[C@@H]1OC[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C2308.7Semi standard non polar33892256
2-O-b-D-Xylopyranosyl-L-arabinose,5TMS,isomer #3C[Si](C)(C)OC1OC[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[C@@H]1OC[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C2307.1Semi standard non polar33892256
2-O-b-D-Xylopyranosyl-L-arabinose,5TMS,isomer #4C[Si](C)(C)OC1OC[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[C@@H]1OC[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C2315.3Semi standard non polar33892256
2-O-b-D-Xylopyranosyl-L-arabinose,5TMS,isomer #5C[Si](C)(C)O[C@H]1[C@H](O[Si](C)(C)C)CO[C@@H](O[C@H]2C(O)OC[C@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C2332.8Semi standard non polar33892256
2-O-b-D-Xylopyranosyl-L-arabinose,5TMS,isomer #6C[Si](C)(C)OC1OC[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[C@@H]1OC[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C2313.5Semi standard non polar33892256
2-O-b-D-Xylopyranosyl-L-arabinose,6TMS,isomer #1C[Si](C)(C)OC1OC[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[C@@H]1OC[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C2366.2Semi standard non polar33892256
2-O-b-D-Xylopyranosyl-L-arabinose,1TBDMS,isomer #1CC(C)(C)[Si](C)(C)O[C@@H]1CO[C@@H](O[C@H]2C(O)OC[C@H](O)[C@@H]2O)[C@H](O)[C@H]1O2633.3Semi standard non polar33892256
2-O-b-D-Xylopyranosyl-L-arabinose,1TBDMS,isomer #2CC(C)(C)[Si](C)(C)OC1OC[C@H](O)[C@H](O)[C@H]1O[C@@H]1OC[C@@H](O)[C@H](O)[C@H]1O2579.7Semi standard non polar33892256
2-O-b-D-Xylopyranosyl-L-arabinose,1TBDMS,isomer #3CC(C)(C)[Si](C)(C)O[C@H]1COC(O)[C@H](O[C@@H]2OC[C@@H](O)[C@H](O)[C@H]2O)[C@H]1O2593.0Semi standard non polar33892256
2-O-b-D-Xylopyranosyl-L-arabinose,1TBDMS,isomer #4CC(C)(C)[Si](C)(C)O[C@H]1[C@@H](O)COC(O)[C@@H]1O[C@@H]1OC[C@@H](O)[C@H](O)[C@H]1O2587.9Semi standard non polar33892256
2-O-b-D-Xylopyranosyl-L-arabinose,1TBDMS,isomer #5CC(C)(C)[Si](C)(C)O[C@H]1[C@H](O[C@H]2C(O)OC[C@H](O)[C@@H]2O)OC[C@@H](O)[C@@H]1O2617.3Semi standard non polar33892256
2-O-b-D-Xylopyranosyl-L-arabinose,1TBDMS,isomer #6CC(C)(C)[Si](C)(C)O[C@H]1[C@H](O)CO[C@@H](O[C@H]2C(O)OC[C@H](O)[C@@H]2O)[C@@H]1O2607.3Semi standard non polar33892256
2-O-b-D-Xylopyranosyl-L-arabinose,2TBDMS,isomer #1CC(C)(C)[Si](C)(C)OC1OC[C@H](O)[C@H](O)[C@H]1O[C@@H]1OC[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O2827.7Semi standard non polar33892256
2-O-b-D-Xylopyranosyl-L-arabinose,2TBDMS,isomer #10CC(C)(C)[Si](C)(C)O[C@H]1[C@H](O)CO[C@@H](O[C@H]2C(O)OC[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]2O)[C@@H]1O2802.1Semi standard non polar33892256
2-O-b-D-Xylopyranosyl-L-arabinose,2TBDMS,isomer #11CC(C)(C)[Si](C)(C)O[C@H]1COC(O)[C@H](O[C@@H]2OC[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)[C@H]1O2815.1Semi standard non polar33892256
2-O-b-D-Xylopyranosyl-L-arabinose,2TBDMS,isomer #12CC(C)(C)[Si](C)(C)O[C@H]1COC(O)[C@H](O[C@@H]2OC[C@@H](O)[C@H](O)[C@H]2O)[C@H]1O[Si](C)(C)C(C)(C)C2794.8Semi standard non polar33892256
2-O-b-D-Xylopyranosyl-L-arabinose,2TBDMS,isomer #13CC(C)(C)[Si](C)(C)O[C@H]1[C@@H](O)COC(O)[C@@H]1O[C@@H]1OC[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O2801.8Semi standard non polar33892256
2-O-b-D-Xylopyranosyl-L-arabinose,2TBDMS,isomer #14CC(C)(C)[Si](C)(C)O[C@H]1[C@@H](O)COC(O)[C@@H]1O[C@@H]1OC[C@@H](O)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C2814.7Semi standard non polar33892256
2-O-b-D-Xylopyranosyl-L-arabinose,2TBDMS,isomer #15CC(C)(C)[Si](C)(C)O[C@H]1[C@H](O)CO[C@@H](O[C@H]2C(O)OC[C@H](O)[C@@H]2O)[C@@H]1O[Si](C)(C)C(C)(C)C2794.9Semi standard non polar33892256
2-O-b-D-Xylopyranosyl-L-arabinose,2TBDMS,isomer #2CC(C)(C)[Si](C)(C)O[C@H]1COC(O)[C@H](O[C@@H]2OC[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]2O)[C@H]1O2826.5Semi standard non polar33892256
2-O-b-D-Xylopyranosyl-L-arabinose,2TBDMS,isomer #3CC(C)(C)[Si](C)(C)O[C@H]1[C@@H](O)COC(O)[C@@H]1O[C@@H]1OC[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O2820.6Semi standard non polar33892256
2-O-b-D-Xylopyranosyl-L-arabinose,2TBDMS,isomer #4CC(C)(C)[Si](C)(C)O[C@@H]1CO[C@@H](O[C@H]2C(O)OC[C@H](O)[C@@H]2O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O2808.9Semi standard non polar33892256
2-O-b-D-Xylopyranosyl-L-arabinose,2TBDMS,isomer #5CC(C)(C)[Si](C)(C)O[C@@H]1CO[C@@H](O[C@H]2C(O)OC[C@H](O)[C@@H]2O)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C2808.6Semi standard non polar33892256
2-O-b-D-Xylopyranosyl-L-arabinose,2TBDMS,isomer #6CC(C)(C)[Si](C)(C)OC1OC[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O[C@@H]1OC[C@@H](O)[C@H](O)[C@H]1O2780.1Semi standard non polar33892256
2-O-b-D-Xylopyranosyl-L-arabinose,2TBDMS,isomer #7CC(C)(C)[Si](C)(C)OC1OC[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[C@@H]1OC[C@@H](O)[C@H](O)[C@H]1O2785.3Semi standard non polar33892256
2-O-b-D-Xylopyranosyl-L-arabinose,2TBDMS,isomer #8CC(C)(C)[Si](C)(C)OC1OC[C@H](O)[C@H](O)[C@H]1O[C@@H]1OC[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O2809.0Semi standard non polar33892256
2-O-b-D-Xylopyranosyl-L-arabinose,2TBDMS,isomer #9CC(C)(C)[Si](C)(C)OC1OC[C@H](O)[C@H](O)[C@H]1O[C@@H]1OC[C@@H](O)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C2819.4Semi standard non polar33892256
2-O-b-D-Xylopyranosyl-L-arabinose,3TBDMS,isomer #1CC(C)(C)[Si](C)(C)OC1OC[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O[C@@H]1OC[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O3018.8Semi standard non polar33892256
2-O-b-D-Xylopyranosyl-L-arabinose,3TBDMS,isomer #10CC(C)(C)[Si](C)(C)O[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)CO[C@@H](O[C@H]2C(O)OC[C@H](O)[C@@H]2O)[C@@H]1O[Si](C)(C)C(C)(C)C3009.9Semi standard non polar33892256
2-O-b-D-Xylopyranosyl-L-arabinose,3TBDMS,isomer #11CC(C)(C)[Si](C)(C)OC1OC[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[C@@H]1OC[C@@H](O)[C@H](O)[C@H]1O2989.9Semi standard non polar33892256
2-O-b-D-Xylopyranosyl-L-arabinose,3TBDMS,isomer #12CC(C)(C)[Si](C)(C)OC1OC[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O[C@@H]1OC[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O3001.4Semi standard non polar33892256
2-O-b-D-Xylopyranosyl-L-arabinose,3TBDMS,isomer #13CC(C)(C)[Si](C)(C)OC1OC[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O[C@@H]1OC[C@@H](O)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C3016.3Semi standard non polar33892256
2-O-b-D-Xylopyranosyl-L-arabinose,3TBDMS,isomer #14CC(C)(C)[Si](C)(C)OC1OC[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[C@@H]1OC[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O3018.8Semi standard non polar33892256
2-O-b-D-Xylopyranosyl-L-arabinose,3TBDMS,isomer #15CC(C)(C)[Si](C)(C)OC1OC[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[C@@H]1OC[C@@H](O)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C3028.2Semi standard non polar33892256
2-O-b-D-Xylopyranosyl-L-arabinose,3TBDMS,isomer #16CC(C)(C)[Si](C)(C)OC1OC[C@H](O)[C@H](O)[C@H]1O[C@@H]1OC[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)C3012.4Semi standard non polar33892256
2-O-b-D-Xylopyranosyl-L-arabinose,3TBDMS,isomer #17CC(C)(C)[Si](C)(C)O[C@H]1[C@H](O)CO[C@@H](O[C@H]2C(O)OC[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]2O[Si](C)(C)C(C)(C)C)[C@@H]1O3036.6Semi standard non polar33892256
2-O-b-D-Xylopyranosyl-L-arabinose,3TBDMS,isomer #18CC(C)(C)[Si](C)(C)O[C@H]1[C@H](O)CO[C@@H](O[C@H]2C(O)OC[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]2O)[C@@H]1O[Si](C)(C)C(C)(C)C3022.3Semi standard non polar33892256
2-O-b-D-Xylopyranosyl-L-arabinose,3TBDMS,isomer #19CC(C)(C)[Si](C)(C)O[C@H]1COC(O)[C@H](O[C@@H]2OC[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)C3043.7Semi standard non polar33892256
2-O-b-D-Xylopyranosyl-L-arabinose,3TBDMS,isomer #2CC(C)(C)[Si](C)(C)OC1OC[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[C@@H]1OC[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O3026.9Semi standard non polar33892256
2-O-b-D-Xylopyranosyl-L-arabinose,3TBDMS,isomer #20CC(C)(C)[Si](C)(C)O[C@H]1[C@@H](O)COC(O)[C@@H]1O[C@@H]1OC[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)C3035.1Semi standard non polar33892256
2-O-b-D-Xylopyranosyl-L-arabinose,3TBDMS,isomer #3CC(C)(C)[Si](C)(C)OC1OC[C@H](O)[C@H](O)[C@H]1O[C@@H]1OC[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O3021.9Semi standard non polar33892256
2-O-b-D-Xylopyranosyl-L-arabinose,3TBDMS,isomer #4CC(C)(C)[Si](C)(C)OC1OC[C@H](O)[C@H](O)[C@H]1O[C@@H]1OC[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C3027.5Semi standard non polar33892256
2-O-b-D-Xylopyranosyl-L-arabinose,3TBDMS,isomer #5CC(C)(C)[Si](C)(C)O[C@H]1COC(O)[C@H](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)[C@H]1O3030.9Semi standard non polar33892256
2-O-b-D-Xylopyranosyl-L-arabinose,3TBDMS,isomer #6CC(C)(C)[Si](C)(C)O[C@H]1COC(O)[C@H](O[C@@H]2OC[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)[C@H]1O3031.4Semi standard non polar33892256
2-O-b-D-Xylopyranosyl-L-arabinose,3TBDMS,isomer #7CC(C)(C)[Si](C)(C)O[C@H]1COC(O)[C@H](O[C@@H]2OC[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]2O)[C@H]1O[Si](C)(C)C(C)(C)C3044.3Semi standard non polar33892256
2-O-b-D-Xylopyranosyl-L-arabinose,3TBDMS,isomer #8CC(C)(C)[Si](C)(C)O[C@H]1[C@@H](O)COC(O)[C@@H]1O[C@@H]1OC[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O3041.9Semi standard non polar33892256
2-O-b-D-Xylopyranosyl-L-arabinose,3TBDMS,isomer #9CC(C)(C)[Si](C)(C)O[C@H]1[C@@H](O)COC(O)[C@@H]1O[C@@H]1OC[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C3044.3Semi standard non polar33892256
2-O-b-D-Xylopyranosyl-L-arabinose,4TBDMS,isomer #1CC(C)(C)[Si](C)(C)OC1OC[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[C@@H]1OC[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O3213.1Semi standard non polar33892256
2-O-b-D-Xylopyranosyl-L-arabinose,4TBDMS,isomer #10CC(C)(C)[Si](C)(C)O[C@H]1[C@@H](O)COC(O)[C@@H]1O[C@@H]1OC[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)C3218.4Semi standard non polar33892256
2-O-b-D-Xylopyranosyl-L-arabinose,4TBDMS,isomer #11CC(C)(C)[Si](C)(C)OC1OC[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[C@@H]1OC[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O3196.6Semi standard non polar33892256
2-O-b-D-Xylopyranosyl-L-arabinose,4TBDMS,isomer #12CC(C)(C)[Si](C)(C)OC1OC[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[C@@H]1OC[C@@H](O)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C3202.4Semi standard non polar33892256
2-O-b-D-Xylopyranosyl-L-arabinose,4TBDMS,isomer #13CC(C)(C)[Si](C)(C)OC1OC[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O[C@@H]1OC[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)C3201.4Semi standard non polar33892256
2-O-b-D-Xylopyranosyl-L-arabinose,4TBDMS,isomer #14CC(C)(C)[Si](C)(C)OC1OC[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[C@@H]1OC[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)C3216.4Semi standard non polar33892256
2-O-b-D-Xylopyranosyl-L-arabinose,4TBDMS,isomer #15CC(C)(C)[Si](C)(C)O[C@H]1[C@H](O)CO[C@@H](O[C@H]2C(O)OC[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]2O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C3222.6Semi standard non polar33892256
2-O-b-D-Xylopyranosyl-L-arabinose,4TBDMS,isomer #2CC(C)(C)[Si](C)(C)OC1OC[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O[C@@H]1OC[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O3209.1Semi standard non polar33892256
2-O-b-D-Xylopyranosyl-L-arabinose,4TBDMS,isomer #3CC(C)(C)[Si](C)(C)OC1OC[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O[C@@H]1OC[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C3215.8Semi standard non polar33892256
2-O-b-D-Xylopyranosyl-L-arabinose,4TBDMS,isomer #4CC(C)(C)[Si](C)(C)OC1OC[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[C@@H]1OC[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O3220.1Semi standard non polar33892256
2-O-b-D-Xylopyranosyl-L-arabinose,4TBDMS,isomer #5CC(C)(C)[Si](C)(C)OC1OC[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[C@@H]1OC[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C3219.3Semi standard non polar33892256
2-O-b-D-Xylopyranosyl-L-arabinose,4TBDMS,isomer #6CC(C)(C)[Si](C)(C)OC1OC[C@H](O)[C@H](O)[C@H]1O[C@@H]1OC[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)C3209.3Semi standard non polar33892256
2-O-b-D-Xylopyranosyl-L-arabinose,4TBDMS,isomer #7CC(C)(C)[Si](C)(C)O[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)CO[C@@H](O[C@H]2C(O)OC[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]2O)[C@@H]1O[Si](C)(C)C(C)(C)C3220.3Semi standard non polar33892256
2-O-b-D-Xylopyranosyl-L-arabinose,4TBDMS,isomer #8CC(C)(C)[Si](C)(C)O[C@H]1COC(O)[C@H](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)[C@H]1O[Si](C)(C)C(C)(C)C3224.9Semi standard non polar33892256
2-O-b-D-Xylopyranosyl-L-arabinose,4TBDMS,isomer #9CC(C)(C)[Si](C)(C)O[C@H]1COC(O)[C@H](O[C@@H]2OC[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)C3230.3Semi standard non polar33892256
2-O-b-D-Xylopyranosyl-L-arabinose,5TBDMS,isomer #1CC(C)(C)[Si](C)(C)OC1OC[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[C@@H]1OC[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O3376.3Semi standard non polar33892256
2-O-b-D-Xylopyranosyl-L-arabinose,5TBDMS,isomer #2CC(C)(C)[Si](C)(C)OC1OC[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[C@@H]1OC[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C3376.6Semi standard non polar33892256
2-O-b-D-Xylopyranosyl-L-arabinose,5TBDMS,isomer #3CC(C)(C)[Si](C)(C)OC1OC[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O[C@@H]1OC[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)C3369.2Semi standard non polar33892256
2-O-b-D-Xylopyranosyl-L-arabinose,5TBDMS,isomer #4CC(C)(C)[Si](C)(C)OC1OC[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[C@@H]1OC[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)C3375.9Semi standard non polar33892256
2-O-b-D-Xylopyranosyl-L-arabinose,5TBDMS,isomer #5CC(C)(C)[Si](C)(C)O[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)CO[C@@H](O[C@H]2C(O)OC[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]2O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C3384.9Semi standard non polar33892256
2-O-b-D-Xylopyranosyl-L-arabinose,5TBDMS,isomer #6CC(C)(C)[Si](C)(C)OC1OC[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[C@@H]1OC[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)C3376.5Semi standard non polar33892256
Spectra

GC-MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted GC-MSPredicted GC-MS Spectrum - 2-O-b-D-Xylopyranosyl-L-arabinose GC-MS (Non-derivatized) - 70eV, Positivesplash10-0fk9-3390000000-057675b763fb71b2d13f2017-09-01Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - 2-O-b-D-Xylopyranosyl-L-arabinose GC-MS (5 TMS) - 70eV, Positivesplash10-004i-2121149000-dcf0ce9206e4a55698142017-10-06Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - 2-O-b-D-Xylopyranosyl-L-arabinose GC-MS (TBDMS_5_6) - 70eV, PositiveNot Available2021-10-12Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - 2-O-b-D-Xylopyranosyl-L-arabinose GC-MS (Non-derivatized) - 70eV, PositiveNot Available2021-10-12Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - 2-O-b-D-Xylopyranosyl-L-arabinose GC-MS ("2-O-b-D-Xylopyranosyl-L-arabinose,5TBDMS,#6" TMS) - 70eV, PositiveNot Available2021-10-14Wishart LabView Spectrum

MS/MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 2-O-b-D-Xylopyranosyl-L-arabinose 10V, Positive-QTOFsplash10-00lr-0690000000-4e6eb6324e7e9fbe2b6f2016-08-01Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 2-O-b-D-Xylopyranosyl-L-arabinose 20V, Positive-QTOFsplash10-001i-0930000000-3c38d1148171468cb4dd2016-08-01Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 2-O-b-D-Xylopyranosyl-L-arabinose 40V, Positive-QTOFsplash10-0fz9-8910000000-5d15386b27b44ac0e6cc2016-08-01Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 2-O-b-D-Xylopyranosyl-L-arabinose 10V, Negative-QTOFsplash10-001i-2690000000-878b83e68ff36a1860a62016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 2-O-b-D-Xylopyranosyl-L-arabinose 20V, Negative-QTOFsplash10-001j-3920000000-8f30e09b2092fcdb96ed2016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 2-O-b-D-Xylopyranosyl-L-arabinose 40V, Negative-QTOFsplash10-0006-9300000000-e4b50cca0ac18b139a8a2016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 2-O-b-D-Xylopyranosyl-L-arabinose 10V, Negative-QTOFsplash10-000y-1970000000-235b34cbed9ea0268ea12021-09-24Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 2-O-b-D-Xylopyranosyl-L-arabinose 20V, Negative-QTOFsplash10-059y-9850000000-ad2b510cd7d87ff8951e2021-09-24Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 2-O-b-D-Xylopyranosyl-L-arabinose 40V, Negative-QTOFsplash10-0006-9100000000-8abcd7e33cb511fd00732021-09-24Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 2-O-b-D-Xylopyranosyl-L-arabinose 10V, Positive-QTOFsplash10-001i-0090000000-62a90e11add1819c92512021-09-24Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 2-O-b-D-Xylopyranosyl-L-arabinose 20V, Positive-QTOFsplash10-001i-4910000000-35875ba6734fa4146c5a2021-09-24Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 2-O-b-D-Xylopyranosyl-L-arabinose 40V, Positive-QTOFsplash10-02ta-9600000000-938bffb6dcabbc73030f2021-09-24Wishart LabView Spectrum

NMR Spectra

Spectrum TypeDescriptionDeposition DateSourceView
Predicted 1D NMR13C NMR Spectrum (1D, 100 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 100 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 1000 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 1000 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 200 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 200 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 300 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 300 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 400 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 400 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 500 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 500 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 600 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 600 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 700 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 700 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 800 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 800 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 900 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 900 MHz, D2O, predicted)2021-09-24Wishart 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 IDFDB018327
KNApSAcK IDNot Available
Chemspider ID35014682
KEGG Compound IDNot Available
BioCyc IDNot Available
BiGG IDNot Available
Wikipedia LinkNot Available
METLIN IDNot Available
PubChem Compound131752484
PDB IDNot Available
ChEBI ID174693
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 References
  1. (). Yannai, Shmuel. (2004) Dictionary of food compounds with CD-ROM: Additives, flavors, and ingredients. Boca Raton: Chapman & Hall/CRC.. .