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Record Information
Version5.0
StatusExpected but not Quantified
Creation Date2012-09-12 01:03:04 UTC
Update Date2022-03-07 02:56:15 UTC
HMDB IDHMDB0039554
Secondary Accession Numbers
  • HMDB39554
Metabolite Identification
Common NameGinsenoside Rh1
DescriptionGinsenoside Rh1, also known as sanchinoside B2, belongs to the class of organic compounds known as triterpenoids. These are terpene molecules containing six isoprene units. Ginsenoside Rh1 is an extremely weak basic (essentially neutral) compound (based on its pKa).
Structure
Data?1563863396
Synonyms
ValueSource
Sanchinoside b2HMDB
Ginsenoside RH(1)HMDB
Ginsenoside g-RH(1)HMDB
Ginsenoside RH1MeSH
Chemical FormulaC36H62O9
Average Molecular Weight638.8721
Monoisotopic Molecular Weight638.439383582
IUPAC Name2-{[5,16-dihydroxy-14-(2-hydroxy-6-methylhept-5-en-2-yl)-2,6,6,10,11-pentamethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadecan-8-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol
Traditional Name2-{[5,16-dihydroxy-14-(2-hydroxy-6-methylhept-5-en-2-yl)-2,6,6,10,11-pentamethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadecan-8-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol
CAS Registry Number63223-86-9
SMILES
CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O)CC1C3(C)CCC(O)C(C)(C)C3C(CC21C)OC1OC(CO)C(O)C(O)C1O
InChI Identifier
InChI=1S/C36H62O9/c1-19(2)10-9-13-36(8,43)20-11-15-34(6)26(20)21(38)16-24-33(5)14-12-25(39)32(3,4)30(33)22(17-35(24,34)7)44-31-29(42)28(41)27(40)23(18-37)45-31/h10,20-31,37-43H,9,11-18H2,1-8H3
InChI KeyRAQNTCRNSXYLAH-UHFFFAOYSA-N
Chemical Taxonomy
Description Belongs to the class of organic compounds known as triterpenoids. These are terpene molecules containing six isoprene units.
KingdomOrganic compounds
Super ClassLipids and lipid-like molecules
ClassPrenol lipids
Sub ClassTriterpenoids
Direct ParentTriterpenoids
Alternative ParentsNot Available
SubstituentsNot Available
Molecular FrameworkAliphatic heteropolycyclic compounds
External DescriptorsNot Available
Ontology
Physiological effectNot Available
Disposition
Process
Role
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 Solubility0.074 g/LALOGPS
logP2.68ALOGPS
logP2.45ChemAxon
logS-3.9ALOGPS
pKa (Strongest Acidic)12.21ChemAxon
pKa (Strongest Basic)-2.8ChemAxon
Physiological Charge0ChemAxon
Hydrogen Acceptor Count9ChemAxon
Hydrogen Donor Count7ChemAxon
Polar Surface Area160.07 ŲChemAxon
Rotatable Bond Count7ChemAxon
Refractivity171.24 m³·mol⁻¹ChemAxon
Polarizability73.42 ųChemAxon
Number of Rings5ChemAxon
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]+245.02131661259
DarkChem[M-H]-234.11831661259
DeepCCS[M-2H]-278.50230932474
DeepCCS[M+Na]+253.61530932474
AllCCS[M+H]+246.332859911
AllCCS[M+H-H2O]+245.632859911
AllCCS[M+NH4]+247.032859911
AllCCS[M+Na]+247.232859911
AllCCS[M-H]-228.432859911
AllCCS[M+Na-2H]-233.132859911
AllCCS[M+HCOO]-238.332859911

Predicted Kovats Retention Indices

Underivatized

MetaboliteSMILESKovats RI ValueColumn TypeReference
Ginsenoside Rh1CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O)CC1C3(C)CCC(O)C(C)(C)C3C(CC21C)OC1OC(CO)C(O)C(O)C1O3242.2Standard polar33892256
Ginsenoside Rh1CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O)CC1C3(C)CCC(O)C(C)(C)C3C(CC21C)OC1OC(CO)C(O)C(O)C1O4239.8Standard non polar33892256
Ginsenoside Rh1CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O)CC1C3(C)CCC(O)C(C)(C)C3C(CC21C)OC1OC(CO)C(O)C(O)C1O4942.3Semi standard non polar33892256

Derivatized

Derivative Name / StructureSMILESKovats RI ValueColumn TypeReference
Ginsenoside Rh1,1TMS,isomer #1CC(C)=CCCC(C)(O[Si](C)(C)C)C1CCC2(C)C1C(O)CC1C3(C)CCC(O)C(C)(C)C3C(OC3OC(CO)C(O)C(O)C3O)CC12C4987.0Semi standard non polar33892256
Ginsenoside Rh1,1TMS,isomer #2CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O[Si](C)(C)C)CC1C3(C)CCC(O)C(C)(C)C3C(OC3OC(CO)C(O)C(O)C3O)CC12C4958.0Semi standard non polar33892256
Ginsenoside Rh1,1TMS,isomer #3CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O)CC1C3(C)CCC(O[Si](C)(C)C)C(C)(C)C3C(OC3OC(CO)C(O)C(O)C3O)CC12C5046.8Semi standard non polar33892256
Ginsenoside Rh1,1TMS,isomer #4CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O)CC1C3(C)CCC(O)C(C)(C)C3C(OC3OC(CO[Si](C)(C)C)C(O)C(O)C3O)CC12C5045.7Semi standard non polar33892256
Ginsenoside Rh1,1TMS,isomer #5CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O)CC1C3(C)CCC(O)C(C)(C)C3C(OC3OC(CO)C(O[Si](C)(C)C)C(O)C3O)CC12C5044.0Semi standard non polar33892256
Ginsenoside Rh1,1TMS,isomer #6CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O)CC1C3(C)CCC(O)C(C)(C)C3C(OC3OC(CO)C(O)C(O[Si](C)(C)C)C3O)CC12C5037.1Semi standard non polar33892256
Ginsenoside Rh1,1TMS,isomer #7CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O)CC1C3(C)CCC(O)C(C)(C)C3C(OC3OC(CO)C(O)C(O)C3O[Si](C)(C)C)CC12C5028.3Semi standard non polar33892256
Ginsenoside Rh1,2TMS,isomer #1CC(C)=CCCC(C)(O[Si](C)(C)C)C1CCC2(C)C1C(O[Si](C)(C)C)CC1C3(C)CCC(O)C(C)(C)C3C(OC3OC(CO)C(O)C(O)C3O)CC12C4844.1Semi standard non polar33892256
Ginsenoside Rh1,2TMS,isomer #10CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O[Si](C)(C)C)CC1C3(C)CCC(O)C(C)(C)C3C(OC3OC(CO)C(O)C(O[Si](C)(C)C)C3O)CC12C4806.5Semi standard non polar33892256
Ginsenoside Rh1,2TMS,isomer #11CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O[Si](C)(C)C)CC1C3(C)CCC(O)C(C)(C)C3C(OC3OC(CO)C(O)C(O)C3O[Si](C)(C)C)CC12C4806.5Semi standard non polar33892256
Ginsenoside Rh1,2TMS,isomer #12CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O)CC1C3(C)CCC(O[Si](C)(C)C)C(C)(C)C3C(OC3OC(CO[Si](C)(C)C)C(O)C(O)C3O)CC12C4956.0Semi standard non polar33892256
Ginsenoside Rh1,2TMS,isomer #13CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O)CC1C3(C)CCC(O[Si](C)(C)C)C(C)(C)C3C(OC3OC(CO)C(O[Si](C)(C)C)C(O)C3O)CC12C4954.0Semi standard non polar33892256
Ginsenoside Rh1,2TMS,isomer #14CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O)CC1C3(C)CCC(O[Si](C)(C)C)C(C)(C)C3C(OC3OC(CO)C(O)C(O[Si](C)(C)C)C3O)CC12C4928.0Semi standard non polar33892256
Ginsenoside Rh1,2TMS,isomer #15CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O)CC1C3(C)CCC(O[Si](C)(C)C)C(C)(C)C3C(OC3OC(CO)C(O)C(O)C3O[Si](C)(C)C)CC12C4920.1Semi standard non polar33892256
Ginsenoside Rh1,2TMS,isomer #16CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O)CC1C3(C)CCC(O)C(C)(C)C3C(OC3OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C3O)CC12C4963.5Semi standard non polar33892256
Ginsenoside Rh1,2TMS,isomer #17CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O)CC1C3(C)CCC(O)C(C)(C)C3C(OC3OC(CO[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C3O)CC12C4949.2Semi standard non polar33892256
Ginsenoside Rh1,2TMS,isomer #18CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O)CC1C3(C)CCC(O)C(C)(C)C3C(OC3OC(CO[Si](C)(C)C)C(O)C(O)C3O[Si](C)(C)C)CC12C4950.1Semi standard non polar33892256
Ginsenoside Rh1,2TMS,isomer #19CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O)CC1C3(C)CCC(O)C(C)(C)C3C(OC3OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O)CC12C4950.1Semi standard non polar33892256
Ginsenoside Rh1,2TMS,isomer #2CC(C)=CCCC(C)(O[Si](C)(C)C)C1CCC2(C)C1C(O)CC1C3(C)CCC(O[Si](C)(C)C)C(C)(C)C3C(OC3OC(CO)C(O)C(O)C3O)CC12C4887.9Semi standard non polar33892256
Ginsenoside Rh1,2TMS,isomer #20CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O)CC1C3(C)CCC(O)C(C)(C)C3C(OC3OC(CO)C(O[Si](C)(C)C)C(O)C3O[Si](C)(C)C)CC12C4937.7Semi standard non polar33892256
Ginsenoside Rh1,2TMS,isomer #21CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O)CC1C3(C)CCC(O)C(C)(C)C3C(OC3OC(CO)C(O)C(O[Si](C)(C)C)C3O[Si](C)(C)C)CC12C4949.8Semi standard non polar33892256
Ginsenoside Rh1,2TMS,isomer #3CC(C)=CCCC(C)(O[Si](C)(C)C)C1CCC2(C)C1C(O)CC1C3(C)CCC(O)C(C)(C)C3C(OC3OC(CO[Si](C)(C)C)C(O)C(O)C3O)CC12C4885.2Semi standard non polar33892256
Ginsenoside Rh1,2TMS,isomer #4CC(C)=CCCC(C)(O[Si](C)(C)C)C1CCC2(C)C1C(O)CC1C3(C)CCC(O)C(C)(C)C3C(OC3OC(CO)C(O[Si](C)(C)C)C(O)C3O)CC12C4883.9Semi standard non polar33892256
Ginsenoside Rh1,2TMS,isomer #5CC(C)=CCCC(C)(O[Si](C)(C)C)C1CCC2(C)C1C(O)CC1C3(C)CCC(O)C(C)(C)C3C(OC3OC(CO)C(O)C(O[Si](C)(C)C)C3O)CC12C4861.6Semi standard non polar33892256
Ginsenoside Rh1,2TMS,isomer #6CC(C)=CCCC(C)(O[Si](C)(C)C)C1CCC2(C)C1C(O)CC1C3(C)CCC(O)C(C)(C)C3C(OC3OC(CO)C(O)C(O)C3O[Si](C)(C)C)CC12C4852.9Semi standard non polar33892256
Ginsenoside Rh1,2TMS,isomer #7CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O[Si](C)(C)C)CC1C3(C)CCC(O[Si](C)(C)C)C(C)(C)C3C(OC3OC(CO)C(O)C(O)C3O)CC12C4832.8Semi standard non polar33892256
Ginsenoside Rh1,2TMS,isomer #8CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O[Si](C)(C)C)CC1C3(C)CCC(O)C(C)(C)C3C(OC3OC(CO[Si](C)(C)C)C(O)C(O)C3O)CC12C4846.8Semi standard non polar33892256
Ginsenoside Rh1,2TMS,isomer #9CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O[Si](C)(C)C)CC1C3(C)CCC(O)C(C)(C)C3C(OC3OC(CO)C(O[Si](C)(C)C)C(O)C3O)CC12C4841.3Semi standard non polar33892256
Ginsenoside Rh1,3TMS,isomer #1CC(C)=CCCC(C)(O[Si](C)(C)C)C1CCC2(C)C1C(O[Si](C)(C)C)CC1C3(C)CCC(O[Si](C)(C)C)C(C)(C)C3C(OC3OC(CO)C(O)C(O)C3O)CC12C4701.7Semi standard non polar33892256
Ginsenoside Rh1,3TMS,isomer #10CC(C)=CCCC(C)(O[Si](C)(C)C)C1CCC2(C)C1C(O)CC1C3(C)CCC(O)C(C)(C)C3C(OC3OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C3O)CC12C4771.4Semi standard non polar33892256
Ginsenoside Rh1,3TMS,isomer #11CC(C)=CCCC(C)(O[Si](C)(C)C)C1CCC2(C)C1C(O)CC1C3(C)CCC(O)C(C)(C)C3C(OC3OC(CO[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C3O)CC12C4748.8Semi standard non polar33892256
Ginsenoside Rh1,3TMS,isomer #12CC(C)=CCCC(C)(O[Si](C)(C)C)C1CCC2(C)C1C(O)CC1C3(C)CCC(O)C(C)(C)C3C(OC3OC(CO[Si](C)(C)C)C(O)C(O)C3O[Si](C)(C)C)CC12C4751.1Semi standard non polar33892256
Ginsenoside Rh1,3TMS,isomer #13CC(C)=CCCC(C)(O[Si](C)(C)C)C1CCC2(C)C1C(O)CC1C3(C)CCC(O)C(C)(C)C3C(OC3OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O)CC12C4748.3Semi standard non polar33892256
Ginsenoside Rh1,3TMS,isomer #14CC(C)=CCCC(C)(O[Si](C)(C)C)C1CCC2(C)C1C(O)CC1C3(C)CCC(O)C(C)(C)C3C(OC3OC(CO)C(O[Si](C)(C)C)C(O)C3O[Si](C)(C)C)CC12C4736.6Semi standard non polar33892256
Ginsenoside Rh1,3TMS,isomer #15CC(C)=CCCC(C)(O[Si](C)(C)C)C1CCC2(C)C1C(O)CC1C3(C)CCC(O)C(C)(C)C3C(OC3OC(CO)C(O)C(O[Si](C)(C)C)C3O[Si](C)(C)C)CC12C4748.9Semi standard non polar33892256
Ginsenoside Rh1,3TMS,isomer #16CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O[Si](C)(C)C)CC1C3(C)CCC(O[Si](C)(C)C)C(C)(C)C3C(OC3OC(CO[Si](C)(C)C)C(O)C(O)C3O)CC12C4696.5Semi standard non polar33892256
Ginsenoside Rh1,3TMS,isomer #17CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O[Si](C)(C)C)CC1C3(C)CCC(O[Si](C)(C)C)C(C)(C)C3C(OC3OC(CO)C(O[Si](C)(C)C)C(O)C3O)CC12C4676.2Semi standard non polar33892256
Ginsenoside Rh1,3TMS,isomer #18CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O[Si](C)(C)C)CC1C3(C)CCC(O[Si](C)(C)C)C(C)(C)C3C(OC3OC(CO)C(O)C(O[Si](C)(C)C)C3O)CC12C4639.6Semi standard non polar33892256
Ginsenoside Rh1,3TMS,isomer #19CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O[Si](C)(C)C)CC1C3(C)CCC(O[Si](C)(C)C)C(C)(C)C3C(OC3OC(CO)C(O)C(O)C3O[Si](C)(C)C)CC12C4647.1Semi standard non polar33892256
Ginsenoside Rh1,3TMS,isomer #2CC(C)=CCCC(C)(O[Si](C)(C)C)C1CCC2(C)C1C(O[Si](C)(C)C)CC1C3(C)CCC(O)C(C)(C)C3C(OC3OC(CO[Si](C)(C)C)C(O)C(O)C3O)CC12C4714.4Semi standard non polar33892256
Ginsenoside Rh1,3TMS,isomer #20CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O[Si](C)(C)C)CC1C3(C)CCC(O)C(C)(C)C3C(OC3OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C3O)CC12C4716.7Semi standard non polar33892256
Ginsenoside Rh1,3TMS,isomer #21CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O[Si](C)(C)C)CC1C3(C)CCC(O)C(C)(C)C3C(OC3OC(CO[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C3O)CC12C4687.8Semi standard non polar33892256
Ginsenoside Rh1,3TMS,isomer #22CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O[Si](C)(C)C)CC1C3(C)CCC(O)C(C)(C)C3C(OC3OC(CO[Si](C)(C)C)C(O)C(O)C3O[Si](C)(C)C)CC12C4699.3Semi standard non polar33892256
Ginsenoside Rh1,3TMS,isomer #23CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O[Si](C)(C)C)CC1C3(C)CCC(O)C(C)(C)C3C(OC3OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O)CC12C4688.8Semi standard non polar33892256
Ginsenoside Rh1,3TMS,isomer #24CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O[Si](C)(C)C)CC1C3(C)CCC(O)C(C)(C)C3C(OC3OC(CO)C(O[Si](C)(C)C)C(O)C3O[Si](C)(C)C)CC12C4678.9Semi standard non polar33892256
Ginsenoside Rh1,3TMS,isomer #25CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O[Si](C)(C)C)CC1C3(C)CCC(O)C(C)(C)C3C(OC3OC(CO)C(O)C(O[Si](C)(C)C)C3O[Si](C)(C)C)CC12C4686.4Semi standard non polar33892256
Ginsenoside Rh1,3TMS,isomer #26CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O)CC1C3(C)CCC(O[Si](C)(C)C)C(C)(C)C3C(OC3OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C3O)CC12C4834.8Semi standard non polar33892256
Ginsenoside Rh1,3TMS,isomer #27CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O)CC1C3(C)CCC(O[Si](C)(C)C)C(C)(C)C3C(OC3OC(CO[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C3O)CC12C4810.7Semi standard non polar33892256
Ginsenoside Rh1,3TMS,isomer #28CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O)CC1C3(C)CCC(O[Si](C)(C)C)C(C)(C)C3C(OC3OC(CO[Si](C)(C)C)C(O)C(O)C3O[Si](C)(C)C)CC12C4810.0Semi standard non polar33892256
Ginsenoside Rh1,3TMS,isomer #29CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O)CC1C3(C)CCC(O[Si](C)(C)C)C(C)(C)C3C(OC3OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O)CC12C4804.7Semi standard non polar33892256
Ginsenoside Rh1,3TMS,isomer #3CC(C)=CCCC(C)(O[Si](C)(C)C)C1CCC2(C)C1C(O[Si](C)(C)C)CC1C3(C)CCC(O)C(C)(C)C3C(OC3OC(CO)C(O[Si](C)(C)C)C(O)C3O)CC12C4697.5Semi standard non polar33892256
Ginsenoside Rh1,3TMS,isomer #30CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O)CC1C3(C)CCC(O[Si](C)(C)C)C(C)(C)C3C(OC3OC(CO)C(O[Si](C)(C)C)C(O)C3O[Si](C)(C)C)CC12C4795.2Semi standard non polar33892256
Ginsenoside Rh1,3TMS,isomer #31CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O)CC1C3(C)CCC(O[Si](C)(C)C)C(C)(C)C3C(OC3OC(CO)C(O)C(O[Si](C)(C)C)C3O[Si](C)(C)C)CC12C4803.6Semi standard non polar33892256
Ginsenoside Rh1,3TMS,isomer #32CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O)CC1C3(C)CCC(O)C(C)(C)C3C(OC3OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O)CC12C4859.2Semi standard non polar33892256
Ginsenoside Rh1,3TMS,isomer #33CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O)CC1C3(C)CCC(O)C(C)(C)C3C(OC3OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C3O[Si](C)(C)C)CC12C4836.5Semi standard non polar33892256
Ginsenoside Rh1,3TMS,isomer #34CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O)CC1C3(C)CCC(O)C(C)(C)C3C(OC3OC(CO[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C3O[Si](C)(C)C)CC12C4850.4Semi standard non polar33892256
Ginsenoside Rh1,3TMS,isomer #35CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O)CC1C3(C)CCC(O)C(C)(C)C3C(OC3OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O[Si](C)(C)C)CC12C4854.9Semi standard non polar33892256
Ginsenoside Rh1,3TMS,isomer #4CC(C)=CCCC(C)(O[Si](C)(C)C)C1CCC2(C)C1C(O[Si](C)(C)C)CC1C3(C)CCC(O)C(C)(C)C3C(OC3OC(CO)C(O)C(O[Si](C)(C)C)C3O)CC12C4672.0Semi standard non polar33892256
Ginsenoside Rh1,3TMS,isomer #5CC(C)=CCCC(C)(O[Si](C)(C)C)C1CCC2(C)C1C(O[Si](C)(C)C)CC1C3(C)CCC(O)C(C)(C)C3C(OC3OC(CO)C(O)C(O)C3O[Si](C)(C)C)CC12C4670.6Semi standard non polar33892256
Ginsenoside Rh1,3TMS,isomer #6CC(C)=CCCC(C)(O[Si](C)(C)C)C1CCC2(C)C1C(O)CC1C3(C)CCC(O[Si](C)(C)C)C(C)(C)C3C(OC3OC(CO[Si](C)(C)C)C(O)C(O)C3O)CC12C4756.6Semi standard non polar33892256
Ginsenoside Rh1,3TMS,isomer #7CC(C)=CCCC(C)(O[Si](C)(C)C)C1CCC2(C)C1C(O)CC1C3(C)CCC(O[Si](C)(C)C)C(C)(C)C3C(OC3OC(CO)C(O[Si](C)(C)C)C(O)C3O)CC12C4744.9Semi standard non polar33892256
Ginsenoside Rh1,3TMS,isomer #8CC(C)=CCCC(C)(O[Si](C)(C)C)C1CCC2(C)C1C(O)CC1C3(C)CCC(O[Si](C)(C)C)C(C)(C)C3C(OC3OC(CO)C(O)C(O[Si](C)(C)C)C3O)CC12C4720.7Semi standard non polar33892256
Ginsenoside Rh1,3TMS,isomer #9CC(C)=CCCC(C)(O[Si](C)(C)C)C1CCC2(C)C1C(O)CC1C3(C)CCC(O[Si](C)(C)C)C(C)(C)C3C(OC3OC(CO)C(O)C(O)C3O[Si](C)(C)C)CC12C4713.8Semi standard non polar33892256
Ginsenoside Rh1,1TBDMS,isomer #1CC(C)=CCCC(C)(O[Si](C)(C)C(C)(C)C)C1CCC2(C)C1C(O)CC1C3(C)CCC(O)C(C)(C)C3C(OC3OC(CO)C(O)C(O)C3O)CC12C5202.3Semi standard non polar33892256
Ginsenoside Rh1,1TBDMS,isomer #2CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O[Si](C)(C)C(C)(C)C)CC1C3(C)CCC(O)C(C)(C)C3C(OC3OC(CO)C(O)C(O)C3O)CC12C5182.0Semi standard non polar33892256
Ginsenoside Rh1,1TBDMS,isomer #3CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O)CC1C3(C)CCC(O[Si](C)(C)C(C)(C)C)C(C)(C)C3C(OC3OC(CO)C(O)C(O)C3O)CC12C5261.9Semi standard non polar33892256
Ginsenoside Rh1,1TBDMS,isomer #4CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O)CC1C3(C)CCC(O)C(C)(C)C3C(OC3OC(CO[Si](C)(C)C(C)(C)C)C(O)C(O)C3O)CC12C5238.9Semi standard non polar33892256
Ginsenoside Rh1,1TBDMS,isomer #5CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O)CC1C3(C)CCC(O)C(C)(C)C3C(OC3OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C3O)CC12C5282.8Semi standard non polar33892256
Ginsenoside Rh1,1TBDMS,isomer #6CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O)CC1C3(C)CCC(O)C(C)(C)C3C(OC3OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C3O)CC12C5265.9Semi standard non polar33892256
Ginsenoside Rh1,1TBDMS,isomer #7CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O)CC1C3(C)CCC(O)C(C)(C)C3C(OC3OC(CO)C(O)C(O)C3O[Si](C)(C)C(C)(C)C)CC12C5263.2Semi standard non polar33892256
Ginsenoside Rh1,2TBDMS,isomer #1CC(C)=CCCC(C)(O[Si](C)(C)C(C)(C)C)C1CCC2(C)C1C(O[Si](C)(C)C(C)(C)C)CC1C3(C)CCC(O)C(C)(C)C3C(OC3OC(CO)C(O)C(O)C3O)CC12C5268.7Semi standard non polar33892256
Ginsenoside Rh1,2TBDMS,isomer #10CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O[Si](C)(C)C(C)(C)C)CC1C3(C)CCC(O)C(C)(C)C3C(OC3OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C3O)CC12C5259.1Semi standard non polar33892256
Ginsenoside Rh1,2TBDMS,isomer #11CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O[Si](C)(C)C(C)(C)C)CC1C3(C)CCC(O)C(C)(C)C3C(OC3OC(CO)C(O)C(O)C3O[Si](C)(C)C(C)(C)C)CC12C5264.4Semi standard non polar33892256
Ginsenoside Rh1,2TBDMS,isomer #12CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O)CC1C3(C)CCC(O[Si](C)(C)C(C)(C)C)C(C)(C)C3C(OC3OC(CO[Si](C)(C)C(C)(C)C)C(O)C(O)C3O)CC12C5362.8Semi standard non polar33892256
Ginsenoside Rh1,2TBDMS,isomer #13CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O)CC1C3(C)CCC(O[Si](C)(C)C(C)(C)C)C(C)(C)C3C(OC3OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C3O)CC12C5400.6Semi standard non polar33892256
Ginsenoside Rh1,2TBDMS,isomer #14CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O)CC1C3(C)CCC(O[Si](C)(C)C(C)(C)C)C(C)(C)C3C(OC3OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C3O)CC12C5377.5Semi standard non polar33892256
Ginsenoside Rh1,2TBDMS,isomer #15CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O)CC1C3(C)CCC(O[Si](C)(C)C(C)(C)C)C(C)(C)C3C(OC3OC(CO)C(O)C(O)C3O[Si](C)(C)C(C)(C)C)CC12C5376.1Semi standard non polar33892256
Ginsenoside Rh1,2TBDMS,isomer #16CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O)CC1C3(C)CCC(O)C(C)(C)C3C(OC3OC(CO[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C(O)C3O)CC12C5391.9Semi standard non polar33892256
Ginsenoside Rh1,2TBDMS,isomer #17CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O)CC1C3(C)CCC(O)C(C)(C)C3C(OC3OC(CO[Si](C)(C)C(C)(C)C)C(O)C(O[Si](C)(C)C(C)(C)C)C3O)CC12C5378.4Semi standard non polar33892256
Ginsenoside Rh1,2TBDMS,isomer #18CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O)CC1C3(C)CCC(O)C(C)(C)C3C(OC3OC(CO[Si](C)(C)C(C)(C)C)C(O)C(O)C3O[Si](C)(C)C(C)(C)C)CC12C5385.4Semi standard non polar33892256
Ginsenoside Rh1,2TBDMS,isomer #19CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O)CC1C3(C)CCC(O)C(C)(C)C3C(OC3OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C3O)CC12C5414.8Semi standard non polar33892256
Ginsenoside Rh1,2TBDMS,isomer #2CC(C)=CCCC(C)(O[Si](C)(C)C(C)(C)C)C1CCC2(C)C1C(O)CC1C3(C)CCC(O[Si](C)(C)C(C)(C)C)C(C)(C)C3C(OC3OC(CO)C(O)C(O)C3O)CC12C5323.5Semi standard non polar33892256
Ginsenoside Rh1,2TBDMS,isomer #20CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O)CC1C3(C)CCC(O)C(C)(C)C3C(OC3OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C3O[Si](C)(C)C(C)(C)C)CC12C5404.5Semi standard non polar33892256
Ginsenoside Rh1,2TBDMS,isomer #21CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O)CC1C3(C)CCC(O)C(C)(C)C3C(OC3OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C3O[Si](C)(C)C(C)(C)C)CC12C5412.5Semi standard non polar33892256
Ginsenoside Rh1,2TBDMS,isomer #3CC(C)=CCCC(C)(O[Si](C)(C)C(C)(C)C)C1CCC2(C)C1C(O)CC1C3(C)CCC(O)C(C)(C)C3C(OC3OC(CO[Si](C)(C)C(C)(C)C)C(O)C(O)C3O)CC12C5305.4Semi standard non polar33892256
Ginsenoside Rh1,2TBDMS,isomer #4CC(C)=CCCC(C)(O[Si](C)(C)C(C)(C)C)C1CCC2(C)C1C(O)CC1C3(C)CCC(O)C(C)(C)C3C(OC3OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C3O)CC12C5329.9Semi standard non polar33892256
Ginsenoside Rh1,2TBDMS,isomer #5CC(C)=CCCC(C)(O[Si](C)(C)C(C)(C)C)C1CCC2(C)C1C(O)CC1C3(C)CCC(O)C(C)(C)C3C(OC3OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C3O)CC12C5304.7Semi standard non polar33892256
Ginsenoside Rh1,2TBDMS,isomer #6CC(C)=CCCC(C)(O[Si](C)(C)C(C)(C)C)C1CCC2(C)C1C(O)CC1C3(C)CCC(O)C(C)(C)C3C(OC3OC(CO)C(O)C(O)C3O[Si](C)(C)C(C)(C)C)CC12C5308.9Semi standard non polar33892256
Ginsenoside Rh1,2TBDMS,isomer #7CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O[Si](C)(C)C(C)(C)C)CC1C3(C)CCC(O[Si](C)(C)C(C)(C)C)C(C)(C)C3C(OC3OC(CO)C(O)C(O)C3O)CC12C5269.6Semi standard non polar33892256
Ginsenoside Rh1,2TBDMS,isomer #8CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O[Si](C)(C)C(C)(C)C)CC1C3(C)CCC(O)C(C)(C)C3C(OC3OC(CO[Si](C)(C)C(C)(C)C)C(O)C(O)C3O)CC12C5254.2Semi standard non polar33892256
Ginsenoside Rh1,2TBDMS,isomer #9CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O[Si](C)(C)C(C)(C)C)CC1C3(C)CCC(O)C(C)(C)C3C(OC3OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C3O)CC12C5293.5Semi standard non polar33892256
Spectra

GC-MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted GC-MSPredicted GC-MS Spectrum - Ginsenoside Rh1 GC-MS (Non-derivatized) - 70eV, Positivesplash10-05fr-4400339000-9f7882207f453de6c5e92017-09-01Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Ginsenoside Rh1 GC-MS (TMS_1_1) - 70eV, PositiveNot Available2021-10-17Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Ginsenoside Rh1 GC-MS (TMS_1_2) - 70eV, PositiveNot Available2021-10-17Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Ginsenoside Rh1 GC-MS (TMS_1_3) - 70eV, PositiveNot Available2021-10-17Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Ginsenoside Rh1 GC-MS (TMS_1_4) - 70eV, PositiveNot Available2021-10-17Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Ginsenoside Rh1 GC-MS (TMS_1_5) - 70eV, PositiveNot Available2021-10-17Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Ginsenoside Rh1 GC-MS (TMS_1_6) - 70eV, PositiveNot Available2021-10-17Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Ginsenoside Rh1 GC-MS (TMS_1_7) - 70eV, PositiveNot Available2021-10-17Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Ginsenoside Rh1 GC-MS (TMS_2_1) - 70eV, PositiveNot Available2021-10-17Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Ginsenoside Rh1 GC-MS (TMS_2_2) - 70eV, PositiveNot Available2021-10-17Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Ginsenoside Rh1 GC-MS (TMS_2_3) - 70eV, PositiveNot Available2021-10-17Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Ginsenoside Rh1 GC-MS (TMS_2_4) - 70eV, PositiveNot Available2021-10-17Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Ginsenoside Rh1 GC-MS (TMS_2_5) - 70eV, PositiveNot Available2021-10-17Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Ginsenoside Rh1 GC-MS (TMS_2_6) - 70eV, PositiveNot Available2021-10-17Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Ginsenoside Rh1 GC-MS (TMS_2_7) - 70eV, PositiveNot Available2021-10-17Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Ginsenoside Rh1 GC-MS (TMS_2_8) - 70eV, PositiveNot Available2021-10-17Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Ginsenoside Rh1 GC-MS (TMS_2_9) - 70eV, PositiveNot Available2021-10-17Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Ginsenoside Rh1 GC-MS (TMS_2_10) - 70eV, PositiveNot Available2021-10-17Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Ginsenoside Rh1 GC-MS (TMS_2_11) - 70eV, PositiveNot Available2021-10-17Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Ginsenoside Rh1 GC-MS (TMS_2_12) - 70eV, PositiveNot Available2021-10-17Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Ginsenoside Rh1 GC-MS (TMS_2_13) - 70eV, PositiveNot Available2021-10-17Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Ginsenoside Rh1 GC-MS (TMS_2_14) - 70eV, PositiveNot Available2021-10-17Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Ginsenoside Rh1 GC-MS (TMS_2_15) - 70eV, PositiveNot Available2021-10-17Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Ginsenoside Rh1 GC-MS (TMS_2_16) - 70eV, PositiveNot Available2021-10-17Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Ginsenoside Rh1 GC-MS (TMS_2_17) - 70eV, PositiveNot Available2021-10-17Wishart LabView Spectrum

MS/MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Ginsenoside Rh1 10V, Positive-QTOFsplash10-0pi0-0000709000-c47fc9449dc5d24bb18f2015-04-24Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Ginsenoside Rh1 20V, Positive-QTOFsplash10-0a4i-0001901000-29b5141f8974ae0c05e82015-04-24Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Ginsenoside Rh1 40V, Positive-QTOFsplash10-0a6r-3102900000-641c8872caa71243d94d2015-04-24Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Ginsenoside Rh1 10V, Positive-QTOFsplash10-0pi0-0000709000-c47fc9449dc5d24bb18f2015-04-24Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Ginsenoside Rh1 20V, Positive-QTOFsplash10-0a4i-0001901000-29b5141f8974ae0c05e82015-04-24Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Ginsenoside Rh1 40V, Positive-QTOFsplash10-0a6r-3102900000-641c8872caa71243d94d2015-04-24Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Ginsenoside Rh1 10V, Positive-QTOFsplash10-0pi0-0000709000-c47fc9449dc5d24bb18f2015-04-24Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Ginsenoside Rh1 20V, Positive-QTOFsplash10-0a4i-0001901000-29b5141f8974ae0c05e82015-04-24Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Ginsenoside Rh1 40V, Positive-QTOFsplash10-0a6r-3102900000-641c8872caa71243d94d2015-04-24Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Ginsenoside Rh1 10V, Negative-QTOFsplash10-052r-0100619000-f72a014cb35ad56ac6172015-04-25Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Ginsenoside Rh1 20V, Negative-QTOFsplash10-0a6r-1100902000-92a0a5324aba767e96572015-04-25Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Ginsenoside Rh1 40V, Negative-QTOFsplash10-0a6r-3001900000-dd99c1cc5d6ff96a3e9e2015-04-25Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Ginsenoside Rh1 10V, Negative-QTOFsplash10-052r-0100619000-f72a014cb35ad56ac6172015-04-25Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Ginsenoside Rh1 20V, Negative-QTOFsplash10-0a6r-1100902000-92a0a5324aba767e96572015-04-25Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Ginsenoside Rh1 40V, Negative-QTOFsplash10-0a6r-3001900000-dd99c1cc5d6ff96a3e9e2015-04-25Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Ginsenoside Rh1 10V, Negative-QTOFsplash10-052r-0100619000-f72a014cb35ad56ac6172015-04-25Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Ginsenoside Rh1 20V, Negative-QTOFsplash10-0a6r-1100902000-92a0a5324aba767e96572015-04-25Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Ginsenoside Rh1 40V, Negative-QTOFsplash10-0a6r-3001900000-dd99c1cc5d6ff96a3e9e2015-04-25Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Ginsenoside Rh1 10V, Positive-QTOFsplash10-0uki-0100129000-b5490daa8c14916851a52021-09-25Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Ginsenoside Rh1 20V, Positive-QTOFsplash10-08g0-6901565000-3a261521134434abde8a2021-09-25Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Ginsenoside Rh1 40V, Positive-QTOFsplash10-014i-9100100000-b1c954b7e0aab81b881e2021-09-25Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Ginsenoside Rh1 10V, Negative-QTOFsplash10-000i-0000009000-8158b86d9eb78664e1f92021-09-25Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Ginsenoside Rh1 20V, Negative-QTOFsplash10-000i-3000169000-5b0ac89fd82fafff02272021-09-25Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Ginsenoside Rh1 40V, Negative-QTOFsplash10-052f-9000031000-81240722da45f7ca003c2021-09-25Wishart LabView Spectrum
Biological Properties
Cellular Locations
  • Extracellular
  • Membrane
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 IDFDB019175
KNApSAcK IDC00030402
Chemspider ID21686433
KEGG Compound IDNot Available
BioCyc IDNot Available
BiGG IDNot Available
Wikipedia LinkNot Available
METLIN IDNot Available
PubChem Compound12855917
PDB IDNot Available
ChEBI IDNot Available
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. Simons K, Toomre D: Lipid rafts and signal transduction. Nat Rev Mol Cell Biol. 2000 Oct;1(1):31-9. [PubMed:11413487 ]
  2. Watson AD: Thematic review series: systems biology approaches to metabolic and cardiovascular disorders. Lipidomics: a global approach to lipid analysis in biological systems. J Lipid Res. 2006 Oct;47(10):2101-11. Epub 2006 Aug 10. [PubMed:16902246 ]
  3. Sethi JK, Vidal-Puig AJ: Thematic review series: adipocyte biology. Adipose tissue function and plasticity orchestrate nutritional adaptation. J Lipid Res. 2007 Jun;48(6):1253-62. Epub 2007 Mar 20. [PubMed:17374880 ]
  4. Lingwood D, Simons K: Lipid rafts as a membrane-organizing principle. Science. 2010 Jan 1;327(5961):46-50. doi: 10.1126/science.1174621. [PubMed:20044567 ]
  5. (). Yannai, Shmuel. (2004) Dictionary of food compounds with CD-ROM: Additives, flavors, and ingredients. Boca Raton: Chapman & Hall/CRC.. .
  6. Gunstone, Frank D., John L. Harwood, and Albert J. Dijkstra (2007). The lipid handbook with CD-ROM. CRC Press.