Hmdb loader
Record Information
Version5.0
StatusExpected but not Quantified
Creation Date2012-09-12 01:01:57 UTC
Update Date2022-03-07 02:56:15 UTC
HMDB IDHMDB0039544
Secondary Accession Numbers
  • HMDB39544
Metabolite Identification
Common Name(20R)-Ginsenoside Rh2
Description(20R)-Ginsenoside Rh2, also known as ginsenoside RH2, belongs to the class of organic compounds known as triterpenoids. These are terpene molecules containing six isoprene units (20R)-Ginsenoside Rh2 is an extremely weak basic (essentially neutral) compound (based on its pKa).
Structure
Data?1563863394
Synonyms
ValueSource
Ginsenoside RH2HMDB
Chemical FormulaC36H62O8
Average Molecular Weight622.8727
Monoisotopic Molecular Weight622.44446896
IUPAC Name2-{[16-hydroxy-14-(2-hydroxy-6-methylhept-5-en-2-yl)-2,6,6,10,11-pentamethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadecan-5-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol
Traditional Name2-{[16-hydroxy-14-(2-hydroxy-6-methylhept-5-en-2-yl)-2,6,6,10,11-pentamethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadecan-5-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol
CAS Registry Number78214-33-2
SMILES
CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O)CC1C3(C)CCC(OC4OC(CO)C(O)C(O)C4O)C(C)(C)C3CCC21C
InChI Identifier
InChI=1S/C36H62O8/c1-20(2)10-9-14-36(8,42)21-11-16-35(7)27(21)22(38)18-25-33(5)15-13-26(32(3,4)24(33)12-17-34(25,35)6)44-31-30(41)29(40)28(39)23(19-37)43-31/h10,21-31,37-42H,9,11-19H2,1-8H3
InChI KeyCKUVNOCSBYYHIS-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 Parents
Substituents
  • Triterpenoid
  • Steroidal glycoside
  • 20-hydroxysteroid
  • 12-hydroxysteroid
  • Hydroxysteroid
  • Steroid
  • Hexose monosaccharide
  • Glycosyl compound
  • O-glycosyl compound
  • Monosaccharide
  • Oxane
  • Tertiary alcohol
  • Cyclic alcohol
  • Secondary alcohol
  • Acetal
  • Organoheterocyclic compound
  • Oxacycle
  • Polyol
  • Alcohol
  • Organooxygen compound
  • Hydrocarbon derivative
  • Organic oxygen compound
  • Primary alcohol
  • Aliphatic heteropolycyclic compound
Molecular FrameworkAliphatic heteropolycyclic compounds
External Descriptors
Ontology
Physiological effectNot Available
Disposition
ProcessNot Available
RoleNot Available
Physical Properties
StateNot Available
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 Solubility0.012 g/LALOGPS
logP3.77ALOGPS
logP3.76ChemAxon
logS-4.7ALOGPS
pKa (Strongest Acidic)12.21ChemAxon
pKa (Strongest Basic)-2.8ChemAxon
Physiological Charge0ChemAxon
Hydrogen Acceptor Count8ChemAxon
Hydrogen Donor Count6ChemAxon
Polar Surface Area139.84 ŲChemAxon
Rotatable Bond Count7ChemAxon
Refractivity169.65 m³·mol⁻¹ChemAxon
Polarizability73.2 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]+238.43331661259
DarkChem[M-H]-232.12131661259
DeepCCS[M-2H]-273.8430932474
DeepCCS[M+Na]+249.26330932474
AllCCS[M+H]+248.832859911
AllCCS[M+H-H2O]+248.032859911
AllCCS[M+NH4]+249.532859911
AllCCS[M+Na]+249.732859911
AllCCS[M-H]-225.632859911
AllCCS[M+Na-2H]-230.332859911
AllCCS[M+HCOO]-235.632859911

Predicted Kovats Retention Indices

Underivatized

MetaboliteSMILESKovats RI ValueColumn TypeReference
(20R)-Ginsenoside Rh2CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O)CC1C3(C)CCC(OC4OC(CO)C(O)C(O)C4O)C(C)(C)C3CCC21C3054.1Standard polar33892256
(20R)-Ginsenoside Rh2CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O)CC1C3(C)CCC(OC4OC(CO)C(O)C(O)C4O)C(C)(C)C3CCC21C4170.8Standard non polar33892256
(20R)-Ginsenoside Rh2CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O)CC1C3(C)CCC(OC4OC(CO)C(O)C(O)C4O)C(C)(C)C3CCC21C4851.2Semi standard non polar33892256

Derivatized

Derivative Name / StructureSMILESKovats RI ValueColumn TypeReference
(20R)-Ginsenoside Rh2,1TMS,isomer #1CC(C)=CCCC(C)(O[Si](C)(C)C)C1CCC2(C)C1C(O)CC1C3(C)CCC(OC4OC(CO)C(O)C(O)C4O)C(C)(C)C3CCC12C4828.7Semi standard non polar33892256
(20R)-Ginsenoside Rh2,1TMS,isomer #1CC(C)=CCCC(C)(O[Si](C)(C)C)C1CCC2(C)C1C(O)CC1C3(C)CCC(OC4OC(CO)C(O)C(O)C4O)C(C)(C)C3CCC12C4538.1Standard non polar33892256
(20R)-Ginsenoside Rh2,1TMS,isomer #2CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O[Si](C)(C)C)CC1C3(C)CCC(OC4OC(CO)C(O)C(O)C4O)C(C)(C)C3CCC12C4803.1Semi standard non polar33892256
(20R)-Ginsenoside Rh2,1TMS,isomer #2CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O[Si](C)(C)C)CC1C3(C)CCC(OC4OC(CO)C(O)C(O)C4O)C(C)(C)C3CCC12C4446.9Standard non polar33892256
(20R)-Ginsenoside Rh2,1TMS,isomer #3CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O)CC1C3(C)CCC(OC4OC(CO[Si](C)(C)C)C(O)C(O)C4O)C(C)(C)C3CCC12C4888.1Semi standard non polar33892256
(20R)-Ginsenoside Rh2,1TMS,isomer #3CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O)CC1C3(C)CCC(OC4OC(CO[Si](C)(C)C)C(O)C(O)C4O)C(C)(C)C3CCC12C4558.4Standard non polar33892256
(20R)-Ginsenoside Rh2,1TMS,isomer #4CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O)CC1C3(C)CCC(OC4OC(CO)C(O[Si](C)(C)C)C(O)C4O)C(C)(C)C3CCC12C4889.0Semi standard non polar33892256
(20R)-Ginsenoside Rh2,1TMS,isomer #4CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O)CC1C3(C)CCC(OC4OC(CO)C(O[Si](C)(C)C)C(O)C4O)C(C)(C)C3CCC12C4509.3Standard non polar33892256
(20R)-Ginsenoside Rh2,1TMS,isomer #5CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O)CC1C3(C)CCC(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O)C(C)(C)C3CCC12C4875.4Semi standard non polar33892256
(20R)-Ginsenoside Rh2,1TMS,isomer #5CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O)CC1C3(C)CCC(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O)C(C)(C)C3CCC12C4503.0Standard non polar33892256
(20R)-Ginsenoside Rh2,1TMS,isomer #6CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O)CC1C3(C)CCC(OC4OC(CO)C(O)C(O)C4O[Si](C)(C)C)C(C)(C)C3CCC12C4862.9Semi standard non polar33892256
(20R)-Ginsenoside Rh2,1TMS,isomer #6CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O)CC1C3(C)CCC(OC4OC(CO)C(O)C(O)C4O[Si](C)(C)C)C(C)(C)C3CCC12C4514.4Standard non polar33892256
(20R)-Ginsenoside Rh2,2TMS,isomer #1CC(C)=CCCC(C)(O[Si](C)(C)C)C1CCC2(C)C1C(O[Si](C)(C)C)CC1C3(C)CCC(OC4OC(CO)C(O)C(O)C4O)C(C)(C)C3CCC12C4709.3Semi standard non polar33892256
(20R)-Ginsenoside Rh2,2TMS,isomer #1CC(C)=CCCC(C)(O[Si](C)(C)C)C1CCC2(C)C1C(O[Si](C)(C)C)CC1C3(C)CCC(OC4OC(CO)C(O)C(O)C4O)C(C)(C)C3CCC12C4495.8Standard non polar33892256
(20R)-Ginsenoside Rh2,2TMS,isomer #10CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O)CC1C3(C)CCC(OC4OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C4O)C(C)(C)C3CCC12C4816.5Semi standard non polar33892256
(20R)-Ginsenoside Rh2,2TMS,isomer #10CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O)CC1C3(C)CCC(OC4OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C4O)C(C)(C)C3CCC12C4573.0Standard non polar33892256
(20R)-Ginsenoside Rh2,2TMS,isomer #11CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O)CC1C3(C)CCC(OC4OC(CO[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C4O)C(C)(C)C3CCC12C4800.2Semi standard non polar33892256
(20R)-Ginsenoside Rh2,2TMS,isomer #11CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O)CC1C3(C)CCC(OC4OC(CO[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C4O)C(C)(C)C3CCC12C4588.0Standard non polar33892256
(20R)-Ginsenoside Rh2,2TMS,isomer #12CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O)CC1C3(C)CCC(OC4OC(CO[Si](C)(C)C)C(O)C(O)C4O[Si](C)(C)C)C(C)(C)C3CCC12C4796.1Semi standard non polar33892256
(20R)-Ginsenoside Rh2,2TMS,isomer #12CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O)CC1C3(C)CCC(OC4OC(CO[Si](C)(C)C)C(O)C(O)C4O[Si](C)(C)C)C(C)(C)C3CCC12C4572.2Standard non polar33892256
(20R)-Ginsenoside Rh2,2TMS,isomer #13CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O)CC1C3(C)CCC(OC4OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O)C(C)(C)C3CCC12C4797.6Semi standard non polar33892256
(20R)-Ginsenoside Rh2,2TMS,isomer #13CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O)CC1C3(C)CCC(OC4OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O)C(C)(C)C3CCC12C4539.8Standard non polar33892256
(20R)-Ginsenoside Rh2,2TMS,isomer #14CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O)CC1C3(C)CCC(OC4OC(CO)C(O[Si](C)(C)C)C(O)C4O[Si](C)(C)C)C(C)(C)C3CCC12C4789.8Semi standard non polar33892256
(20R)-Ginsenoside Rh2,2TMS,isomer #14CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O)CC1C3(C)CCC(OC4OC(CO)C(O[Si](C)(C)C)C(O)C4O[Si](C)(C)C)C(C)(C)C3CCC12C4566.4Standard non polar33892256
(20R)-Ginsenoside Rh2,2TMS,isomer #15CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O)CC1C3(C)CCC(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O[Si](C)(C)C)C(C)(C)C3CCC12C4801.8Semi standard non polar33892256
(20R)-Ginsenoside Rh2,2TMS,isomer #15CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O)CC1C3(C)CCC(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O[Si](C)(C)C)C(C)(C)C3CCC12C4524.0Standard non polar33892256
(20R)-Ginsenoside Rh2,2TMS,isomer #2CC(C)=CCCC(C)(O[Si](C)(C)C)C1CCC2(C)C1C(O)CC1C3(C)CCC(OC4OC(CO[Si](C)(C)C)C(O)C(O)C4O)C(C)(C)C3CCC12C4755.8Semi standard non polar33892256
(20R)-Ginsenoside Rh2,2TMS,isomer #2CC(C)=CCCC(C)(O[Si](C)(C)C)C1CCC2(C)C1C(O)CC1C3(C)CCC(OC4OC(CO[Si](C)(C)C)C(O)C(O)C4O)C(C)(C)C3CCC12C4594.0Standard non polar33892256
(20R)-Ginsenoside Rh2,2TMS,isomer #3CC(C)=CCCC(C)(O[Si](C)(C)C)C1CCC2(C)C1C(O)CC1C3(C)CCC(OC4OC(CO)C(O[Si](C)(C)C)C(O)C4O)C(C)(C)C3CCC12C4747.5Semi standard non polar33892256
(20R)-Ginsenoside Rh2,2TMS,isomer #3CC(C)=CCCC(C)(O[Si](C)(C)C)C1CCC2(C)C1C(O)CC1C3(C)CCC(OC4OC(CO)C(O[Si](C)(C)C)C(O)C4O)C(C)(C)C3CCC12C4554.8Standard non polar33892256
(20R)-Ginsenoside Rh2,2TMS,isomer #4CC(C)=CCCC(C)(O[Si](C)(C)C)C1CCC2(C)C1C(O)CC1C3(C)CCC(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O)C(C)(C)C3CCC12C4718.8Semi standard non polar33892256
(20R)-Ginsenoside Rh2,2TMS,isomer #4CC(C)=CCCC(C)(O[Si](C)(C)C)C1CCC2(C)C1C(O)CC1C3(C)CCC(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O)C(C)(C)C3CCC12C4554.6Standard non polar33892256
(20R)-Ginsenoside Rh2,2TMS,isomer #5CC(C)=CCCC(C)(O[Si](C)(C)C)C1CCC2(C)C1C(O)CC1C3(C)CCC(OC4OC(CO)C(O)C(O)C4O[Si](C)(C)C)C(C)(C)C3CCC12C4718.0Semi standard non polar33892256
(20R)-Ginsenoside Rh2,2TMS,isomer #5CC(C)=CCCC(C)(O[Si](C)(C)C)C1CCC2(C)C1C(O)CC1C3(C)CCC(OC4OC(CO)C(O)C(O)C4O[Si](C)(C)C)C(C)(C)C3CCC12C4563.8Standard non polar33892256
(20R)-Ginsenoside Rh2,2TMS,isomer #6CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O[Si](C)(C)C)CC1C3(C)CCC(OC4OC(CO[Si](C)(C)C)C(O)C(O)C4O)C(C)(C)C3CCC12C4706.6Semi standard non polar33892256
(20R)-Ginsenoside Rh2,2TMS,isomer #6CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O[Si](C)(C)C)CC1C3(C)CCC(OC4OC(CO[Si](C)(C)C)C(O)C(O)C4O)C(C)(C)C3CCC12C4507.5Standard non polar33892256
(20R)-Ginsenoside Rh2,2TMS,isomer #7CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O[Si](C)(C)C)CC1C3(C)CCC(OC4OC(CO)C(O[Si](C)(C)C)C(O)C4O)C(C)(C)C3CCC12C4695.1Semi standard non polar33892256
(20R)-Ginsenoside Rh2,2TMS,isomer #7CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O[Si](C)(C)C)CC1C3(C)CCC(OC4OC(CO)C(O[Si](C)(C)C)C(O)C4O)C(C)(C)C3CCC12C4469.3Standard non polar33892256
(20R)-Ginsenoside Rh2,2TMS,isomer #8CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O[Si](C)(C)C)CC1C3(C)CCC(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O)C(C)(C)C3CCC12C4658.7Semi standard non polar33892256
(20R)-Ginsenoside Rh2,2TMS,isomer #8CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O[Si](C)(C)C)CC1C3(C)CCC(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O)C(C)(C)C3CCC12C4470.8Standard non polar33892256
(20R)-Ginsenoside Rh2,2TMS,isomer #9CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O[Si](C)(C)C)CC1C3(C)CCC(OC4OC(CO)C(O)C(O)C4O[Si](C)(C)C)C(C)(C)C3CCC12C4663.2Semi standard non polar33892256
(20R)-Ginsenoside Rh2,2TMS,isomer #9CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O[Si](C)(C)C)CC1C3(C)CCC(OC4OC(CO)C(O)C(O)C4O[Si](C)(C)C)C(C)(C)C3CCC12C4478.0Standard non polar33892256
(20R)-Ginsenoside Rh2,3TMS,isomer #1CC(C)=CCCC(C)(O[Si](C)(C)C)C1CCC2(C)C1C(O[Si](C)(C)C)CC1C3(C)CCC(OC4OC(CO[Si](C)(C)C)C(O)C(O)C4O)C(C)(C)C3CCC12C4616.9Semi standard non polar33892256
(20R)-Ginsenoside Rh2,3TMS,isomer #1CC(C)=CCCC(C)(O[Si](C)(C)C)C1CCC2(C)C1C(O[Si](C)(C)C)CC1C3(C)CCC(OC4OC(CO[Si](C)(C)C)C(O)C(O)C4O)C(C)(C)C3CCC12C4542.9Standard non polar33892256
(20R)-Ginsenoside Rh2,3TMS,isomer #10CC(C)=CCCC(C)(O[Si](C)(C)C)C1CCC2(C)C1C(O)CC1C3(C)CCC(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O[Si](C)(C)C)C(C)(C)C3CCC12C4644.8Semi standard non polar33892256
(20R)-Ginsenoside Rh2,3TMS,isomer #10CC(C)=CCCC(C)(O[Si](C)(C)C)C1CCC2(C)C1C(O)CC1C3(C)CCC(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O[Si](C)(C)C)C(C)(C)C3CCC12C4560.8Standard non polar33892256
(20R)-Ginsenoside Rh2,3TMS,isomer #11CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O[Si](C)(C)C)CC1C3(C)CCC(OC4OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C4O)C(C)(C)C3CCC12C4603.0Semi standard non polar33892256
(20R)-Ginsenoside Rh2,3TMS,isomer #11CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O[Si](C)(C)C)CC1C3(C)CCC(OC4OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C4O)C(C)(C)C3CCC12C4524.0Standard non polar33892256
(20R)-Ginsenoside Rh2,3TMS,isomer #12CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O[Si](C)(C)C)CC1C3(C)CCC(OC4OC(CO[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C4O)C(C)(C)C3CCC12C4567.7Semi standard non polar33892256
(20R)-Ginsenoside Rh2,3TMS,isomer #12CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O[Si](C)(C)C)CC1C3(C)CCC(OC4OC(CO[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C4O)C(C)(C)C3CCC12C4538.4Standard non polar33892256
(20R)-Ginsenoside Rh2,3TMS,isomer #13CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O[Si](C)(C)C)CC1C3(C)CCC(OC4OC(CO[Si](C)(C)C)C(O)C(O)C4O[Si](C)(C)C)C(C)(C)C3CCC12C4579.4Semi standard non polar33892256
(20R)-Ginsenoside Rh2,3TMS,isomer #13CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O[Si](C)(C)C)CC1C3(C)CCC(OC4OC(CO[Si](C)(C)C)C(O)C(O)C4O[Si](C)(C)C)C(C)(C)C3CCC12C4530.0Standard non polar33892256
(20R)-Ginsenoside Rh2,3TMS,isomer #14CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O[Si](C)(C)C)CC1C3(C)CCC(OC4OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O)C(C)(C)C3CCC12C4561.7Semi standard non polar33892256
(20R)-Ginsenoside Rh2,3TMS,isomer #14CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O[Si](C)(C)C)CC1C3(C)CCC(OC4OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O)C(C)(C)C3CCC12C4492.8Standard non polar33892256
(20R)-Ginsenoside Rh2,3TMS,isomer #15CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O[Si](C)(C)C)CC1C3(C)CCC(OC4OC(CO)C(O[Si](C)(C)C)C(O)C4O[Si](C)(C)C)C(C)(C)C3CCC12C4559.6Semi standard non polar33892256
(20R)-Ginsenoside Rh2,3TMS,isomer #15CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O[Si](C)(C)C)CC1C3(C)CCC(OC4OC(CO)C(O[Si](C)(C)C)C(O)C4O[Si](C)(C)C)C(C)(C)C3CCC12C4516.9Standard non polar33892256
(20R)-Ginsenoside Rh2,3TMS,isomer #16CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O[Si](C)(C)C)CC1C3(C)CCC(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O[Si](C)(C)C)C(C)(C)C3CCC12C4565.7Semi standard non polar33892256
(20R)-Ginsenoside Rh2,3TMS,isomer #16CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O[Si](C)(C)C)CC1C3(C)CCC(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O[Si](C)(C)C)C(C)(C)C3CCC12C4484.9Standard non polar33892256
(20R)-Ginsenoside Rh2,3TMS,isomer #17CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O)CC1C3(C)CCC(OC4OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O)C(C)(C)C3CCC12C4736.8Semi standard non polar33892256
(20R)-Ginsenoside Rh2,3TMS,isomer #17CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O)CC1C3(C)CCC(OC4OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O)C(C)(C)C3CCC12C4589.9Standard non polar33892256
(20R)-Ginsenoside Rh2,3TMS,isomer #18CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O)CC1C3(C)CCC(OC4OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C4O[Si](C)(C)C)C(C)(C)C3CCC12C4707.6Semi standard non polar33892256
(20R)-Ginsenoside Rh2,3TMS,isomer #18CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O)CC1C3(C)CCC(OC4OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C4O[Si](C)(C)C)C(C)(C)C3CCC12C4620.3Standard non polar33892256
(20R)-Ginsenoside Rh2,3TMS,isomer #19CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O)CC1C3(C)CCC(OC4OC(CO[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C4O[Si](C)(C)C)C(C)(C)C3CCC12C4728.7Semi standard non polar33892256
(20R)-Ginsenoside Rh2,3TMS,isomer #19CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O)CC1C3(C)CCC(OC4OC(CO[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C4O[Si](C)(C)C)C(C)(C)C3CCC12C4584.3Standard non polar33892256
(20R)-Ginsenoside Rh2,3TMS,isomer #2CC(C)=CCCC(C)(O[Si](C)(C)C)C1CCC2(C)C1C(O[Si](C)(C)C)CC1C3(C)CCC(OC4OC(CO)C(O[Si](C)(C)C)C(O)C4O)C(C)(C)C3CCC12C4596.3Semi standard non polar33892256
(20R)-Ginsenoside Rh2,3TMS,isomer #2CC(C)=CCCC(C)(O[Si](C)(C)C)C1CCC2(C)C1C(O[Si](C)(C)C)CC1C3(C)CCC(OC4OC(CO)C(O[Si](C)(C)C)C(O)C4O)C(C)(C)C3CCC12C4510.7Standard non polar33892256
(20R)-Ginsenoside Rh2,3TMS,isomer #20CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O)CC1C3(C)CCC(OC4OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O[Si](C)(C)C)C(C)(C)C3CCC12C4730.6Semi standard non polar33892256
(20R)-Ginsenoside Rh2,3TMS,isomer #20CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O)CC1C3(C)CCC(OC4OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O[Si](C)(C)C)C(C)(C)C3CCC12C4540.0Standard non polar33892256
(20R)-Ginsenoside Rh2,3TMS,isomer #3CC(C)=CCCC(C)(O[Si](C)(C)C)C1CCC2(C)C1C(O[Si](C)(C)C)CC1C3(C)CCC(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O)C(C)(C)C3CCC12C4565.9Semi standard non polar33892256
(20R)-Ginsenoside Rh2,3TMS,isomer #3CC(C)=CCCC(C)(O[Si](C)(C)C)C1CCC2(C)C1C(O[Si](C)(C)C)CC1C3(C)CCC(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O)C(C)(C)C3CCC12C4519.3Standard non polar33892256
(20R)-Ginsenoside Rh2,3TMS,isomer #4CC(C)=CCCC(C)(O[Si](C)(C)C)C1CCC2(C)C1C(O[Si](C)(C)C)CC1C3(C)CCC(OC4OC(CO)C(O)C(O)C4O[Si](C)(C)C)C(C)(C)C3CCC12C4563.6Semi standard non polar33892256
(20R)-Ginsenoside Rh2,3TMS,isomer #4CC(C)=CCCC(C)(O[Si](C)(C)C)C1CCC2(C)C1C(O[Si](C)(C)C)CC1C3(C)CCC(OC4OC(CO)C(O)C(O)C4O[Si](C)(C)C)C(C)(C)C3CCC12C4527.1Standard non polar33892256
(20R)-Ginsenoside Rh2,3TMS,isomer #5CC(C)=CCCC(C)(O[Si](C)(C)C)C1CCC2(C)C1C(O)CC1C3(C)CCC(OC4OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C4O)C(C)(C)C3CCC12C4672.3Semi standard non polar33892256
(20R)-Ginsenoside Rh2,3TMS,isomer #5CC(C)=CCCC(C)(O[Si](C)(C)C)C1CCC2(C)C1C(O)CC1C3(C)CCC(OC4OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C4O)C(C)(C)C3CCC12C4601.3Standard non polar33892256
(20R)-Ginsenoside Rh2,3TMS,isomer #6CC(C)=CCCC(C)(O[Si](C)(C)C)C1CCC2(C)C1C(O)CC1C3(C)CCC(OC4OC(CO[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C4O)C(C)(C)C3CCC12C4650.7Semi standard non polar33892256
(20R)-Ginsenoside Rh2,3TMS,isomer #6CC(C)=CCCC(C)(O[Si](C)(C)C)C1CCC2(C)C1C(O)CC1C3(C)CCC(OC4OC(CO[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C4O)C(C)(C)C3CCC12C4616.5Standard non polar33892256
(20R)-Ginsenoside Rh2,3TMS,isomer #7CC(C)=CCCC(C)(O[Si](C)(C)C)C1CCC2(C)C1C(O)CC1C3(C)CCC(OC4OC(CO[Si](C)(C)C)C(O)C(O)C4O[Si](C)(C)C)C(C)(C)C3CCC12C4643.9Semi standard non polar33892256
(20R)-Ginsenoside Rh2,3TMS,isomer #7CC(C)=CCCC(C)(O[Si](C)(C)C)C1CCC2(C)C1C(O)CC1C3(C)CCC(OC4OC(CO[Si](C)(C)C)C(O)C(O)C4O[Si](C)(C)C)C(C)(C)C3CCC12C4605.0Standard non polar33892256
(20R)-Ginsenoside Rh2,3TMS,isomer #8CC(C)=CCCC(C)(O[Si](C)(C)C)C1CCC2(C)C1C(O)CC1C3(C)CCC(OC4OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O)C(C)(C)C3CCC12C4638.6Semi standard non polar33892256
(20R)-Ginsenoside Rh2,3TMS,isomer #8CC(C)=CCCC(C)(O[Si](C)(C)C)C1CCC2(C)C1C(O)CC1C3(C)CCC(OC4OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O)C(C)(C)C3CCC12C4570.5Standard non polar33892256
(20R)-Ginsenoside Rh2,3TMS,isomer #9CC(C)=CCCC(C)(O[Si](C)(C)C)C1CCC2(C)C1C(O)CC1C3(C)CCC(OC4OC(CO)C(O[Si](C)(C)C)C(O)C4O[Si](C)(C)C)C(C)(C)C3CCC12C4629.2Semi standard non polar33892256
(20R)-Ginsenoside Rh2,3TMS,isomer #9CC(C)=CCCC(C)(O[Si](C)(C)C)C1CCC2(C)C1C(O)CC1C3(C)CCC(OC4OC(CO)C(O[Si](C)(C)C)C(O)C4O[Si](C)(C)C)C(C)(C)C3CCC12C4596.9Standard non polar33892256
(20R)-Ginsenoside Rh2,1TBDMS,isomer #1CC(C)=CCCC(C)(O[Si](C)(C)C(C)(C)C)C1CCC2(C)C1C(O)CC1C3(C)CCC(OC4OC(CO)C(O)C(O)C4O)C(C)(C)C3CCC12C5051.7Semi standard non polar33892256
(20R)-Ginsenoside Rh2,1TBDMS,isomer #1CC(C)=CCCC(C)(O[Si](C)(C)C(C)(C)C)C1CCC2(C)C1C(O)CC1C3(C)CCC(OC4OC(CO)C(O)C(O)C4O)C(C)(C)C3CCC12C4805.8Standard non polar33892256
(20R)-Ginsenoside Rh2,1TBDMS,isomer #2CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O[Si](C)(C)C(C)(C)C)CC1C3(C)CCC(OC4OC(CO)C(O)C(O)C4O)C(C)(C)C3CCC12C5025.6Semi standard non polar33892256
(20R)-Ginsenoside Rh2,1TBDMS,isomer #2CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O[Si](C)(C)C(C)(C)C)CC1C3(C)CCC(OC4OC(CO)C(O)C(O)C4O)C(C)(C)C3CCC12C4714.5Standard non polar33892256
(20R)-Ginsenoside Rh2,1TBDMS,isomer #3CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O)CC1C3(C)CCC(OC4OC(CO[Si](C)(C)C(C)(C)C)C(O)C(O)C4O)C(C)(C)C3CCC12C5084.4Semi standard non polar33892256
(20R)-Ginsenoside Rh2,1TBDMS,isomer #3CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O)CC1C3(C)CCC(OC4OC(CO[Si](C)(C)C(C)(C)C)C(O)C(O)C4O)C(C)(C)C3CCC12C4821.9Standard non polar33892256
(20R)-Ginsenoside Rh2,1TBDMS,isomer #4CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O)CC1C3(C)CCC(OC4OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C4O)C(C)(C)C3CCC12C5122.5Semi standard non polar33892256
(20R)-Ginsenoside Rh2,1TBDMS,isomer #4CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O)CC1C3(C)CCC(OC4OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C4O)C(C)(C)C3CCC12C4765.4Standard non polar33892256
(20R)-Ginsenoside Rh2,1TBDMS,isomer #5CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O)CC1C3(C)CCC(OC4OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C4O)C(C)(C)C3CCC12C5102.2Semi standard non polar33892256
(20R)-Ginsenoside Rh2,1TBDMS,isomer #5CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O)CC1C3(C)CCC(OC4OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C4O)C(C)(C)C3CCC12C4757.3Standard non polar33892256
(20R)-Ginsenoside Rh2,1TBDMS,isomer #6CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O)CC1C3(C)CCC(OC4OC(CO)C(O)C(O)C4O[Si](C)(C)C(C)(C)C)C(C)(C)C3CCC12C5097.2Semi standard non polar33892256
(20R)-Ginsenoside Rh2,1TBDMS,isomer #6CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O)CC1C3(C)CCC(OC4OC(CO)C(O)C(O)C4O[Si](C)(C)C(C)(C)C)C(C)(C)C3CCC12C4767.9Standard non polar33892256
(20R)-Ginsenoside Rh2,2TBDMS,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(OC4OC(CO)C(O)C(O)C4O)C(C)(C)C3CCC12C5136.9Semi standard non polar33892256
(20R)-Ginsenoside Rh2,2TBDMS,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(OC4OC(CO)C(O)C(O)C4O)C(C)(C)C3CCC12C4959.4Standard non polar33892256
(20R)-Ginsenoside Rh2,2TBDMS,isomer #10CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O)CC1C3(C)CCC(OC4OC(CO[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C(O)C4O)C(C)(C)C3CCC12C5254.7Semi standard non polar33892256
(20R)-Ginsenoside Rh2,2TBDMS,isomer #10CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O)CC1C3(C)CCC(OC4OC(CO[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C(O)C4O)C(C)(C)C3CCC12C5035.3Standard non polar33892256
(20R)-Ginsenoside Rh2,2TBDMS,isomer #11CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O)CC1C3(C)CCC(OC4OC(CO[Si](C)(C)C(C)(C)C)C(O)C(O[Si](C)(C)C(C)(C)C)C4O)C(C)(C)C3CCC12C5227.2Semi standard non polar33892256
(20R)-Ginsenoside Rh2,2TBDMS,isomer #11CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O)CC1C3(C)CCC(OC4OC(CO[Si](C)(C)C(C)(C)C)C(O)C(O[Si](C)(C)C(C)(C)C)C4O)C(C)(C)C3CCC12C5046.2Standard non polar33892256
(20R)-Ginsenoside Rh2,2TBDMS,isomer #12CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O)CC1C3(C)CCC(OC4OC(CO[Si](C)(C)C(C)(C)C)C(O)C(O)C4O[Si](C)(C)C(C)(C)C)C(C)(C)C3CCC12C5235.4Semi standard non polar33892256
(20R)-Ginsenoside Rh2,2TBDMS,isomer #12CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O)CC1C3(C)CCC(OC4OC(CO[Si](C)(C)C(C)(C)C)C(O)C(O)C4O[Si](C)(C)C(C)(C)C)C(C)(C)C3CCC12C5035.7Standard non polar33892256
(20R)-Ginsenoside Rh2,2TBDMS,isomer #13CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O)CC1C3(C)CCC(OC4OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C4O)C(C)(C)C3CCC12C5261.1Semi standard non polar33892256
(20R)-Ginsenoside Rh2,2TBDMS,isomer #13CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O)CC1C3(C)CCC(OC4OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C4O)C(C)(C)C3CCC12C4996.0Standard non polar33892256
(20R)-Ginsenoside Rh2,2TBDMS,isomer #14CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O)CC1C3(C)CCC(OC4OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C4O[Si](C)(C)C(C)(C)C)C(C)(C)C3CCC12C5254.2Semi standard non polar33892256
(20R)-Ginsenoside Rh2,2TBDMS,isomer #14CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O)CC1C3(C)CCC(OC4OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C4O[Si](C)(C)C(C)(C)C)C(C)(C)C3CCC12C5018.4Standard non polar33892256
(20R)-Ginsenoside Rh2,2TBDMS,isomer #15CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O)CC1C3(C)CCC(OC4OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C4O[Si](C)(C)C(C)(C)C)C(C)(C)C3CCC12C5265.1Semi standard non polar33892256
(20R)-Ginsenoside Rh2,2TBDMS,isomer #15CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O)CC1C3(C)CCC(OC4OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C4O[Si](C)(C)C(C)(C)C)C(C)(C)C3CCC12C4980.1Standard non polar33892256
(20R)-Ginsenoside Rh2,2TBDMS,isomer #2CC(C)=CCCC(C)(O[Si](C)(C)C(C)(C)C)C1CCC2(C)C1C(O)CC1C3(C)CCC(OC4OC(CO[Si](C)(C)C(C)(C)C)C(O)C(O)C4O)C(C)(C)C3CCC12C5177.5Semi standard non polar33892256
(20R)-Ginsenoside Rh2,2TBDMS,isomer #2CC(C)=CCCC(C)(O[Si](C)(C)C(C)(C)C)C1CCC2(C)C1C(O)CC1C3(C)CCC(OC4OC(CO[Si](C)(C)C(C)(C)C)C(O)C(O)C4O)C(C)(C)C3CCC12C5061.9Standard non polar33892256
(20R)-Ginsenoside Rh2,2TBDMS,isomer #3CC(C)=CCCC(C)(O[Si](C)(C)C(C)(C)C)C1CCC2(C)C1C(O)CC1C3(C)CCC(OC4OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C4O)C(C)(C)C3CCC12C5192.3Semi standard non polar33892256
(20R)-Ginsenoside Rh2,2TBDMS,isomer #3CC(C)=CCCC(C)(O[Si](C)(C)C(C)(C)C)C1CCC2(C)C1C(O)CC1C3(C)CCC(OC4OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C4O)C(C)(C)C3CCC12C5007.1Standard non polar33892256
(20R)-Ginsenoside Rh2,2TBDMS,isomer #4CC(C)=CCCC(C)(O[Si](C)(C)C(C)(C)C)C1CCC2(C)C1C(O)CC1C3(C)CCC(OC4OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C4O)C(C)(C)C3CCC12C5160.1Semi standard non polar33892256
(20R)-Ginsenoside Rh2,2TBDMS,isomer #4CC(C)=CCCC(C)(O[Si](C)(C)C(C)(C)C)C1CCC2(C)C1C(O)CC1C3(C)CCC(OC4OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C4O)C(C)(C)C3CCC12C5002.6Standard non polar33892256
(20R)-Ginsenoside Rh2,2TBDMS,isomer #5CC(C)=CCCC(C)(O[Si](C)(C)C(C)(C)C)C1CCC2(C)C1C(O)CC1C3(C)CCC(OC4OC(CO)C(O)C(O)C4O[Si](C)(C)C(C)(C)C)C(C)(C)C3CCC12C5164.5Semi standard non polar33892256
(20R)-Ginsenoside Rh2,2TBDMS,isomer #5CC(C)=CCCC(C)(O[Si](C)(C)C(C)(C)C)C1CCC2(C)C1C(O)CC1C3(C)CCC(OC4OC(CO)C(O)C(O)C4O[Si](C)(C)C(C)(C)C)C(C)(C)C3CCC12C5019.5Standard non polar33892256
(20R)-Ginsenoside Rh2,2TBDMS,isomer #6CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O[Si](C)(C)C(C)(C)C)CC1C3(C)CCC(OC4OC(CO[Si](C)(C)C(C)(C)C)C(O)C(O)C4O)C(C)(C)C3CCC12C5119.9Semi standard non polar33892256
(20R)-Ginsenoside Rh2,2TBDMS,isomer #6CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O[Si](C)(C)C(C)(C)C)CC1C3(C)CCC(OC4OC(CO[Si](C)(C)C(C)(C)C)C(O)C(O)C4O)C(C)(C)C3CCC12C4980.8Standard non polar33892256
(20R)-Ginsenoside Rh2,2TBDMS,isomer #7CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O[Si](C)(C)C(C)(C)C)CC1C3(C)CCC(OC4OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C4O)C(C)(C)C3CCC12C5145.0Semi standard non polar33892256
(20R)-Ginsenoside Rh2,2TBDMS,isomer #7CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O[Si](C)(C)C(C)(C)C)CC1C3(C)CCC(OC4OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C4O)C(C)(C)C3CCC12C4930.8Standard non polar33892256
(20R)-Ginsenoside Rh2,2TBDMS,isomer #8CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O[Si](C)(C)C(C)(C)C)CC1C3(C)CCC(OC4OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C4O)C(C)(C)C3CCC12C5102.2Semi standard non polar33892256
(20R)-Ginsenoside Rh2,2TBDMS,isomer #8CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O[Si](C)(C)C(C)(C)C)CC1C3(C)CCC(OC4OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C4O)C(C)(C)C3CCC12C4928.2Standard non polar33892256
(20R)-Ginsenoside Rh2,2TBDMS,isomer #9CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O[Si](C)(C)C(C)(C)C)CC1C3(C)CCC(OC4OC(CO)C(O)C(O)C4O[Si](C)(C)C(C)(C)C)C(C)(C)C3CCC12C5113.0Semi standard non polar33892256
(20R)-Ginsenoside Rh2,2TBDMS,isomer #9CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O[Si](C)(C)C(C)(C)C)CC1C3(C)CCC(OC4OC(CO)C(O)C(O)C4O[Si](C)(C)C(C)(C)C)C(C)(C)C3CCC12C4942.8Standard non polar33892256
Spectra

GC-MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted GC-MSPredicted GC-MS Spectrum - (20R)-Ginsenoside Rh2 GC-MS (Non-derivatized) - 70eV, Positivesplash10-0a4l-6611479000-d65beba914679bda47302017-09-01Wishart LabView Spectrum

MS/MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (20R)-Ginsenoside Rh2 10V, Positive-QTOFsplash10-06rf-0000935000-72e79458b189eee0befe2015-04-24Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (20R)-Ginsenoside Rh2 20V, Positive-QTOFsplash10-0006-1101900000-5766366e4d9a892f488d2015-04-24Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (20R)-Ginsenoside Rh2 40V, Positive-QTOFsplash10-0296-3223900000-9c43c30f74a5dc7a192e2015-04-24Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (20R)-Ginsenoside Rh2 10V, Negative-QTOFsplash10-00dl-1100829000-fcc0f11fc191610bb5d62015-04-25Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (20R)-Ginsenoside Rh2 20V, Negative-QTOFsplash10-052f-1100901000-fc81da55658166ad081a2015-04-25Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (20R)-Ginsenoside Rh2 40V, Negative-QTOFsplash10-052f-3002900000-d35f2e9734fcbb871f352015-04-25Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (20R)-Ginsenoside Rh2 10V, Negative-QTOFsplash10-00di-0000009000-2e1102fd6ff7161b17862021-09-22Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (20R)-Ginsenoside Rh2 20V, Negative-QTOFsplash10-00di-4000339000-29459647dfbbd85a0a3d2021-09-22Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (20R)-Ginsenoside Rh2 40V, Negative-QTOFsplash10-0a4i-9000121000-048ed11e4b13f460d3f32021-09-22Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (20R)-Ginsenoside Rh2 10V, Positive-QTOFsplash10-05du-0102935000-14966d53e5413a3b69da2021-09-22Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (20R)-Ginsenoside Rh2 20V, Positive-QTOFsplash10-03kc-6906342000-692461ca603e830e059e2021-09-22Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (20R)-Ginsenoside Rh2 40V, Positive-QTOFsplash10-014i-9200000000-88ee720056493df588b02021-09-22Wishart 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 IDFDB019163
KNApSAcK IDNot Available
Chemspider ID24784756
KEGG Compound IDNot Available
BioCyc IDNot Available
BiGG IDNot Available
Wikipedia LinkNot Available
METLIN IDNot Available
PubChem Compound14081290
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.