Hmdb loader
Record Information
Version5.0
StatusExpected but not Quantified
Creation Date2012-09-11 23:31:46 UTC
Update Date2022-03-07 02:55:41 UTC
HMDB IDHMDB0038244
Secondary Accession Numbers
  • HMDB38244
Metabolite Identification
Common NamePanaxatriol
DescriptionPanaxatriol is found in beverages. Panaxatriol is present in ginseng Panaxatriol is an organic coumpound characterizing a group of ginsenosides. It is a dammarane-type tetracyclic triterpene sapogenin found in ginseng (Panax ginseng) and in notoginseng (Panax pseudoginseng). It is formed by the dehydration of protopanaxatriol.
Structure
Data?1563863163
SynonymsNot Available
Chemical FormulaC30H52O4
Average Molecular Weight476.7315
Monoisotopic Molecular Weight476.386560152
IUPAC Name2,6,6,10,11-pentamethyl-14-(2,6,6-trimethyloxan-2-yl)tetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadecane-5,8,16-triol
Traditional Name2,6,6,10,11-pentamethyl-14-(2,6,6-trimethyloxan-2-yl)tetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadecane-5,8,16-triol
CAS Registry NumberNot Available
SMILES
CC12CCC(C1C(O)CC1C3(C)CCC(O)C(C)(C)C3C(O)CC21C)C1(C)CCCC(C)(C)O1
InChI Identifier
InChI=1S/C30H52O4/c1-25(2)12-9-13-30(8,34-25)18-10-15-28(6)23(18)19(31)16-21-27(5)14-11-22(33)26(3,4)24(27)20(32)17-29(21,28)7/h18-24,31-33H,9-17H2,1-8H3
InChI KeyQFJUYMMIBFBOJY-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
  • 3-hydroxysteroid
  • 12-hydroxysteroid
  • 6-hydroxysteroid
  • Hydroxysteroid
  • Steroid
  • Oxane
  • Cyclic alcohol
  • Secondary alcohol
  • Dialkyl ether
  • Ether
  • Oxacycle
  • Organoheterocyclic compound
  • Polyol
  • Alcohol
  • Hydrocarbon derivative
  • Organic oxygen compound
  • Organooxygen compound
  • Aliphatic heteropolycyclic compound
Molecular FrameworkAliphatic heteropolycyclic compounds
External DescriptorsNot Available
Ontology
Physiological effectNot Available
Disposition
Process
Role
Physical Properties
StateSolid
Experimental Molecular Properties
PropertyValueReference
Melting Point238 - 239 °CNot Available
Boiling PointNot AvailableNot Available
Water SolubilityNot AvailableNot Available
LogPNot AvailableNot Available
Experimental Chromatographic PropertiesNot Available
Predicted Molecular Properties
PropertyValueSource
Water Solubility0.0021 g/LALOGPS
logP4.59ALOGPS
logP4.32ChemAxon
logS-5.4ALOGPS
pKa (Strongest Acidic)14.35ChemAxon
pKa (Strongest Basic)-2.8ChemAxon
Physiological Charge0ChemAxon
Hydrogen Acceptor Count4ChemAxon
Hydrogen Donor Count3ChemAxon
Polar Surface Area69.92 ŲChemAxon
Rotatable Bond Count1ChemAxon
Refractivity136.3 m³·mol⁻¹ChemAxon
Polarizability57.36 ųChemAxon
Number of Rings5ChemAxon
BioavailabilityYesChemAxon
Rule of FiveYesChemAxon
Ghose FilterNoChemAxon
Veber's RuleNoChemAxon
MDDR-like RuleNoChemAxon
Predicted Chromatographic Properties

Predicted Collision Cross Sections

PredictorAdduct TypeCCS Value (Å2)Reference
DarkChem[M+H]+208.51131661259
DarkChem[M-H]-202.01131661259
DeepCCS[M-2H]-256.83830932474
DeepCCS[M+Na]+232.06530932474
AllCCS[M+H]+217.532859911
AllCCS[M+H-H2O]+215.932859911
AllCCS[M+NH4]+219.032859911
AllCCS[M+Na]+219.432859911
AllCCS[M-H]-215.032859911
AllCCS[M+Na-2H]-217.732859911
AllCCS[M+HCOO]-220.732859911

Predicted Kovats Retention Indices

Underivatized

MetaboliteSMILESKovats RI ValueColumn TypeReference
PanaxatriolCC12CCC(C1C(O)CC1C3(C)CCC(O)C(C)(C)C3C(O)CC21C)C1(C)CCCC(C)(C)O12504.8Standard polar33892256
PanaxatriolCC12CCC(C1C(O)CC1C3(C)CCC(O)C(C)(C)C3C(O)CC21C)C1(C)CCCC(C)(C)O13254.5Standard non polar33892256
PanaxatriolCC12CCC(C1C(O)CC1C3(C)CCC(O)C(C)(C)C3C(O)CC21C)C1(C)CCCC(C)(C)O13909.0Semi standard non polar33892256

Derivatized

Derivative Name / StructureSMILESKovats RI ValueColumn TypeReference
Panaxatriol,1TMS,isomer #1CC1(C)CCCC(C)(C2CCC3(C)C2C(O[Si](C)(C)C)CC2C4(C)CCC(O)C(C)(C)C4C(O)CC23C)O13843.1Semi standard non polar33892256
Panaxatriol,1TMS,isomer #2CC1(C)CCCC(C)(C2CCC3(C)C2C(O)CC2C4(C)CCC(O[Si](C)(C)C)C(C)(C)C4C(O)CC23C)O13851.6Semi standard non polar33892256
Panaxatriol,1TMS,isomer #3CC1(C)CCCC(C)(C2CCC3(C)C2C(O)CC2C4(C)CCC(O)C(C)(C)C4C(O[Si](C)(C)C)CC23C)O13843.3Semi standard non polar33892256
Panaxatriol,2TMS,isomer #1CC1(C)CCCC(C)(C2CCC3(C)C2C(O[Si](C)(C)C)CC2C4(C)CCC(O[Si](C)(C)C)C(C)(C)C4C(O)CC23C)O13767.4Semi standard non polar33892256
Panaxatriol,2TMS,isomer #2CC1(C)CCCC(C)(C2CCC3(C)C2C(O[Si](C)(C)C)CC2C4(C)CCC(O)C(C)(C)C4C(O[Si](C)(C)C)CC23C)O13738.4Semi standard non polar33892256
Panaxatriol,2TMS,isomer #3CC1(C)CCCC(C)(C2CCC3(C)C2C(O)CC2C4(C)CCC(O[Si](C)(C)C)C(C)(C)C4C(O[Si](C)(C)C)CC23C)O13794.7Semi standard non polar33892256
Panaxatriol,3TMS,isomer #1CC1(C)CCCC(C)(C2CCC3(C)C2C(O[Si](C)(C)C)CC2C4(C)CCC(O[Si](C)(C)C)C(C)(C)C4C(O[Si](C)(C)C)CC23C)O13678.8Semi standard non polar33892256
Panaxatriol,1TBDMS,isomer #1CC1(C)CCCC(C)(C2CCC3(C)C2C(O[Si](C)(C)C(C)(C)C)CC2C4(C)CCC(O)C(C)(C)C4C(O)CC23C)O14069.1Semi standard non polar33892256
Panaxatriol,1TBDMS,isomer #2CC1(C)CCCC(C)(C2CCC3(C)C2C(O)CC2C4(C)CCC(O[Si](C)(C)C(C)(C)C)C(C)(C)C4C(O)CC23C)O14077.5Semi standard non polar33892256
Panaxatriol,1TBDMS,isomer #3CC1(C)CCCC(C)(C2CCC3(C)C2C(O)CC2C4(C)CCC(O)C(C)(C)C4C(O[Si](C)(C)C(C)(C)C)CC23C)O14072.0Semi standard non polar33892256
Panaxatriol,2TBDMS,isomer #1CC1(C)CCCC(C)(C2CCC3(C)C2C(O[Si](C)(C)C(C)(C)C)CC2C4(C)CCC(O[Si](C)(C)C(C)(C)C)C(C)(C)C4C(O)CC23C)O14216.8Semi standard non polar33892256
Panaxatriol,2TBDMS,isomer #2CC1(C)CCCC(C)(C2CCC3(C)C2C(O[Si](C)(C)C(C)(C)C)CC2C4(C)CCC(O)C(C)(C)C4C(O[Si](C)(C)C(C)(C)C)CC23C)O14169.2Semi standard non polar33892256
Panaxatriol,2TBDMS,isomer #3CC1(C)CCCC(C)(C2CCC3(C)C2C(O)CC2C4(C)CCC(O[Si](C)(C)C(C)(C)C)C(C)(C)C4C(O[Si](C)(C)C(C)(C)C)CC23C)O14232.4Semi standard non polar33892256
Panaxatriol,3TBDMS,isomer #1CC1(C)CCCC(C)(C2CCC3(C)C2C(O[Si](C)(C)C(C)(C)C)CC2C4(C)CCC(O[Si](C)(C)C(C)(C)C)C(C)(C)C4C(O[Si](C)(C)C(C)(C)C)CC23C)O14308.8Semi standard non polar33892256
Spectra

GC-MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted GC-MSPredicted GC-MS Spectrum - Panaxatriol GC-MS (Non-derivatized) - 70eV, Positivesplash10-03ei-1121900000-adbd038c291ec781e8252017-09-01Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Panaxatriol GC-MS (3 TMS) - 70eV, Positivesplash10-004i-2001029000-df0a5af6b69c89e7201f2017-10-06Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Panaxatriol GC-MS (Non-derivatized) - 70eV, PositiveNot Available2021-10-12Wishart LabView Spectrum

MS/MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Panaxatriol 10V, Positive-QTOFsplash10-0a4l-0000900000-4b3f6574a373023ba0d02016-08-01Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Panaxatriol 20V, Positive-QTOFsplash10-054x-5005900000-0a5c39d96fd3f64224a42016-08-01Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Panaxatriol 40V, Positive-QTOFsplash10-004l-6156900000-ce0f57315c84d5f562192016-08-01Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Panaxatriol 10V, Negative-QTOFsplash10-004i-0000900000-2b8f18115e339182ceeb2016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Panaxatriol 20V, Negative-QTOFsplash10-0a6r-2001900000-3f4bf9f77dcba83923962016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Panaxatriol 40V, Negative-QTOFsplash10-0a4r-8009800000-7a464a30fbcda04c03a22016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Panaxatriol 10V, Positive-QTOFsplash10-004i-0001900000-22be9c698de518a123e92021-09-24Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Panaxatriol 20V, Positive-QTOFsplash10-0a6u-1311900000-6322917bb5a0607d278c2021-09-24Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Panaxatriol 40V, Positive-QTOFsplash10-0006-9814000000-cc8a082fb8bf88d394982021-09-24Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Panaxatriol 10V, Negative-QTOFsplash10-004i-0000900000-9871cb200f8d99e952cb2021-09-24Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Panaxatriol 20V, Negative-QTOFsplash10-004i-0000900000-f0dbbe6e23aebf4fc58d2021-09-24Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Panaxatriol 40V, Negative-QTOFsplash10-004i-0000900000-cb78a87a66288f7228192021-09-24Wishart 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 IDFDB017536
KNApSAcK IDNot Available
Chemspider ID291218
KEGG Compound IDNot Available
BioCyc IDNot Available
BiGG IDNot Available
Wikipedia LinkPanaxatriol
METLIN IDNot Available
PubChem Compound328779
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.