(20S)-Protopanaxadiol

Type: Metabolite
PubChem: 11213350
DrugBank: None
IUPAC: (3S,5R,8R,9R,10R,12R,13R,14R,17S)-17-[(2S)-2-hydroxy-6-methylhept-5-en-2-yl]-4,4,8,10,14-pentamethyl-2,3,5,6,7,9,11,12,13,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthrene-3,12-diol
Standard InChI: InChI=1S/C30H52O3/c1-19(2)10-9-14-30(8,33)20-11-16-29(7)25(20)21(31)18-23-27(5)15-13-24(32)26(3,4)22(27)12-17-28(23,29)6/h10,20-25,31-33H,9,11-18H2,1-8H3/t20-,21+,22-,23+,24-,25-,27-,28+,29+,30-/m0/s1
Standard InChIKey: PYXFVCFISTUSOO-HKUCOEKDSA-N
SMILES: CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O)CC1C3(C)CCC(O)C(C)(C)C3CCC12C

Parent compounds

Chemical Structure Parent compounds name Reaction name Genus Species Reference
Ginsenoside RcHydrolysisFusobacteriumUnknown10.1016/j.jgr.2017.04.011
Ginsenoside RcHydrolysisBacteroidesUnknown10.1016/j.jgr.2017.04.011
Ginsenoside Rb2HydrolysisEubacteriumUnknown10.1016/j.jgr.2017.04.011
Ginsenoside Rb2HydrolysisBifidobacteriumUnknown10.1016/j.jgr.2017.04.011
Ginsenoside Rg3HydrolysisBifidobacteriumUnknown10.1016/j.jgr.2017.04.011
Ginsenoside Rg3HydrolysisEubacteriumUnknown10.1016/j.jgr.2017.04.011
Ginsenoside Rg3HydrolysisBacteroidesUnknown10.1016/j.jgr.2017.04.011
Ginsenoside Rb1HydrolysisFusobacteriumUnknown10.1016/j.jgr.2017.04.011
Ginsenoside Rb1HydrolysisBacteroidesUnknown10.1016/j.jgr.2017.04.011
Ginsenoside Rb1HydrolysisBifidobacteriumUnknown10.1016/j.jgr.2017.04.011
Ginsenoside Rb1HydrolysisEubacteriumUnknown10.1016/j.jgr.2017.04.011