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(20S)-Protopanaxadiol metabolite M1-2

PubChem CID: 12314836

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Compound Synonyms C37X3X4NMW, (20S)-Protopanaxadiol metabolite M1-2, UNII-C37X3X4NMW, (20S,24S)-Epoxydammarane-3,12,25-triol, 141979-08-0, 20,24-Epoxydammarane-3beta,12beta,25-triol, (20S,24S)-, (20S,24S)-20,24-Epoxydammarane-3beta,12beta,25-triol, (3beta,12beta,20S,24S)-20,24-Epoxydammarane-3,12,25-triol, Dammarane-3,12,25-triol, 20,24-epoxy-, (3beta,12beta,24S)-, CHEMBL466363, (20S,24S)-20,24-EPOXYDAMMARANE-3.BETA.,12.BETA.,25-TRIOL, 20,24-EPOXYDAMMARANE-3.BETA.,12.BETA.,25-TRIOL, (20S,24S)-, (3.BETA.,12.BETA.,20S,24S)-20,24-EPOXYDAMMARANE-3,12,25-TRIOL, DAMMARANE-3,12,25-TRIOL, 20,24-EPOXY-, (3.BETA.,12.BETA.,24S)-
Topological Polar Surface Area 69.9
Hydrogen Bond Donor Count 3.0
Heavy Atom Count 34.0
Isotope Atom Count 0.0
Molecular Complexity 823.0
Database Name cmaup_ingredients;npass_chem_all;pubchem
Defined Atom Stereocenter Count 11.0
Uniprot Id n.a., P08183
Iupac Name (3S,5R,8R,9R,10R,12R,13R,14R,17S)-17-[(2S,5S)-5-(2-hydroxypropan-2-yl)-2-methyloxolan-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
Prediction Hob 1.0
Xlogp 5.9
Molecular Formula C30H52O4
Prediction Swissadme 0.0
Inchi Key DOAJFZJEGHSYOI-BVGXOPESSA-N
Fcsp3 1.0
Logs -4.429
Rotatable Bond Count 2.0
Logd 4.745
Compound Name (20S)-Protopanaxadiol metabolite M1-2
Prediction Hob Swissadme 0.0
Exact Mass 476.387
Formal Charge 0.0
Monoisotopic Mass 476.387
Hydrogen Bond Acceptor Count 4.0
Molecular Weight 476.7
Covalent Unit Count 1.0
Total Atom Stereocenter Count 11.0
Total Bond Stereocenter Count 0.0
Esol -6.380800400000002
Inchi InChI=1S/C30H52O4/c1-25(2)20-10-15-28(6)21(27(20,5)13-11-22(25)32)17-19(31)24-18(9-14-29(24,28)7)30(8)16-12-23(34-30)26(3,4)33/h18-24,31-33H,9-17H2,1-8H3/t18-,19+,20-,21+,22-,23-,24-,27-,28+,29+,30-/m0/s1
Smiles C[C@]1(CC[C@H](O1)C(C)(C)O)[C@H]2CC[C@@]3([C@@H]2[C@@H](C[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)O)C)C)O)C
Nring 5.0
Defined Bond Stereocenter Count 0.0