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(3S,5S,8S,9S,10S,13R,14S,17R)-10,13-dimethyl-17-[(2R)-6-methylheptan-2-yl]-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-ol

PubChem CID: 7157118

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Compound Synonyms (3S,5S,8S,9S,10S,13R,14S,17R)-10,13-dimethyl-17-[(2R)-6-methylheptan-2-yl]-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-ol, CHOLESTANOL, 5 alpha Cholestan 3 alpha ol
Ghose Rule False
Classyfire Kingdom Organic compounds
Topological Polar Surface Area 20.2
Hydrogen Bond Donor Count 1.0
Pfizer 3 75 Rule False
Scaffold Graph Level C1CCC2C(C1)CCC1C3CCCC3CCC21
Np Classifier Class Cholestane steroids
Deep Smiles CCCCC[C@H][C@H]CC[C@@H][C@]5C)CC[C@H][C@@H]6CC[C@@H][C@]6C)CC[C@@H]C6)O)))))))))))))))))C)))))C
Heavy Atom Count 28.0
Classyfire Class Steroids and steroid derivatives
Scaffold Graph Node Level C1CCC2C(C1)CCC1C3CCCC3CCC21
Classyfire Subclass Cholestane steroids
Isotope Atom Count 0.0
Molecular Complexity 540.0
Database Name imppat_phytochem;pubchem
Defined Atom Stereocenter Count 9.0
Iupac Name (3S,5S,8S,9S,10S,13R,14S,17R)-10,13-dimethyl-17-[(2R)-6-methylheptan-2-yl]-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-ol
Veber Rule True
Classyfire Superclass Lipids and lipid-like molecules
Xlogp 9.4
Gsk 4 400 Rule False
Molecular Formula C27H48O
Scaffold Graph Node Bond Level C1CCC2C(C1)CCC1C3CCCC3CCC21
Inchi Key QYIXCDOBOSTCEI-PNIPQYGLSA-N
Silicos It Class Moderately soluble
Rotatable Bond Count 5.0
Synonyms cholestanol
Esol Class Poorly soluble
Functional Groups CO
Compound Name (3S,5S,8S,9S,10S,13R,14S,17R)-10,13-dimethyl-17-[(2R)-6-methylheptan-2-yl]-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-ol
Exact Mass 388.371
Formal Charge 0.0
Monoisotopic Mass 388.371
Hydrogen Bond Acceptor Count 1.0
Molecular Weight 388.7
Gi Absorption False
Covalent Unit Count 1.0
Total Atom Stereocenter Count 9.0
Total Bond Stereocenter Count 0.0
Lipinski Rule Of 5 True
Inchi InChI=1S/C27H48O/c1-18(2)7-6-8-19(3)23-11-12-24-22-10-9-20-17-21(28)13-15-26(20,4)25(22)14-16-27(23,24)5/h18-25,28H,6-17H2,1-5H3/t19-,20+,21+,22-,23-,24+,25+,26+,27-/m1/s1
Smiles C[C@H](CCCC(C)C)[C@H]1CC[C@@H]2[C@@]1(CC[C@H]3[C@@H]2CC[C@@H]4[C@@]3(CC[C@@H](C4)O)C)C
Np Classifier Biosynthetic Pathway Terpenoids
Defined Bond Stereocenter Count 0.0
Egan Rule False
Np Classifier Superclass Steroids

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