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(1S,3R,8R,11S,12S,14S,15R,16R)-15-(4,5-dihydroxy-5,6-dimethylheptan-2-yl)-14-hydroxy-7,7,12,16-tetramethylpentacyclo[9.7.0.01,3.03,8.012,16]octadecan-6-one

PubChem CID: 101306915

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Ghose Rule False
Classyfire Kingdom Organic compounds
Topological Polar Surface Area 77.8
Hydrogen Bond Donor Count 3.0
Pfizer 3 75 Rule False
Scaffold Graph Level CC1CCC23CC24CCC2CCCC2C4CCC3C1
Np Classifier Class Cycloartane triterpenoids
Deep Smiles CC[C@H][C@@H]O)C[C@@][C@]5C)CC[C@][C@H]6CC[C@@H][C@]6C7)CCC=O)C6C)C))))))))))))))C)))))CCCCC)C))O)C))O
Heavy Atom Count 35.0
Classyfire Class Steroids and steroid derivatives
Scaffold Graph Node Level OC1CCC23CC24CCC2CCCC2C4CCC3C1
Classyfire Subclass Cycloartanols and derivatives
Isotope Atom Count 0.0
Molecular Complexity 896.0
Database Name imppat_phytochem;pubchem
Defined Atom Stereocenter Count 8.0
Iupac Name (1S,3R,8R,11S,12S,14S,15R,16R)-15-(4,5-dihydroxy-5,6-dimethylheptan-2-yl)-14-hydroxy-7,7,12,16-tetramethylpentacyclo[9.7.0.01,3.03,8.012,16]octadecan-6-one
Veber Rule True
Classyfire Superclass Lipids and lipid-like molecules
Xlogp 6.2
Gsk 4 400 Rule False
Molecular Formula C31H52O4
Scaffold Graph Node Bond Level O=C1CCC23CC24CCC2CCCC2C4CCC3C1
Inchi Key UQLZMKVTQRWWBV-YCRULZMASA-N
Silicos It Class Moderately soluble
Rotatable Bond Count 5.0
Synonyms argentatin c
Esol Class Poorly soluble
Functional Groups CC(C)=O, CO
Compound Name (1S,3R,8R,11S,12S,14S,15R,16R)-15-(4,5-dihydroxy-5,6-dimethylheptan-2-yl)-14-hydroxy-7,7,12,16-tetramethylpentacyclo[9.7.0.01,3.03,8.012,16]octadecan-6-one
Exact Mass 488.387
Formal Charge 0.0
Monoisotopic Mass 488.387
Hydrogen Bond Acceptor Count 4.0
Molecular Weight 488.7
Gi Absorption True
Covalent Unit Count 1.0
Total Atom Stereocenter Count 11.0
Total Bond Stereocenter Count 0.0
Lipinski Rule Of 5 True
Inchi InChI=1S/C31H52O4/c1-18(2)29(8,35)24(34)15-19(3)25-20(32)16-28(7)22-10-9-21-26(4,5)23(33)11-12-30(21)17-31(22,30)14-13-27(25,28)6/h18-22,24-25,32,34-35H,9-17H2,1-8H3/t19?,20-,21-,22-,24?,25-,27+,28-,29?,30+,31-/m0/s1
Smiles CC(C)C(C)(C(CC(C)[C@H]1[C@H](C[C@@]2([C@@]1(CC[C@]34[C@H]2CC[C@@H]5[C@]3(C4)CCC(=O)C5(C)C)C)C)O)O)O
Np Classifier Biosynthetic Pathway Terpenoids
Defined Bond Stereocenter Count 0.0
Egan Rule True
Np Classifier Superclass Triterpenoids