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Homalomenol B

PubChem CID: 101634633

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Compound Synonyms Homalomenol B, 145400-04-0, (+)-homalomenol B, CHEBI:132901, DTXSID801123582, (1R,3aR,4R,7S,7aR)-3a,7-dimethyl-1-(2-methylprop-2-en-1-yl)octahydro-1H-indene-4,7-diol
Ghose Rule True
Classyfire Kingdom Organic compounds
Topological Polar Surface Area 40.5
Hydrogen Bond Donor Count 2.0
Pfizer 3 75 Rule False
Scaffold Graph Level C1CCC2CCCC2C1
Np Classifier Class Oppositane sesquiterpenoids
Deep Smiles CC=C)C[C@H]CC[C@@][C@@H]5[C@@]C)O)CC[C@H]6O))))))C
Heavy Atom Count 17.0
Classyfire Class Prenol lipids
Scaffold Graph Node Level C1CCC2CCCC2C1
Classyfire Subclass Sesquiterpenoids
Isotope Atom Count 0.0
Molecular Complexity 325.0
Database Name imppat_phytochem;npass_chem_all;pubchem
Defined Atom Stereocenter Count 5.0
Iupac Name (3R,3aR,4S,7R,7aR)-4,7a-dimethyl-3-(2-methylprop-2-enyl)-2,3,3a,5,6,7-hexahydro-1H-indene-4,7-diol
Veber Rule True
Classyfire Superclass Lipids and lipid-like molecules
Xlogp 3.2
Gsk 4 400 Rule True
Molecular Formula C15H26O2
Scaffold Graph Node Bond Level C1CCC2CCCC2C1
Inchi Key PECCCWAOADXQBC-ZSAUSMIDSA-N
Silicos It Class Soluble
Rotatable Bond Count 2.0
Synonyms homalomenol b
Esol Class Soluble
Functional Groups C=C(C)C, CO
Compound Name Homalomenol B
Exact Mass 238.193
Formal Charge 0.0
Monoisotopic Mass 238.193
Hydrogen Bond Acceptor Count 2.0
Molecular Weight 238.37
Gi Absorption True
Covalent Unit Count 1.0
Total Atom Stereocenter Count 5.0
Total Bond Stereocenter Count 0.0
Lipinski Rule Of 5 True
Inchi InChI=1S/C15H26O2/c1-10(2)9-11-5-7-14(3)12(16)6-8-15(4,17)13(11)14/h11-13,16-17H,1,5-9H2,2-4H3/t11-,12-,13-,14+,15+/m1/s1
Smiles CC(=C)C[C@H]1CC[C@@]2([C@@H]1[C@@](CC[C@H]2O)(C)O)C
Np Classifier Biosynthetic Pathway Terpenoids
Defined Bond Stereocenter Count 0.0
Egan Rule True
Np Classifier Superclass Sesquiterpenoids