(3aS,4S,7aS)-4-[2-(2,3-dihydroxy-6-methylphenyl)ethyl]-7a-methyl-octahydro-1H-indene-1,5-dione

• ChemBase ID: 6152
• Molecular Formular: C19H24O4
• Molecular Mass: 316.39146
• Monoisotopic Mass: 316.16745925
• SMILES: O=C1CC[C@@H]2[C@]1(C)CCC(=O)[C@H]2CCc1c(O)c(O)ccc1C
• Canonical SMILES: O=C1CC[C@]2([C@H]([C@@H]1CCc1c(C)ccc(c1O)O)CCC2=O)C
• InChI: InChI=1S/C19H24O4/c1-11-3-7-16(21)18(23)12(11)4-5-13-14-6-8-17(22)19(14,2)10-9-15(13)20/h3,7,13-14,21,23H,4-6,8-10H2,1-2H3/t13-,14-,19-/m0/s1
• InChIKey: YUHVBHDSVLKFNI-NJSLBKSFSA-N

NAMES AND DATABASE IDS

Names

• IUPAC name: (3aS,4S,7aS)-4-[2-(2,3-dihydroxy-6-methylphenyl)ethyl]-7a-methyl-octahydro-1H-indene-1,5-dione
• IUPAC Traditional name: DHSA
• Synonyms: 3,4-dihydroxy-9,10-secoandrosta-1(10),2,4-triene-9,17-dione

Database IDs

• PubChem SID: 160969577; 99445013
• PubChem CID: 440483

CALCULATED PROPERTIES

JChem

• Acid pKa: 9.435305
• H Acceptors: 4
• H Donor: 2
• LogD (pH = 5.5): 4.1480074
• LogD (pH = 7.4): 4.1440973
• Log P: 4.1480575
• Molar Refractivity: 88.1862 cm^3
• Polarizability: 34.09317 Å^3
• Polar Surface Area: 74.6 Å^2
• Rotatable Bonds: 3
• Lipinski's Rule of Five: true

ALOGPS 2.1

• Log P: 3.17
• LOG S: -4.02
• Solubility (Water): 3.06e-02 g/l

DETAILS

DrugBank - DB08542

Drug information: experimental