ID: ALA3289881

Max Phase: Preclinical

Molecular Formula: C18H14O3S

Molecular Weight: 310.37

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  O=C(Cc1cccc(O)c1)c1ccc(-c2cccc(O)c2)s1

Standard InChI:  InChI=1S/C18H14O3S/c19-14-5-1-3-12(9-14)10-16(21)18-8-7-17(22-18)13-4-2-6-15(20)11-13/h1-9,11,19-20H,10H2

Standard InChI Key:  IWYSVLAKANDCDX-UHFFFAOYSA-N

Associated Targets(Human)

Estradiol 17-beta-dehydrogenase 2 1671 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Estradiol 17-beta-dehydrogenase 1 2224 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Estradiol 17-beta-dehydrogenase 2 138 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: Small moleculeTopical: NoFirst In Class: NoBlack Box: No
Chirality: NoAvailability: NoProdrug: No

Drug Indications

MESH IDMESH Heading EFO IDsEFO TermsMax Phase for IndicationReferences

Mechanisms of Action

Mechanism of ActionAction Typetarget IDTarget NameTarget TypeTarget OrganismBinding Site NameReferences

Properties

Molecular Weight: 310.37Molecular Weight (Monoisotopic): 310.0664AlogP: 4.25#Rotatable Bonds: 4
Polar Surface Area: 57.53Molecular Species: NEUTRALHBA: 4HBD: 2
#RO5 Violations: 0HBA (Lipinski): 3HBD (Lipinski): 2#RO5 Violations (Lipinski): 0
CX Acidic pKa: 9.05CX Basic pKa: CX LogP: 4.31CX LogD: 4.31
Aromatic Rings: 3Heavy Atoms: 22QED Weighted: 0.71Np Likeness Score: -0.16

References

1. Perspicace E, Cozzoli L, Gargano EM, Hanke N, Carotti A, Hartmann RW, Marchais-Oberwinkler S..  (2014)  Novel, potent and selective 17β-hydroxysteroid dehydrogenase type 2 inhibitors as potential therapeutics for osteoporosis with dual human and mouse activities.,  83  [PMID:24974351] [10.1016/j.ejmech.2014.06.036]

Source