ID: ALA3287190

Max Phase: Preclinical

Molecular Formula: C15H12N2O

Molecular Weight: 236.27

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  CC(=O)n1ccc2cc(-c3cccnc3)ccc21

Standard InChI:  InChI=1S/C15H12N2O/c1-11(18)17-8-6-13-9-12(4-5-15(13)17)14-3-2-7-16-10-14/h2-10H,1H3

Standard InChI Key:  MYHBLSHQWVTDMP-UHFFFAOYSA-N

Associated Targets(Human)

Cytochrome P450 11B2 2325 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Cytochrome P450 11B1 1750 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Cytochrome P450 17A1 3627 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Cytochrome P450 19A1 6099 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: 236.27Molecular Weight (Monoisotopic): 236.0950AlogP: 3.36#Rotatable Bonds: 1
Polar Surface Area: 34.89Molecular Species: NEUTRALHBA: 3HBD: 0
#RO5 Violations: 0HBA (Lipinski): 3HBD (Lipinski): 0#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: 4.72CX LogP: 1.82CX LogD: 1.82
Aromatic Rings: 3Heavy Atoms: 18QED Weighted: 0.65Np Likeness Score: -1.04

References

1. Yin L, Hu Q, Emmerich J, Lo MM, Metzger E, Ali A, Hartmann RW..  (2014)  Novel pyridyl- or isoquinolinyl-substituted indolines and indoles as potent and selective aldosterone synthase inhibitors.,  57  (12): [PMID:24899257] [10.1021/jm500140c]

Source