Drug Information
Drug General Information | |||||
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Drug ID |
D0K2DR
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Former ID |
DNC009638
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Drug Name |
5-Pyridin-3-yl-1,3-dihydro-2H-indol-2-one
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Drug Type |
Small molecular drug
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Indication | Discovery agent | Investigative | [1] | ||
Structure |
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Download2D MOL |
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Formula |
C13H10N2O
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Canonical SMILES |
C1C2=C(C=CC(=C2)C3=CN=CC=C3)NC1=O
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InChI |
1S/C13H10N2O/c16-13-7-11-6-9(3-4-12(11)15-13)10-2-1-5-14-8-10/h1-6,8H,7H2,(H,15,16)
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InChIKey |
LRXSVYIRRDZVNQ-UHFFFAOYSA-N
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PubChem Compound ID | |||||
Target and Pathway | |||||
Target(s) | Cytochrome P450 19 | Target Info | Inhibitor | [1] | |
Cytochrome P450 11B1, mitochondrial | Target Info | Inhibitor | [1] | ||
BioCyc Pathway | Superpathway of steroid hormone biosynthesis | ||||
Estradiol biosynthesis II | |||||
Estradiol biosynthesis IPWY-7305:Superpathway of steroid hormone biosynthesis | |||||
Glucocorticoid biosynthesis | |||||
Mineralocorticoid biosynthesis | |||||
KEGG Pathway | Steroid hormone biosynthesis | ||||
Metabolic pathways | |||||
Ovarian steroidogenesishsa00140:Steroid hormone biosynthesis | |||||
NetPath Pathway | FSH Signaling Pathway | ||||
PANTHER Pathway | Androgen/estrogene/progesterone biosynthesis | ||||
PathWhiz Pathway | Androgen and Estrogen MetabolismPW000141:Steroidogenesis | ||||
Reactome | Endogenous sterolsR-HSA-194002:Glucocorticoid biosynthesis | ||||
Endogenous sterols | |||||
WikiPathways | Metapathway biotransformation | ||||
Tryptophan metabolism | |||||
Oxidation by Cytochrome P450 | |||||
Ovarian Infertility Genes | |||||
Metabolism of steroid hormones and vitamin D | |||||
FSH signaling pathway | |||||
Integrated Breast Cancer Pathway | |||||
Phase 1 - Functionalization of compoundsWP702:Metapathway biotransformation | |||||
Corticotropin-releasing hormone | |||||
References | |||||
REF 1 | J Med Chem. 2008 Dec 25;51(24):8077-87.In vivo active aldosterone synthase inhibitors with improved selectivity: lead optimization providing a series of pyridine substituted 3,4-dihydro-1H-quinolin-2-one derivatives. | ||||
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