Drug General Information |
Drug ID |
D0N1PQ
|
Former ID |
DNC005715
|
Drug Name |
3-(6-methoxynaphthalen-2-yl)pyridine
|
Drug Type |
Small molecular drug
|
Indication |
Discovery agent
|
Investigative |
[1]
|
Structure |
|
Download
2D MOL
3D MOL
|
Formula |
C16H13NO
|
Canonical SMILES |
COC1=CC2=C(C=C1)C=C(C=C2)C3=CN=CC=C3
|
InChI |
1S/C16H13NO/c1-18-16-7-6-12-9-13(4-5-14(12)10-16)15-3-2-8-17-11-15/h2-11H,1H3
|
InChIKey |
DCVWYSMRLGKIJB-UHFFFAOYSA-N
|
PubChem Compound ID |
|
Target and Pathway |
Target(s) |
Cytochrome P450 19 |
Target Info |
Inhibitor |
[1]
|
Cytochrome P450 11B1, mitochondrial |
Target Info |
Inhibitor |
[2]
|
17 alpha-hydroxylase-C17, 20-lyase |
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 biosynthesisPWY-7305:Superpathway of steroid hormone biosynthesis
|
Androgen biosynthesis
|
KEGG Pathway
|
Steroid hormone biosynthesis
|
Metabolic pathways
|
Ovarian steroidogenesishsa00140:Steroid hormone biosynthesis
|
Metabolic pathwayshsa00140:Steroid hormone biosynthesis
|
Ovarian steroidogenesis
|
Prolactin signaling pathway
|
NetPath Pathway
|
FSH Signaling Pathway
|
PANTHER Pathway
|
Androgen/estrogene/progesterone biosynthesis
|
PathWhiz Pathway
|
Androgen and Estrogen MetabolismPW000141:SteroidogenesisPW000045:Androgen and Estrogen Metabolism
|
Steroidogenesis
|
Reactome
|
Endogenous sterolsR-HSA-194002:Glucocorticoid biosynthesis
|
Endogenous sterolsR-HSA-193048:Androgen biosynthesis
|
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 hormoneWP702:Metapathway biotransformation
|
Steroid Biosynthesis
|
Glucocorticoid & Mineralcorticoid Metabolism
|
Prostate Cancer
|
Phase 1 - Functionalization of compounds
|
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. |
---|
REF 2 | J Med Chem. 2008 Oct 9;51(19):6138-49. Epub 2008 Sep 3.Novel aldosterone synthase inhibitors with extended carbocyclic skeleton by a combined ligand-based and structure-based drug design approach. |