Drug General Information |
Drug ID |
D0R0TE
|
Former ID |
DNC005718
|
Drug Name |
3-(6-Ethoxy-naphthalen-2-yl)-pyridine
|
Drug Type |
Small molecular drug
|
Indication |
Discovery agent
|
Investigative |
[1]
|
Structure |
|
Download
2D MOL
3D MOL
|
Formula |
C17H15NO
|
Canonical SMILES |
CCOC1=CC2=C(C=C1)C=C(C=C2)C3=CN=CC=C3
|
InChI |
1S/C17H15NO/c1-2-19-17-8-7-13-10-14(5-6-15(13)11-17)16-4-3-9-18-12-16/h3-12H,2H2,1H3
|
InChIKey |
CQLHDOYGDGBDQA-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]
|
17 alpha-hydroxylase-C17, 20-lyase |
Target Info |
Inhibitor |
[1]
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BioCyc Pathway
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Superpathway of steroid hormone biosynthesis
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Estradiol biosynthesis II
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Estradiol biosynthesis IPWY-7305:Superpathway of steroid hormone biosynthesis
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Glucocorticoid biosynthesis
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Mineralocorticoid biosynthesisPWY-7305:Superpathway of steroid hormone biosynthesis
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Androgen biosynthesis
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KEGG Pathway
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Steroid hormone biosynthesis
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Metabolic pathways
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Ovarian steroidogenesishsa00140:Steroid hormone biosynthesis
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Metabolic pathwayshsa00140:Steroid hormone biosynthesis
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Ovarian steroidogenesis
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Prolactin signaling pathway
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NetPath Pathway
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FSH Signaling Pathway
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PANTHER Pathway
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Androgen/estrogene/progesterone biosynthesis
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PathWhiz Pathway
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Androgen and Estrogen MetabolismPW000141:SteroidogenesisPW000045:Androgen and Estrogen Metabolism
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Steroidogenesis
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Reactome
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Endogenous sterolsR-HSA-194002:Glucocorticoid biosynthesis
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Endogenous sterolsR-HSA-193048:Androgen biosynthesis
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Glucocorticoid biosynthesis
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Endogenous sterols
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WikiPathways
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Metapathway biotransformation
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Tryptophan metabolism
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Oxidation by Cytochrome P450
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Ovarian Infertility Genes
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Metabolism of steroid hormones and vitamin D
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FSH signaling pathway
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Integrated Breast Cancer Pathway
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Phase 1 - Functionalization of compoundsWP702:Metapathway biotransformation
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Corticotropin-releasing hormoneWP702:Metapathway biotransformation
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Steroid Biosynthesis
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Glucocorticoid & Mineralcorticoid Metabolism
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Prostate Cancer
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Phase 1 - Functionalization of compounds
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References |
REF 1 | J Med Chem. 2005 Oct 20;48(21):6632-42.Heteroaryl-substituted naphthalenes and structurally modified derivatives: selective inhibitors of CYP11B2 for the treatment of congestive heart failure and myocardial fibrosis. |