Drug General Information |
Drug ID |
D06JYY
|
Former ID |
DNC008927
|
Drug Name |
3-[3-(4-Methoxybenzyl)naphthalen-2-yl]pyridine
|
Drug Type |
Small molecular drug
|
Indication |
Discovery agent
|
Investigative |
[1]
|
Structure |
|
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2D MOL
3D MOL
|
Formula |
C23H19NO
|
Canonical SMILES |
COC1=CC=C(C=C1)CC2=CC3=CC=CC=C3C=C2C4=CN=CC=C4
|
InChI |
1S/C23H19NO/c1-25-22-10-8-17(9-11-22)13-21-14-18-5-2-3-6-19(18)15-23(21)20-7-4-12-24-16-20/h2-12,14-16H,13H2,1H3
|
InChIKey |
GOGQHVZGANJJDF-UHFFFAOYSA-N
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PubChem Compound ID |
|
Target and Pathway |
Target(s) |
Cytochrome P450 11B1, mitochondrial |
Target Info |
Inhibitor |
[1]
|
Cytochrome P450 3A4 |
Target Info |
Inhibitor |
[1]
|
BioCyc Pathway
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Superpathway of steroid hormone biosynthesis
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Glucocorticoid biosynthesis
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Mineralocorticoid biosynthesis
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KEGG Pathway
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Steroid hormone biosynthesis
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Metabolic pathwayshsa00140:Steroid hormone biosynthesis
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Linoleic acid metabolism
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Retinol metabolism
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Metabolism of xenobiotics by cytochrome P450
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Drug metabolism - cytochrome P450
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Drug metabolism - other enzymes
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Metabolic pathways
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Bile secretion
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Chemical carcinogenesis
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PathWhiz Pathway
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SteroidogenesisPW000015:Caffeine Metabolism
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Retinol Metabolism
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Reactome
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Glucocorticoid biosynthesis
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Endogenous sterolsR-HSA-211981:Xenobiotics
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Aflatoxin activation and detoxification
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WikiPathways
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Metapathway biotransformation
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Oxidation by Cytochrome P450
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Metabolism of steroid hormones and vitamin D
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Corticotropin-releasing hormoneWP702:Metapathway biotransformation
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Aflatoxin B1 metabolism
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Estrogen metabolism
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Benzo(a)pyrene metabolism
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Tamoxifen metabolism
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Tryptophan metabolism
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Nuclear Receptors in Lipid Metabolism and Toxicity
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Nuclear Receptors Meta-Pathway
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Farnesoid X Receptor Pathway
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Vitamin D Receptor Pathway
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Felbamate Metabolism
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Lidocaine metabolism
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Nifedipine Activity
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Colchicine Metabolic Pathway
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Irinotecan Pathway
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Drug Induction of Bile Acid Pathway
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Fatty Acid Omega Oxidation
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Codeine and Morphine Metabolism
|
References |
REF 1 | 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. |