Drug Information
Drug General Information | |||||
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Drug ID |
D0Z3GX
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Former ID |
DNC011109
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Drug Name |
4-(4-(thiophen-3-yl)benzyl)pyridine
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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 |
C16H13NS
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Canonical SMILES |
C1=CC(=CC=C1CC2=CC=NC=C2)C3=CSC=C3
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InChI |
1S/C16H13NS/c1-3-15(16-7-10-18-12-16)4-2-13(1)11-14-5-8-17-9-6-14/h1-10,12H,11H2
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InChIKey |
JZVKRZVTIHAZFG-UHFFFAOYSA-N
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PubChem Compound ID | |||||
Target and Pathway | |||||
Target(s) | Cytochrome P450 11B1, mitochondrial | Target Info | Inhibitor | [1] | |
17 alpha-hydroxylase-C17, 20-lyase | Target Info | Inhibitor | [1] | ||
BioCyc Pathway | Superpathway of steroid hormone biosynthesis | ||||
Glucocorticoid biosynthesis | |||||
Mineralocorticoid biosynthesisPWY-7305:Superpathway of steroid hormone biosynthesis | |||||
Androgen biosynthesis | |||||
KEGG Pathway | Steroid hormone biosynthesis | ||||
Metabolic pathwayshsa00140:Steroid hormone biosynthesis | |||||
Metabolic pathways | |||||
Ovarian steroidogenesis | |||||
Prolactin signaling pathway | |||||
PathWhiz Pathway | SteroidogenesisPW000045:Androgen and Estrogen Metabolism | ||||
Steroidogenesis | |||||
Reactome | Glucocorticoid biosynthesis | ||||
Endogenous sterolsR-HSA-193048:Androgen biosynthesis | |||||
Endogenous sterols | |||||
WikiPathways | Metapathway biotransformation | ||||
Oxidation by Cytochrome P450 | |||||
Metabolism of steroid hormones and vitamin D | |||||
Corticotropin-releasing hormoneWP702:Metapathway biotransformation | |||||
Steroid Biosynthesis | |||||
Glucocorticoid & Mineralcorticoid Metabolism | |||||
Prostate Cancer | |||||
Phase 1 - Functionalization of compounds | |||||
References | |||||
REF 1 | J Med Chem. 2010 Aug 12;53(15):5749-58.Replacement of imidazolyl by pyridyl in biphenylmethylenes results in selective CYP17 and dual CYP17/CYP11B1 inhibitors for the treatment of prostate cancer. | ||||
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