Drug General Information |
Drug ID |
D03EXD
|
Former ID |
DNC011103
|
Drug Name |
4-[(4'-Hydroxybiphenyl-4-yl)methyl]pyridine
|
Drug Type |
Small molecular drug
|
Indication |
Discovery agent
|
Investigative |
[1]
|
Structure |
|
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2D MOL
3D MOL
|
Formula |
C18H15NO2
|
Canonical SMILES |
C1=CC(=CC=C1C2=CC=C(C=C2)O)C(C3=CC=NC=C3)O
|
InChI |
1S/C18H15NO2/c20-17-7-5-14(6-8-17)13-1-3-15(4-2-13)18(21)16-9-11-19-12-10-16/h1-12,18,20-21H
|
InChIKey |
ABUNZHUAYBOXCN-UHFFFAOYSA-N
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PubChem Compound ID |
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Target and Pathway |
Target(s) |
17 alpha-hydroxylase-C17, 20-lyase |
Target Info |
Inhibitor |
[1]
|
Cytochrome P450 11B1, mitochondrial |
Target Info |
Inhibitor |
[1]
|
Cytochrome P450 19 |
Target Info |
Inhibitor |
[1]
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BioCyc Pathway
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Superpathway of steroid hormone biosynthesis
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Glucocorticoid biosynthesis
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Androgen biosynthesisPWY-7305:Superpathway of steroid hormone biosynthesis
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Mineralocorticoid biosynthesisPWY-7305:Superpathway of steroid hormone biosynthesis
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Estradiol biosynthesis II
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Estradiol biosynthesis I
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KEGG Pathway
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Steroid hormone biosynthesis
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Metabolic pathways
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Ovarian steroidogenesis
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Prolactin signaling pathwayhsa00140:Steroid hormone biosynthesis
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Metabolic pathwayshsa00140:Steroid hormone biosynthesis
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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 Metabolism
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SteroidogenesisPW000141:SteroidogenesisPW000045:Androgen and Estrogen Metabolism
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Reactome
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Androgen biosynthesis
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Glucocorticoid biosynthesis
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Endogenous sterolsR-HSA-194002:Glucocorticoid biosynthesis
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Endogenous sterolsR-HSA-211976:Endogenous sterols
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WikiPathways
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Metapathway biotransformation
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Steroid Biosynthesis
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Oxidation by Cytochrome P450
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Metabolism of steroid hormones and vitamin D
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Glucocorticoid & Mineralcorticoid Metabolism
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Prostate Cancer
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Phase 1 - Functionalization of compoundsWP702:Metapathway biotransformation
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Corticotropin-releasing hormoneWP702:Metapathway biotransformation
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Tryptophan metabolism
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Ovarian Infertility Genes
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FSH signaling pathway
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Integrated Breast Cancer Pathway
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Phase 1 - Functionalization of compounds
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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. |