Drug Information
Drug General Information | |||||
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Drug ID |
D03TRM
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Former ID |
DNC004643
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Drug Name |
5-Indan-(1E)-ylidenemethyl-1H-imidazole
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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 |
C13H12N2
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Canonical SMILES |
C1CC(=CC2=CN=CN2)C3=CC=CC=C31
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InChI |
1S/C13H12N2/c1-2-4-13-10(3-1)5-6-11(13)7-12-8-14-9-15-12/h1-4,7-9H,5-6H2,(H,14,15)/b11-7+
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InChIKey |
FXLOWXDBTSZJFZ-YRNVUSSQSA-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] | ||
BioCyc Pathway | Superpathway of steroid hormone biosynthesis | ||||
Estradiol biosynthesis II | |||||
Estradiol biosynthesis IPWY-7305:Superpathway of steroid hormone biosynthesis | |||||
Glucocorticoid biosynthesis | |||||
Mineralocorticoid biosynthesis | |||||
KEGG Pathway | Steroid hormone biosynthesis | ||||
Metabolic pathways | |||||
Ovarian steroidogenesishsa00140:Steroid hormone biosynthesis | |||||
NetPath Pathway | FSH Signaling Pathway | ||||
PANTHER Pathway | Androgen/estrogene/progesterone biosynthesis | ||||
PathWhiz Pathway | Androgen and Estrogen MetabolismPW000141:Steroidogenesis | ||||
Reactome | Endogenous sterolsR-HSA-194002: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 hormone | |||||
References | |||||
REF 1 | J Med Chem. 2005 Mar 24;48(6):1796-805.Synthesis and evaluation of imidazolylmethylenetetrahydronaphthalenes and imidazolylmethyleneindanes: potent inhibitors of aldosterone synthase. | ||||
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