Drug Information
| Drug General Information | Top | |||
|---|---|---|---|---|
| Drug ID |
D09TTR
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| Former ID |
DNC013125
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| Drug Name |
1-(3-phenylpropyl)-1H-imidazole
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| Synonyms |
1-(3-phenylpropyl)-1H-imidazole; CHEMBL380271; 1-(3-phenylpropyl)imidazole; 1H-Imidazole, 1-(3-phenylpropyl)-; SCHEMBL3160306; DDGQVFKVBFAACE-UHFFFAOYSA-N; BDBM50191796; AKOS009137296
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| Drug Type |
Small molecular drug
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| Indication | Discovery agent [ICD-11: N.A.] | Investigative | [1] | |
| Structure |
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Download2D MOL |
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| Formula |
C12H14N2
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| Canonical SMILES |
C1=CC=C(C=C1)CCCN2C=CN=C2
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| InChI |
1S/C12H14N2/c1-2-5-12(6-3-1)7-4-9-14-10-8-13-11-14/h1-3,5-6,8,10-11H,4,7,9H2
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| InChIKey |
DDGQVFKVBFAACE-UHFFFAOYSA-N
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| CAS Number |
CAS 56643-92-6
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| PubChem Compound ID | ||||
| Target and Pathway | Top | |||
|---|---|---|---|---|
| Target(s) | Steroid 17-alpha-monooxygenase (S17AH) | Target Info | Inhibitor | [1] |
| BioCyc | Superpathway of steroid hormone biosynthesis | |||
| Glucocorticoid biosynthesis | ||||
| Androgen biosynthesis | ||||
| KEGG Pathway | Steroid hormone biosynthesis | |||
| Metabolic pathways | ||||
| Ovarian steroidogenesis | ||||
| Prolactin signaling pathway | ||||
| Pathwhiz Pathway | Androgen and Estrogen Metabolism | |||
| Steroidogenesis | ||||
| Reactome | Androgen biosynthesis | |||
| Glucocorticoid biosynthesis | ||||
| Endogenous sterols | ||||
| WikiPathways | Metapathway biotransformation | |||
| Steroid Biosynthesis | ||||
| Oxidation by Cytochrome P450 | ||||
| Metabolism of steroid hormones and vitamin D | ||||
| Glucocorticoid & Mineralcorticoid Metabolism | ||||
| Prostate Cancer | ||||
| Phase 1 - Functionalization of compounds | ||||
| References | Top | |||
|---|---|---|---|---|
| REF 1 | Synthesis, biochemical evaluation and rationalisation of the inhibitory activity of a range of 4-substituted phenyl alkyl imidazole-based inhibitor... Bioorg Med Chem Lett. 2006 Sep 15;16(18):4752-6. | |||
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