Drug Information
| Drug General Information | Top | |||
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| Drug ID |
D0AK9S
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| Former ID |
DNC010503
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| Drug Name |
3-[1-(4-Bromobenzyl)-1H-imidazol-5-yl]-1-propanol
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| Synonyms |
CHEMBL598810; SCHEMBL3823053; 3-[1-(4-Bromobenzyl)-1H-imidazol-5-yl]-1-propanol; HNOJMJNDVRPLSW-UHFFFAOYSA-N; BDBM50307229; 1-p-Bromobenzyl-5-(3-hydroxypropyl)-1H-imidazole
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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 |
C13H15BrN2O
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| Canonical SMILES |
C1=CC(=CC=C1CN2C=NC=C2CCCO)Br
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| InChI |
1S/C13H15BrN2O/c14-12-5-3-11(4-6-12)9-16-10-15-8-13(16)2-1-7-17/h3-6,8,10,17H,1-2,7,9H2
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| InChIKey |
HNOJMJNDVRPLSW-UHFFFAOYSA-N
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| PubChem Compound ID | ||||
| Target and Pathway | Top | |||
|---|---|---|---|---|
| Target(s) | Steroid 11-beta-hydroxylase (CYP11B1) | Target Info | Inhibitor | [1] |
| BioCyc | Superpathway of steroid hormone biosynthesis | |||
| Glucocorticoid biosynthesis | ||||
| Mineralocorticoid biosynthesis | ||||
| KEGG Pathway | Steroid hormone biosynthesis | |||
| Metabolic pathways | ||||
| Pathwhiz Pathway | Steroidogenesis | |||
| Reactome | Glucocorticoid biosynthesis | |||
| Endogenous sterols | ||||
| WikiPathways | Metapathway biotransformation | |||
| Oxidation by Cytochrome P450 | ||||
| Metabolism of steroid hormones and vitamin D | ||||
| Corticotropin-releasing hormone | ||||
| References | Top | |||
|---|---|---|---|---|
| REF 1 | Synthesis, biological evaluation, and molecular modeling of 1-benzyl-1H-imidazoles as selective inhibitors of aldosterone synthase (CYP11B2). J Med Chem. 2010 Feb 25;53(4):1712-25. | |||
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