Drug Information
Drug General Information | Top | |||
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Drug ID |
D0PH1G
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Former ID |
DNC010502
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Drug Name |
3-[1-(4-Cyanobenzyl)-1H-imidazol-5-yl]-1-propanol
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Synonyms |
CHEMBL598399; SCHEMBL3822518; 3-[1-(4-Cyanobenzyl)-1H-imidazol-5-yl]-1-propanol; ACOYOVQVLSTOMH-UHFFFAOYSA-N; ZINC34123980; BDBM50307226; AKOS027324260; 1-p-Cyanophenylmethyl-5-(3-hydroxypropyl)-1H-imidazole; 1-(p-cyanophenylmethyl)-5-(3-hydroxypropyl)-1H-imidazole; 1-(p-Cyanophenylmethyl)-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 |
Download2D MOL |
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Formula |
C14H15N3O
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Canonical SMILES |
C1=CC(=CC=C1CN2C=NC=C2CCCO)C#N
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InChI |
1S/C14H15N3O/c15-8-12-3-5-13(6-4-12)10-17-11-16-9-14(17)2-1-7-18/h3-6,9,11,18H,1-2,7,10H2
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InChIKey |
ACOYOVQVLSTOMH-UHFFFAOYSA-N
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PubChem Compound ID |
Target and Pathway | Top | |||
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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 | |||
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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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