Drug Information
| Drug General Information | Top | |||
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| Drug ID |
D0G3RD
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| Former ID |
DNC011429
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| Drug Name |
2-Methyl-1,2-di-pyridin-3-yl-propane
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| Synonyms |
CHEMBL54171; 87372-71-2; 2-Methyl-1,2-di-pyridin-3-yl-propane; CTK3C4533; DTXSID60658228; ZINC29551986; BDBM50028165; 3,3'-(2-Methylpropane-1,2-diyl)dipyridine; Pyridine, 3,3'-(1,1-dimethyl-1,2-ethanediyl)bis-
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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 |
C14H16N2
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| Canonical SMILES |
CC(C)(CC1=CN=CC=C1)C2=CN=CC=C2
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| InChI |
1S/C14H16N2/c1-14(2,13-6-4-8-16-11-13)9-12-5-3-7-15-10-12/h3-8,10-11H,9H2,1-2H3
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| InChIKey |
PKJNPGGSGKBGGS-UHFFFAOYSA-N
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| CAS Number |
CAS 87372-71-2
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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 | Structure-activity relationship study of the inhibition of adrenal cortical 11 beta-hydroxylase by new metyrapone analogues. J Med Chem. 1984 Jan;27(1):15-9. | |||
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