Drug Information
| Drug General Information | Top | |||
|---|---|---|---|---|
| Drug ID |
D0Y2AK
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| Former ID |
DNC011474
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| Drug Name |
1-Phenyl-2-pyridin-3-yl-propan-1-one
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| Synonyms |
CHEMBL53248; 62144-16-5; 1-phenyl-2-pyridin-3-yl-propan-1-one; alpha-(3-Pyridyl)propiophenone; SCHEMBL4810062; CTK2C6291; DTXSID40463372; BDBM50028159; 1-phenyl-2-(3-pyridinyl)-1-propanone; 1-Propanone, 1-phenyl-2-(3-pyridinyl)-
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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 |
C14H13NO
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| Canonical SMILES |
CC(C1=CN=CC=C1)C(=O)C2=CC=CC=C2
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| InChI |
1S/C14H13NO/c1-11(13-8-5-9-15-10-13)14(16)12-6-3-2-4-7-12/h2-11H,1H3
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| InChIKey |
NFHIPZYAYZPXJE-UHFFFAOYSA-N
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| CAS Number |
CAS 62144-16-5
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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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