Drug Information
Drug General Information | Top | |||
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Drug ID |
D08UWI
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Former ID |
DNC011434
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Drug Name |
2-Methyl-1-phenyl-2-pyridin-3-yl-propan-1-one
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Synonyms |
87372-75-6; 2-Methyl-1-phenyl-2-(3-pyridinyl)-1-propanone; CHEMBL294460; 2-Mppp; 2-Methyl-1-phenyl-2-pyridin-3-yl-propan-1-one; AC1L37C5; SCHEMBL12260655; CTK5F8302; DTXSID50236312; ZINC5138212; BDBM50028170; KB-231336; 2-methyl-1-phenyl-2-pyridin-3-ylpropan-1-one
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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 |
C15H15NO
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Canonical SMILES |
CC(C)(C1=CN=CC=C1)C(=O)C2=CC=CC=C2
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InChI |
1S/C15H15NO/c1-15(2,13-9-6-10-16-11-13)14(17)12-7-4-3-5-8-12/h3-11H,1-2H3
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InChIKey |
GWWVZTFGCNLAOV-UHFFFAOYSA-N
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CAS Number |
CAS 87372-75-6
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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 | 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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