Drug Information
| Drug General Information | Top | |||
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| Drug ID |
D03PXS
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| Former ID |
DNC009094
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| Drug Name |
2-oxo-N-phenyl-2H-chromene-3-carboxamide
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| Synonyms |
2-oxo-N-phenyl-2H-chromene-3-carboxamide; NSC375104; 2-oxo-N-phenylchromene-3-carboxamide; 54396-25-7; AC1L7UQ9; Oprea1_247443; Oprea1_472798; CBDivE_011982; JMC521935 Compound 6; SCHEMBL831792; IFLab1_001129; CHEMBL494795; NIOSH/DJ2267500; Coumarin, 3-(anilinocarbonyl)-; BDBM23543; ZINC42178; DTXSID80321427; MolPort-000-375-218; HMS1415D07; (2-oxochromen-3-yl)-N-benzamide; 3-Carboxamide-coumarin deriv., 18; STK337557; AKOS000511884; 2-oxo-N-phenyl-chromene-3-carboxamide; NSC-375104; MCULE-7275389335; IDI1_008996
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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 |
C16H11NO3
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| Canonical SMILES |
C1=CC=C(C=C1)NC(=O)C2=CC3=CC=CC=C3OC2=O
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| InChI |
1S/C16H11NO3/c18-15(17-12-7-2-1-3-8-12)13-10-11-6-4-5-9-14(11)20-16(13)19/h1-10H,(H,17,18)
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| InChIKey |
IMFBGZCBLOPVCJ-UHFFFAOYSA-N
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| CAS Number |
CAS 54396-25-7
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| PubChem Compound ID | ||||
| References | Top | |||
|---|---|---|---|---|
| REF 1 | Synthesis, molecular modeling, and selective inhibitory activity against human monoamine oxidases of 3-carboxamido-7-substituted coumarins. J Med Chem. 2009 Apr 9;52(7):1935-42. | |||
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