Drug Information
| Drug General Information | Top | |||
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| Drug ID |
D0B1WD
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| Former ID |
DNC009097
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| Drug Name |
N-(4-Ethylphenyl)-2-oxo-2H-chromene-3-carboxamide
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| Synonyms |
N-(4-ethylphenyl)-2-oxo-2H-chromene-3-carboxamide; 2-Oxo-2H-chromene-3-carboxylic acid (4-ethyl-phenyl)-amide; AC1LF7IS; ChemDiv3_001051; AC1Q2TK3; 3-carboxamido coumarin, 13; Oprea1_789803; Oprea1_049912; CHEMBL469583; BDBM29163; MolPort-000-375-251; HMS1475P17; ZINC130255; STK421228; AKOS000533669; MCULE-8672204127; IDI1_020017; BAS 00837926; ST45140661; EU-0002704; N-(4-ethylphenyl)-2-oxochromene-3-carboxamide; SR-01000410412; N-(4-ethylphenyl)(2-oxochromen-3-yl)carboxamide; SR-01000410412-1
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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 |
C18H15NO3
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| Canonical SMILES |
CCC1=CC=C(C=C1)NC(=O)C2=CC3=CC=CC=C3OC2=O
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| InChI |
1S/C18H15NO3/c1-2-12-7-9-14(10-8-12)19-17(20)15-11-13-5-3-4-6-16(13)22-18(15)21/h3-11H,2H2,1H3,(H,19,20)
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| InChIKey |
CCRNXJJERVYHEO-UHFFFAOYSA-N
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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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