Drug Information
| Drug General Information | Top | |||
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| Drug ID |
D00XJA
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| Former ID |
DNC010058
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| Drug Name |
6-methoxy-2-oxo-2H-chromene-3-carboxylic acid
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| Synonyms |
6-Methoxy-2-oxo-2H-chromene-3-carboxylic acid; 35924-44-8; 6-methoxy-2-oxochromene-3-carboxylic acid; CHEMBL568416; 6-methoxy-2-oxo-2H-1-benzopyran-3-carboxylic acid; MLS000061036; AC1LEG8M; CBMicro_000141; Oprea1_705276; Oprea1_357602; 6-methoxy-3-carboxy-coumarin; SCHEMBL978456; CTK1B0306; DTXSID90351856; XIQQAIQZABTSNZ-UHFFFAOYSA-N; MolPort-000-467-024; ZINC103684; HMS2443I11; HMS1607B10; SMSF0006060; ZX-AL001956; STL553633; SBB043625; BDBM50303489; AKOS000274154; CB01296; MCULE-7757033841; BAS 00518708; SMR000069802
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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 |
C11H8O5
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| Canonical SMILES |
COC1=CC2=C(C=C1)OC(=O)C(=C2)C(=O)O
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| InChI |
1S/C11H8O5/c1-15-7-2-3-9-6(4-7)5-8(10(12)13)11(14)16-9/h2-5H,1H3,(H,12,13)
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| InChIKey |
XIQQAIQZABTSNZ-UHFFFAOYSA-N
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| CAS Number |
CAS 35924-44-8
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| PubChem Compound ID | ||||
| References | Top | |||
|---|---|---|---|---|
| REF 1 | Deciphering the mechanism of carbonic anhydrase inhibition with coumarins and thiocoumarins. J Med Chem. 2010 Jan 14;53(1):335-44. | |||
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