Drug Information
| Drug General Information | Top | |||
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| Drug ID |
D0N8LR
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| Former ID |
DNC005750
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| Drug Name |
N-(4-Sulfamoyl-phenyl)-propionamide
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| Synonyms |
N-(4-sulfamoylphenyl)propanamide; 4-propionamidobenzenesulfonamide; CHEMBL278395; 4708-37-6; AC1LI2CK; SCHEMBL13263684; aromatic sulfonamide compound 10; 4-Propionamido-benzenesulfonamide; BDBM16645; MolPort-001-490-167; ZINC381801; AKOS003252339; N-[4-(aminosulfonyl)phenyl]propanamide; MCULE-9928658311; ST45021659; AO-080/11989809
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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 |
C9H12N2O3S
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| Canonical SMILES |
CCC(=O)NC1=CC=C(C=C1)S(=O)(=O)N
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| InChI |
1S/C9H12N2O3S/c1-2-9(12)11-7-3-5-8(6-4-7)15(10,13)14/h3-6H,2H2,1H3,(H,11,12)(H2,10,13,14)
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| InChIKey |
KEFCIQSZJXXOLO-UHFFFAOYSA-N
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| PubChem Compound ID | ||||
| References | Top | |||
|---|---|---|---|---|
| REF 1 | Carbonic anhydrase inhibitors: inhibition of the tumor-associated isozymes IX and XII with a library of aromatic and heteroaromatic sulfonamides. Bioorg Med Chem Lett. 2005 Nov 1;15(21):4862-6. | |||
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