Drug Information
| Drug General Information | Top | |||
|---|---|---|---|---|
| Drug ID |
D01XFH
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| Former ID |
DNC006917
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| Drug Name |
N-propynyl amidebenzenesulphonide
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| Synonyms |
N-(prop-2-ynyl)-4-sulfamoylbenzamide
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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 |
C10H10N2O3S
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| Canonical SMILES |
C#CCNC(=O)C1=CC=C(C=C1)S(=O)(=O)N
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| InChI |
1S/C10H10N2O3S/c1-2-7-12-10(13)8-3-5-9(6-4-8)16(11,14)15/h1,3-6H,7H2,(H,12,13)(H2,11,14,15)
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| InChIKey |
KRDXLVUMSYUYOP-UHFFFAOYSA-N
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| PubChem Compound ID | ||||
| References | Top | |||
|---|---|---|---|---|
| REF 1 | A novel class of carbonic anhydrase inhibitors: glycoconjugate benzene sulfonamides prepared by "click-tailing". J Med Chem. 2006 Nov 2;49(22):6539-48. | |||
| REF 2 | Inhibition of membrane-associated carbonic anhydrase isozymes IX, XII and XIV with a library of glycoconjugate benzenesulfonamides. Bioorg Med Chem Lett. 2007 Feb 15;17(4):987-92. | |||
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