Drug Information
| Drug General Information | Top | |||
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| Drug ID |
D0X6IE
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| Former ID |
DNC009157
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| Drug Name |
4-amino-N-(4-sulfamoylbenzyl)benzenesulfonamide
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| Synonyms |
CHEMBL266026; 4-[[(4-aminophenyl)sulfonylamino]methyl]benzenesulfonamide; AC1NA7ER; SCHEMBL3789773; BDBM10871; ZINC6392199; aromatic/heteroaromatic sulfonamide 16; AKOS024362676; MCULE-5136189306; ST50993685; N-(4-Sulfamoylbenzyl)-4-aminobenzenesulfonamide; 4-amino-N-[(4-sulfamoylphenyl)methyl]benzene-1-sulfonamide; 4-({[(4-aminophenyl)sulfonyl]amino}methyl)benzenesulfonamide; Benzenesulfonamide, 4-amino-N-[[4-(aminosulfonyl)phenyl]methyl]-
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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 |
C13H15N3O4S2
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| Canonical SMILES |
C1=CC(=CC=C1CNS(=O)(=O)C2=CC=C(C=C2)N)S(=O)(=O)N
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| InChI |
1S/C13H15N3O4S2/c14-11-3-7-13(8-4-11)22(19,20)16-9-10-1-5-12(6-2-10)21(15,17)18/h1-8,16H,9,14H2,(H2,15,17,18)
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| InChIKey |
HHCXOFYGBAPOJR-UHFFFAOYSA-N
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| PubChem Compound ID | ||||
| References | Top | |||
|---|---|---|---|---|
| REF 1 | Cloning, expression, post-translational modifications and inhibition studies on the latest mammalian carbonic anhydrase isoform, CA XV. J Med Chem. 2009 Feb 12;52(3):646-54. | |||
| REF 2 | Carbonic anhydrase inhibitors. Inhibition studies of a coral secretory isoform by sulfonamides. Bioorg Med Chem. 2009 Jul 15;17(14):5054-8. | |||
| REF 3 | Carbonic anhydrase inhibitors. Characterization and inhibition studies of the most active beta-carbonic anhydrase from Mycobacterium tuberculosis, ... Bioorg Med Chem Lett. 2009 Dec 1;19(23):6649-54. | |||
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