Drug Information
| Drug General Information | Top | |||
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| Drug ID |
D0Z1HY
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| Former ID |
DNC005901
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| Drug Name |
4-amino-6-chlorobenzene-1,3-disulfonamide
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| Synonyms |
121-30-2; 4-Amino-6-chlorobenzene-1,3-disulfonamide; 4-Amino-6-chloro-1,3-benzenedisulfonamide; Chloraminophenamide; Idorese; Salmid; Chloroaminophenamide; 1,3-Benzenedisulfonamide, 4-amino-6-chloro-; 5-Chloro-2,4-disulfamylaniline; 4-Amino-6-chloro-m-benzenedisulfonamide; 3-Chloro-4,6-disulfamoylaniline; 5-Chloro-2,4-disulfamoylaniline; UNII-3A52O8YREJ; Su 5683; 4-Amino-6-Chloro-1,3-Benzendisulfonamide; 3A52O8YREJ; CHEBI:3602; CHEMBL266240; 4-Amino-6-chlorobenzene-1,3-disulphonamide
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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 |
C6H8ClN3O4S2
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| Canonical SMILES |
C1=C(C(=CC(=C1Cl)S(=O)(=O)N)S(=O)(=O)N)N
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| InChI |
1S/C6H8ClN3O4S2/c7-3-1-4(8)6(16(10,13)14)2-5(3)15(9,11)12/h1-2H,8H2,(H2,9,11,12)(H2,10,13,14)
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| InChIKey |
IHJCXVZDYSXXFT-UHFFFAOYSA-N
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| CAS Number |
CAS 121-30-2
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| PubChem Compound ID | ||||
| ChEBI ID |
CHEBI:3602
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| 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 | Mutation of Phe91 to Asn in human carbonic anhydrase I unexpectedly enhanced both catalytic activity and affinity for sulfonamide inhibitors. Bioorg Med Chem. 2010 Aug 1;18(15):5498-503. | |||
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