Therapeutic Targets Database
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TTD Drug ID: DAP000601

Drug Information
NameDichlorphenamide    
SynonymsDichlorphenamid; SBB058142; Diclofenamida [INN-Spanish]; Prestwick3_000809; Dichlorophenamide (DCP); Daranide; CHEMBL17; Prestwick0_000809; Oratrol; EINECS 204-440-6; AC1L1F18; UNII-VVJ6673MHY; BSPBio_000677; DB07948; MLS002154010; ZINC00896918; Diclofenamida; Merck Brand of Dichlorphenamide; NCGC00016371-02; Glajust; Diclofenamide; DB01144; Dichlorphenamide (USP); Diclofenamidum [INN-Latin]; BPBio1_000745; Glaumid; LS-30043; Antidrasi; 120-97-8; Llorens Brand of Dichlorphenamide; HMS1570B19; Daranide (TN); Dichlorophenamide; 3,4-Dichloro-5-sulfamylbenzenesulfonamide; Diclofenamidum; I7A; CHEBI:101085; Barastonin; BRN 2703329; NCGC00016371-01; CB 8000; 1,3-Disulfamoyl-4,5-dichlorobenzene; SMR001233338; C07459; BRD-K71499074-001-03-8; 4,5-Dichloro-benzene-1,3-disulfonic acid diamide; Prestwick2_000809; m-Benzenedisulfonamide, 4,5-dichloro-; Diclofenamid; 1,3-Benzenedisulfonamide, 4,5-dichloro-; 4,5-Dichloro-m-benzenedisulfonamide; S2177_Selleck; Diclofenamide (JP15/INN); Glaucol; D004005; Prestwick_1071; FT-0084528; 4,5-Dichloro-1,3-disulfamoylbenzene; 1,3-Disulfamyl-4,5-dichlorobenzene; CAS-120-97-8; 4,5-Dichloro-1,3-benzenedisulfonamide; dichlorphenamide; Dasanide; Dichlorphenamide [BAN]; 2pou; Glauconide; 4,5-dichlorobenzene-1,3-disulfonamide; Glafco; HSDB 3267; MolPort-004-285-635; Dichlofenamide; D00518; CID3038; C6H6Cl2N2O4S2; Prestwick1_000809; SPBio_002598    
IndicationChronic glaucomaApproved    [1]
Structure

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Therapeutic ClassAntiglaucomic Agents    
CAS NumberCAS 120-97-8
FormularC6H6Cl2N2O4S2    
PubChem Compound IDCID 3038.    
PubChem Substance IDSID 9662.    
SuperDrug ATC IDS01EC02;    
SuperDrug CAS ID000120978;    
TargetCarbonic anhydraseInhibitor[2][3][4]
Ref 1FDA Approved Drug Products from FDA Official Website. 2009. Application Number: (NDA) 011366 To Reference
Ref 2Bioorg Med Chem. 2009 Jul 15;17(14):5054-8. Epub 2009 May 30.Carbonic anhydrase inhibitors. Inhibition studies of a coral secretory isoform by sulfonamides. To Reference
Ref 3Carbonic anhydrase inhibitors. Cloning, characterization, and inhibition studies of a new beta-carbonic anhydrase from Mycobacterium tuberculosis. J Med Chem. 2009 May 14;52(9):3116-20. To Reference
Ref 4Molecular cloning, characterization, and inhibition studies of the Rv1284 beta-carbonic anhydrase from Mycobacterium tuberculosis with sulfonamides and a sulfamate. J Med Chem. 2009 Apr 23;52(8):2226-32. To Reference



 

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