Therapeutic Targets Database
BIDD Pharmainformatics Databases


TTD Drug ID: DAP000146

Drug Information
Synonymscefotaxime; Cefotaxima; AC1OC9NB; Spectrum4_000268; SPBio_000138; Prestwick0_000139; AC1L9UKL; STK383264; BSPBio_000218; Cefotaximum [INN-Latin]; CE3; Claforan; HMS2090M11; SPBio_002157; KBioGR_000736; Cefotaxime (INN); Lopac0_000278; C16H17N5O7S2; BSPBio_001961; AC1NSF5T; CID5742673; Spectrum_000108; BRD-K99586414-236-02-3; DivK1c_000767; 63527-53-7; KBio2_000548; CID6604086; AC1O7G8N; BIDD:GT0681; Cefotaxim; Cephotaxime; AC1NX3QV; CID5916965; MolPort-006-834-754; DB00493; KBio2_003116; Cefotaximum; KBioSS_000548; Prestwick1_000139; AC1NZU9Q; AC1L1E42; Cefotaxim Hikma (TN); Spectrum2_000119; RU 24662; Claforan (*Sodium salt*); Cefotaxim Hikma; CID7566336; AC1O712I; CHEBI:204928; Ru-24756; NCGC00021126-01; KBio3_001181; CID6540461; KBio1_000767; Spectrum3_000331; AC1NUIF8; Klaforan; KBio2_005684; NINDS_000767; Cefotaxime [INN:BAN]; Prestwick2_000139; C06885; EINECS 264-299-1; Spectrum5_000667; D07647; MolPort-002-339-742; LS-187246; Cefotaxima [INN-Spanish]; MolPort-005-934-578; AC1NSF6T; 64485-93-4 (mono-hydrochloride salt); CID9868614; AKOS003286450; LS-149920; AC-217; IDI1_000767; CID5479527; CHEMBL102; Cefotaxime acid; UNII-N2GI8B1GK7; BRD-K78364995-236-03-5; CID5361354; CID2632; CID5361298; 60846-21-1; BPBio1_000240; CID6914272; Cephotaxim; 63527-52-6; Prestwick3_000139; CID456256    
Trade NameClaforan    
CompanyRoussel Uclaf    
IndicationBacterial InfectionApproved    [1]

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Therapeutic ClassAnti-Bacterial Agents    
CAS NumberCAS 63527-52-6
PubChem Compound IDCID 2632.    
PubChem Substance IDSID 6538280.    
SuperDrug ATC IDJ01DD01;    
SuperDrug CAS ID064485934;    
TargetD-alanyl-D-alanine carboxypeptidaseInhibitor[2][3]
Ref 1FDA Approved Drug Products from FDA Official Website. 2009. Application Number: (ANDA) 064200 To Reference
Ref 2Extended-spectrum cephalosporinases: structure, detection and epidemiology. Future Microbiol. 2007 Jun;2:297-307. To Reference
Ref 3Binding of cephalothin and cefotaxime to D-ala-D-ala-peptidase reveals a functional basis of a natural mutation in a low-affinity penicillin-binding protein and in extended-spectrum beta-lactamases. Biochemistry. 1995 Jul 25;34(29):9532-40. To Reference


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