Cloxacillin-13C4 Sodium Salt

CAS : 642-78-4

Ref. TR-C587462

Informations sur le produit

• Nom: Cloxacillin-13C4 Sodium Salt
• Synonymes: (2S,5R,6R)-6-[[[3-(2-Chlorophenyl)-5-methyl-4-isoxazolyl]carbonyl]amino]-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic Acid-13C4 Sodium Salt, 3-(o-Chlorophenyl)-5-methyl-4-isoxazolylpenicillin sodium salt, 4-Thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid, 6-[3-(o-chlorophenyl)-5-methyl-4-isoxazolecarboxamido]-3,3-dimethyl-7-oxo-, monosodium salt, 4-Thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid, 6-[[[3-(2-chlorophenyl)-5-methyl-4-isoxazolyl]carbonyl]amino]-3,3-dimethyl-7-oxo-, monosodium salt, (2S,5R,6R)-, 4-Thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid, 6-[[[3-(2-chlorophenyl)-5-methyl-4-isoxazolyl]carbonyl]amino]-3,3-dimethyl-7-oxo-, monosodium salt, [2S-(2α,5α,6β)]-, 4-Thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid, 6-[[[3-(2-chlorophenyl)-5-methyl-4-isoxazolyl]carbonyl]amino]-3,3-dimethyl-7-oxo-, sodium salt (1:1), (2S,5R,6R)-, 4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid, 6-[[[3-(2-chlorophenyl)-5-methyl-4-isoxazolyl]carbonyl]amino]-3,3-dimethyl-7-oxo-, sodium salt, (2S,5R,6R)- (1:1), Ankerbin, Austrastaph, BRL 1621 sodium salt, Cloxacillin sodium, Cloxapen, Ekvacillin, Gelstaph, Monosodium cloxacillin, Neoclox, Orbenin, Orbenin sodium, Prevencilina P, Prostaphilin A, Prostaphlin A, Sodium (2S,5R,6R)-6-({[3-(2-chlorophenyl)-5-methyl-1,2-oxazol-4-yl]carbonyl}amino)-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate, Sodium 3-(O-chlorophenyl)-5-methyl-4-isoxazolylpenicillin, Sodium cloxacillin, Sodium orbenin, Sodium syntarpen, Staphybiotic, Syntarpen sodium salt, Tegopen, [(5R,6R)-6-({[3-(2,6-dichlorophenyl)-5-methyl-1,2-oxazol-4-yl]carbonyl}amino)-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylato-kappaO]sodium hydrate (1:1)

Description

Stability Hygroscopic
Applications Labelled analogue of Cloxacillin, an antibiotic that belongs to the group of the isoxazolylpenicillins. Cloxacillin is used to treat infections caused by species of staphylococci that produce beta-lactamase due to its inhibitory effects on beta-lactamase binding.
References Gibbs, D.L. et al.: Curr. Microbiol., 2, 239 (1979); Dmitrova, D. et al.: Farmat., 48, 28 (2001); Craven, N. et al.: Res. Vet. Sci., 29, 57 (1980);

• Marque: TRC

Propriétés chimiques

• Masse moléculaire: 461.83
• Formule: C₁₅C₄H₁₇ClN₃NaO₅S
• Couleur/Forme: Off-White
• InChI: InChI=1S/C19H18ClN3O5S.Na/c1-8-11(12(22-28-8)9-6-4-5-7-10(9)20)15(24)21-13-16(25)23-14(18(26)27)19(2,3)29-17(13)23;/h4-7,13-14,17H,1-3H3,(H,21,24)(H,26,27);/q;+1/p-1/t13-,14+,17-;/m1./s1/i1+1,8+1,11+1,15+1
• Code InChI: InChIKey=SCLZRKVZRBKZCR-QSLPWVMZSA-M
• SMILES: CC1(C)S[C@@H]2[C@H](N[13C](=O)[13c]3c(-c4ccccc4Cl)no[13c]3[13CH3])C(=O)N2[C@H]1C(=O)O[Na]