Cloxacillin sodium salt monohydrate, beta-lactamase-resistant antibiotic

Code: c9393-5g D2-231

Not available outside of the UK & Ireland.

Application

Cloxacillin is effective against infections caused by penicillin G-resistant staphylococci. It was used in studies of topical antibacterial agents for burn and cr...


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Your Price
£250.00 5G

Not available outside of the UK & Ireland.

Application

Cloxacillin is effective against infections caused by penicillin G-resistant staphylococci. It was used in studies of topical antibacterial agents for burn and crush wounds.

Biochem/physiol Actions

Cloxacillin is a semi-synthetic antibiotic and a chlorinated derivative of oxacillin. It inhibits the last stage of bacterial cell wall synthesis by binding to penicillin-binding proteins (PBPs), which results in cell lysis. Cell lysis is mediated by bacterial cell wall autolytic enzymes. Cloxacillin is often used as AmpC β-lactamase inhibitor in combination with β-lactam antibiotics.

General description

Chemical structure: ß-lactam

Other Notes

Keep container tightly closed in a dry and well-ventilated place.

antibiotic activity spectrumGram-positive bacteria
formpowder or crystals
InChI keyKCUWTKOTPIUBRI-VICXVTCVSA-M
InChI1S/C19H18ClN3O5S.Na.H2O/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);;1H2/q;+1;/p-1/t13-,14+,17-;;/m1../s1
mode of actioncell wall synthesis | interferes
Quality Level200
SMILES stringO.[Na+].Cc1onc(-c2ccccc2Cl)c1C(=O)N[C@H]3[C@H]4SC(C)(C)[C@@H](N4C3=O)C([O-])=O
storage temp.2-8°C
Code
Description
Unit Size
List Price
Qty
C9393-1G
Unit:1G
List Price: £69.70
Source:List Price
ADD
Cas Number7081-44-9
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