CAS 5250-39-5: Flucloxacillin
Formula:C19H17ClFN3O5S
InChI:InChI=1S/C19H17ClFN3O5S/c1-7-10(12(23-29-7)11-8(20)5-4-6-9(11)21)15(25)22-13-16(26)24-14(18(27)28)19(2,3)30-17(13)24/h4-6,13-14,17H,1-3H3,(H,22,25)(H,27,28)/t13-,14+,17-/m1/s1
InChI key:InChIKey=UIOFUWFRIANQPC-JKIFEVAISA-N
SMILES:C(O)(=O)[C@@H]1N2[C@@]([C@H](NC(=O)C=3C(=NOC3C)C4=C(Cl)C=CC=C4F)C2=O)(SC1(C)C)[H]
Synonyms:- (2S,5R,6R)-6-[[[3-(2-Chloro-6-fluorophenyl)-5-methyl-4-isoxazolyl]carbonyl]amino]-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid
- 4-Thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid, 6-[3-(2-chloro-6-fluorophenyl)-5-methyl-4-isoxazolecarboxamido]-3,3-dimethyl-7-oxo-
- 4-Thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid, 6-[[[3-(2-chloro-6-fluorophenyl)-5-methyl-4-isoxazolyl]carbonyl]amino]-3,3-dimethyl-7-oxo-, (2S,5R,6R)-
- 4-Thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid, 6-[[[3-(2-chloro-6-fluorophenyl)-5-methyl-4-isoxazolyl]carbonyl]amino]-3,3-dimethyl-7-oxo-, [2S-(2α,5α,6β)]-
- 6-[3-(2-Chloro-6-fluorophenyl)-5-methyl-4-isoxazolecarboxamido]-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid
- 6-[3-(2-Chloro-6-fluorophenyl)-5-methyl-4-isoxazolecarboxamido]penicillanic acid
- Abboflox
- Brl 2039
- Culpen
- Fk 900
- Flopen
- See more synonyms
Sort by
Found 3 products.
Flucloxacillin
CAS:Flucloxacillin is a beta-lactam antibiotic, which is derived from the penicillin family. It is synthetically produced through chemical modification to enhance its stability against beta-lactamase enzymes. The mode of action of flucloxacillin involves inhibiting bacterial cell wall synthesis. It binds to penicillin-binding proteins (PBPs) located inside the bacterial cell wall, which in turn inhibits the transpeptidation or cross-linking of peptidoglycan chains. This action leads to cell lysis and ultimately, bacterial death. Flucloxacillin is predominantly used against Gram-positive bacteria, especially staphylococci, including penicillinase-producing strains resistant to other penicillins. It is employed in the treatment of various infections such as skin and soft tissue infections, respiratory tract infections, and osteomyelitis. Due to its specific activity and resistance to the action of beta-lactamase, flucloxacillin is often chosen in cases where methicillin-resistant strains are not suspected. Its clinical utility is critical, particularly in the context of penicillinase-producing Staphylococcus aureus.Formula:C19H17ClFN3O5SPurity:Min. 95%Molecular weight:453.87 g/molFlucloxacillin
CAS:Flucloxacillin, an antibiotic, effectively combats both gram-positive and gram-negative bacteria [1] [2].Formula:C19H17ClFN3O5SColor and Shape:SolidMolecular weight:453.87
