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53950-14-4

53950-14-4 Structure

53950-14-4 Structure
IdentificationBack Directory
[Name]

L-lysine mono[[6R-[6alpha,7beta(R*)]]-7-[(aminophenylacetyl)amino]-3-methyl-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate]
[CAS]

53950-14-4
[Synonyms]

Cefalexin lysine
Cefalexinlysinate
L-lysine mono[[6R-[6alpha,7beta(R*)]]-7-[(aminophenylacetyl)amino]-3-methyl-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate]
[EINECS(EC#)]

258-880-9
[Molecular Formula]

C22H31N5O6S
[MDL Number]

MFCD22380972
[MOL File]

53950-14-4.mol
[Molecular Weight]

493.576
Hazard InformationBack Directory
[Uses]

Cephalexin (Cefalexin) lysine is a potent, orally active new semisynthetic cephalosporin antibiotic with a broad antibacterial spectrum. Cephalexin lysine has antibacterial activity against a wide variety of gram-positive and gram-negative bacteria. Cephalexin lysine targets penicillin-binding proteins (PBPs) to inhibit bacterial cell wall assembly. Cephalexin lysine is used for the research of pneumonia, strep throat, and bacterial endocarditis, et al[1][2].
[in vivo]

Cephalexin lysine (0-50 mg/kg; p.o.; for 3.5 hours) has antibacterial activity in male Swiss-Webster mice with infected bacterial[2].

Animal Model:Male Swiss-Webster mice with infected bacterial[2]
Dosage:0-50 mg/kg
Administration:Oral administration; for 3.5 hours
Result:Had antibacterial activity against Streptococcus pyogenes, Streptococcus pneumoniae, Staphylococcus aureus and several gram-negative species mice.
[IC 50]

β-lactam
[References]

[1] Cho H, et, al. Beta-lactam antibiotics induce a lethal malfunctioning of the bacterial cell wall synthesis machinery. Cell. 2014 Dec 4;159(6):1300-11. DOI:10.1016/j.cell.2014.11.017
[2] Buck RE, et, al. Cefadroxil, a new broad-spectrum cephalosporin. Antimicrob Agents Chemother. 1977 Feb;11(2):324-30. DOI:10.1128/AAC.11.2.324
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