-
Detailed Description
CAS Number: 33075-00-2
Molecular Formula: C19H28N4O6S2
Molecular Weight: 472.58
Mechanism of Action: Like β-lactams, cephalosporins interfere with PBP (penicillin binding protein) activity involved in the final phase of peptidoglycan synthesis. PBP’s are enzymes which catalyze a pentaglycine crosslink between alanine and lysine residues providing additional strength to the cell wall. Without a pentaglycine crosslink, the integrity of the cell wall is severely compromised and ultimately leads to cell lysis and death. Resistance to cephalosporins is commonly due to cells containing plasmid encoded β-lactamases.
Storage Conditions: -20C (hygroscopic)
-
Applications
Spectrum: Gram-positive, Gram-negative
Microbiology Applications: Cefathiamidine has a similar antibacterial spectrum as Cefalotin.
-
Specifications
Form: Solid
Appearance: White to off-white crystalline powder
Source: Synthetic
Purity Level: ≥97.0% (anhydrous basis)
CAS Number: 33075-00-2
Molecular Formula: C19H28N4O6S2
Molecular Weight: 472.58
Mechanism of Action: Like β-lactams, cephalosporins interfere with PBP (penicillin binding protein) activity involved in the final phase of peptidoglycan synthesis. PBP’s are enzymes which catalyze a pentaglycine crosslink between alanine and lysine residues providing additional strength to the cell wall. Without a pentaglycine crosslink, the integrity of the cell wall is severely compromised and ultimately leads to cell lysis and death. Resistance to cephalosporins is commonly due to cells containing plasmid encoded β-lactamases.
Storage Conditions: -20C (hygroscopic)
Spectrum: Gram-positive, Gram-negative
Microbiology Applications: Cefathiamidine has a similar antibacterial spectrum as Cefalotin.
Form: Solid
Appearance: White to off-white crystalline powder
Source: Synthetic
Purity Level: ≥97.0% (anhydrous basis)