cephalosporin c

Cephalosporin C zinc salt was a potent inhibitor of SAMHD1 (IC50 : 1.1 ± 0.1 µM), and this inhibition was largely attributable to the presence of zinc.

Cephalosporin C exhibits relatively weak resistance to Gram-positive and Gram-negative bacteria. It is stable against penicillinase, but can be decomposed by cephalosporinase. When hydrolyzed to remove its side chain, it yields 7-amino-cefenoic acid (7-ACA), which is an essential raw material for the production of semisynthetic cephalosporins.

Cephalosporin Canalog-1 is an analogue of Cephalosporin C, which exhibits relatively weak resistance to both Gram-positive and Gram-negative bacteria. Cephalosporin C is stable against penicillinase but can be decomposed by cephalosporinase. Through hydrolysis, its side chain can be removed to yield 7-amino-cefenoic acid (7-ACA), an essential raw material for producing semi-synthetic cephalosporins.

Cephalosporin Canalog-1 (sodium) is an analogue of Cephalosporin C, which demonstrates weak resistance against both Gram-positive and Gram-negative bacteria. It is stable to penicillinase and can be broken down by cephalosporinase. Hydrolysis removes the side chain to yield 7-amino-cefenoic acid (7-ACA), a crucial precursor for synthesizing semi-synthetic cephalosporins.

AMG 118 Immobilized cephalosporin C acylase is an enzyme in immobilized form used primarily in industrial catalysis for the production of the vital pharmaceutical intermediate, 7-aminocephalosporanic acid (7-ACA). The CPC acylase it contains is a highly specialized β-lactam acylase or peptidase capable of cleaving the amide bond within β-lactams.

AMK-EX (Immobilized cephalosporin C or 7-ACA esterase) is an immobilized enzyme where cephalosporin C/7-ACA esterases are enzymes capable of hydrolyzing cephalosporin or 7-ACA ester bonds. Immobilized enzymes involve a technique that anchors enzymes onto carriers, facilitating easy separation and recovery, while enhancing the enzyme's stability, activity, and reusability.

Cefaloridine is a first-generation semisynthetic derivative of cephalosporin C. It is unique among cephalosporins in that it exists as a zwitterion. Cephaloridine was very effective to cure pneumococcal pneumonia. It has a high clinical and bacteriologica

LB 11058 is a novel injectable cephalosporin featuring a C-3 pyridyl-substituted vinyl sulfide and a C-7 2-amino-5-chloro-1,3-thiazole group. This compound exhibits exceptional activity against Streptococcus pneumoniae and demonstrates similar efficacy against β-hemolytic streptococci. The inhibition pattern for LB 11058 with S. aureus is consistent, as all isolates are inhibited under this pattern.

Cefcapene is an orally active cephalosporin antibiotic. It is capable of inactivating chromosomally encoded class C β-lactamases. Cefcapene is applicable in antibacterial research.

ETX0282 is an orally available, broad spectrum inhibitor of class A and C β-lactamases. Entasis is developing ETX0282 in combination with cefpodoxime proxetil, an orally available cephalosporin approved for treatment of a variety of bacterial infections.