Date published: 2025-12-7

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Cefotetan (CAS 69712-56-7)

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Alternate Names:
(6R,7S)-7-[[[4-(2-Amino-1-carboxy-2-oxoethylidene)-1,3-dithietan-2-yl]carbonyl]amino]-7-methoxy-3-[[(1-methyl-1H-tetrazol-5-yl)thio]methyl]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic Acid; Apacef
Application:
Cefotetan is an antibiotic related to Cephalosporin used to treat bacterial infections
CAS Number:
69712-56-7
Molecular Weight:
575.62
Molecular Formula:
C17H17N7O8S4
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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Cefotetan, a second-generation cephalosporin antibiotic, has been a subject of extensive scientific research due to its potent antimicrobial activity and unique mechanism of action. Recent studies have explaind its mechanism, revealing its ability to inhibit bacterial cell wall synthesis by binding to penicillin-binding proteins (PBPs). Cefotetan targets specific PBPs, particularly PBP3, which plays a crucial role in the final stages of peptidoglycan synthesis during bacterial cell wall assembly. By binding to PBP3, cefotetan disrupts the cross-linking of peptidoglycan chains, leading to weakened bacterial cell walls and eventual cell lysis. This mechanism confers broad-spectrum activity against a wide range of Gram-positive and Gram-negative bacteria, including many clinically relevant pathogens. Moreover, cefotetan has been investigated for its potential applications in combination therapies and synergistic interactions with other antibiotics. Additionally, researchers have utilized cefotetan as a tool compound in microbiology research, facilitating the study of bacterial cell wall biosynthesis and mechanisms of antibiotic resistance. Its potent antimicrobial activity and unique mechanism make cefotetan a valuable asset in antimicrobial research, offering insights into bacterial cell biology and potential strategies for combating antibiotic-resistant infections.


Cefotetan (CAS 69712-56-7) References

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  2. Activities of cefoxitin and cefotetan against Mycobacterium fortuitum infections in mice.  |  Saito, H., et al. 1984. Antimicrob Agents Chemother. 26: 270-1. PMID: 6592999
  3. Comparison of cefoxitin, cefotetan, and ampicillin/sulbactam as prophylaxis for polymicrobial infection in mice.  |  Brook, I. 1995. Clin Infect Dis. 20 Suppl 2: S376-7. PMID: 7548603
  4. Comparison of cefoxitin, cefotetan and the combination of ampicillin with sulbactam in the therapy of polymicrobial infection in mice.  |  Brook, I. 1994. J Antimicrob Chemother. 34: 791-6. PMID: 7706175
  5. Prophylaxis of and therapy for polymicrobial infection in mice with cefoxitin, cefotetan, and cefmetazole.  |  Brook, I. 1993. Clin Infect Dis. 16 Suppl 4: S425-6. PMID: 8324161
  6. Use of cephalosporins for prophylaxis and therapy of polymicrobial infection in mice.  |  Brook, I. 1993. Antimicrob Agents Chemother. 37: 1531-5. PMID: 8363386
  7. In-vitro susceptibility and in-vivo efficacy of antimicrobials in the treatment of intraabdominal sepsis in mice.  |  Brook, I. and Gillmore, JD. 1993. J Antimicrob Chemother. 31: 393-401. PMID: 8486573
  8. Persistence of vancomycin-resistant Enterococcus faecium gastrointestinal tract colonization in antibiotic-treated mice.  |  Dever, LL. and Handwerger, S. 1996. Microb Drug Resist. 2: 415-21. PMID: 9158812
  9. Bacterial filamentation of Yersinia pestis by beta-lactam antibiotics in experimentally infected mice.  |  Davis, KJ., et al. 1997. Arch Pathol Lab Med. 121: 865-8. PMID: 9278616
  10. Antibiotic treatment of experimental pneumonic plague in mice.  |  Byrne, WR., et al. 1998. Antimicrob Agents Chemother. 42: 675-81. PMID: 9517950

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Cefotetan, 10 mg

sc-391583
10 mg
$320.00