Date published: 2025-12-5

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Cefdinir (CAS 91832-40-5)

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Application:
Cefdinir is a cephalosporin antibiotic structurally similar to cefixime
CAS Number:
91832-40-5
Purity:
≥97%
Molecular Weight:
395.41
Molecular Formula:
C14H13N5O5S2
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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Cefdinir, cataloged under CAS number 91832-40-5, is a third-generation cephalosporin, notable for its broad spectrum of activity and enhanced stability against β-lactamase enzymes compared to earlier cephalosporins. Structurally, cefdinir contains a β-lactam ring, which is crucial for its antibacterial activity, and a side chain that increases its resistance to degradation by β-lactamase enzymes. The primary mechanism by which cefdinir functions involves the inhibition of bacterial cell wall synthesis. It achieves this by binding to specific penicillin-binding proteins (PBPs) within the bacterial cell wall. This binding interferes with the final transpeptidation step of peptidoglycan synthesis, which is essential for cell wall strength and integrity. As a result, the disrupted cell wall synthesis leads to bacterial cell lysis and death. In research settings, cefdinir has been employed to study the kinetics of bacterial cell wall synthesis and degradation, particularly focusing on the action of PBPs and the resistance mechanisms developed by bacteria against cephalosporins. Furthermore, investigations involving cefdinir have contributed to a deeper understanding of the molecular interactions between cephalosporins and PBPs, providing insights that are vital for the development of new antibacterial agents with improved efficacy and stability. These studies are instrumental in advancing the field of bacterial resistance and adaptation, particularly in understanding how cephalosporins can be modified to overcome resistance.


Cefdinir (CAS 91832-40-5) References

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  2. [In vitro antibacterial activity of cefdinir against isolates of respiratory tract pathogens in children].  |  Lu, Q., et al. 2004. Zhonghua Er Ke Za Zhi. 42: 697-700. PMID: 15482675
  3. RU 29 246, the active compound of the cephalosporin-prodrug-ester HR 916. I. Antibacterial activity in vitro.  |  Bauernfeind, A., et al. 1992. J Antibiot (Tokyo). 45: 505-20. PMID: 1592683
  4. Comparative in vitro activities of seven new beta-lactams, alone and in combination with beta-lactamase inhibitors, against clinical isolates resistant to third generation cephalosporins.  |  Gupta, V., et al. 2006. Braz J Infect Dis. 10: 22-5. PMID: 16767311
  5. Antibacterial activity of cefpodoxime in comparison with cefixime, cefdinir, cefetamet, ceftibuten, loracarbef, cefprozil, BAY 3522, cefuroxime, cefaclor and cefadroxil.  |  Bauernfeind, A. and Jungwirth, R. 1991. Infection. 19: 353-62. PMID: 1800377
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  7. Antibiotic effects against periodontal bacteria in organ cultured tissue.  |  Takeshita, M., et al. 2017. Clin Exp Dent Res. 3: 5-12. PMID: 29744173
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Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Cefdinir, 10 mg

sc-217854
10 mg
$150.00