Date published: 2026-2-1

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Cefprozil (CAS 92665-29-7)

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Alternate Names:
Cefprozilum; Brisoral; Arzimol
Application:
Cefprozil is an antibacterial
CAS Number:
92665-29-7
Molecular Weight:
389.43
Molecular Formula:
C18H19N3O5S
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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Cefprozil, identified by CAS number 92665-29-7, is a second-generation cephalosporin that has been extensively used in microbiological research to study the dynamics of bacterial cell wall synthesis and the mechanisms of bacterial resistance. Cefprozil functions by targeting and inhibiting specific penicillin-binding proteins (PBPs), which are crucial enzymes involved in the biosynthesis of the bacterial cell wall. These PBPs catalyze the cross-linking of peptidoglycan layers that provide structural integrity to the bacterial cell wall. By binding to these PBPs, cefprozil interferes with the normal construction process of the cell wall, resulting in the weakening and eventual rupture of the wall, leading to bacterial cell lysis and death. In research contexts, cefprozil is particularly valuable for its efficacy against a broad range of Gram-positive and some Gram-negative bacteria, which allows for comparative studies on PBP target specificity and the impact of structural variations on antibiotic efficacy. Additionally, cefprozil has been employed in studies focused on the evolution of beta-lactamase enzymes, particularly those that confer resistance to cephalosporins. Through such research, insights into genetic mutations that lead to enhanced bacterial resistance are gained, aiding in the development of strategies to counteract these resistant strains and to understand the molecular basis of antibiotic action further.


Cefprozil (CAS 92665-29-7) References

  1. Development of pH-responsive polymer and citrate aqueous two-phase system for extractive bioconversion of cefprozil.  |  Chen, J., et al. 2017. Talanta. 174: 256-264. PMID: 28738576
  2. Chemometrics for resolving spectral data of cephalosporines and tracing their residue in waste water samples.  |  Yehia, AM., et al. 2019. Spectrochim Acta A Mol Biomol Spectrosc. 219: 436-443. PMID: 31063958
  3. Lipophilicity study of different cephalosporins: Computational prediction of minimum inhibitory concentration using salting-out chromatography.  |  AboulMagd, AM., et al. 2021. J Pharm Biomed Anal. 206: 114358. PMID: 34534866
  4. Proteomic analysis of Penicillin G acylases and resulting residues in semi-synthetic β-lactam antibiotics using liquid chromatography - tandem mass spectrometry.  |  Wang, Y., et al. 2022. J Chromatogr A. 1678: 463365. PMID: 35907366
  5. Quantification of 16 cephalosporins in the aquatic environment by liquid chromatography-tandem mass spectrometry.  |  Kaddah, MMY., et al. 2022. J Sep Sci. 45: 4052-4069. PMID: 36095323
  6. Heterologous expression, purification, and characterization of thermo- and alkali-tolerant laccase-like multicopper oxidase from Bacillus mojavensis TH309 and determination of its antibiotic removal potential.  |  Adigüzel, AO., et al. 2023. Arch Microbiol. 205: 287. PMID: 37454356
  7. Aquasomes nanoformulation for controlled release of drug and improved effectiveness against bacterial infections.  |  Shanmugam, B. and Srinivasan, UM. 2024. Ther Deliv. 15: 95-107. PMID: 38174590
  8. Identification and characterization of domain-specific inhibitors of DENV NS3 and NS5 proteins by in silico screening methods.  |  Samuel, J., et al. 2024. J Biomol Struct Dyn. 1-15. PMID: 38334186

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Cefprozil, 10 mg

sc-211046
10 mg
$205.00