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Cefteram Pivoxil (CAS 82547-81-7)

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Alternate Names:
Tomiron
Application:
Cefteram Pivoxil is a third generation cephalosporin antibiotic and antibacterial
CAS Number:
82547-81-7
Molecular Weight:
593.64
Molecular Formula:
C22H27N9O7S2
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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Cefteram Pivoxil, with the CAS number 82547-81-7, is an esterified prodrug form of the cephalosporin antibiotic cefteram. This chemical modification enhances the oral bioavailability of the compound. Once administered, cefteram pivoxil is metabolized in the body to release cefteram, which is the active moiety. Cefteram exerts its antibacterial action primarily through the inhibition of bacterial cell wall synthesis, a critical process for bacterial cell viability. It achieves this by binding to specific penicillin-binding proteins (PBPs) located inside the bacterial cell wall. These PBPs play a crucial role in the final stages of assembling the bacterial cell wall and in reshaping during cell growth and division. By inhibiting these proteins, cefteram disrupts the cell wall synthesis, leading to cell lysis and bacterial death. In research settings, cefteram pivoxil has been extensively utilized to study the pharmacokinetics and dynamics of prodrug conversion in cephalosporins, offering insights into how esterification can be used to enhance drug delivery and absorption. Furthermore, research involving this compound has contributed to understanding the spectrum of activity against various bacterial pathogens and the mechanisms underlying resistance to cephalosporin antibiotics. Such studies are pivotal in guiding the development of next-generation cephalosporins to combat resistant bacterial strains effectively.


Cefteram Pivoxil (CAS 82547-81-7) References

  1. Effect of antacid pretreatment on the pharmacokinetics of AS-924, a novel ester-type cephem antibiotic--comparison with cefteram-pivoxil.  |  Totsuka, K., et al. 2001. Int J Antimicrob Agents. 18: 477-82. PMID: 11711264
  2. Antimicrobial activities of six new oral cephem antibiotics.  |  Chang, SC., et al. 1990. J Formos Med Assoc. 89: 661-5. PMID: 1981227
  3. Synthesis and oral activity of ME1207, a new orally active cephalosporin.  |  Sakagami, K., et al. 1990. J Antibiot (Tokyo). 43: 1047-50. PMID: 2211357
  4. Antimicrobial activity and stability to beta-lactamase of BMY-28271, a new oral cephalosporin ester.  |  Matsui, H., et al. 1990. Antimicrob Agents Chemother. 34: 555-61. PMID: 2344162
  5. Some Pharmacodynamic Aspects of Cefepime.  |  Elsayed, MG., et al. 2013. J Pharm (Cairo). 2013: 381910. PMID: 26555975
  6. In vitro activity of cefteram against predominantly enteropathogenic and glucose nonfermentative gram-negatives.  |  Hohl, P., et al. 1989. Chemotherapy. 35: 242-5. PMID: 2766865
  7. [The influence of cefteram pivoxil on the intestinal bacterial flora].  |  Iwata, S., et al. 1989. Jpn J Antibiot. 42: 1761-79. PMID: 2810740
  8. Impurity profiling of Cefteram pivoxil based on Fourier transform ion cyclotron resonance MS.  |  Yue, Y., et al. 2020. J Pharm Biomed Anal. 191: 113591. PMID: 32889346
  9. Efficacy of CS-834 against experimental pneumonia caused by penicillin-susceptible and -resistant Streptococcus pneumoniae in mice.  |  Fukuoka, T., et al. 1998. Antimicrob Agents Chemother. 42: 23-7. PMID: 9449255
  10. Effects of fluoroquinolones on experimental pneumonia caused by penicillin-resistant Streptococcus pneumoniae in mice.  |  Tamada and Sadao, et al. 1998. Journal of Infection and Chemotherapy. 4.3: 116-120.

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Cefteram Pivoxil, 5 mg

sc-211047
5 mg
$400.00