Date published: 2025-10-1

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7-Amino-3 chloromethyl-3-cephem-4-carboxylic Acid p-Methoxybenzyl Ester Hydrochloride (CAS 113479-65-5)

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Alternate Names:
(6R,7R)-7-Amino-3-(chloromethyl)-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid (4-Methoxyphenyl)methyl ester hydrochloride
CAS Number:
113479-65-5
Molecular Weight:
405.30
Molecular Formula:
C16H18Cl2N2O4S
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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7-Amino-3 chloromethyl-3-cephem-4-carboxylic Acid p-Methoxybenzyl Ester Hydrochloride, a chemical compound, has been extensively researched for its potential applications in antimicrobial research and drug development. Its mechanism of action involves inhibition of bacterial cell wall synthesis by irreversibly binding to penicillin-binding proteins (PBPs), particularly those involved in cross-linking peptidoglycan, thereby disrupting the structural integrity of bacterial cell walls and leading to bacterial cell lysis. This mechanism makes it effective against a broad spectrum of Gram-positive and Gram-negative bacteria. In scientific research, this compound has been utilized as a tool to explain the molecular mechanisms underlying bacterial cell wall synthesis and antibiotic resistance. Additionally, it has served as a scaffold for the development of novel cephalosporin derivatives with improved pharmacokinetic properties and enhanced antimicrobial activity. Furthermore, research efforts have explored its potential synergistic effects in combination therapy regimens, aiming to overcome bacterial resistance mechanisms and enhance antimicrobial efficacy. Overall, this compound holds promise as a valuable asset in antimicrobial research, contributing to advancements in understanding bacterial physiology and the development of novel antimicrobial agents.


7-Amino-3 chloromethyl-3-cephem-4-carboxylic Acid p-Methoxybenzyl Ester Hydrochloride (CAS 113479-65-5) References

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  3. Novel fluorescent cephalosporins: synthesis, antimicrobial activity and photodynamic inactivation of antibiotic resistant bacteria.  |  Xiao, JM., et al. 2013. Eur J Med Chem. 59: 150-9. PMID: 23220643
  4. Antimicrobial Activity of Novel Synthetic Peptides Derived from Indolicidin and Ranalexin against Streptococcus pneumoniae.  |  Jindal, HM., et al. 2015. PLoS One. 10: e0128532. PMID: 26046345
  5. Novel broad-spectrum and long-acting parenteral cephalosporins having an acyl cyanamide moiety at the C-3 terminal: Synthesis and structure-activity relationships.  |  Yokoo, K., et al. 2016. Eur J Med Chem. 124: 698-712. PMID: 27639362
  6. Macrocycle-Antibiotic Hybrids: A Path to Clinical Candidates.  |  Surur, AS. and Sun, D. 2021. Front Chem. 9: 659845. PMID: 33996753
  7. β-Lactamase-Responsive Hydrogel Drug Delivery Platform for Bacteria-Triggered Cargo Release.  |  Alkekhia, D., et al. 2022. ACS Appl Mater Interfaces. 14: 27538-27550. PMID: 35675049
  8. In Vitro and In Vivo Development of a β-Lactam-Metallo-β-Lactamase Inhibitor: Targeting Carbapenem-Resistant Enterobacterales.  |  Peters, BK., et al. 2023. ACS Infect Dis. 9: 486-496. PMID: 36786013
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Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

7-Amino-3 chloromethyl-3-cephem-4-carboxylic Acid p-Methoxybenzyl Ester Hydrochloride, 10 mg

sc-210590
10 mg
$320.00