Date published: 2026-4-24

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Azlocillin (CAS 37091-66-0)

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CAS Number:
37091-66-0
Molecular Weight:
461.497
Molecular Formula:
C20H23N5O6S
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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Azlocillin, a semisynthetic penicillin derivative, has been extensively studied in scientific research for its potent antimicrobial properties and its mechanism of action against bacterial pathogens. It functions by inhibiting bacterial cell wall synthesis through binding irreversibly to penicillin-binding proteins (PBPs), particularly PBP-1a and PBP-1b, which are essential enzymes involved in peptidoglycan cross-linking. This action disrupts the integrity of the bacterial cell wall, leading to cell lysis and ultimately bacterial death. Research on azlocillin has focused on elucidating its spectrum of activity against a wide range of Gram-positive and Gram-negative bacteria, including Pseudomonas aeruginosa, Enterobacter species, and Proteus mirabilis, among others. Moreover, investigations into the pharmacokinetic properties of azlocillin have been conducted to optimize dosing regimens and assess its bioavailability, distribution, metabolism, and excretion in various biological systems. Additionally, azlocillin has been utilized as a valuable tool in microbiological research to explore bacterial resistance mechanisms, characterize structure-activity relationships of β-lactam antibiotics, and develop strategies to combat antimicrobial resistance. Ongoing research endeavors continue to delve into the pharmacological and microbiological aspects of azlocillin, aiming to expand its utility in the fight against infectious diseases and address emerging challenges posed by antibiotic resistance.


Azlocillin (CAS 37091-66-0) References

  1. Comparative in vitro activity of azlocillin, ampicillin, mezlocillin, piperacillin, and ticarcillin, alone and in combination with an aminoglycoside.  |  White, GW., et al. 1979. Antimicrob Agents Chemother. 15: 540-3. PMID: 111616
  2. Azlocillin: in vitro studies of a new semisynthetic penicillin.  |  Stewart, D. and Bodey, GP. 1977. Antimicrob Agents Chemother. 11: 865-70. PMID: 18083
  3. Comparative efficacy of ciprofloxacin, azlocillin, imipenem/cilastatin and tobramycin in a model of experimental septicemia due to Pseudomonas aeruginosa in neutropenic mice.  |  Ulrich, E., et al. 1989. Infection. 17: 311-5. PMID: 2599653
  4. Synergy of ciprofloxacin and azlocillin in vitro and in a neutropenic mouse model of infection.  |  Chin, NX., et al. 1986. Eur J Clin Microbiol. 5: 23-8. PMID: 2938945
  5. Control of Pseudomonas sepsis in mice with azlocillin combined with gentamicin.  |  Polívková, L. and Holá, V. 1986. Czech Med. 9: 200-2. PMID: 3102185
  6. In vitro selection of DNA aptamers and their integration in a competitive voltammetric biosensor for azlocillin determination in waste water.  |  Chinnappan, R., et al. 2020. Anal Chim Acta. 1101: 149-156. PMID: 32029106
  7. Comparison of the antibacterial activity of azlocillin and ticarcillin in vitro and in irradiated neutropenic mice.  |  van der Voet, GB., et al. 1985. J Antimicrob Chemother. 16: 605-13. PMID: 3935638
  8. Evaluation of azlocillin in vitro and in discriminative animal models of infection.  |  Scheld, WM., et al. 1983. J Antimicrob Chemother. 11 Suppl B: 51-68. PMID: 6619033
  9. Excretion of azlocillin and mezlocillin by the normal pancreas and in acute pancreatitis in dogs and rats.  |  Demol, P., et al. 1983. Digestion. 27: 93-9. PMID: 6628842
  10. In vitro activity of azlocillin, metronidazole and its hydroxy metabolite against anaerobes. Bacteriostatic synergism studies.  |  Werner, H., et al. 1983. Arzneimittelforschung. 33: 574-7. PMID: 6683537

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Azlocillin, 10 g

sc-337545
10 g
$1400.00