Date published: 2025-12-18

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Aztreonam (CAS 78110-38-0)

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Alternate Names:
Azthreonam
Application:
Aztreonam is a synthetic monocyclic β-lactam antibiotic
CAS Number:
78110-38-0
Purity:
≥96%
Molecular Weight:
435.43
Molecular Formula:
C13H17N5O8S2
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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Aztreonam, with the CAS number 78110-38-0, is a synthetic monocyclic beta-lactam antibiotic belonging to the monobactam subclass that is specifically designed to target Gram-negative bacteria. Its action mechanism is distinctively focused on inhibiting bacterial cell wall synthesis. Aztreonam achieves this by binding with high affinity to penicillin-binding protein 3 (PBP3), which plays a critical role in the synthesis of the bacterial cell wall. By interfering with PBP3′s activity, aztreonam inhibits the cross-linking of the peptidoglycan layer, which is essential for maintaining cell wall integrity. This disruption leads to the prevention of cell wall construction, culminating in bacterial cell lysis and death. In research, aztreonam is particularly valued for its stability against beta-lactamases, enzymes produced by many bacteria that degrade beta-lactam antibiotics, making it an excellent candidate for studying resistance mechanisms. Researchers utilize aztreonam to explore how bacteria evolve to resist antibiotics, examining genetic mutations and protein expression changes that confer resistance. Additionally, its unique structure compared to other beta-lactams makes aztreonam a useful tool in studying the specificity and binding dynamics of beta-lactam antibiotics with PBPs, thereby contributing to broader research into antibiotic design and bacterial resistance strategies.


Aztreonam (CAS 78110-38-0) References

  1. Effect of various antibiotics on modulation of intestinal microbiota and bile acid profile in mice.  |  Zhang, Y., et al. 2014. Toxicol Appl Pharmacol. 277: 138-45. PMID: 24657338
  2. Targeted Metabolomics Analysis Identifies Intestinal Microbiota-Derived Urinary Biomarkers of Colonization Resistance in Antibiotic-Treated Mice.  |  Obrenovich, ME., et al. 2017. Antimicrob Agents Chemother. 61: PMID: 28584146
  3. Urinary Metabolites of Green Tea as Potential Markers of Colonization Resistance to Pathogenic Gut Bacteria in Mice.  |  Obrenovich, ME., et al. 2019. Pathog Immun. 4: 271-293. PMID: 31773068
  4. Effect of the Short-Term Use of Fluoroquinolone and β-Lactam Antibiotics on Mouse Gut Microbiota.  |  Gu, SL., et al. 2020. Infect Drug Resist. 13: 4547-4558. PMID: 33376361
  5. Functional features of KPC-109, a novel 270-loop KPC-3 mutant mediating resistance to avibactam-based β-lactamase inhibitor combinations and cefiderocol.  |  Di Pilato, V., et al. 2024. Int J Antimicrob Agents. 63: 107030. PMID: 37931849
  6. The MSMEG_1586 of M. smegmatis Is a Penicillin-Interactive Enzyme That Can Potentially Hydrolyse Aztreonam and Cephalosporins.  |  Panda, AP., et al. 2023. Curr Microbiol. 81: 26. PMID: 38041782
  7. Effect of hyperbaric oxygen on the growth and susceptibility of facultatively anaerobic bacteria and bacteria with oxidative metabolism to selected antibiotics.  |  Chmelař, D., et al. 2024. Folia Microbiol (Praha). 69: 101-108. PMID: 38100018
  8. Unveiling distinct genetic features in multidrug-resistant Escherichia coli isolated from mammary tissue and gut of mastitis induced mice.  |  Hoque, MN., et al. 2024. Heliyon. 10: e26723. PMID: 38434354
  9. Characterization of β-lactamase and virulence genes in Pseudomonas aeruginosa isolated from clinical, environmental and poultry sources in Bangladesh.  |  Islam, R., et al. 2024. PLoS One. 19: e0296542. PMID: 38626002
  10. Iron efflux by IetA enhances β-lactam aztreonam resistance and is linked to oxidative stress through cellular respiration in Riemerella anatipestifer.  |  Liu, M., et al. 2024. J Antimicrob Chemother. 79: 1385-1396. PMID: 38629469

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Aztreonam, 10 mg

sc-210856
10 mg
$150.00