Date published: 2025-10-20

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Leucomycin A5 (CAS 18361-45-0)

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Alternate Names:
Kitasamycin
Application:
Leucomycin A5 is a potent macrocyclic lactone antibiotic
CAS Number:
18361-45-0
Purity:
≥95%
Molecular Weight:
771.9
Molecular Formula:
C39H65NO14
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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Leucomycin A5, a member of the macrolide antibiotic family, has been extensively studied in scientific research due to its distinctive mechanism of action and potential applications in microbiology and antimicrobial drug development. Mechanistically, Leucomycin A5 inhibits bacterial protein synthesis by binding to the 50S ribosomal subunit of bacteria, thus preventing the elongation of the peptide chain during translation. This interference disrupts bacterial growth and proliferation. Leucomycin A5′s mechanism of action sets it apart from other antibiotics and makes it effective against a wide range of gram-positive bacteria, including antibiotic-resistant strains. In research, Leucomycin A5 has been instrumental in elucidating the structural and functional properties of the bacterial ribosome, providing insights into the molecular basis of antibiotic activity and bacterial resistance mechanisms. Additionally, Leucomycin A5 has been employed as a tool in microbiological studies to investigate ribosome function, translation regulation, and bacterial physiology. Furthermore, Leucomycin A5 and its derivatives have been explored for their potential applications in drug discovery programs targeting bacterial infections and antibiotic resistance. Ongoing research continues to explore the diverse research applications of Leucomycin A5, offering promising avenues for understanding bacterial biology and developing novel antimicrobial agents.


Leucomycin A5 (CAS 18361-45-0) References

  1. High-throughput screening for multi-class veterinary drug residues in animal muscle using liquid chromatography/tandem mass spectrometry with on-line solid-phase extraction.  |  Tang, HP., et al. 2006. Rapid Commun Mass Spectrom. 20: 2565-72. PMID: 16878343
  2. Spatiotemporal heterogeneity of antibiotic pollution and ecological risk assessment in Taihu Lake Basin, China.  |  Xu, Z., et al. 2018. Sci Total Environ. 643: 12-20. PMID: 29935359
  3. Testing the efficacy of kitasamycin for use in the control and treatment of swine dysentery in experimentally infected pigs.  |  La, T., et al. 2019. Aust Vet J. 97: 452-464. PMID: 31529470
  4. Effect of kitasamycin and nitrofurantoin at subinhibitory concentrations on quorum sensing regulated traits of Chromobacterium violaceum.  |  Ibrahim, YM., et al. 2020. Antonie Van Leeuwenhoek. 113: 1601-1615. PMID: 32889593
  5. Development of a monoclonal-based ic-ELISA for the determination of kitasamycin in animal tissues and simulation studying its molecular recognition mechanism.  |  Li, L., et al. 2021. Food Chem. 363: 129465. PMID: 34247034
  6. The Antibiotic Kitasamycin-A Potential Agent for Specific Fibrosis Preventing Therapy after Fistulating Glaucoma Surgery?  |  Sterenczak, KA., et al. 2023. Pharmaceutics. 15: PMID: 36839651
  7. Functional Proteomics Analysis of Norfloxacin-Resistant Edwardsiella tarda.  |  Wu, JH., et al. 2023. J Proteome Res. 22: 3489-3498. PMID: 37856871
  8. Subtherapeutic Kitasamycin Promoted Fat Accumulation in the Longissimus Dorsi Muscle in Growing-Finishing Pigs.  |  Han, G., et al. 2024. Animals (Basel). 14: PMID: 38612296
  9. Acyl derivatives of 16-membered macrolides. I. Synthesis and biological properties of 3'-O-propionylleucomycin A5 (TMS-19-Q).  |  Sakakibara, H., et al. 1981. J Antibiot (Tokyo). 34: 1001-10. PMID: 7319915
  10. Development of a pH-paralleling approach of quantifying six-category pharmaceuticals in surface water using SPE-HPLC-MS/MS  |  Hong, B., et al. 2021. Watershed ecology and the environment. 3: 1-16.

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Leucomycin A5, 1 mg

sc-362763
1 mg
$153.00