Date published: 2026-2-14

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Leucomycins (CAS 1392-21-8)

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CAS Number:
1392-21-8
Molecular Weight:
785.96
Molecular Formula:
C40H67NO14
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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Leucomycins, also known as Kitasamycins, are a group of macrolide antibiotics that have been extensively used in scientific research to study their antibacterial mechanisms and broader biological effects. These compounds function primarily by binding to the 50S ribosomal subunit of susceptible bacteria, inhibiting protein synthesis by blocking the translocation step in mRNA translation. This interaction prevents the growth of bacteria by disrupting their ability to produce essential proteins, making leucomycins valuable tools for studying the ribosomal function and antibiotic interaction. In research settings, leucomycins are used to explore the intricacies of ribosome structure and function, particularly how modifications to ribosomal RNA or proteins can confer resistance to macrolide antibiotics. These studies are crucial for understanding the development of bacterial resistance and for designing new antibiotics that can overcome these resistance mechanisms. Additionally, leucomycins are employed in investigations of microbial ecology, where their impact on bacterial communities within various environments can provide insights into the natural roles of antibiotics and the evolutionary pressures that shape microbial populations. Furthermore, leucomycins have been used in gene expression studies, particularly in systems where bacterial genes are modified to be sensitive or resistant to these antibiotics, allowing researchers to control gene expression through antibiotic administration. This application facilitates the study of gene function and regulation in a controlled manner, enhancing our understanding of bacterial genetics and the potential for genetic manipulation. Through these diverse research applications, leucomycins contribute significantly to the field of microbiology and molecular biology, advancing knowledge in antibiotic action and microbial dynamics.


Leucomycins (CAS 1392-21-8) References

  1. Effect of leucomycins and analogues on binding [14C ]erythromycin to Escherichia coli ribosomes.  |  Pestka, S., et al. 1974. Antimicrob Agents Chemother. 6: 606-12. PMID: 15825314
  2. The effect of surfactant on fermentation of kitasamycin in Streptomyces kitasatoensis.  |  Zheng, Q. and Gao, S. 2016. Biotechnol Appl Biochem. 63: 895-900. PMID: 26339801
  3. 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
  4. Quantitative analysis of impurities in leucomycin bulk drugs and tablets: A high performance liquid chromatography-charged aerosol detection method and its conversion to ultraviolet detection method.  |  Liu, G., et al. 2021. J Pharm Biomed Anal. 202: 114148. PMID: 34052548
  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. A green and rapid analytical method for determination of kitasamycin in animal feedstuffs by ultra-high performance liquid chromatography tandem mass spectrometry.  |  Xu, F., et al. 2022. J Chromatogr A. 1676: 463203. PMID: 35753112
  7. Novel dimeric derivatives of leucomycins and tylosin, sixteen-membered macrolides.  |  Omura, S., et al. 1982. J Med Chem. 25: 271-5. PMID: 7040661
  8. Binding of [3H]tetrahydroleucomycin A3 to Escherichia coli ribosomes and the effect of 3'-O-acyl derivatives of leucomycins on the binding.  |  Omura, S., et al. 1982. J Antibiot (Tokyo). 35: 491-6. PMID: 7047480
  9. Stimulation of leucomycin production by magnesium phosphate and its relevance to nitrogen catabolite regulation.  |  Omura, S., et al. 1980. Antimicrob Agents Chemother. 18: 691-5. PMID: 7447425
  10. Inhibition of the biosynthesis of leucomycin, a macrolide antibiotic, by cerulenin.  |  Takeshima, H., et al. 1977. J Biochem. 81: 1127-32. PMID: 881413

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Leucomycins, 5 g

sc-295356
5 g
$57.00

Leucomycins, 25 g

sc-295356A
25 g
$189.00