Date published: 2026-1-19

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Corynecin I (CAS 4423-58-9)

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Alternate Names:
Dechlorochloramphenicol
Application:
Corynecin I is a chloramphenicol-like acyl nitrophenylpropylamine
CAS Number:
4423-58-9
Molecular Weight:
254.24
Molecular Formula:
C11H14N2O5
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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Corynecin I is an antibiotic produced by Corynebacterium spp., noted for its role in microbiological and biochemical research. The mechanism of action of Corynecin I involves inhibiting bacterial protein synthesis by binding to the bacterial ribosome, thus interfering with the translation process. This inhibition prevents the formation of essential proteins needed for bacterial growth and survival. Corynecin I has been used extensively in studies focusing on understanding the dynamics of protein synthesis and the specific interactions between antibiotics and ribosomal subunits. Researchers have employed Corynecin I to investigate bacterial resistance mechanisms, particularly how mutations in ribosomal RNA or proteins can confer resistance to antibiotics. Advanced techniques such as X-ray crystallography and cryo-electron microscopy have been utilized to explain the detailed structure of ribosomal complexes bound with Corynecin I, providing insights into its binding sites and the conformational changes induced upon binding. Additionally, Corynecin I serves as a model compound in studies aiming to design new antibiotics with improved efficacy and reduced resistance. Its role in probing the fundamental aspects of ribosome function and antibiotic resistance underscores its importance in the development of novel antimicrobial agents and the broader understanding of bacterial translation mechanisms.


Corynecin I (CAS 4423-58-9) References

  1. Rhodococcus comparative genomics reveals a phylogenomic-dependent non-ribosomal peptide synthetase distribution: insights into biosynthetic gene cluster connection to an orphan metabolite.  |  Undabarrena, A., et al. 2021. Microb Genom. 7: PMID: 34241590
  2. Exploring the Diversity and Antibacterial Potentiality of Cultivable Actinobacteria from the Soil of the Saxaul Forest in Southern Gobi Desert in Mongolia.  |  Liu, SW., et al. 2022. Microorganisms. 10: PMID: 35630432
  3. iChip-Inspired Isolation, Bioactivities and Dereplication of Actinomycetota from Portuguese Beach Sediments.  |  Dos Santos, JDN., et al. 2022. Microorganisms. 10: PMID: 35889190
  4. Phylogenomics, phenotypic, and functional traits of five novel (Earth-derived) bacterial species isolated from the International Space Station and their prevalence in metagenomes.  |  Simpson, AC., et al. 2023. Sci Rep. 13: 19207. PMID: 37932283
  5. Recent Advances in Chemistry and Bioactivities of Secondary Metabolites from the Genus Acremonium.  |  Qin, Y., et al. 2024. J Fungi (Basel). 10: PMID: 38248947
  6. Biotechnological Key Genes of the Rhodococcus erythropolis MGMM8 Genome: Genes for Bioremediation, Antibiotics, Plant Protection, and Growth Stimulation.  |  Afordoanyi, DM., et al. 2023. Microorganisms. 12: PMID: 38257915
  7. Complete genome sequence of a novel Prescottella sp. R16 isolate from deep-sea sediments in the western Pacific.  |  Ma, L., et al. 2024. Front Genet. 15: 1356956. PMID: 38549861
  8. Corynecin (chloramphenicol analogs) fermentation studies: selective production of Corynecin I by Corynebacterium hydrocarboclastus grown on acetate.  |  Nakano, H., et al. 1977. Biotechnol Bioeng. 19: 1009-18. PMID: 884230
  9. Production of Corynecins by Mutants Defective in Glycolipids Synthesis and Increased in Corynecin I  |  H Nakano, F Tomita, T Suzuki. 1974. Agricultural and Biological Chemistry. 38: 2471–2475.
  10. Biosynthesis of Corynecins by Corynebacterium hydrocarboclastus: On the Origin of the N-Acyl Group Get access Arrow  |  H Nakano, F Tomita, T Suzuki. 1976. Agricultural and Biological Chemistry. 40: 331–336.

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Corynecin I, 5 mg

sc-391470
5 mg
$475.00

Corynecin I, 1 mg

sc-391470A
1 mg
$75.00