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Reveromycin B (CAS 144860-68-4)

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Application:
Reveromycin B is a novel polyketide type antibiotic shown inhibit mitogenic activity
CAS Number:
144860-68-4
Purity:
>90%
Molecular Weight:
660.8
Molecular Formula:
C36H52O11
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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Reveromycin B, with the CAS number 144860-68-4, is a member of the reveromycin class of compounds, which are isolated from the fermentation broth of various Streptomyces species. This compound is characterized by a spiroacetal enol ether structure, which is essential for its biological activity. The primary mechanism of action of Reveromycin B involves the inhibition of isoleucyl-tRNA synthetase, an enzyme critical for protein synthesis. By specifically targeting this enzyme, Reveromycin B disrupts the incorporation of the amino acid isoleucine into proteins, which impedes protein production and affects cell growth and proliferation. This specific inhibition makes it a useful tool for researchers studying the role of aminoacyl-tRNA synthetases in protein synthesis and cellular metabolism. In research environments, Reveromycin B has been employed to probe the effects of inhibited protein synthesis on cellular processes, particularly in the context of cell cycle regulation and apoptosis. Studies using this compound help explain the complex balance of protein synthesis and its impact on cell behavior, providing insights into the fundamental mechanisms that govern cellular growth and death. Through these investigations, Reveromycin B contributes to a deeper understanding of molecular biology and biochemistry, especially in deciphering how cells manage protein synthesis under various physiological and pathological conditions.


Reveromycin B (CAS 144860-68-4) References

  1. Enantioselective synthesis of the [6,6] spiroketal core of reveromycin A.  |  Drouet, KE., et al. 2000. Org Lett. 2: 207-10. PMID: 10814283
  2. Total synthesis of reveromycin A.  |  Shimizu, T., et al. 2000. Org Lett. 2: 2153-6. PMID: 10891254
  3. Stereoselective total synthesis of reveromycin B and C19-epi-reveromycin B.  |  Drouet, KE. and Theodorakis, EA. 2000. Chemistry. 6: 1987-2001. PMID: 10894398
  4. Identification of Saccharomyces cerevisiae isoleucyl-tRNA synthetase as a target of the G1-specific inhibitor Reveromycin A.  |  Miyamoto, Y., et al. 2002. J Biol Chem. 277: 28810-4. PMID: 12050165
  5. Chemical modification of reveromycin A and its biological activities.  |  Shimizu, T., et al. 2002. Bioorg Med Chem Lett. 12: 3363-6. PMID: 12419362
  6. Reveromycins, new inhibitors of eukaryotic cell growth. I. Producing organism, fermentation, isolation and physico-chemical properties.  |  Takahashi, H., et al. 1992. J Antibiot (Tokyo). 45: 1409-13. PMID: 1429225
  7. Reveromycins, new inhibitors of eukaryotic cell growth. II. Biological activities.  |  Takahashi, H., et al. 1992. J Antibiot (Tokyo). 45: 1414-9. PMID: 1429226
  8. Reveromycins, new inhibitors of eukaryotic cell growth. III. Structures of reveromycins A, B, C and D.  |  Koshino, H., et al. 1992. J Antibiot (Tokyo). 45: 1420-7. PMID: 1429227
  9. Reveromycins revealed: new polyketide spiroketals from Australian marine-derived and terrestrial Streptomyces spp. A case of natural products vs. artifacts.  |  Fremlin, L., et al. 2011. Org Biomol Chem. 9: 1201-11. PMID: 21152660
  10. Identification and delineation of action mechanism of antifungal agents: Reveromycin E and its new derivative isolated from Streptomyces sp. JCK-6141.  |  Nguyen and Hang Thi Thu, et al. 2021. Postharvest Biology and Technology. 182: 111700.

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Reveromycin B, 250 µg

sc-202315
250 µg
$390.00