Date published: 2026-4-5

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beta-Rubromycin (CAS 27267-70-5)

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Application:
β-Rubromycin is a quinone antibiotic agent that inhibits reverse transcriptase
CAS Number:
27267-70-5
Molecular Weight:
536.45
Molecular Formula:
C27H20O12
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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β-Rubromycin, a natural anthraquinone compound isolated from Streptomyces spp., demonstrates notable biochemical significance due to its unique structural features and biological activities, primarily within the realm of scientific research. The core mechanism of action for β-Rubromycin involves its interaction with DNA through intercalation, a process where the planar molecules insert between DNA base pairs. This binding disrupts the double helical structure of DNA, affecting various biochemical pathways related to DNA replication and transcription. In research environments, β-Rubromycin has been extensively used as a tool to study these fundamental cellular processes. Furthermore, β-Rubromycin exhibits potent inhibitory effects on RNA polymerase, an enzyme critical for the transcription process. By hindering RNA synthesis, it provides a valuable mechanism for studying transcriptional regulation. This property is particularly useful in molecular biology research, where understanding the dynamics of enzyme inhibition can reveal much about gene expression control mechanisms. In addition to its primary activities, β-Rubromycin is also employed in the study of oxidative stress responses due to its generation of reactive oxygen species when intercalated within DNA. These characteristics make it an interesting subject for examining cellular responses to oxidative damage and the pathways that cells utilize to mitigate such stress.


beta-Rubromycin (CAS 27267-70-5) References

  1. Inhibition of human telomerase by rubromycins: implication of spiroketal system of the compounds as an active moiety.  |  Ueno, T., et al. 2000. Biochemistry. 39: 5995-6002. PMID: 10821671
  2. The biochemical mode of inhibition of DNA polymerase beta by alpha-rubromycin.  |  Mizushina, Y., et al. 2000. Biochim Biophys Acta. 1523: 172-81. PMID: 11042381
  3. Facile synthesis of naphthoquinone spiroketals by diastereoselective oxidative [3 + 2] cycloaddition.  |  Wu, KL., et al. 2007. Org Lett. 9: 5537-40. PMID: 18044909
  4. Anti-cancer targeting telomerase inhibitors: β-rubromycin and oleic acid.  |  Mizushina, Y., et al. 2012. Mini Rev Med Chem. 12: 1135-43. PMID: 22876944
  5. New strategies for natural products containing chroman spiroketals.  |  Green, JC., et al. 2012. Pure Appl Chem. 84: 1621-1631. PMID: 25554712
  6. Structure Determination, Functional Characterization, and Biosynthetic Implications of Nybomycin Metabolites from a Mining Reclamation Site-Associated Streptomyces.  |  Wang, X., et al. 2019. J Nat Prod. 82: 3469-3476. PMID: 31833370
  7. Chemical genetic approach using β-rubromycin reveals that a RIO kinase-like protein is involved in morphological development in Phytophthora infestans.  |  Tani, S., et al. 2020. Sci Rep. 10: 22326. PMID: 33339950
  8. Genome mining of Streptomyces sp. CB00271 as a natural high-producer of β-rubromycin and the resulting discovery of β-rubromycin acid.  |  Yi, L., et al. 2021. Biotechnol Bioeng. 118: 2243-2254. PMID: 33629382
  9. Identification of tuoromycin with beta-rubromycin.  |  De Barros Côelho, JS., et al. 1970. Farmaco Sci. 25: 721-6. PMID: 5484775

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

beta-Rubromycin, 1 mg

sc-204636
1 mg
$177.00

beta-Rubromycin, 5 mg

sc-204636A
5 mg
$712.00