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Reductiomycin (CAS 68748-55-0)

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Alternate Names:
AM-6201; S 551II; (E)-4-(3-((2-Hydroxy-5-oxocyclopent-1-en-1-yl)amino)-3-oxoprop-1-en-1-yl)-2,3-dihydrofuran-2-yl acetate
Application:
Reductiomycin is an antibiotic with antimicrobial effects
CAS Number:
68748-55-0
Molecular Weight:
293.3
Molecular Formula:
C14H15NO6
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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Reductiomycin, cataloged under the CAS number 68748-55-0, is an antibiotic compound derived from the actinomycete Streptomyces. It is distinguished by a naphthoquinone core structure, which plays a crucial role in its biochemical activity. Reductiomycin exhibits a unique mechanism of action primarily through its ability to interact with DNA, where it binds irreversibly to the nucleic acid strands. This binding is believed to involve the formation of free radicals, which can cause breaks in the DNA strands, thereby inhibiting the replication and transcription processes within cells. The compound′s action is particularly noteworthy because it involves redox cycling, a process that generates reactive oxygen species (ROS) as byproducts. These ROS further contribute to its activity by causing oxidative damage to cellular components, including lipids, proteins, and nucleic acids. In research settings, reductiomycin has been utilized as a tool to study the cellular responses to oxidative stress and DNA damage. This research has provided insights into the mechanisms of cell death and survival under oxidative conditions, contributing to a broader understanding of cellular defense mechanisms against oxidative stress. By studying reductiomycin′s interactions and effects within biological systems, researchers gain valuable information on the potential impacts of oxidative agents on cells, which is essential for fields like molecular biology and genetics.


Reductiomycin (CAS 68748-55-0) References

  1. Iminonitroso Diels-Alder reactions for efficient derivatization and functionalization of complex diene-containing natural products.  |  Li, F., et al. 2007. Org Lett. 9: 2923-6. PMID: 17602642
  2. Screening, isolation, taxonomy and fermentation of an antibiotic producer Streptomyces xinghaiensis from soil capable of acting against linezolid resistant strains.  |  Kumar, KS., et al. 2012. Indian J Exp Biol. 50: 718-28. PMID: 23214266
  3. Studies on the biosynthesis of antibiotics.  |  Floss, HG., et al. 1986. J Nat Prod. 49: 957-70. PMID: 3553432
  4. Reductiomycin, a new antibiotic. I. Taxonomy, fermentation, isolation, characterization and biological activities.  |  Shimizu, K. and Tamura, G. 1981. J Antibiot (Tokyo). 34: 649-53. PMID: 7275849
  5. Reductiomycin, a new antibiotic. II. Structural elucidation by spectroscopic studies.  |  Shimizu, K. and Tamura, G. 1981. J Antibiot (Tokyo). 34: 654-7. PMID: 7275850
  6. Structure of antitumor alkaloid AM-6201.  |  Konda, Y., et al. 1981. J Antibiot (Tokyo). 34: 1222-3. PMID: 7328062
  7. Crystal and molecular structure of reductiomycin.  |  Donohue, et al. 1984. Journal of crystallographic and spectroscopic research. 14: 35-43.
  8. Biosynthesis of the antiobiotic reductiomycin.  |  Beale and John M., et al. 1986. Journal of the American Chemical Society. 108.2: 31-332.

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Reductiomycin, 1 mg

sc-203235
1 mg
$90.00

Reductiomycin, 5 mg

sc-203235A
5 mg
$360.00