Date published: 2026-6-4

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Fusapyrone (CAS 156856-31-4)

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Application:
Fusapyrone is a broad specrum antifungal metabolite with low zoo-toxicity
CAS Number:
156856-31-4
Molecular Weight:
606.79
Molecular Formula:
C34H54O9
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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Fusapyrone is a secondary metabolite produced by the filamentous fungus Fusarium semitectum, notable for its role in chemical ecology and as a subject of interest in the study of natural products. This compound belongs to the class of alpha-pyrones, characterized by a distinctive six-membered lactone ring structure. Fusapyrone operates through a mechanism involving the inhibition of protein synthesis in competing microbial species, thereby acting as an antimicrobial agent within its ecological niche. The unique mode of action of fusapyrone is particularly significant because it targets specific stages of protein assembly, which can disrupt the overall metabolic processes of susceptible organisms. In research settings, fusapyrone has been used to explore its bioactive properties, particularly its role in interspecies microbial interactions. Studies focus on how fusapyrone and similar compounds influence microbial community dynamics, competition, and survival strategies in various environments. This research contributes to a broader understanding of the ecological roles of fungal metabolites and their potential applications in managing microbial populations. Additionally, the study of fusapyrone enhances knowledge about the biosynthesis of alpha-pyrones and their evolutionary significance in fungal defense strategies, providing insights into the complex interplay between chemical structure and biological function.


Fusapyrone (CAS 156856-31-4) References

  1. High performance liquid chromatography for the analysis of fusapyrone and deoxyfusapyrone, two antifungal alpha-pyrones from Fusarium semitectum.  |  Evidente, A., et al. 1999. Nat Toxins. 7: 133-7. PMID: 10797640
  2. Biological characterization of fusapyrone and deoxyfusapyrone, two bioactive secondary metabolites of Fusarium semitectum.  |  Altomare, C., et al. 2000. J Nat Prod. 63: 1131-5. PMID: 10978211
  3. Isolation and characterization of bioactive metabolites from marine-derived filamentous fungi collected from tropical and sub-tropical coral reefs.  |  Namikoshi, M., et al. 2000. Chem Pharm Bull (Tokyo). 48: 1452-7. PMID: 11045449
  4. Structure-activity relationships of derivatives of fusapyrone, an antifungal metabolite of Fusarium semitectum.  |  Altomare, C., et al. 2004. J Agric Food Chem. 52: 2997-3001. PMID: 15137845
  5. Isolation and structure elucidation of neofusapyrone from a marine-derived Fusarium species, and structural revision of fusapyrone and deoxyfusapyrone.  |  Hiramatsu, F., et al. 2006. J Antibiot (Tokyo). 59: 704-9. PMID: 17256469
  6. Inhibition of species of the Aspergillus section Nigri and ochratoxin a production in grapes by fusapyrone.  |  Favilla, M., et al. 2008. Appl Environ Microbiol. 74: 2248-53. PMID: 18263739
  7. Novel neofusapyrones isolated from Verticillium dahliae as potent antifungal substances.  |  Honma, M., et al. 2010. Bioorg Med Chem Lett. 20: 709-12. PMID: 19962895
  8. Resolving a Natural Product Cold Case: Elucidation of Fusapyrone Structure and Absolute Configuration and Demonstration of Their Fungal Biofilm Disrupting Properties.  |  Kil, YS., et al. 2023. J Org Chem. 88: 9167-9186. PMID: 37343240
  9. Biosynthesis of Fusapyrone Depends on the H3K9 Methyltransferase, FmKmt1, in Fusarium mangiferae.  |  Atanasoff-Kardjalieff, AK., et al. 2021. Front Fungal Biol. 2: 671796. PMID: 37744112
  10. Fusapyrone and deoxyfusapyrone, two antifungal alpha-pyrones from Fusarium semitectum.  |  Evidente, A., et al. 1994. Nat Toxins. 2: 4-13. PMID: 8032694

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Fusapyrone, 1 mg

sc-391553
1 mg
$250.00

Fusapyrone, 5 mg

sc-391553A
5 mg
$835.00