Date published: 2025-12-5

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Aspinonene (CAS 157676-96-5)

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Application:
Aspinonene is a multifunctional epoxide fungal metabolite
CAS Number:
157676-96-5
Molecular Weight:
188.2
Molecular Formula:
C9H16O4
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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Aspinonene is characterized by its unique molecular structure which includes multiple ring systems and a diverse set of functional groups that contribute to its complex chemical behavior. This compound is part of a broader class of organic compounds known as terpenes, which are widely studied for their extensive roles in natural processes and their applications in non-medical research fields. The mechanisms of action of aspinonene are largely defined by its ability to participate in biochemical signaling pathways within plants, influencing various physiological responses such as growth, defense, and adaptation to environmental stresses. In research contexts, aspinonene has been utilized as a model compound to explore the synthesis and function of sesquiterpenes, providing insights into the ecological roles of these compounds in plant biology and interactions within ecosystems. Moreover, studies involving aspinonene contribute to the understanding of terpene biosynthesis, a crucial area in plant biochemistry that has implications for biotechnology and agricultural sciences. By investigating the pathways and enzymes involved in aspinonene synthesis, researchers can develop better strategies for enhancing crop resistance and understanding plant resilience, making aspinonene a valuable tool in non-medical scientific inquiries and applications in fields such as environmental science and green chemistry.


Aspinonene (CAS 157676-96-5) References

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  2. Pentaketides relating to aspinonene and dihydroaspyrone from a marine-derived fungus, Aspergillus ostianus.  |  Kito, K., et al. 2007. J Nat Prod. 70: 2022-5. PMID: 17994702
  3. Triggering cryptic natural product biosynthesis in microorganisms.  |  Scherlach, K. and Hertweck, C. 2009. Org Biomol Chem. 7: 1753-60. PMID: 19590766
  4. Nine new and five known polyketides derived from a deep sea-sourced Aspergillus sp. 16-02-1.  |  Chen, XW., et al. 2014. Mar Drugs. 12: 3116-37. PMID: 24871461
  5. Extending the 'One Strain Many Compounds' (OSMAC) Principle to Marine Microorganisms.  |  Romano, S., et al. 2018. Mar Drugs. 16: PMID: 30041461
  6. Aspergillus ochraceus: Metabolites, Bioactivities, Biosynthesis, and Biotechnological Potential.  |  Hareeri, RH., et al. 2022. Molecules. 27: PMID: 36235292
  7. Deciphering mechanisms of production of natural compounds using inducer-producer microbial consortia.  |  Gasparek, M., et al. 2023. Biotechnol Adv. 64: 108117. PMID: 36813010
  8. Phytochemical analysis and anti-infective potential of fungal endophytes isolated from Nigella sativa seeds.  |  Shady, NH., et al. 2023. BMC Microbiol. 23: 343. PMID: 37974074
  9. OSMAC Strategy: A promising way to explore microbial cyclic peptides.  |  Zhang, Y., et al. 2024. Eur J Med Chem. 268: 116175. PMID: 38377824
  10. Secondary metabolites by chemical screening, 28. Aspinonene, a new multifunctional fungal metabolite  |  Fuchser, J., et al. 1994. Liebigs Annalen der Chemie. 1994(8): 831-835.

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Aspinonene, 1 mg

sc-202068
1 mg
$175.00

Aspinonene, 5 mg

sc-202068A
5 mg
$693.00