Date published: 2025-12-18

1-800-457-3801

SCBT Portrait Logo
Seach Input

Altenusin (CAS 31186-12-6)

0.0(0)
Write a reviewAsk a question

Alternate Names:
MS 341
Application:
Altenusin is an antifungal penicillide and strong pp60c-Src inhibitor
CAS Number:
31186-12-6
Purity:
≥97%
Molecular Weight:
290.3
Molecular Formula:
C15H14O6
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

QUICK LINKS

Altenusin is a naturally occurring bibenzyl compound initially isolated from various fungal species, including Alternaria species. It exhibits intriguing biological activities due to its unique structural features. Chemically, altenusin is characterized by two connected aromatic rings, which contribute to its potent biological properties. The molecular structure includes hydroxyl groups that play a crucial role in its interaction with various biological substrates. In scientific research, altenusin has primarily been explored for its ability to interfere with certain biochemical pathways. Specifically, it acts as an inhibitor of DNA methyltransferase, an enzyme responsible for adding methyl groups to the DNA molecule, which is crucial for gene expression regulation. This mechanism of action makes altenusin a valuable tool in epigenetic studies, where it is used to understand the role of DNA methylation in gene expression. Furthermore, altenusin has been found to inhibit the synthesis of melanin in vitro, which has prompted studies into its role in cellular pigment processes. Its impact on melanin synthesis suggests potential applications in understanding pigment formation and regulation at the molecular level. The research into altenusin is a vibrant field that contributes significantly to the broader understanding of molecular interactions and enzymatic regulation in biological systems.


Altenusin (CAS 31186-12-6) References

  1. Alutenusin, a specific neutral sphingomyelinase inhibitor, produced by Penicillium sp. FO-7436.  |  Uchida, R., et al. 1999. J Antibiot (Tokyo). 52: 572-4. PMID: 10470682
  2. Studies in the biochemistry of micro-organisms. 103. Metabolites of Alternaria tenuis auct; culture filtrate products.  |  ROSETT, T., et al. 1957. Biochem J. 67: 390-400. PMID: 13479395
  3. Studies in the biosynthesis of fungal metabolites. 4. Alternariol monomethyl ether and its relation to other phenolic metabolites of Alternaria tenuis.  |  THOMAS, R. 1961. Biochem J. 80: 234-40. PMID: 13776530
  4. Isolation, structure, and HIV-1-integrase inhibitory activity of structurally diverse fungal metabolites.  |  Singh, SB., et al. 2003. J Ind Microbiol Biotechnol. 30: 721-31. PMID: 14714192
  5. HIV-1 integrase inhibitors: 2003-2004 update.  |  Dayam, R., et al. 2006. Med Res Rev. 26: 271-309. PMID: 16496343
  6. Altenusin, a biphenyl isolated from the endophytic fungus Alternaria sp., inhibits trypanothione reductase from Trypanosoma cruzi.  |  Cota, BB., et al. 2008. FEMS Microbiol Lett. 285: 177-82. PMID: 18557945
  7. The Polyphenol Altenusin Inhibits in Vitro Fibrillization of Tau and Reduces Induced Tau Pathology in Primary Neurons.  |  Chua, SW., et al. 2017. ACS Chem Neurosci. 8: 743-751. PMID: 28067492
  8. Altenusin, a Nonsteroidal Microbial Metabolite, Attenuates Nonalcoholic Fatty Liver Disease by Activating the Farnesoid X Receptor.  |  Zheng, Z., et al. 2017. Mol Pharmacol. 92: 425-436. PMID: 28739572
  9. Altenusin, a fungal metabolite, alleviates TGF-β1-induced EMT in renal proximal tubular cells and renal fibrosis in unilateral ureteral obstruction.  |  Thipboonchoo, N., et al. 2024. Heliyon. 10: e24983. PMID: 38318047
  10. Isolation of myosin light chain kinase inhibitors from microorganisms: dehydroaltenusin, altenusin, atrovenetinone, and cyclooctasulfur.  |  Nakanishi, S., et al. 1995. Biosci Biotechnol Biochem. 59: 1333-5. PMID: 7670197

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Altenusin, 1 mg

sc-202454
1 mg
$286.00

Altenusin, 5 mg

sc-202454A
5 mg
$1020.00