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15-Acetoxyscirpenol (CAS 2623-22-5)

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Alternate Names:
15-Acetoxyscirpen-3,4-diol
Application:
15-Acetoxyscirpenol is a trichothecene mycotoxin and an apoptosis inducer
CAS Number:
2623-22-5
Molecular Weight:
324.37
Molecular Formula:
C17H24O6
Supplemental Information:
This is as a Dangerous Good for transport and may be subject to additional shipping charges.
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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15-Acetoxy Scirpenol, a trichothecene mycotoxin exhibits the ability to induce apoptotic cell death in human Jurkat T cells. It is also known as 15-Acetoxyscirpenol, which is classified as a trichothecene mycotoxin and an apoptosis inducer. Furthermore, another trichothecene mycotoxin called Monoacetoxyscirpenol, also referred to as 4-deacetylanguidin or 15-acetylscirpenetriol, falls within the category of organic compounds known as trichothecenes. These compounds are characterized by the presence of an epoxide ring and a benzopyran derivative, which may have varying numbers of hydroxyl, acetyl, or other substituents.


15-Acetoxyscirpenol (CAS 2623-22-5) References

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  2. Simultaneous quantification of A-trichothecene mycotoxins in grains using liquid chromatography-atmospheric pressure chemical ionisation mass spectrometry.  |  Razzazi-Fazeli, E., et al. 2002. J Chromatogr A. 968: 129-42. PMID: 12236496
  3. The use of tissue culture for the detection of mycotoxins.  |  Robb, J., et al. 1990. Lett Appl Microbiol. 10: 161-5. PMID: 1366585
  4. Induction of apoptosis by disturbing mitochondrial-membrane potential and cleaving PARP in Jurkat T cells through treatment with acetoxyscirpenol mycotoxins.  |  Lee, DH., et al. 2006. Biol Pharm Bull. 29: 648-54. PMID: 16595895
  5. Inhibition of sodium glucose cotransporter-I expressed in Xenopus laevis oocytes by 4-acetoxyscirpendiol from Cordyceps takaomantana (anamorph = Paecilomyces tenuipes).  |  Yoo, O. and Lee, DH. 2006. Med Mycol. 44: 79-85. PMID: 16805097
  6. First Report on the Occurrence of Fusarium langsethiae Isolated from Wheat Kernels in Poland.  |  Lukanowski, A., et al. 2008. Plant Dis. 92: 488. PMID: 30769700
  7. Development of a sensitive enzyme-linked immunosorbent assay for the detection of diacetoxyscirpenol.  |  Klaffer, U., et al. 1988. Int J Food Microbiol. 6: 9-17. PMID: 3079464
  8. Fusarium Species Pathogenic to Barley and Their Associated Mycotoxins.  |  Salas, B., et al. 1999. Plant Dis. 83: 667-674. PMID: 30845619
  9. Production and characterization of a monoclonal antibody to the trichothecene mycotoxin diacetoxyscirpenol.  |  Pauly, JU., et al. 1988. Biol Chem Hoppe Seyler. 369: 487-92. PMID: 3202955
  10. Combination of Extrusion and Fermentation with Lactobacillus plantarum and L. uvarum Strains for Improving the Safety Characteristics of Wheat Bran.  |  Bartkiene, E., et al. 2021. Toxins (Basel). 13: PMID: 33669853
  11. Trichothecene structure and toxicity to the green alga Chlorella pyrenoidosa.  |  Ikawa, M., et al. 1985. Toxicon. 23: 535-7. PMID: 4024150
  12. Production of 3-acetoxyscirpene-4,15-diol from anguidine (4,15-diacetoxyscirpene-3-ol) by Fusarium oxysporum f.sp. vasinfectum.  |  Claridge, CA. and Schmitz, H. 1979. Appl Environ Microbiol. 37: 693-6. PMID: 453837
  13. Structure-activity relationships and interactions among trichothecene mycotoxins as assessed by yeast bioassay.  |  Madhyastha, MS., et al. 1994. Toxicon. 32: 1147-52. PMID: 7801350
  14. Molecular phylogenetic, morphological, and mycotoxin data support reidentification of the Quorn mycoprotein fungus as Fusarium venenatum.  |  O'Donnell, K., et al. 1998. Fungal Genet Biol. 23: 57-67. PMID: 9501477

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

15-Acetoxyscirpenol, 1 mg

sc-391528
1 mg
$175.00