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ProductsBack/Nivalenol [23282-20-4]

Nivalenol [23282-20-4]

Research Use Only
N3584
LKT Laboratories
Estimated Purity≥99%, TLC
Product group Chemicals
€ 241,00
1 mg
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Overview

  • Supplier
    LKT Laboratories
  • Product Name
    Nivalenol [23282-20-4]
  • Delivery Days Customer
    7
  • Certification
    Research Use Only
  • Estimated Purity
    ≥99%, TLC
  • Format
    DMSO, Methanol, dichloromethane. Slightly soluble in water.
  • Scientific Description
    Trichothecene mycotoxin produced by Fusarium; peptide chain initiation inhibitor.
  • Storage Instruction
    -20°C
  • UNSPSC
    12352200

References

  • Alassane-Kpembi I, Kolf-Clauw M, Gauthier T, et al. New insights into mycotoxin mixtures: the toxicity of low doses of Type B trichothecenes on intestinal epithelial cells is synergistic. Toxicol Appl Pharmacol. 2013 Oct 1;272(1):191-8. PMID: 23735874. Wu W, Flannery BM, Sugita-Konishi Y, et al. Comparison of murine anorectic responses to the 8-ketotrichothecenes 3-acetyldeoxynivalenol, 15-acetyldeoxynivalenol, fusarenon X and nivalenol. Food Chem Toxicol. 2012 Jun;50(6):2056-61. PMID: 22465835. Nagashima H, Kushiro M, Nakagawa H. Nuclear factor-kappaB inhibitors alleviate nivalenol-induced cytotoxicity in HL60 cells. Environ Toxicol Pharmacol. 2011 Jan;31(1):258-61. PMID: 21787693. Marzocco S, Russo R, Bianco G, et al. Pro-apoptotic effects of nivalenol and deoxynivalenol trichothecenes in J774A.1 murine macrophages. Toxicol Lett. 2009 Aug 25;189(1):21-6. PMID: 19410639. Nasri T, Bosch RR, Voorde St, et al. Differential induction of apoptosis by type A and B trichothecenes in Jurkat T-lymphocytes. Toxicol In Vitro. 2006 Sep;20(6):832-40. PMID: 16472964. Cundliffe E, Cannon M, Davies J. Mechanism of inhibition of eukaryotic protein synthesis by trichothecene fungal toxins. Proc Natl Acad Sci U S A. 1974 Jan;71(1):30-4. PMID: 4521056.