D0156

Deoxynivalenol

Protein synthesis inhibitor, powder

• Synonim(y): 3α,7α,15-Trihydroxy-12,13-epoxytrichothec-9-en-8-one, Vomitoxin
• Wzór empiryczny (zapis Hilla): C₁₅H₂₀O₆
• Numer CAS: 51481-10-8
• Masa cząsteczkowa: 296.32
• UNSPSC Code: 12352200
• PubChem Substance ID: 24893213
• NACRES: NA.77
• MDL number: MFCD09039270
• Form: powder

Właściwości

• Nazwa produktu: Deoxynivalenol,
• form: powder
• Quality Segment: 300
• storage temp.: 2-8°C
• SMILES string: [H][C@]12O[C@]3([H])[C@H](O)C[C@@](C)([C@]34CO4)[C@@]1(CO)[C@H](O)C(=O)C(C)=C2
• InChI: 1S/C15H20O6/c1-7-3-9-14(5-16,11(19)10(7)18)13(2)4-8(17)12(21-9)15(13)6-20-15/h3,8-9,11-12,16-17,19H,4-6H2,1-2H3/t8-,9-,11-,12-,13-,14-,15+/m1/s1
• InChI key: LINOMUASTDIRTM-QGRHZQQGSA-N

Opis

General description

Deoxynivalenol (DON) is a natural mycotoxin found in Fusarium graminearum and Fusarium culmorum. It belongs to the B-trichothecenes family of mycotoxins.

Application

Deoxynivalenol has been used:

• as a mycotoxin to induce cytotoxicity in porcine jejunal epithelial cells and study the protective effects of Saccharomyces cerevisiae on the cell viability of host cells.[1]
• to induce toxicity in nude mice to study the effect of probiotics (Lactobacillus rhamnosus GG (LGG) or Lactobacillus acidophilus (LA)) supplementation on host protection[2]
• as a thyroid hormone receptor (TRβ) antagonist in cell-based luciferase reporter gene (CALUX) assay[3]

Biochem/physiol Actions

Deoxynivalenol (DON) blocks the synthesis of DNA and RNA by inhibiting the process of translation.

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Informacja o środkach bezpieczeństwa

• pictograms: GHS06
• signalword: Danger
• hcodes: H300
• pcodes: P264 - P270 - P301 + P310 - P405 - P501
• Hazard Classifications: Acute Tox. 2 Oral
• Klasa składowania: 6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials
• wgk: WGK 3
• flash_point_f: Not applicable
• flash_point_c: Not applicable
• ppe: Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges