| Weight | 296.319 g/mol |
|---|---|
| Formula | C15H20O6 |
| Hydrogen Acceptors | 6 |
| Hydrogen Donors | 3 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 1 |
DEOXYNIVALENOL (51481-10-8)
Score:
#591 in Biology
,
#627 in Chemistry
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- Sigma-Aldrich - DEOXYNIVALENOL82.90 - 495.50 USD
- Fisher Scientific - Search for DEOXYNIVALENOL
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- Invited Review: TOXICOLOGY OF DEOXYNIVALENOL (VOMITOXIN) (Journal of Toxicology and Environmental Health, 1996)
- Toxicology of deoxynivalenol (Vomitoxin) (Journal of Toxicology and Environmental Health, 1996)
- Deoxynivalenol: Toxicology and Potential Effects on Humans (Journal of Toxicology and Environmental Health-part B-critical Reviews, 2005)
- Deoxynivalenol: mechanisms of action, human exposure, and toxicological relevance (Archives of Toxicology, 2010)
- Detoxification of the Fusarium mycotoxin deoxynivalenol by a UDP-glucosyltransferase from Arabidopsis thaliana. (Journal of Biological Chemistry, 2003)
- Worldwide contamination of cereals by the Fusarium mycotoxins nivalenol, deoxynivalenol, and zearalenone. 1. Survey of 19 countries (Journal of Agricultural and Food Chemistry, 1988)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCC1=CC2C(C(C1=O)O)(C3(CC(C(C34CO4)O2)O)C)CO
-
InChIKeyLINOMUASTDIRTM-UHFFFAOYSA-N
- Pubchem - DEOXYNIVALENOL
- Wikipedia - deoxynivalenol
Vomitoxin, also known as deoxynivalenol (DON), is a type B trichothecene, an epoxy-sesquiterpenoid. This mycotoxin occurs predominantly in grains such as wheat, barley, oats, rye, and corn, and less often in rice, sorghum, and triticale. The occurrence of deoxynivalenol is associated primarily with Fusarium graminearum (Gibberella zeae) and F.
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