| Weight | 296.319 g/mol |
|---|---|
| Formula | C15H20O6 |
| Hydrogen Acceptors | 6 |
| Hydrogen Donors | 3 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 1 |
Vomitoxin (51481-10-8)
Score:
#621 in Biology
,
#661 in Chemistry
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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)
- Effects of 8-week exposure of the B6C3F1 mouse to dietary deoxynivalenol (vomitoxin) and zearalenone (Food and Chemical Toxicology, 1986)
- Effect of milling and baking on deoxynivalenol (vomitoxin) content of eastern Canadian wheats (Journal of Agricultural and Food Chemistry, 1984)
- Vomitoxin-Induced Cyclooxygenase-2 Gene Expression in Macrophages Mediated by Activation of ERK and p38 but Not JNK Mitogen-Activated Protein Kinases (Toxicological Sciences, 2002)
- Rapid, Sequential Activation of Mitogen-Activated Protein Kinases and Transcription Factors Precedes Proinflammatory Cytokine mRNA Expression in Spleens of Mice Exposed to the Trichothecene Vomitoxin (Toxicological Sciences, 2003)
-
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
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