| Weight | 312.318 g/mol |
|---|---|
| Formula | C15H20O7 |
| Hydrogen Acceptors | 7 |
| Hydrogen Donors | 4 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 1 |
NIVALENOL (23282-20-4)
Score:
#279 in Biochemistry
,
#1067 in Biology
,
#1195 in Chemistry
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- Worldwide contamination of cereals by the Fusarium mycotoxins nivalenol, deoxynivalenol, and zearalenone. 1. Survey of 19 countries (Journal of Agricultural and Food Chemistry, 1988)
- Tri13 and Tri7 Determine Deoxynivalenol- and Nivalenol-Producing Chemotypes of Gibberella zeae (Applied and Environmental Microbiology, 2002)
- Identification of deoxynivalenol- and nivalenol-producing chemotypes of Gibberella zeae by using PCR. (Applied and Environmental Microbiology, 2001)
- Comparative cytotoxicity of deoxynivalenol, nivalenol, their acetylated derivatives and de-epoxy metabolites (Food and Chemical Toxicology, 2004)
- Toxicity and apoptosis induced by the mycotoxins nivalenol, deoxynivalenol and fumonisin B1 in a human erythroleukemia cell line (Toxicology in Vitro, 2004)
- Evaluation of the intestinal absorption of deoxynivalenol and nivalenol by an in vitro gastrointestinal model, and the binding efficacy of activated carbon and other adsorbent materials (Food and Chemical Toxicology, 2004)
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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(C(C(C(C34CO4)O2)O)O)C)CO
-
InChIKeyUKOTXHQERFPCBU-UHFFFAOYSA-N
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