| Weight | 354.355 g/mol |
|---|---|
| Formula | C17H22O8 |
| Hydrogen Acceptors | 8 |
| Hydrogen Donors | 3 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 2 |
Fusarenone X (23255-69-8)
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- Formation of fusarenone X, nivalenol, zearalenone, alpha-trans-zearalenol, beta-trans-zearalenol, and fusarin C by Fusarium crookwellense. (Applied and Environmental Microbiology, 1988)
- Differential-pulse polarography of trichothecene mycotoxins : Determination of Deoxynivalenol, Nivalenol and Fusarenone-X in Maize (Analytica Chimica Acta, 1984)
- Production of Nivalenol and Fusarenone-X by Fusarium tricinctum Fn-2B on a Rice Substrate. (Applied and Environmental Microbiology, 1984)
- Biosynthesis, isolation, purification and separation of nivalenol, fusarenone X and zearalenone (Mycotoxin Research, 1991)
- Nivalenol and fusarenone X in kernels of maize hybrids inoculated with Fusarium poae [Peck] Wollenw. (1994)
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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)OC(=O)C)C)CO
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InChIKeyXGCUCFKWVIWWNW-UHFFFAOYSA-N
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