| Weight | 721.838 g/mol |
|---|---|
| Formula | C34H59NO15 |
| Hydrogen Acceptors | 12 |
| Hydrogen Donors | 8 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 29 |
fumonisin b1 (116355-83-0)
fumonisin B(1) · fumonisin-B1
Score:
#1850 in Biology
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#2218 in Chemistry
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- Pulmonary Edema and Hydrothorax in Swine Produced by Fumonisin B1, a Toxic Metabolite of Fusarium Moniliforme (Journal of Veterinary Diagnostic Investigation, 1990)
- Toxicity and carcinogenicity of the Fusanum monilzforine metabolite, fumonisin B1, in rats (Carcinogenesis, 1991)
- Simultaneous occurrence of fumonisin B1 and other mycotoxins in moldy corn collected from the People's Republic of China in regions with high incidences of esophageal cancer. (Applied and Environmental Microbiology, 1994)
- Fumonisin B1Induced Cell Death in Arabidopsis Protoplasts Requires Jasmonate-, Ethylene-, and Salicylate-Dependent Signaling Pathways (The Plant Cell, 2000)
- Fumonisin B1 inhibits sphingosine (sphinganine) N-acyltransferase and de novo sphingolipid biosynthesis in cultured neurons in situ. (Journal of Biological Chemistry, 1993)
- Upstream of growth and differentiation factor 1 (uog1), a mammalian homolog of the yeast longevity assurance gene 1 (LAG1), regulates N-stearoyl-sphinganine (C18-(dihydro)ceramide) synthesis in a fumonisin B1-independent manner in mammalian cells. (Journal of Biological Chemistry, 2002)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - fumonisin B(1)
- fumonisin-B1
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SMILESCCCCC(C)C(C(CC(C)CC(CCCCC(CC(C(C)N)O)O)O)OC(=O)CC(CC(=O)O)C(=O)O)OC(=O)CC(CC(=O)O)C(=O)O
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InChIKeyUVBUBMSSQKOIBE-UHFFFAOYSA-N
- Pubchem - fumonisin b1
- Wikipedia - Fumonisin B1
Fumonisin B1 is the most prevalent member of a family of toxins, known as fumonisins, produced by several species of Fusarium molds, such as Fusarium verticillioides, which occur mainly in maize (corn), wheat and other cereals. Fumonisin B1 contamination of maize has been reported worldwide at mg/kg levels. Human exposure occurs at levels of micrograms to milligrams per day and is greatest in regions where maize products are the dietary staple.
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Tricarballylic acid
+
Reactant
(Ester from carboxilic acid(SN2))
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