Mycotoxin.
Product Details
| Alternative Name: | 1-Hydroxycyclobut-1-ene-3,4-dione . sodium salt |
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| Formula: | C4HO3 . Na |
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| MW: | 97.1 . 23.0 |
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| Source: | Isolated from Fusarium moniliforme. |
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| CAS: | 71376-34-6 |
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| RTECS: | GU1815000 |
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| Purity: | ≥98% (TLC) |
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| Identity: | Identity determined by NMR. |
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| Appearance: | Light yellow powder. |
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| Solubility: | Soluble in water, methanol or DMSO. |
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| Shipping: | Ambient Temperature |
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| Long Term Storage: | -20°C |
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| Regulatory Status: | RUO - Research Use Only |
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Product Literature References
Effects of moniliformin in presence of cyclohexadepsipeptides on isolated mammalian tissue and cells: M.R. Kamyar, et al.; Toxicol. In Vitro
20, 1284 (2006),
Abstract;
Genotoxic effects of three Fusarium mycotoxins, fumonisin B1, moniliformin and vomitoxin in bacteria and in primary cultures of rat hepatocytes: S. Knasmuller, et al.; Mutat. Res.
391, 39 (1997),
Abstract;
Comparative cytotoxicity of fumonisin B1 and moniliformin in chicken primary cell cultures: W. Wu, et al.; Mycopathologia
132, 111 (1995),
Abstract;
Moniliformin: the result of storing a citric acid cycle intermediate: M.E. Forster; Biochem. Med. Metab. Biol.
47, 279 (1992),
Abstract;
Effect of moniliformin on myocardial contractility in rats: L.L. Fan, et al.; Biomed. Environ. Sci.
4, 290 (1991),
Abstract;
Moniliformin, a metabolite of Fusarium moniliforme NRRL 6322: purification and toxicity: H.R. Burmeister, et al.; Appl. Environ. Microbiol.
37, 11 (1979),
Abstract;
Full Text
A molecular mechanism for the toxic action of moniliformin, a mycotoxin produced by Fusarium moniliforme: P.G. Thiel; Biochem. Pharmacol.
27, 483 (1978),
Abstract;
Isolation and purification of moniliformin: M. Steyn, et al.; J. Assoc. Off. Anal. Chem.
61, 578 (1978),
Abstract;
Moniliformin, a mycotoxin from Fusarium fusarioides: C.J. Rabie, et al.; J. Agric. Food Chem.
26, 375 (1978),
Abstract;
Structure and synthesis of moniliformin, a novel cyclobutane microbial toxin: J.P. Springer, et al.; JACS
96, 2267 (1974),
Abstract;
