3-Nitropropionic acid
Chemical compound From Wikipedia, the free encyclopedia
3-Nitropropionic acid (3-NPA) is a mycotoxin, a potent mitochondrial inhibitor,[1] which is toxic to humans. It is produced by a number of fungi, and may be found in food such as in sugar cane as well as Japanese fungally fermented staples, including miso, soy sauce, katsuobushi,[2] coconuts[3] and some traditional Chinese medicines.[4]
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Names | |
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Preferred IUPAC name
3-Nitropropanoic acid | |
Other names
3-NPA β-Nitropropionic acid Hiptagenic acid Bovinocidin | |
Identifiers | |
3D model (JSmol) |
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ChemSpider | |
ECHA InfoCard | 100.007.276 |
PubChem CID |
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UNII | |
CompTox Dashboard (EPA) |
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Properties | |
C3H5NO4 | |
Molar mass | 119.076 g·mol−1 |
Melting point | 65–67 °C (149–153 °F; 338–340 K) |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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It can be caused by extreme weather, stressed crop growth conditions, as well as storage conditions (like moisture),[5] which can give a further rise under global warming conditions.[6] Fungi of the genus Arthrinium are known to produce 3-nitropropanoic acid.[7]
Fatal 3-NPA poisoning as a result of drinking coconut water has been reported in a case where a pre-prepared coconut had been stored at room temperature for a month, instead of being refrigerated.[8]
It is found that 3-nitropropionic acid is a mitochondrial toxin and produces striatal alterations in rats similar to those observed in the brain of Huntington's disease patients, and administration of the cannabinoid receptor agonist WIN55212-2 to rats for six consecutive days, before the 3-NPA injection, exerted preventive effects on all alterations elicited by the toxin, like mitochondrial dysfunction and lipid peroxidation, by activation of the CB1 receptor.[9]
References
Further reading
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