3-Nitropropionic acid

Chemical compound From Wikipedia, the free encyclopedia

3-Nitropropionic acid

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]

Quick Facts Names, Identifiers ...
β-Nitropropionic acid
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Names
Preferred IUPAC name
3-Nitropropanoic acid
Other names
3-NPA
β-Nitropropionic acid
Hiptagenic acid
Bovinocidin
Identifiers
3D model (JSmol)
ChemSpider
ECHA InfoCard 100.007.276
UNII
  • InChI=1S/C3H5NO4/c5-3(6)1-2-4(7)8/h1-2H2,(H,5,6)
    Key: WBLZUCOIBUDNBV-UHFFFAOYSA-N
  • C(C[N+](=O)[O-])C(=O)O
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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