| Secondary metabolites trivial name - ochratoxin C | ||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Species | A. ochraceus | |||||||||||||
| Systematic name | Ochratoxin A ethyl ester Alanine, N-((5-chloro-8-hydroxy-3-methyl-1-oxo-7-isochromanyl)carbonyl)-3-phenyl-, ethyl ester, L- L-Phenylalanine, N-((5-chloro-3,4-dihydro-8-hydroxy-3-methyl-1-oxo-1H-2-benzopyran-7-yl)carbonyl)-, ethyl ester, (R)- | |||||||||||||
| Molecular formulae | C22H22ClNO6 | |||||||||||||
| Molecular weight | 431.866 | |||||||||||||
| Chemical abstracts number | 4865-85-4 | |||||||||||||
| Selected references | Fuchs R, Hult K, Peraica M, Radic B, Plestina R. Conversion of ochratoxin C into ochratoxin A in vivo. Appl Environ Microbiol. 1984 Jul;48(1):41-2. Xiao H, Marquardt RR, Abramson D, Frohlich AA. Related Articles, Links Metabolites of ochratoxins in rat urine and in a culture of Aspergillus ochraceus. Appl Environ Microbiol. 1996 Feb;62(2):648-55. | |||||||||||||
| Toxicity | Because it is readily hydrolysed to ochratoxin A in the animal body, ochratoxin C has similar toxicity to ochratoxin A. | |||||||||||||
| Structure diagram | ![]() | |||||||||||||
| 3D Structure | ![]() | |||||||||||||
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