Results 121 to 130 of about 2,684 (181)
Mycotoxin Residues in Chicken Breast Muscle and Liver. [PDF]
FoodsLešić T +4 more
europepmc +1 more source
Mycotoxins and Beyond: Unveiling Multiple Organic Contaminants in Pet Feeds Through HRMS Suspect Screening. [PDF]
Toxins (Basel)Dematati D +3 more
europepmc +1 more source
The role of global DNA methylation in citrinin induced toxicity: <i>In vitro</i> and <i>in silico</i> approach. [PDF]
Toxicol RepCakir MC, Ozden S.
europepmc +1 more source
On the alkaline salts of citrinin
The Journal of Antibiotics, Series B, 1953 openaire +1 more source
Citrinin inhibits the function of Leydig cells in male rats in prepuberty
Ecotoxicology and Environmental Safety, 2023 Citrinin, a mycotoxin existing in fruits, has nephrotoxicity, hepatotoxicity and embryotoxicity. The effects of citrinin on Leydig cell development in prepuberty remains unclear.
Ren-Shan Ge, Yiyan Wang, Mengyun Wang
exaly +3 more sources
A Major Decomposition Product, Citrinin H2, from Citrinin on Heating with Moisture
Bioscience, Biotechnology and Biochemistry, 2002 Citrinin is one of the mycotoxins produced by Penicillium citrinum. We examined the decomposition products after heating citrinin in water at 140 degrees C and isolated a major product, citrinin H2 (3-(3,5-dihydroxy-2-methylphenyl)-2-formyloxy-butane).
Alka Mehta +2 more
exaly +3 more sources
Frontiers in Microbiology, 2018 Monascus purpureus YY-1 is widely used in food colorant production in China. Our previous study clearly illustrated the whole-genome data for YY-1 and provided useful insight into evolutionary research and industrial applications.
Bin Liang, Xin-Jun Du
exaly +3 more sources
Four New Citrinin Derivatives from a Marine-Derived Penicillium sp. Fungal Strain
Molecules, 2013 Four new citrinin derivatives, including two citrinin dimers and two citrinin monomer derivatives, were isolated and identified from a marine-derived fungal strain Penicillium sp. ML226 along with six known related compounds.
Zhong Zheng
exaly +3 more sources
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Nature, 1949
FOLLOWING upon the development of a new structural formula for citrinin described in a communication1 submitted to Nature on March 17, 1948, we have now been able to effect a synthesis of citrinin, thereby confirming our earlier deductions.
N J, CARTWRIGHT +2 more
openaire +2 more sources
FOLLOWING upon the development of a new structural formula for citrinin described in a communication1 submitted to Nature on March 17, 1948, we have now been able to effect a synthesis of citrinin, thereby confirming our earlier deductions.
N J, CARTWRIGHT +2 more
openaire +2 more sources
Nature, 1948
IN view of the recent communication on this topic by Cram1 to the editor of the Journal of the American Chemical Society, we wish to record that in the course of an extensive investigation on the chemistry of citrinin initiated in these laboratories in 1945, the synthesis of 4-methyl-5-ethylresorcinol2, m.p.
J. P. BROWN +3 more
openaire +2 more sources
IN view of the recent communication on this topic by Cram1 to the editor of the Journal of the American Chemical Society, we wish to record that in the course of an extensive investigation on the chemistry of citrinin initiated in these laboratories in 1945, the synthesis of 4-methyl-5-ethylresorcinol2, m.p.
J. P. BROWN +3 more
openaire +2 more sources