1990
DOI: 10.1584/jpestics.15.579
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Isotope Effects on the Metabolic <i>N</i>-Demethylation of Diuron and Monuron in Hepatocytes and Liver Microsomes of Rats

Abstract: Deuterium isotope effects on the metabolic N-demethylation of diuron and monuron were measured in hepatocytes and in liver microsomes of rats. The intermolecular isotope effects were close to unity but the intramolecular effects on the reaction with diuron were 1.99 in hepatocytes (2.33 with monuron) and 2.47 in microsomes. The finding indicated that one electron was removed from nitrogen in the first step of reaction followed by deprotonation. A rapid interchange of two N-methyl groups in the substrate molecu… Show more

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“…Cryopreserved rat hepatocytes maintained nearly all of their N-demethylation activity for up to 23 days of freezing -but NADPH addition was required to restore full activity (diuron as substrate) (ref. 21). In contrast when aminopyrine was used as substrate Ndemethylation activity was retained after two days of storage but decreased to 10% after 21 days of storage (ref.…”
Section: Immobilization and Cryopreservation Of Cellsmentioning
confidence: 99%
“…Cryopreserved rat hepatocytes maintained nearly all of their N-demethylation activity for up to 23 days of freezing -but NADPH addition was required to restore full activity (diuron as substrate) (ref. 21). In contrast when aminopyrine was used as substrate Ndemethylation activity was retained after two days of storage but decreased to 10% after 21 days of storage (ref.…”
Section: Immobilization and Cryopreservation Of Cellsmentioning
confidence: 99%