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triflupéridol

chimie / santé / général - iate.europa.eu eur-lex.europa.eu
Electrochemical and enzymatic in vitro studies on reactive drug metabolites synthesis, characterization and avoidance... Metabolic studies on haloperidol and trifluperidol, in comparison with their corresponding silicon analogues, were performed in liver microsomes and hepatocytes....
général - core.ac.uk - PDF: core.ac.uk
Dopamine receptor subtypes in renal brush border and basolateral membranes ... DA-1 receptors were quantitated by the specific binding of 125I-SCH 23982, a DA-1 antagonist (defined by 20 µM SCH 23390, a DA-1 antagonist) and DA-2 receptors by the specific binding of 3H-methyl-spiroperidol or 3H-spiroperidol (defined by 30 µM trifluperidol, a predominantly DA-2 antagonist)....
Characterization of haloperidol and trifluperidol as subtype-selective nmethyl-d-aspartate receptor antagonists using [3h]tcp and [3h]ifenprodil binding in rat brain membranes[3H]TCP and [3H]ifenprodil binding to N-methyl-D-aspartate (NMDA) receptors in rat forebrain membranes was used to compare the inhibition of haloperidol and trifluperidol with that of ifenprodil and eliprodil....
Flupentixol and trifluperidol reduce interleukin-1 � and interleukin-2 release by rat mixed glial andFlupentixol and trifluperidol reduce interleukin-1β and interleukin-2 release by rat mixed glial and microglial cell cultures....


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