Pages that link to "Q39140964"
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The following pages link to Synthesis and pharmacological properties of a series of antidopaminergic piperidyl benzamides (Q39140964):
Displayed 15 items.
- Effect of substituted benzamide drugs on rat striatal tyrosine hydroxylase (Q39212850) (← links)
- Differential activities of some benzamide derivatives on peripheral and intracerebral administration (Q39227798) (← links)
- Multiple Dopamine Receptors in Brain and the Pharmacological Action of Substituted Benzamide Drugs (Q40093313) (← links)
- Differential effects of benzamides and thioxanthenes on dopamine-elicited accumulation of cyclic AMP in isolated rabbit retina (Q40161735) (← links)
- Stereocontrolled dopamine receptor binding and subtype selectivity of clebopride analogues synthesized from aspartic acid (Q44570469) (← links)
- Comparison of the potencies of clebopride and other substituted benzamide drugs on isolated gastrointestinal tract of the guinea-pig and rat (Q46208844) (← links)
- Substituted benzamides as cerebral dopamine antagonists in rodents (Q48296371) (← links)
- Effects of clozapine in a selective muscarinic bioassay and on single cells of the rat hippocampus (Q48924444) (← links)
- Rapid thin-layer chromatographic photodensitometric method for the determination of metoclopramide and clebopride in the presence of some of their metabolic products (Q67004532) (← links)
- Simultaneous determination of clebopride and a major metabolite N-desbenzylclebopride in plasma by capillary gas chromatography—negative-ion chemical ionization mass spectrometry (Q67926717) (← links)
- Determination of clebopride in plasma by capillary gas chromatography-negative-ion chemical ionization mass spectrometry (Q68023098) (← links)
- On the mechanism of metabolic N-dealkylation. Isolation of a relatively stable carbinolamine (Q72433791) (← links)
- The pharmacokinetics of a new benzamide drug, clebopride, in the rat and the dog (Q72493473) (← links)
- Potent lipophilic substituted benzamide drugs are not selective D-1 dopamine receptor antagonists in the rat (Q72558027) (← links)
- Crystal structure of human PLD1 provides insight into activation by PI(4,5)P2 and RhoA (Q90547099) (← links)