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The Journal of Pharmacology and Experimental Therapeutics|April 1, 1991
In vivo binding of SCH 39166: a D-1 selective antagonistR D McQuade, R A Duffy, V L Coffin, et al.
Neuroscience Letters|June 15, 1984
Behavioral interaction of adenosine and methylxanthines on central purinergic systemsV L Coffin, J A Taylor, J W Phillis, et al.
The Journal of Pharmacology and Experimental Therapeutics|December 1, 1988
Pharmacological profile of SCH39166: a dopamine D1 selective benzonaphthazepine with potential antipsychotic activityR E Chipkin, L C Iorio, V L Coffin, et al.
Journal of Neurochemistry|December 1, 1991
[3H]SCH 39166, a new D1-selective radioligand: in vitro and in vivo binding analysesR D McQuade, R A Duffy, C C Anderson, et al.
Bioorganic & Medicinal Chemistry Letters|January 2, 2001
Benzylidene ketal derivatives as M2 muscarinic receptor antagonistsC D Boyle, S Chackalamannil, L Y Chen, et al.
Bioorganic & Medicinal Chemistry Letters|August 31, 2001
Metabolic stabilization of benzylidene ketal M(2) muscarinic receptor antagonists via halonaphthoic acid substitutionC D Boyle, S Chackalamannil, J W Clader, et al.
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