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Research Communications in Molecular Pathology and Pharmacology|July 1, 1995

In vivo disposition and in vitro metabolism of an anxiolytic compound, BMS-184111, in ratsK Yeleswaram, K J Volk, R Rourick, et al.

Journal of Medicinal Chemistry|November 1, 1980

Substituted 6,7-dihydroimidazo[1,2-a]purin-9(4H)-onesD L Temple, J P Yevich, J D Catt, et al.

Nuclear Medicine and Biology|July 1, 1993

Synthesis of (+/-)-[18F]BMY 14802, its enantiomers and their anatomical distributions in rodentsC Y Shiue, L Q Bai, G G Shiue, et al.

Journal of Medicinal Chemistry|November 1, 1990

Synthesis, biological profile, and quantitative structure-activity relationship of a series of novel 3-hydroxy-3-methylglutaryl coenzyme A reductase inhibitorsS Y Sit, R A Parker, I Motoc, et al.

Journal of Medicinal Chemistry|March 1, 1986

Synthesis and biological evaluation of 1-(1,2-benzisothiazol-3-yl)- and (1,2-benzisoxazol-3-yl)piperazine derivatives as potential antipsychotic agentsJ P Yevich, J S New, D W Smith, et al.

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Showing results (1-10 of 5) with videos related to

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Research Communications in Molecular Pathology and Pharmacology|July 1, 1995

In vivo disposition and in vitro metabolism of an anxiolytic compound, BMS-184111, in ratsK Yeleswaram, K J Volk, R Rourick, et al.

Journal of Medicinal Chemistry|November 1, 1980

Substituted 6,7-dihydroimidazo[1,2-a]purin-9(4H)-onesD L Temple, J P Yevich, J D Catt, et al.

Nuclear Medicine and Biology|July 1, 1993

Synthesis of (+/-)-[18F]BMY 14802, its enantiomers and their anatomical distributions in rodentsC Y Shiue, L Q Bai, G G Shiue, et al.

Journal of Medicinal Chemistry|November 1, 1990

Synthesis, biological profile, and quantitative structure-activity relationship of a series of novel 3-hydroxy-3-methylglutaryl coenzyme A reductase inhibitorsS Y Sit, R A Parker, I Motoc, et al.

Journal of Medicinal Chemistry|March 1, 1986

Synthesis and biological evaluation of 1-(1,2-benzisothiazol-3-yl)- and (1,2-benzisoxazol-3-yl)piperazine derivatives as potential antipsychotic agentsJ P Yevich, J S New, D W Smith, et al.

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