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C G Wermuth

Showing results (21-30 of 45) with videos related to

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Journal De Pharmacologie|April 1, 1986
[Pharmacologic profile of an original psychotropic drug. Minaprine: comparison with six reference antidepressives]P Worms, J P Kan, A Perio, et al.
Pharmacology, Biochemistry, and Behavior|January 1, 1990
Anxiolytic and sedative properties of BW A78U, a novel anticonvulsant adenine derivativeM Willard, R Misslin, E Vogel, et al.
Journal of Medicinal Chemistry|March 3, 1999
Aminopyridazines as acetylcholinesterase inhibitorsJ M Contreras, Y M Rival, S Chayer, et al.
Journal of Medicinal Chemistry|February 17, 1998
5-HT3 antagonists derived from aminopyridazine-type muscarinic M1 agonistsY Rival, R Hoffmann, B Didier, et al.
Journal of Neurochemistry|June 1, 1982
A high-affinity, Na+-dependent uptake system for gamma-hydroxybutyrate in membrane vesicles prepared from rat brainJ Benavides, J F Rumigny, J J Bourguignon, et al.
Brain Research|October 8, 1986
Biochemical characterization of the interaction of three pyridazinyl-GABA derivatives with the GABAA receptor siteM Heaulme, J P Chambon, R Leyris, et al.
Journal of Medicinal Chemistry|May 1, 1988
Analogues of gamma-hydroxybutyric acid. Synthesis and binding studiesJ J Bourguignon, A Schoenfelder, M Schmitt, et al.
European Journal of Pharmacology|December 15, 1987
The sensitivity of gamma-aminobutyric acid antagonists to thiocyanate is related to the absence of a functional anionic group in their structureC G Wermuth, J P Chambon, M Heaulme, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 1, 1985
An arylaminopyridazine derivative of gamma-aminobutyric acid (GABA) is a selective and competitive antagonist at the GABAA receptor siteJ P Chambon, P Feltz, M Heaulme, et al.
British Journal of Pharmacology|July 1, 1977
A potent new beta2-adrenoceptor blocking agentJ L Imbs, F Miesch, J Schwartz, et al.
Pageof 5

Showing results (21-30 of 45) with videos related to

Sort By:
Pageof 5
Journal De Pharmacologie|April 1, 1986
[Pharmacologic profile of an original psychotropic drug. Minaprine: comparison with six reference antidepressives]P Worms, J P Kan, A Perio, et al.
Pharmacology, Biochemistry, and Behavior|January 1, 1990
Anxiolytic and sedative properties of BW A78U, a novel anticonvulsant adenine derivativeM Willard, R Misslin, E Vogel, et al.
Journal of Medicinal Chemistry|March 3, 1999
Aminopyridazines as acetylcholinesterase inhibitorsJ M Contreras, Y M Rival, S Chayer, et al.
Journal of Medicinal Chemistry|February 17, 1998
5-HT3 antagonists derived from aminopyridazine-type muscarinic M1 agonistsY Rival, R Hoffmann, B Didier, et al.
Journal of Neurochemistry|June 1, 1982
A high-affinity, Na+-dependent uptake system for gamma-hydroxybutyrate in membrane vesicles prepared from rat brainJ Benavides, J F Rumigny, J J Bourguignon, et al.
Brain Research|October 8, 1986
Biochemical characterization of the interaction of three pyridazinyl-GABA derivatives with the GABAA receptor siteM Heaulme, J P Chambon, R Leyris, et al.
Journal of Medicinal Chemistry|May 1, 1988
Analogues of gamma-hydroxybutyric acid. Synthesis and binding studiesJ J Bourguignon, A Schoenfelder, M Schmitt, et al.
European Journal of Pharmacology|December 15, 1987
The sensitivity of gamma-aminobutyric acid antagonists to thiocyanate is related to the absence of a functional anionic group in their structureC G Wermuth, J P Chambon, M Heaulme, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 1, 1985
An arylaminopyridazine derivative of gamma-aminobutyric acid (GABA) is a selective and competitive antagonist at the GABAA receptor siteJ P Chambon, P Feltz, M Heaulme, et al.
British Journal of Pharmacology|July 1, 1977
A potent new beta2-adrenoceptor blocking agentJ L Imbs, F Miesch, J Schwartz, et al.
Pageof 5