Zobrazeno 1 - 10
of 39
pro vyhledávání: '"J. M. Vigouret"'
Autor:
H. P. Weber, A. R. Dravid, J. M. Vigouret, H. O. Kalkman, A. Hofmann, A. L. Jaton, J. Nozulak, Malcolm D. Walkinshaw
Publikováno v:
ChemInform. 23
Publikováno v:
Advances in pharmacology (San Diego, Calif.). 35
Publikováno v:
Journal of Medicinal Chemistry. 21:754-757
A new two-step sequence for the epimerization of methyl dihydrolysergate (5) at C-8 leading to methyl dihydroisolysergate (7) is presented. The latter compound was used as a starting material for the synthesis of various ergolines, of which (5R,8R,10
Publikováno v:
Journal of Neural Transmission. 69:179-199
CK 204-933 displaces [3H]dopamine and [3H]spiperone with high affinity from D-1 and D-2 recognition sites in membranes of calf caudate. Results from functional in vitro tests suggest that it is a partial agonist at D-1 receptors and an antagonist at
Autor:
A, Yotis, J M, Vigouret
Publikováno v:
Agressologie: revue internationale de physio-biologie et de pharmacologie appliquees aux effets de l'agression. 23
Publikováno v:
Triangle; the Sandoz journal of medical science. 14(2)
Autor:
A L, Jaton, J M, Vigouret
Publikováno v:
Journal de pharmacologie. 16
Rats were trained in 4 consecutive trials to obtain a liquid reward in a labyrinth system. Drugs were given s.c. 2-4 hours before each trial, and starting time (ST), running time (RT) and number of errors (NE) were recorded on the fourth trial. Hyder
Publikováno v:
Chemischer Informationsdienst. 17
5-Hydroxy-2-aminotetralin derivatives in which one N-alkyl substituent carries a functional group have been prepared and their dopaminergic activities compared with those of 5-hydroxy-2-(di-n-propylamino)tetralin (5-OH-DPAT) and known ergolines. Seve
Publikováno v:
British journal of pharmacology. 56(3)