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Autor:
Max P. Seiler, Beat H. Gähwiler, Heinz H. Büscher, Albert Enz, Roger W. Foote, Dietmar Römer, Hansjörg Wüthrich, Richard Maurer, Gary T. Shearman
Publikováno v:
Life Sciences. 42:137-152
Here we describe the potent antinociceptive action of the indolophenanthridine, CY 208-243, which has high affinities to the dopamine D1 binding and the opioid sites as well as to the 5-HT1A site. The antinociceptive action was comparable to that of