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Interaction of Opiate and Phencyclidine Derivatives with the Acetylcholine Receptor

机译:阿片和苯环利定衍生物与乙酰胆碱受体的相互作用

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The purpose of this work was to define the structural and biochemical environment of the AChR/I and the relationship of drug structure to the resultant pharmacological response. A number of drugs were tested using both biochemical and electrophysiological tests. For the most part, compounds consisted of benzomorphan and phencyclidine analogs, with the benzomorphans being the more thoroughly tested. Several important portions of the benzomorphan structure were identified, and the results of varying substitutents suggested that hydrophobicity parameters were the most important determinants of binding affinity.

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