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Molecular Pharmacology, Vol 10, 425-437, Copyright © 1974 by the American Society for Pharmacology and Experimental Therapeutics
1 Laboratoire de Chimie Physique et de Cristallographie, Institut Lavoisier, Université de Louvain,
Belgium
A study of the conformation of neuroleptic durgs by X-ray diffraction and simple conformational calculations has revealed some relationships among the relative arrangements of possible pharmacodynamic groups for these substances. A hydrogen bond donor at an appropriate distance from the basic nitrogen common to most neuroleptics often results in an enhancement of activity.
Note:
ACKNOWLEDGMENTS
I am much indebted to Dr. P. A. J. Janssen
and Dr. J. Tollenaere for stimulating discussions.
I also thank Professor M. Van Meerssche for his
interest in this work.
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