Structure-affinity relationship studies on 5-HT1A receptor ligands. 2. Heterobicyclic phenylpiperazines with N4-aralkyl substituents

…, I Van Wijngaarden, MTM Tulp, W Soudijn

Index: Van Steen; Van Wijngaarden; Tulp; Soudijn Journal of Medicinal Chemistry, 1994 , vol. 37, # 17 p. 2761 - 2773

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Citation Number: 47

Abstract

(4). Their affinities for~-HT~ A receptors range from 0.15 to 28 nM and thus emphasize the importance of N4-substitution. By combining the SAR of these N4-aralkyl series with the recently publishedll SAR of the N4-alkyl-substituted phenylpiperazines, the nature of the interaction of the N4-substituted phenylpiperazines and the B-HT~ A receptor was further examined using comparative molecular field analysis (CoMFA). To discriminate between ...