A comparison between the conformation of dexclamol and the tricyclic and butyrophenone type dopamine antagonists

Author:

Moereels H.,Tollenaere J.P.

Publisher

Elsevier BV

Subject

General Pharmacology, Toxicology and Pharmaceutics,General Biochemistry, Genetics and Molecular Biology,General Medicine

Cited by 13 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Structural requirements of Na+-dependent antidopaminergic agents: Tropapride, Piquindone, Zetidoline, and Metoclopramide Comparison with Na+-independent ligands;Journal of Computer-Aided Molecular Design;1989-03

2. Topology of Dopamine Receptors;Basic and Clinical Aspects of Neuroscience;1989

3. Structure analyses of R48455 a potent D2 antagonist and its inactive isomer R49399;European Journal of Medicinal Chemistry;1988-01

4. Molecular Characterization of Anti-Neuroleptic Idiotypes and Anti-Idiotypes;Anti-Idiotypes, Receptors, and Molecular Mimicry;1988

5. Conformation of dibenzo[b,f]heteroepin drugs and related compounds;Journal of Crystallographic and Spectroscopic Research;1984-10

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