Model-based LFER parameters and QSAR of Ligand Î²-Adrenoceptor Interactions II. Estimation and QSAR of Agonistic Potency and Receptor Affinity in a Series of Î²-Adrenergic phenethanolamines-Reference-Cited by-同舟云学术

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Model-based LFER parameters and QSAR of Ligand Î²-Adrenoceptor Interactions II. Estimation and QSAR of Agonistic Potency and Receptor Affinity in a Series of Î²-Adrenergic phenethanolamines

Published:1991 Issue:1 Volume:10 Page:23-30
ISSN:0931-8771
Container-title:Quantitative Structure-Activity Relationships
language:en
Short-container-title:Quant. Struct.-Act. Relat.

Author:

Dove Stefan,Franke Rainer

Publisher

Wiley

Subject

Pharmacology

Reference22 articles.

1. Model-based LFER Parameters and QSAR of Ligand-Î²-Adrenoceptor Interactions I. Equlibrium Models and Parameters of Î²-Adrenergic Effectuation

2. Structure-binding—Activity analysis of beta-adrenergic amines—I

3. Mode of coupling between the β-adrenergic receptor and adenylate cyclase in turkey erythrocytes

Cited by 3 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. Linear Free-Energy Relationships for the Alkyl Radical Affinities of Nitroxides: A Theoretical Study;Macromolecules;2010-03-25

2. Structure-Activity Relationship Studies of CNS Agents, Part 25: 4,6-Di(heteroaryl)-2-(N-methylpiperazino)pyrimidines as New, Potent 5-HT2A Receptor Ligands: A Verification of the Topographic Model;Archiv der Pharmazie;1995

3. Model-based LFER Parameters and QSAR of Ligand-Î²-Adrenoceptor Interactions I. Equlibrium Models and Parameters of Î²-Adrenergic Effectuation;Quantitative Structure-Activity Relationships;1991

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