Synthesis and structure activity relationships of alkyl substituted analogues of the functional M1 selective muscarinic receptor agonist xanomeline-Reference-Cited by-同舟云学术

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Synthesis and structure activity relationships of alkyl substituted analogues of the functional M1 selective muscarinic receptor agonist xanomeline

Published:1994-09 Issue:18 Volume:4 Page:2205-2210
ISSN:0960-894X
Container-title:Bioorganic & Medicinal Chemistry Letters
language:en
Short-container-title:Bioorganic & Medicinal Chemistry Letters

Author:

Quimby Steven J.,Shannon Harlan E.,Bymaster Frank P.,Sauerberg Per,Olesen Preben H,Sheardown Malcolm J.,Suzdak Peter D.,Mitch Charles H.

Publisher

Elsevier BV

Subject

Organic Chemistry,Clinical Biochemistry,Drug Discovery,Pharmaceutical Science,Molecular Biology,Molecular Medicine,Biochemistry

Reference12 articles.

1. Cholinomimetics and Alzheimer's disease

2. Novel functional M1 selective muscarinic agonists. Synthesis and structure-activity relationships of 3-(1,2,5-thiadiazolyl)-1,2,5,6-tetrahydro-1-methylpyridines

3. Synthesis and structure-activity relationships of heterocyclic analogues of the functional M1 selective muscarinic agonist hexyloxy-TZTP

Cited by 8 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. ChemInform Abstract: Synthesis and Structure Activity Relationships of Alkyl Substituted Analogues of the Functional M1 Selective Muscarinic Receptor Agonist Xanomeline.;ChemInform;2010-08-18

2. Thiadiazole Carbamates: Potent Inhibitors of Lysosomal Acid Lipase and Potential Niemann−Pick Type C Disease Therapeutics;Journal of Medicinal Chemistry;2010-06-17

3. A new synthesis of 3,4-disubstituted 1,2,5-thiadiazoles;Tetrahedron Letters;2007-07

4. Studies on Three-dimensional QSAR of Muscarinic Receptor Agonists;Acta Physico-Chimica Sinica;2005

5. 1-(1,2,5-Thiadiazol-4-yl)-4-azatricyclo[2.2.1.02,6]heptanes as New Potent Muscarinic M1 Agonists: Structure−Activity Relationship for 3-Aryl-2-propyn-1-yloxy and 3-Aryl-2-propyn-1-ylthio Derivatives;Journal of Medicinal Chemistry;1999-05-08

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