Synthesis and optimization of novel and selective muscarinic M3 receptor antagonists-Reference-Cited by-同舟云学术

Synthesis and optimization of novel and selective muscarinic M3 receptor antagonists

Published:2007-09 Issue:18 Volume:17 Page:5256-5260
ISSN:0960-894X
Container-title:Bioorganic & Medicinal Chemistry Letters
language:en
Short-container-title:Bioorganic & Medicinal Chemistry Letters

Author:

Kumar Naresh,Kaur Kirandeep,Aeron Shelly,Dharmarajan Sankaranarayanan,Silamkoti Arun D.V.,Mehta Anita,Gupta Suman,Chugh Anita,Gupta Jang B.,Salman Mohammad,Palle Venkata P.,Cliffe Ian A.

Publisher

Elsevier BV

Subject

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

Reference14 articles.

1. The subtypes of muscarinic receptors for neurogenic bladder contraction in rats

2. Darifenacin: a novel M3muscarinic selective receptor antagonist for the treatment of overactive bladder

3. Synthesis and Antimuscarinic Properties of Quinuclidin-3-yl 1,2,3,4-Tetrahydroisoquinoline-2-carboxylate Derivatives as Novel Muscarinic Receptor Antagonists

4. Discovery of 2-Aminothiazole-4-carboxamides, a Novel Class of Muscarinic M3 Selective Antagonists, through Solution-Phase Parallel Synthesis

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