The effect of absolute configuration on activity, subtype selectivity (M3/M2) of 3α-acyloxy-6β-acetoxyltropane derivatives as muscarinic M3 receptor antagonists-Reference-Cited by-同舟云学术

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The effect of absolute configuration on activity, subtype selectivity (M3/M2) of 3α-acyloxy-6β-acetoxyltropane derivatives as muscarinic M3 receptor antagonists

Published:2013-03 Issue:5 Volume:21 Page:1234-1239
ISSN:0968-0896
Container-title:Bioorganic & Medicinal Chemistry
language:en
Short-container-title:Bioorganic & Medicinal Chemistry

Author:

Wang Zhi-Peng,Liu Hui-Zhong,Zhu Liang,Hu You-Min,Cui Yong-Yao,Niu Yin-Yao,Lu Yang,Chen Hong-Zhuan

Publisher

Elsevier BV

Subject

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

Reference17 articles.

1. Contractile role of M2 and M3 muscarinic receptors in gastrointestinal, airway and urinary bladder smooth muscle

2. Muscarinic receptor subtypes of the bladder and gastrointestinal tract

3. Functional M3muscarinic acetylcholine receptors in mammalian hearts

4. Muscarinic M3 receptor antagonists with (2R)-2-[(1R)-3,3-Difluorocyclopentyl]-2-hydroxyphenylacetamide Structures. Part 2

5. A new series of M3 muscarinic antagonists based on the 4-amino-piperidine scaffold

Cited by 2 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. Enantioseparation of 3 α -acyloxy-6 β -acetoxyltropane compounds with Chiralpak AD and Chiralcel OD-H chiral stationary phases;Chinese Journal of Chromatography;2015

2. Muscarinic acetylcholine receptor modulators derived from natural toxins and diverse interaction modes;Science China Chemistry;2013-08-31

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