Selective inhibition of TRPM2 channel by two novel synthesized ADPR analogues-Reference-Cited by-同舟云学术

Selective inhibition of TRPM2 channel by two novel synthesized ADPR analogues

Published:2017-11-15 Issue:2 Volume:91 Page:552-566
ISSN:1747-0277
Container-title:Chemical Biology & Drug Design
language:en
Short-container-title:Chem Biol Drug Des

Author:

Luo Xiao¹^ORCID,Li Meng²,Zhan Kaiyu³,Yang Wei³,Zhang Lihe¹,Wang KeWei²⁴,Yu Peilin⁵,Zhang Liangren¹

Affiliation:

1. State Key Laboratory of Natural and Biomimetic Drugs; Peking University; Beijing China

2. Department of Neurobiology; Neuroscience Research Institute; Peking University Health Science Center; Peking University School of Pharmaceutical Sciences; Beijing China

3. Department of Neurobiology; Zhejiang University School of Medicine; Hangzhou Zhejiang China

4. Department of Pharmacology; School of Pharmacy; Qingdao University; Qingdao China

5. Department of Toxicology; School of Public Health; Zhejiang University; Hangzhou Zhejiang China

Funder

National Natural Science Foundation of China

Ministry of Science and Technology

Publisher

Wiley

Subject

Molecular Medicine,Biochemistry,Drug Discovery,Pharmacology,Organic Chemistry

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/cbdd.13119/fullpdf

Reference40 articles.

1. Neuronal TRP channels: thermometers, pathfinders and life-savers

2. Transient Receptor Potential Channels and Mechanosensation

3. New Molecular Mechanisms on the Activation of TRPM2 Channels by Oxidative Stress and ADP-Ribose

4. TRPM2: a multifunctional ion channel for calcium signalling

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