The spinal anti-allodynic effects of endomorphin analogs with C-terminal hydrazide modification in neuropathic pain model-Reference-Cited by-同舟云学术

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The spinal anti-allodynic effects of endomorphin analogs with C-terminal hydrazide modification in neuropathic pain model

Published:2020-12 Issue: Volume:134 Page:170407
ISSN:0196-9781
Container-title:Peptides
language:en
Short-container-title:Peptides

Author:

Zhang Yu-zhe,Yang Wen-jiao,Wang Xiao-fang,Wang Meng-meng,Zhang Yao,Gu Ning,Wang Chang-lin

Publisher

Elsevier BV

Subject

Cellular and Molecular Neuroscience,Endocrinology,Physiology,Biochemistry

Reference35 articles.

1. A potent and selective endogenous agonist for the mu-opiate receptor;Zadina;Nature,1997

2. Spinal analgesic actions of the new endogenous opioid peptides endomorphin-1 and -2;Stone;Neuroreport,1997

3. Differential antinociceptive effects of endomorphin-1 and endomorphin-2 in the mouse;Tseng;J. Pharmacol. Exp. Ther.,2000

4. Pain inhibition by endomorphins;Przewłocki;Ann. N. Y. Acad. Sci.,1999

5. Antiallodynic effects of Endomorphin-1 and Endomorphin-2 in the spared nerve injury model of neuropathic pain in mice;Wang;Anesth. Analg.,2017

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. Synthesis, Pharmacological Evaluation, and Computational Studies of Cyclic Opioid Peptidomimetics Containing β3-Lysine;Molecules;2021-12-28

2. Novel Cyclic Endomorphin Analogues with Multiple Modifications and Oligoarginine Vector Exhibit Potent Antinociception with Reduced Opioid-like Side Effects;Journal of Medicinal Chemistry;2021-11-16

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