Structure-constrained endomorphin analogs display differential antinociceptive mechanisms in mice after spinal administration-Reference-Cited by-同舟云学术

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Structure-constrained endomorphin analogs display differential antinociceptive mechanisms in mice after spinal administration

Published:2017-05 Issue: Volume:91 Page:40-48
ISSN:0196-9781
Container-title:Peptides
language:en
Short-container-title:Peptides

Author:

Wang Yuan,Zhou Jingjing,Liu Xin,Zhao Long,Wang Zhaojuan,Zhang Xianghui,Wang Kezhou,Wang Linqing,Wang Rui

Funder

National Natural Science Foundation of China

Program for Changjiang Scholars and Innovative Research Team in University

Fundamental Research Funds for the Central Universities

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. Endomorphins: potential roles and therapeutic indications in the development of opioid peptide analgesic drugs;Liu;Med. Res. Rev.,2012

3. Opioid receptors and their ligands;Janecka;Curr. Top. Med. Chem.,2004

4. The endogenous opioid system and clinical pain management;Holden;AACN Clin. Issues,2005

5. Endomorphin analogs;Janecka;Curr. Med. Chem.,2007

Cited by 4 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. Development of Multifunctional and Orally Active Cyclic Peptide Agonists of Opioid/Neuropeptide FF Receptors that Produce Potent, Long-Lasting, and Peripherally Restricted Antinociception with Diminished Side Effects;Journal of Medicinal Chemistry;2021-09-01

2. Contribution of the μ opioid receptor and enkephalin to the antinociceptive actions of endomorphin-1 analogs with unnatural amino acid modifications in the spinal cord;Peptides;2021-07

3. Endogenous opiates and behavior: 2017;Peptides;2020-02

4. MEL-N16: A Series of Novel Endomorphin Analogs with Good Analgesic Activity and a Favorable Side Effect Profile;ACS Chemical Neuroscience;2017-08-10

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