Synthesis and in vitro pharmacological studies of new C(2) modified salvinorin A analogues-Reference-Cited by-同舟云学术

Synthesis and in vitro pharmacological studies of new C(2) modified salvinorin A analogues

Published:2005-08 Issue:16 Volume:15 Page:3744-3747
ISSN:0960-894X
Container-title:Bioorganic & Medicinal Chemistry Letters
language:en
Short-container-title:Bioorganic & Medicinal Chemistry Letters

Author:

Lee David Y.W.,Karnati Vishnu V.R.,He Minsheng,Liu-Chen Lee-Yuan,Kondaveti Leelakrishna,Ma Zhongze,Wang Yulin,Chen Yong,Beguin Cecile,Carlezon William A.,Cohen Bruce

Publisher

Elsevier BV

Subject

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

Reference25 articles.

1. Disruption of the kappa -opioid receptor gene in mice enhances sensitivity to chemical visceral pain, impairs pharmacological actions of the selective kappa -agonist U-50,488H and attenuates morphine withdrawal

2. Motivational Effects of Cannabinoids Are Mediated by μ-Opioid and κ-Opioid Receptors

Cited by 59 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. From Plant to Chemistry: Sources of Active Opioid Antinociceptive Principles for Medicinal Chemistry and Drug Design;Molecules;2023-10-14

2. Ligand and G-protein selectivity in the.-opioid receptor;NATURE;2023

3. Ligand and G-protein selectivity in the κ-opioid receptor;Nature;2023-05-03

4. Solving an Old Puzzle: Elucidation and Evaluation of the Binding Mode of Salvinorin A at the Kappa Opioid Receptor;Molecules;2023-01-11

5. Clerodane furanoditerpenoids from the stems of Tinospora sinensis;Archives of Pharmacal Research;2022-04-27