Design, synthesis, and biological evaluation of structurally constrained hybrid analogues containing ropinirole moiety as a novel class of potent and selective dopamine D3 receptor ligands-Reference-Cited by-同舟云学术

Design, synthesis, and biological evaluation of structurally constrained hybrid analogues containing ropinirole moiety as a novel class of potent and selective dopamine D3 receptor ligands

Published:2018-07-01 Issue:3 Volume:92 Page:1597-1609
ISSN:1747-0277
Container-title:Chemical Biology & Drug Design
language:en
Short-container-title:Chem Biol Drug Des

Author:

Zhou Benhua¹²,Hong Kwon Ho³,Ji Min⁴⁵,Cai Jin¹⁵^ORCID

Affiliation:

1. School of Chemistry and Chemical Engineering; Southeast University; Nanjing Jiangsu China

2. School of Chemistry and Chemical Engineering; Yancheng Institute of Technology; Yancheng China

3. Department of Medicinal Chemistry and the Institute for Therapeutics Discovery and Development; University of Minnesota; Minneapolis Minnesota

4. School of Biological Science & Medical Engineering, Southeast University; Nanjing China

5. Suzhou Key Laboratory of Biomaterials and Technologies & Collaborative Innovation Center of Suzhou Nano Science and Technology; Suzhou China

Funder

Natural Science Foundation of Jiangsu Province

Publisher

Wiley

Subject

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

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/cbdd.13324/fullpdf

Reference36 articles.

1. Molecular cloning and characterization of a novel dopamine receptor (D3) as a target for neuroleptics

2. The Physiology, Signaling, and Pharmacology of Dopamine Receptors

3. Selective Antagonism at Dopamine D3 Receptors as a Target for Drug Addiction Pharmacotherapy: A Review of Preclinical Evidence

4. Targeting the dopamine D3 receptor: an overview of drug design strategies

5. The novel dopamine D3 receptor antagonist, SR 21502, reduces cocaine conditioned place preference in rats

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