Structural Studies on D2 Dopamine Receptors: Mutation of a Histidine Residue Specifically Affects the Binding of a Subgroup of Substituted Benzamide Drugs-Reference-Cited by-同舟云学术

Structural Studies on D2 Dopamine Receptors: Mutation of a Histidine Residue Specifically Affects the Binding of a Subgroup of Substituted Benzamide Drugs

Published:2008-06-28 Issue:5 Volume:62 Page:1664-1669
ISSN:0022-3042
Container-title:Journal of Neurochemistry
language:en
Short-container-title:

Author:

Woodward Robert,Daniell Sarah J.,Strange Philip G.,Naylor Louise H.

Publisher

Wiley

Subject

Cellular and Molecular Neuroscience,Biochemistry

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1046/j.1471-4159.1994.62051664.x/fullpdf

Reference19 articles.

1. Cloning and expression of a rat D2 dopamine receptor;Bunzow;Nature,1988

2. Differences in the ligand binding properties of the short and long versions of the D2 dopamine receptor;Castro;J. Neurochem.,1993

3. Molecular diversity of the dopamine receptors;Civelli;Annu. Rev. Pharmacol. Toxicol.,1993

4. Contributions of conserved serine residues to the interactions of ligands with dopamine D2 receptors;Cox;J. Neurochem.,1992

5. Interaction of neuroleptic drugs with rat striatal D-1 and D-2 dopamine receptors: a quantitative structure-affinity relationship study;El Tayar;Eur. J. Med. Chem.,1988

Cited by 29 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. Abolishing Dopamine D2long/D3 Receptor Affinity of Subtype-Selective Carbamoylguanidine-Type Histamine H2 Receptor Agonists;Journal of Medicinal Chemistry;2021-06-10

2. Impaired Clearance From the Brain Increases the Brain Exposure to Metoclopramide in Elderly Subjects;Clinical Pharmacology & Therapeutics;2020-10-14

3. Aminergic GPCR–Ligand Interactions: A Chemical and Structural Map of Receptor Mutation Data;Journal of Medicinal Chemistry;2018-10-17

4. P-Glycoprotein (ABCB1) Inhibits the Influx and Increases the Efflux of 11C-Metoclopramide Across the Blood–Brain Barrier: A PET Study on Nonhuman Primates;Journal of Nuclear Medicine;2018-05-10

5. In vitro, molecular modeling and behavioral studies of 3-{[4-(5-methoxy-1H-indol-3-yl)-1,2,3,6-tetrahydropyridin-1-yl]methyl}-1,2-dihydroquinolin-2-one (D2AAK1) as a potential antipsychotic;Neurochemistry International;2016-06