In Silico Analysis of FDA Drugs as P2X4 Modulators for the Treatment of Alcohol Use Disorder-Reference-Cited by-同舟云学术

In Silico Analysis of FDA Drugs as P2X4 Modulators for the Treatment of Alcohol Use Disorder

Published:2020-06-08 Issue:9 Volume:39 Page:1900111
ISSN:1868-1743
Container-title:Molecular Informatics
language:en
Short-container-title:Mol. Inf.

Author:

Reyes‐Espinosa Francisco¹,Nieto‐Pescador María G.²,Bocanegra‐García Virgilio¹,Lozano‐Guzmán Eduardo²,Rivera Gildardo¹^ORCID

Affiliation:

1. Laboratorio de Biotecnología Farmacéutica Centro de Biotecnología Genómica Instituto Politécnico Nacional 88710 Reynosa México

2. Facultad de Ciencias Químicas Universidad Juárez del Estado de Durango 34120 Durango México

Funder

National Council of Science and Technology

Publisher

Wiley

Subject

Organic Chemistry,Computer Science Applications,Drug Discovery,Molecular Medicine,Structural Biology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/minf.201900111

Reference45 articles.

1. National Institute on Alcohol Abuse and Alcoholism (NIAAA). Available online: https://www.niaaa.nih.gov/alcohol-health/overview-alcohol-consumption/alcohol-use-disorders (accessed 1 March 2019).

2. Allosteric Control of Gating and Kinetics at P2X4Receptor Channels

3. Ivermectin Antagonizes Ethanol Inhibition in Purinergic P2X4 Receptors

4. Cross-talk between P2X4 and γ-Aminobutyric Acid, Type A Receptors Determines Synaptic Efficacy at a Central Synapse

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