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5/31/2023 7:59:32 AM | Browse: 56 | Download: 0
Publication Name World Journal of Pharmacology
Manuscript ID 84146
Country Brazil
Category Biochemistry & Molecular Biology
Manuscript Type Basic Study
Article Title In silico insight into Amurensinine - an N-Methyl-D-Aspartate receptor antagonist
Manuscript Source Unsolicited Manuscript
All Author List Cinthia Façanha Wendel, Queren Hapuque Oliveira Alencar, Rafaela Viana Vieira and Kádima Nayara Teixeira
Funding Agency and Grant Number
Corresponding Author Kádima Nayara Teixeira, PhD, Professor, Campus Toledo, Universidade Federal do Paraná, Max Planck 3796, Toledo 85.919-899, Paraná, Brazil. kadimateixeira@ufpr.br
Key Words Amurensinine; Bioinformatics analysis; Isopavines; Molecular docking; N-methyl-D-Aspartate receptor
Core Tip Amurensinine binds to a region of the amino terminal domain on the N-methyl-D-Aspartate receptor and the interaction is stabilized mainly by covalent bonds, which confer an affinity energy of significant value to the receptor/Ligand complex. The interaction between Amurensinine and the receptor, which is involved in neurological diseases, suggests that this isopavine may interfere with its function, so it may have therapeutic potential in this area.
Citation Façanha Wendel C, Hapuque Oliveira Alencar Q, Viana Vieira R, Teixeira KN. In silico insight into Amurensinine - an N-Methyl-D-Aspartate receptor antagonist. World J Pharmacol 2023; 12(3): 25-34
Received
2023-03-02 20:04
Peer-Review Started
2023-03-01 18:46
To Make the First Decision
Return for Revision
2023-04-13 08:16
Revised
2023-05-05 21:42
Second Decision
2023-05-31 03:10
Accepted by Journal Editor-in-Chief
Accepted by Company Editor-in-Chief
2023-05-31 07:59
Articles in Press
2023-05-31 07:59
Publication Fee Transferred
Edit the Manuscript by Language Editor
Typeset the Manuscript
2023-06-14 01:45
ISSN 2220-3192 (online)
Open Access This article is an open-access article that was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution NonCommercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: https://creativecommons.org/Licenses/by-nc/4.0/
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