S-3-hydroxyphenyl (N-hydroxycarbamamido) (diphenyl) ethanethioate derivatives as potential inhibitors of 5 -Lipoxygenase (5-LOX)
DOI:
https://doi.org/10.18687/LACCEI2023.1.1.1222Keywords:
5-Lipoxygenase, molecular docking, anti-inflammatory drugsAbstract
We have designed and docked derivatives of a new anti-inflammatory compound into the crystal structure of the Lipoxygenase-5 (LOX-5) enzyme. We found that four derivatives have the same ability to inhibit the activity of the enzyme as the anti-inflammatory drug Zileuton. This information may help us develop new compounds to treat inflammation.Downloads
Published
2023-07-27
Issue
Section
Articles
Copyright
Copyright (c) 2023 LACCEI
License
This work is licensed under a Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International License.
LACCEI retains copyright of all published articles under the terms of its copyright transfer agreement. As the copyright holder, LACCEI distributes the articles to the public under the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International License (CC BY-NC-SA 4.0).
How to Cite
Ariza-Rua, Danilo, Rebollo, Juan Alberto, Chavarro-Mesa, Edisson, & Ballestas-Casallas, Yamil. (2023). S-3-hydroxyphenyl (N-hydroxycarbamamido) (diphenyl) ethanethioate derivatives as potential inhibitors of 5 -Lipoxygenase (5-LOX). LACCEI, 1(8). https://doi.org/10.18687/LACCEI2023.1.1.1222