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Covalent Warheads Targeting Cysteine Residue: The Promising Approach in Drug Development
Cysteine is one of the least abundant amino acids in proteins of many organisms, which plays a crucial role in catalysis, signal transduction, and redox regulation of gene expression. The thiol group of cysteine possesses the ability to perform nucleophilic and redox-active functions that are not fe...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9694382/ https://www.ncbi.nlm.nih.gov/pubmed/36431829 http://dx.doi.org/10.3390/molecules27227728 |
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author | Huang, Fangjiao Han, Xiaoli Xiao, Xiaohui Zhou, Jinming |
author_facet | Huang, Fangjiao Han, Xiaoli Xiao, Xiaohui Zhou, Jinming |
author_sort | Huang, Fangjiao |
collection | PubMed |
description | Cysteine is one of the least abundant amino acids in proteins of many organisms, which plays a crucial role in catalysis, signal transduction, and redox regulation of gene expression. The thiol group of cysteine possesses the ability to perform nucleophilic and redox-active functions that are not feasible for other natural amino acids. Cysteine is the most common covalent amino acid residue and has been shown to react with a variety of warheads, especially Michael receptors. These unique properties have led to widespread interest in this nucleophile, leading to the development of a variety of cysteine-targeting warheads with different chemical compositions. Herein, we summarized the various covalent warheads targeting cysteine residue and their application in drug development. |
format | Online Article Text |
id | pubmed-9694382 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-96943822022-11-26 Covalent Warheads Targeting Cysteine Residue: The Promising Approach in Drug Development Huang, Fangjiao Han, Xiaoli Xiao, Xiaohui Zhou, Jinming Molecules Review Cysteine is one of the least abundant amino acids in proteins of many organisms, which plays a crucial role in catalysis, signal transduction, and redox regulation of gene expression. The thiol group of cysteine possesses the ability to perform nucleophilic and redox-active functions that are not feasible for other natural amino acids. Cysteine is the most common covalent amino acid residue and has been shown to react with a variety of warheads, especially Michael receptors. These unique properties have led to widespread interest in this nucleophile, leading to the development of a variety of cysteine-targeting warheads with different chemical compositions. Herein, we summarized the various covalent warheads targeting cysteine residue and their application in drug development. MDPI 2022-11-10 /pmc/articles/PMC9694382/ /pubmed/36431829 http://dx.doi.org/10.3390/molecules27227728 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Huang, Fangjiao Han, Xiaoli Xiao, Xiaohui Zhou, Jinming Covalent Warheads Targeting Cysteine Residue: The Promising Approach in Drug Development |
title | Covalent Warheads Targeting Cysteine Residue: The Promising Approach in Drug Development |
title_full | Covalent Warheads Targeting Cysteine Residue: The Promising Approach in Drug Development |
title_fullStr | Covalent Warheads Targeting Cysteine Residue: The Promising Approach in Drug Development |
title_full_unstemmed | Covalent Warheads Targeting Cysteine Residue: The Promising Approach in Drug Development |
title_short | Covalent Warheads Targeting Cysteine Residue: The Promising Approach in Drug Development |
title_sort | covalent warheads targeting cysteine residue: the promising approach in drug development |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9694382/ https://www.ncbi.nlm.nih.gov/pubmed/36431829 http://dx.doi.org/10.3390/molecules27227728 |
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