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Research Progress of H(2)S Donors Conjugate Drugs Based on ADTOH
H(2)S is an endogenous gas signaling molecule and its multiple biological effects have been demonstrated. The abnormal level of H(2)S is closely related to the occurrence and development of many diseases, and H(2)S donors has important pharmacological implications. In recent years, H(2)S donors repr...
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/PMC9822322/ https://www.ncbi.nlm.nih.gov/pubmed/36615525 http://dx.doi.org/10.3390/molecules28010331 |
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author | Wen, Shuai Cao, Changchang Ge, Jianwen Yang, Wenzhe Wang, Yan Mou, Yi |
author_facet | Wen, Shuai Cao, Changchang Ge, Jianwen Yang, Wenzhe Wang, Yan Mou, Yi |
author_sort | Wen, Shuai |
collection | PubMed |
description | H(2)S is an endogenous gas signaling molecule and its multiple biological effects have been demonstrated. The abnormal level of H(2)S is closely related to the occurrence and development of many diseases, and H(2)S donors has important pharmacological implications. In recent years, H(2)S donors represented by ADTOH (5-(4-hydroxyphenyl)-3H-1,2-dithiole-3-thione) are often used to synthesize new ‘conjugate’ compounds that can release H(2)S and parent drugs. These hybrids retain the pharmacological activity of the parent drugs and H(2)S and have a synergistic effect. ADTOH and parent drug hybrids have become one of the important strategies for the development of H(2)S donor conjugate drugs. This review summarizes molecular hybrids between ADTOH and clinical drugs to provide new ideas for the study of H(2)S donor drug design. |
format | Online Article Text |
id | pubmed-9822322 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-98223222023-01-07 Research Progress of H(2)S Donors Conjugate Drugs Based on ADTOH Wen, Shuai Cao, Changchang Ge, Jianwen Yang, Wenzhe Wang, Yan Mou, Yi Molecules Review H(2)S is an endogenous gas signaling molecule and its multiple biological effects have been demonstrated. The abnormal level of H(2)S is closely related to the occurrence and development of many diseases, and H(2)S donors has important pharmacological implications. In recent years, H(2)S donors represented by ADTOH (5-(4-hydroxyphenyl)-3H-1,2-dithiole-3-thione) are often used to synthesize new ‘conjugate’ compounds that can release H(2)S and parent drugs. These hybrids retain the pharmacological activity of the parent drugs and H(2)S and have a synergistic effect. ADTOH and parent drug hybrids have become one of the important strategies for the development of H(2)S donor conjugate drugs. This review summarizes molecular hybrids between ADTOH and clinical drugs to provide new ideas for the study of H(2)S donor drug design. MDPI 2022-12-31 /pmc/articles/PMC9822322/ /pubmed/36615525 http://dx.doi.org/10.3390/molecules28010331 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 Wen, Shuai Cao, Changchang Ge, Jianwen Yang, Wenzhe Wang, Yan Mou, Yi Research Progress of H(2)S Donors Conjugate Drugs Based on ADTOH |
title | Research Progress of H(2)S Donors Conjugate Drugs Based on ADTOH |
title_full | Research Progress of H(2)S Donors Conjugate Drugs Based on ADTOH |
title_fullStr | Research Progress of H(2)S Donors Conjugate Drugs Based on ADTOH |
title_full_unstemmed | Research Progress of H(2)S Donors Conjugate Drugs Based on ADTOH |
title_short | Research Progress of H(2)S Donors Conjugate Drugs Based on ADTOH |
title_sort | research progress of h(2)s donors conjugate drugs based on adtoh |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9822322/ https://www.ncbi.nlm.nih.gov/pubmed/36615525 http://dx.doi.org/10.3390/molecules28010331 |
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