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Synthesis, Characterization, and Application of 2-((3-(Chloromethyl)-benzoyl)oxy)benzoic Acid: A Review
[Image: see text] Salicylic acid (SA) derivate is well-known for its anti-inflammatory and analgesic activity through cyclooxygenase (COX)-inhibition. Previous studies pointed toward gastric toxicity induced by most salicylic acid derivative compounds, particularly acetylsalicylic acid (ASA). Despit...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9835159/ https://www.ncbi.nlm.nih.gov/pubmed/36643478 http://dx.doi.org/10.1021/acsomega.2c05566 |
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author | Tjahjono, Yudy Caroline, Foe, Kuncoro Karnati, Srikanth Ergün, Süleyman Esar, Senny Yesery Wijaya, Hendy Hadinugroho, Wuryanto Kusindarta, Dwi Liliek Wihadmadyatami, Hevi |
author_facet | Tjahjono, Yudy Caroline, Foe, Kuncoro Karnati, Srikanth Ergün, Süleyman Esar, Senny Yesery Wijaya, Hendy Hadinugroho, Wuryanto Kusindarta, Dwi Liliek Wihadmadyatami, Hevi |
author_sort | Tjahjono, Yudy |
collection | PubMed |
description | [Image: see text] Salicylic acid (SA) derivate is well-known for its anti-inflammatory and analgesic activity through cyclooxygenase (COX)-inhibition. Previous studies pointed toward gastric toxicity induced by most salicylic acid derivative compounds, particularly acetylsalicylic acid (ASA). Despite the adverse effect, ASA is still used due to price affordability and additional advantages in preventing platelet aggregation. Recently, a novel salicylic acid derivative called 2-((3 (chloromethyl)benzoyl)oxy)benzoic acid (3-CH(2)Cl) was introduced as a potential alternative compound to substitute ASA. Preliminary assessment results of COX-2 specificity, toxicity profile, analgesic, anti-inflammatory, and antiplatelet activity have made 3-CH(2)Cl a promising compound for “new” drug development. This review focuses on the discovery, potential activity, and benefits of 3-CH(2)Cl and the possible molecular mechanisms of its regulations in health and disease. Thus, this review may prove to be beneficial for the utilization of 3-CH(2)Cl as a potential alternative drug to substitute ASA. |
format | Online Article Text |
id | pubmed-9835159 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-98351592023-01-13 Synthesis, Characterization, and Application of 2-((3-(Chloromethyl)-benzoyl)oxy)benzoic Acid: A Review Tjahjono, Yudy Caroline, Foe, Kuncoro Karnati, Srikanth Ergün, Süleyman Esar, Senny Yesery Wijaya, Hendy Hadinugroho, Wuryanto Kusindarta, Dwi Liliek Wihadmadyatami, Hevi ACS Omega [Image: see text] Salicylic acid (SA) derivate is well-known for its anti-inflammatory and analgesic activity through cyclooxygenase (COX)-inhibition. Previous studies pointed toward gastric toxicity induced by most salicylic acid derivative compounds, particularly acetylsalicylic acid (ASA). Despite the adverse effect, ASA is still used due to price affordability and additional advantages in preventing platelet aggregation. Recently, a novel salicylic acid derivative called 2-((3 (chloromethyl)benzoyl)oxy)benzoic acid (3-CH(2)Cl) was introduced as a potential alternative compound to substitute ASA. Preliminary assessment results of COX-2 specificity, toxicity profile, analgesic, anti-inflammatory, and antiplatelet activity have made 3-CH(2)Cl a promising compound for “new” drug development. This review focuses on the discovery, potential activity, and benefits of 3-CH(2)Cl and the possible molecular mechanisms of its regulations in health and disease. Thus, this review may prove to be beneficial for the utilization of 3-CH(2)Cl as a potential alternative drug to substitute ASA. American Chemical Society 2022-12-28 /pmc/articles/PMC9835159/ /pubmed/36643478 http://dx.doi.org/10.1021/acsomega.2c05566 Text en © 2022 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by-nc-nd/4.0/Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Tjahjono, Yudy Caroline, Foe, Kuncoro Karnati, Srikanth Ergün, Süleyman Esar, Senny Yesery Wijaya, Hendy Hadinugroho, Wuryanto Kusindarta, Dwi Liliek Wihadmadyatami, Hevi Synthesis, Characterization, and Application of 2-((3-(Chloromethyl)-benzoyl)oxy)benzoic Acid: A Review |
title | Synthesis, Characterization, and Application of 2-((3-(Chloromethyl)-benzoyl)oxy)benzoic
Acid: A Review |
title_full | Synthesis, Characterization, and Application of 2-((3-(Chloromethyl)-benzoyl)oxy)benzoic
Acid: A Review |
title_fullStr | Synthesis, Characterization, and Application of 2-((3-(Chloromethyl)-benzoyl)oxy)benzoic
Acid: A Review |
title_full_unstemmed | Synthesis, Characterization, and Application of 2-((3-(Chloromethyl)-benzoyl)oxy)benzoic
Acid: A Review |
title_short | Synthesis, Characterization, and Application of 2-((3-(Chloromethyl)-benzoyl)oxy)benzoic
Acid: A Review |
title_sort | synthesis, characterization, and application of 2-((3-(chloromethyl)-benzoyl)oxy)benzoic
acid: a review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9835159/ https://www.ncbi.nlm.nih.gov/pubmed/36643478 http://dx.doi.org/10.1021/acsomega.2c05566 |
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