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Utilization of transition metal fluoride-based solid support catalysts for the synthesis of sulfonamides: carbonic anhydrase inhibitory activity and in silico study
The applications of solid support catalysts in catalyzing organic reactions are well-evident. In the present study, we explored a transition metal fluoride (FeF(3)) adsorbed on molecular sieves (4 Å) as a solid support catalyst for the preparation of sulfonamides 3a–3o. The solid support catalyst wa...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8979346/ https://www.ncbi.nlm.nih.gov/pubmed/35425332 http://dx.doi.org/10.1039/d1ra07844e |
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author | Ali, Deedar Amjad, Sayyeda Tayyeba Shafique, Zainab Naseer, Muhammad Moazzam al-Rashida, Mariya Sindhu, Tayyaba Allamgir Iftikhar, Shafia Shah, Muhammad Raza Hameed, Abdul Iqbal, Jamshed |
author_facet | Ali, Deedar Amjad, Sayyeda Tayyeba Shafique, Zainab Naseer, Muhammad Moazzam al-Rashida, Mariya Sindhu, Tayyaba Allamgir Iftikhar, Shafia Shah, Muhammad Raza Hameed, Abdul Iqbal, Jamshed |
author_sort | Ali, Deedar |
collection | PubMed |
description | The applications of solid support catalysts in catalyzing organic reactions are well-evident. In the present study, we explored a transition metal fluoride (FeF(3)) adsorbed on molecular sieves (4 Å) as a solid support catalyst for the preparation of sulfonamides 3a–3o. The solid support catalyst was characterized via X-ray diffraction and AFM analysis. The catalyst was further explored for the synthesis of indoles 6a–h, 1H-tetrazoles and 1,4-dihydropyridines. The sulfonamides prepared herein were investigated for their potential to inhibit carbonic anhydrase (hCA II, hCA IX and hCA XII). All compounds were found to be active inhibitors with IC(50) values in the low micromolar range. Some compounds were even found to be highly selective inhibitors. Compound 3i only inhibited hCA II (IC(50) = 2.76 ± 1.1 μM) and had <27% inhibition against hCA IX and hCA XII. Similarly, 3e (IC(50) = 0.63 ± 0.14 μM) only inhibited hCA XII and showed <31% inhibition against hCA II and hCA IX. Molecular docking studies were carried out to rationalize the ligand-binding site interactions. Given the lack of selective CA inhibitors, compounds 3e and 3i can provide significant leads for the further development of highly selective CA inhibitors. |
format | Online Article Text |
id | pubmed-8979346 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-89793462022-04-13 Utilization of transition metal fluoride-based solid support catalysts for the synthesis of sulfonamides: carbonic anhydrase inhibitory activity and in silico study Ali, Deedar Amjad, Sayyeda Tayyeba Shafique, Zainab Naseer, Muhammad Moazzam al-Rashida, Mariya Sindhu, Tayyaba Allamgir Iftikhar, Shafia Shah, Muhammad Raza Hameed, Abdul Iqbal, Jamshed RSC Adv Chemistry The applications of solid support catalysts in catalyzing organic reactions are well-evident. In the present study, we explored a transition metal fluoride (FeF(3)) adsorbed on molecular sieves (4 Å) as a solid support catalyst for the preparation of sulfonamides 3a–3o. The solid support catalyst was characterized via X-ray diffraction and AFM analysis. The catalyst was further explored for the synthesis of indoles 6a–h, 1H-tetrazoles and 1,4-dihydropyridines. The sulfonamides prepared herein were investigated for their potential to inhibit carbonic anhydrase (hCA II, hCA IX and hCA XII). All compounds were found to be active inhibitors with IC(50) values in the low micromolar range. Some compounds were even found to be highly selective inhibitors. Compound 3i only inhibited hCA II (IC(50) = 2.76 ± 1.1 μM) and had <27% inhibition against hCA IX and hCA XII. Similarly, 3e (IC(50) = 0.63 ± 0.14 μM) only inhibited hCA XII and showed <31% inhibition against hCA II and hCA IX. Molecular docking studies were carried out to rationalize the ligand-binding site interactions. Given the lack of selective CA inhibitors, compounds 3e and 3i can provide significant leads for the further development of highly selective CA inhibitors. The Royal Society of Chemistry 2022-01-24 /pmc/articles/PMC8979346/ /pubmed/35425332 http://dx.doi.org/10.1039/d1ra07844e Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/ |
spellingShingle | Chemistry Ali, Deedar Amjad, Sayyeda Tayyeba Shafique, Zainab Naseer, Muhammad Moazzam al-Rashida, Mariya Sindhu, Tayyaba Allamgir Iftikhar, Shafia Shah, Muhammad Raza Hameed, Abdul Iqbal, Jamshed Utilization of transition metal fluoride-based solid support catalysts for the synthesis of sulfonamides: carbonic anhydrase inhibitory activity and in silico study |
title | Utilization of transition metal fluoride-based solid support catalysts for the synthesis of sulfonamides: carbonic anhydrase inhibitory activity and in silico study |
title_full | Utilization of transition metal fluoride-based solid support catalysts for the synthesis of sulfonamides: carbonic anhydrase inhibitory activity and in silico study |
title_fullStr | Utilization of transition metal fluoride-based solid support catalysts for the synthesis of sulfonamides: carbonic anhydrase inhibitory activity and in silico study |
title_full_unstemmed | Utilization of transition metal fluoride-based solid support catalysts for the synthesis of sulfonamides: carbonic anhydrase inhibitory activity and in silico study |
title_short | Utilization of transition metal fluoride-based solid support catalysts for the synthesis of sulfonamides: carbonic anhydrase inhibitory activity and in silico study |
title_sort | utilization of transition metal fluoride-based solid support catalysts for the synthesis of sulfonamides: carbonic anhydrase inhibitory activity and in silico study |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8979346/ https://www.ncbi.nlm.nih.gov/pubmed/35425332 http://dx.doi.org/10.1039/d1ra07844e |
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