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Synthesis of Thiazolo[5,4-f]quinazolin-9(8H)-ones as Multi-Target Directed Ligands of Ser/Thr Kinases
A library of thirty novel thiazolo[5,4-f]quinazolin-9(8H)-one derivatives belonging to four series designated as 12, 13, 14 and 15 was efficiently prepared, helped by microwave-assisted technology when required. The efficient multistep synthesis of methyl 6-amino-2-cyano- benzo[d]thiazole-7-carboxyl...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6273584/ https://www.ncbi.nlm.nih.gov/pubmed/27144552 http://dx.doi.org/10.3390/molecules21050578 |
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author | Hédou, Damien Godeau, Julien Loaëc, Nadège Meijer, Laurent Fruit, Corinne Besson, Thierry |
author_facet | Hédou, Damien Godeau, Julien Loaëc, Nadège Meijer, Laurent Fruit, Corinne Besson, Thierry |
author_sort | Hédou, Damien |
collection | PubMed |
description | A library of thirty novel thiazolo[5,4-f]quinazolin-9(8H)-one derivatives belonging to four series designated as 12, 13, 14 and 15 was efficiently prepared, helped by microwave-assisted technology when required. The efficient multistep synthesis of methyl 6-amino-2-cyano- benzo[d]thiazole-7-carboxylate (1) has been reinvestigated and performed on a multigram scale. The inhibitory potency of the final products against five kinases involved in Alzheimer’s disease was evaluated. This study demonstrates that some molecules of the 12 and 13 series described in this paper are particularly promising for the development of new multi-target inhibitors of kinases. |
format | Online Article Text |
id | pubmed-6273584 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-62735842018-12-28 Synthesis of Thiazolo[5,4-f]quinazolin-9(8H)-ones as Multi-Target Directed Ligands of Ser/Thr Kinases Hédou, Damien Godeau, Julien Loaëc, Nadège Meijer, Laurent Fruit, Corinne Besson, Thierry Molecules Article A library of thirty novel thiazolo[5,4-f]quinazolin-9(8H)-one derivatives belonging to four series designated as 12, 13, 14 and 15 was efficiently prepared, helped by microwave-assisted technology when required. The efficient multistep synthesis of methyl 6-amino-2-cyano- benzo[d]thiazole-7-carboxylate (1) has been reinvestigated and performed on a multigram scale. The inhibitory potency of the final products against five kinases involved in Alzheimer’s disease was evaluated. This study demonstrates that some molecules of the 12 and 13 series described in this paper are particularly promising for the development of new multi-target inhibitors of kinases. MDPI 2016-04-30 /pmc/articles/PMC6273584/ /pubmed/27144552 http://dx.doi.org/10.3390/molecules21050578 Text en © 2016 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Hédou, Damien Godeau, Julien Loaëc, Nadège Meijer, Laurent Fruit, Corinne Besson, Thierry Synthesis of Thiazolo[5,4-f]quinazolin-9(8H)-ones as Multi-Target Directed Ligands of Ser/Thr Kinases |
title | Synthesis of Thiazolo[5,4-f]quinazolin-9(8H)-ones as Multi-Target Directed Ligands of Ser/Thr Kinases |
title_full | Synthesis of Thiazolo[5,4-f]quinazolin-9(8H)-ones as Multi-Target Directed Ligands of Ser/Thr Kinases |
title_fullStr | Synthesis of Thiazolo[5,4-f]quinazolin-9(8H)-ones as Multi-Target Directed Ligands of Ser/Thr Kinases |
title_full_unstemmed | Synthesis of Thiazolo[5,4-f]quinazolin-9(8H)-ones as Multi-Target Directed Ligands of Ser/Thr Kinases |
title_short | Synthesis of Thiazolo[5,4-f]quinazolin-9(8H)-ones as Multi-Target Directed Ligands of Ser/Thr Kinases |
title_sort | synthesis of thiazolo[5,4-f]quinazolin-9(8h)-ones as multi-target directed ligands of ser/thr kinases |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6273584/ https://www.ncbi.nlm.nih.gov/pubmed/27144552 http://dx.doi.org/10.3390/molecules21050578 |
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