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Current progress, challenges and future prospects of indazoles as protein kinase inhibitors for the treatment of cancer

The indazole core is an interesting pharmacophore due to its applications in medicinal chemistry. In the past few years, this moiety has been used for the synthesis of kinase inhibitors. Many researchers have demonstrated the use of indazole derivatives as specific kinase inhibitors, including tyros...

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Autores principales: Tandon, Nitin, Luxami, Vijay, Kant, Divya, Tandon, Runjhun, Paul, Kamaldeep
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9037120/
https://www.ncbi.nlm.nih.gov/pubmed/35478899
http://dx.doi.org/10.1039/d1ra03979b
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author Tandon, Nitin
Luxami, Vijay
Kant, Divya
Tandon, Runjhun
Paul, Kamaldeep
author_facet Tandon, Nitin
Luxami, Vijay
Kant, Divya
Tandon, Runjhun
Paul, Kamaldeep
author_sort Tandon, Nitin
collection PubMed
description The indazole core is an interesting pharmacophore due to its applications in medicinal chemistry. In the past few years, this moiety has been used for the synthesis of kinase inhibitors. Many researchers have demonstrated the use of indazole derivatives as specific kinase inhibitors, including tyrosine kinase and serine/threonine kinases. A number of anticancer drugs with an indazole core are commercially available, e.g. axitinib, linifanib, niraparib, and pazopanib. Indazole derivatives are applied for the targeted treatment of lung, breast, colon, and prostate cancers. In this review, we compile the current development of indazole derivatives as kinase inhibitors and their application as anticancer agents in the past five years.
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spelling pubmed-90371202022-04-26 Current progress, challenges and future prospects of indazoles as protein kinase inhibitors for the treatment of cancer Tandon, Nitin Luxami, Vijay Kant, Divya Tandon, Runjhun Paul, Kamaldeep RSC Adv Chemistry The indazole core is an interesting pharmacophore due to its applications in medicinal chemistry. In the past few years, this moiety has been used for the synthesis of kinase inhibitors. Many researchers have demonstrated the use of indazole derivatives as specific kinase inhibitors, including tyrosine kinase and serine/threonine kinases. A number of anticancer drugs with an indazole core are commercially available, e.g. axitinib, linifanib, niraparib, and pazopanib. Indazole derivatives are applied for the targeted treatment of lung, breast, colon, and prostate cancers. In this review, we compile the current development of indazole derivatives as kinase inhibitors and their application as anticancer agents in the past five years. The Royal Society of Chemistry 2021-07-20 /pmc/articles/PMC9037120/ /pubmed/35478899 http://dx.doi.org/10.1039/d1ra03979b Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/
spellingShingle Chemistry
Tandon, Nitin
Luxami, Vijay
Kant, Divya
Tandon, Runjhun
Paul, Kamaldeep
Current progress, challenges and future prospects of indazoles as protein kinase inhibitors for the treatment of cancer
title Current progress, challenges and future prospects of indazoles as protein kinase inhibitors for the treatment of cancer
title_full Current progress, challenges and future prospects of indazoles as protein kinase inhibitors for the treatment of cancer
title_fullStr Current progress, challenges and future prospects of indazoles as protein kinase inhibitors for the treatment of cancer
title_full_unstemmed Current progress, challenges and future prospects of indazoles as protein kinase inhibitors for the treatment of cancer
title_short Current progress, challenges and future prospects of indazoles as protein kinase inhibitors for the treatment of cancer
title_sort current progress, challenges and future prospects of indazoles as protein kinase inhibitors for the treatment of cancer
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9037120/
https://www.ncbi.nlm.nih.gov/pubmed/35478899
http://dx.doi.org/10.1039/d1ra03979b
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