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2000
Volume 9, Issue 7
  • ISSN: 1871-5206
  • E-ISSN: 1875-5992

Abstract

Protein kinases are one of the largest known families of enzyme characterized by having a well conserved ATP binding pocket. Most of the synthetic kinase inhibitors are ATP-competitive, but display some potential problems, like selectivity, discrepancy between the in vitro and in vivo inhibition assays and an high risk of developing mutation inside the ATP-binding pocket. Recently some new inhibitors with a non-competitive mechanism of action were reported, with intresting results both in vitro and in vivo.

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/content/journals/acamc/10.2174/187152009789056930
2009-09-01
2025-04-21
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/content/journals/acamc/10.2174/187152009789056930
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  • Article Type:
    Research Article
Keyword(s): anticancer drugs; ATP non-competitive; drug discovery; Ser/Thr kinase inhibitors
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