Literature DB >> 21599421

Checkpoint kinase inhibitors: a patent review (2009 - 2010).

Michael Lainchbury1, Ian Collins.   

Abstract

INTRODUCTION: Cells that suffer DNA damage activate the checkpoint kinases CHK1 and CHK2, which signal to initiate repair processes, limit cell-cycle progression and prevent cell replication, until the damaged DNA is repaired. Due to their potential application as novel anticancer therapies, inhibitors of CHK1 and CHK2 have become the focus of numerous drug discovery projects. AREAS COVERED: This patent review examines the chemical structures and biological activities of recently reported CHK1 and CHK2 inhibitors. The chemical abstract and patent databases SciFinder and esp@cenet were used to locate patent applications that were published between September 2008 and December 2010, claiming chemical structures for use as CHK1 or CHK2 inhibitors. EXPERT OPINION: This is an exciting time for checkpoint kinase inhibitors, with several currently in Phase I or II clinical trials. Many of the CHK1 inhibitors contained within this patent review have shown preclinical efficacy in combination with DNA-damaging chemotherapies. CHK1 inhibitors have recently been demonstrated to be efficacious as single agents in preclinical models of tumors with constitutive activation of CHK1 or high intrinsic DNA damage due to replication stress. The level of newly published patent applications covering CHK1 and CHK2 inhibitors remains high and a diverse range of scaffolds has been claimed.

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Year:  2011        PMID: 21599421     DOI: 10.1517/13543776.2011.586632

Source DB:  PubMed          Journal:  Expert Opin Ther Pat        ISSN: 1354-3776            Impact factor:   6.674


  8 in total

Review 1.  Cell Cycle Regulation and Melanoma.

Authors:  Wen Xu; Grant McArthur
Journal:  Curr Oncol Rep       Date:  2016-06       Impact factor: 5.075

Review 2.  Structure-based design, discovery and development of checkpoint kinase inhibitors as potential anticancer therapies.

Authors:  Thomas P Matthews; Alan M Jones; Ian Collins
Journal:  Expert Opin Drug Discov       Date:  2013-04-18       Impact factor: 6.098

3.  Benzimidazole inhibitors of the protein kinase CHK2: clarification of the binding mode by flexible side chain docking and protein-ligand crystallography.

Authors:  Cornelis Matijssen; M Cris Silva-Santisteban; Isaac M Westwood; Samerene Siddique; Vanessa Choi; Peter Sheldrake; Rob L M van Montfort; Julian Blagg
Journal:  Bioorg Med Chem       Date:  2012-09-21       Impact factor: 3.641

4.  Deacetylation of CHK2 by SIRT1 protects cells from oxidative stress-dependent DNA damage response.

Authors:  Jiyun Kwon; Suhee Lee; Yong-Nyun Kim; In Hye Lee
Journal:  Exp Mol Med       Date:  2019-03-22       Impact factor: 8.718

5.  CCT244747 is a novel potent and selective CHK1 inhibitor with oral efficacy alone and in combination with genotoxic anticancer drugs.

Authors:  Mike I Walton; Paul D Eve; Angela Hayes; Melanie R Valenti; Alexis K De Haven Brandon; Gary Box; Albert Hallsworth; Elizabeth L Smith; Kathy J Boxall; Michael Lainchbury; Thomas P Matthews; Yann Jamin; Simon P Robinson; G Wynne Aherne; John C Reader; Louis Chesler; Florence I Raynaud; Suzanne A Eccles; Ian Collins; Michelle D Garrett
Journal:  Clin Cancer Res       Date:  2012-08-28       Impact factor: 12.531

6.  Discovery of 3-alkoxyamino-5-(pyridin-2-ylamino)pyrazine-2-carbonitriles as selective, orally bioavailable CHK1 inhibitors.

Authors:  Michael Lainchbury; Thomas P Matthews; Tatiana McHardy; Kathy J Boxall; Michael I Walton; Paul D Eve; Angela Hayes; Melanie R Valenti; Alexis K de Haven Brandon; Gary Box; G Wynne Aherne; John C Reader; Florence I Raynaud; Suzanne A Eccles; Michelle D Garrett; Ian Collins
Journal:  J Med Chem       Date:  2012-10-19       Impact factor: 7.446

7.  The clinical development candidate CCT245737 is an orally active CHK1 inhibitor with preclinical activity in RAS mutant NSCLC and Eµ-MYC driven B-cell lymphoma.

Authors:  Mike I Walton; Paul D Eve; Angela Hayes; Alan T Henley; Melanie R Valenti; Alexis K De Haven Brandon; Gary Box; Kathy J Boxall; Matthew Tall; Karen Swales; Thomas P Matthews; Tatiana McHardy; Michael Lainchbury; James Osborne; Jill E Hunter; Neil D Perkins; G Wynne Aherne; John C Reader; Florence I Raynaud; Suzanne A Eccles; Ian Collins; Michelle D Garrett
Journal:  Oncotarget       Date:  2016-01-19

8.  A radiosensitizing effect of RAD51 inhibition in glioblastoma stem-like cells.

Authors:  Anaïs Balbous; Ulrich Cortes; Karline Guilloteau; Pierre Rivet; Baptiste Pinel; Mathilde Duchesne; Julie Godet; Odile Boissonnade; Michel Wager; René Jean Bensadoun; Jean-Claude Chomel; Lucie Karayan-Tapon
Journal:  BMC Cancer       Date:  2016-08-05       Impact factor: 4.430

  8 in total

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