4.5 Article

Novel approaches for targeting kinases: allosteric inhibition, allosteric activation and pseudokinases

Journal

FUTURE MEDICINAL CHEMISTRY
Volume 6, Issue 5, Pages 541-561

Publisher

FUTURE SCI LTD
DOI: 10.4155/fmc.13.216

Keywords

-

Funding

  1. SGC
  2. Canadian Institutes for Health Research [1097737]
  3. Canada Foundation for Innovation
  4. Genome Canada
  5. GlaxoSmithKline
  6. Pfizer
  7. Eli Lilly
  8. Takeda
  9. AbbVie
  10. Novartis Research Foundation
  11. Ontario Ministry of Research and Innovation
  12. Wellcome Trust [092809/Z/10/Z]

Ask authors/readers for more resources

Protein kinases are involved in many essential cellular processes and their deregulation can lead to a variety of diseases, including cancer. The pharmaceutical industry has invested heavily in the identification of kinase inhibitors to modulate these disease-promoting pathways, resulting in several successful drugs. However, the field is challenging as it is difficult to identify novel selective inhibitors with good pharmacokinetic/pharmacodynamic properties. In addition, resistance to kinase inhibitor treatment frequently arises. The identification of non-ATP site targeting (allosteric') inhibitors, the identification of kinase activators and the expansion of kinase target space to include the less studied members of the family, including atypical- and pseudo-kinases, are potential avenues to overcome these challenges. In this perspective, the opportunities and challenges of following these approaches and others will be discussed.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.5
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available