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Non-kinase targets of protein kinase inhibitors

Nature Reviews Drug Discovery, 2017
Kinome-wide profiling platforms have comprehensively identified the relevant kinases that are targeted by numerous protein kinase inhibitors. However, recent projects have begun to discover non-kinase targets of kinase inhibitors. These non-kinase targets can contribute to the desired or undesired activities of inhibitors, or act as silent bystanders ...
L. Munoz
semanticscholar   +4 more sources

Protein Kinase Inhibitors [PDF]

open access: possible, 2014
The article contains sections titled: 1. Introduction 2. Approved Kinase Inhibitors and Their Syntheses 3.
A. Kleemann
semanticscholar   +2 more sources

Discovery of Cysteine-targeting Covalent Protein Kinase Inhibitors.

Journal of Medicinal Chemistry, 2021
Small molecule covalent kinase inhibitors (CKIs) have entered a new era in drug discovery, which have the advantage for sustained target inhibition and high selectivity.
Xiaoyun Lu   +3 more
semanticscholar   +1 more source

Irreversible protein kinase inhibitors.

Current Medicinal Chemistry, 2011
Targeting cancer with small molecule irreversible inhibitors of kinases represents an emerging challenge in drug discovery. Irreversible inhibitors bind to kinase active site in a covalent and irreversible form, most frequently by reacting with a nucleophilic cysteine residue, located near the ATP binding pocket.
L. Garuti, M. Roberti, G. Bottegoni
semanticscholar   +5 more sources

Protein kinase inhibitors in melanoma

Expert Opinion on Pharmacotherapy, 2013
The most commonly mutated oncogene identified to date in melanoma is BRAF (∼ 50%), an upstream mediator of the mitogen-activated protein kinase (MAPK) pathway. Recently, BRAF-kinase inhibitors as well as MEK-kinase inhibitors were introduced into the clinics.Substantial Phase II and III clinical trials were searched in patients with advanced melanoma ...
Claus Garbe   +2 more
openaire   +3 more sources

Inhibitors of protein tyrosine kinases

Current Opinion in Biotechnology, 1995
The description in the past year of several novel protein tyrosine kinase inhibitors, which exhibit dramatic improvements in potency and specificity over earlier agents, will be considered a major turning point in the field. These compounds appear to have the necessary pharmacological properties to finally allow clarification of whether suppression of ...
David W. Fry, Alexander James Bridges
openaire   +3 more sources

Paullones as Inhibitors of Protein Kinases

Current Topics in Medicinal Chemistry, 2011
Paullones are a class of molecules structurally based on the 7,12-dihydroindolo[3,2-d][1]benzazepin-6(5H)-one parent scaffold. Many of these structures are inhibitors of certain protein kinases, namely cyclin-dependent kinases and glycogen synthase kinase-3. Being well referenced in the literature on the one hand and commercially available on the other
Conrad Kunick, Nadine Tolle
openaire   +3 more sources

Inhibitors of protein kinases and phosphatases

Trends in Biochemical Sciences, 1994
Inhibitors of eukaryotic protein kinases and phosphatases are a chemically diverse array of natural and synthetic compounds, including medicines, potions and poisons. These substances are valuable pharmacological probes and affinity ligands for the kinases and phosphatases of signalling pathways, enhancing our knowledge of the cellular effects of the ...
MacKintosh, Carol, MacKintosh, Robert W.
openaire   +4 more sources

Protein kinase C inhibitors

Current Oncology Reports, 2002
Protein kinase C (PKC) is a family of serine-threonine protein kinases that are involved in signal transduction pathways that regulate growth factor response, proliferation, and apoptosis. Its central role in these processes, which are closely involved in tumor initiation, progression, and response to antitumor agents, makes it an attractive ...
Stanley B. Kaye, Helen C. Swannie
openaire   +3 more sources

An inhibitor protein of nuclear protein kinases

Nature, 1979
THE cyclical phosphorylation and dephosphorylation of proteins, catalysed by protein kinases and phosphoprotein phosphatases, respectively, are important ways in which cells regulate many of their metabolic activities. Cells seem to have at least two distinct phosphorylation systems, one in the cytoplasm, the other in the nucleus.
Francoise Farron-Furstenthal   +1 more
openaire   +3 more sources

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