Results 281 to 290 of about 4,906,436 (344)
Some of the next articles are maybe not open access.

Kinase inhibitors: the road ahead

Nature Reviews Drug Discovery, 2018
Fleur M Ferguson, Nathanael S Gray
exaly   +2 more sources

Properties of FDA-approved small molecule protein kinase inhibitors: a 2021 update.

Pharmacological Research, 2021
Owing to the dysregulation of protein kinase activity in many diseases including cancer, the protein kinase enzyme family has become one of the most important drug targets in the 21st century.
R. Roskoski
semanticscholar   +1 more source

Tyrosine Kinase Inhibitors

Current Cancer Drug Targets, 2010
Over the last ten years, several new and therapeutically relevant cancer drugs targeting tyrosine kinases signaling pathways have been developed. Tyrosine kinase inhibitors (TKIs) are a pharmaceutical class of small molecules, orally available, well-tolerated, worldwide approved drugs for the treatment of several neoplasms, including lung, breast ...
NATOLI, Clara   +5 more
openaire   +3 more sources

Multi-Kinase Inhibitors

Current Medicinal Chemistry, 2015
The limitations of many mono-kinase inhibitors can be overcome by agents with multi-target action. An important advantage of targeting more than one kinase, is an increase in potency, due to the synergistic effect. Moreover, this approach can reduce the possibility of developing drug resistance.
GARUTI, LAURA   +2 more
openaire   +3 more sources

Advances in covalent kinase inhibitors.

Chemical Society Reviews, 2020
Over the past decade, covalent kinase inhibitors (CKI) have seen a resurgence in drug discovery. Covalency affords a unique set of advantages as well as challenges relative to their non-covalent counterpart.
Ayah Abdeldayem   +4 more
semanticscholar   +1 more source

Properties of FDA-approved small molecule protein kinase inhibitors.

Pharmacological Research, 2019
Because mutations, overexpression, and dysregulation of protein kinases play essential roles in the pathogenesis of many illnesses, this enzyme family has become one of the most important drug targets in the past 20 years.
R. Roskoski
semanticscholar   +1 more source

Properties of FDA-approved small molecule protein kinase inhibitors: a 2020 update.

Pharmacological Research, 2019
Because genetic alterations including mutations, overexpression, translocations, and dysregulation of protein kinases are involved in the pathogenesis of many illnesses, this enzyme family is currently the subject of many drug discovery programs in the ...
R. Roskoski
semanticscholar   +1 more source

Aurora kinase inhibitors

Critical Reviews in Oncology/Hematology, 2010
Most human cancer cells are characterized by changes in the amount or organization of DNA resulting in chromosome instability and aneuploidy. Several mitotic kinases, Aurora kinases amongst others, regulate the progression of the cell through mitosis. So far three Aurora kinases have been identified in man: Aurora-A, Aurora-B and Aurora-C.
Kitzen, JJEM (Jos)   +2 more
openaire   +2 more sources

Acute Lung Injury: the therapeutic role of Rho kinase inhibitors.

Pharmacological Research, 2020
Acute lung injury (ALI) is a pulmonary illness with high rates of mortality and morbidity. Rho GTPase and its downstream effector, Rho kinase (ROCK), have been demonstrated to be involved in cell adhesion, motility, and contraction which can play a role ...
F. Abedi   +3 more
semanticscholar   +1 more source

Inhibitors of tyrosine kinase

Current Opinion in Oncology, 1997
This review covers the literature on significant studies of small molecule inhibitors of the epidermal growth factor receptor (EGFR), platelet-derived growth factor receptor (PDGFR), fibroblast growth factor receptor (FGFR), Flk-1, and src family tyrosine kinases from 1996 through mid-1997. During this period, there has been substantial progress in the
W D, Klohs, D W, Fry, A J, Kraker
openaire   +2 more sources

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