Literature DB >> 21446845

Targeting the DFG-in kinase conformation: a new trend emerging from a patent analysis.

Mauro Angiolini1.   

Abstract

Aberrant kinase signaling leads to a multitude of disease states. The clinical and commercial success of agents typified by imatinib or dasatinib in the treatment of hematological malignancies has further validated kinase inhibition as a useful clinical strategy. This increased interest in kinases as therapeutic targets is evidenced by the rapidly increasing number of patent applications and peer-reviewed articles. This article discusses recent Patent that describe small molecules targeting the DFG-in active kinase conformation, by the so-called 'Type I½' inhibitor, against a small set of clinically relevant targets such as B-Raf, p38α, Jak2 and EphB4. Preclinical and clinical data are also highlighted for the most promising new molecular entities.

Entities:  

Mesh:

Substances:

Year:  2011        PMID: 21446845     DOI: 10.4155/fmc.10.294

Source DB:  PubMed          Journal:  Future Med Chem        ISSN: 1756-8919            Impact factor:   3.808


  6 in total

1.  Virtual screening using a conformationally flexible target protein: models for ligand binding to p38α MAPK.

Authors:  Natalie B Vinh; Jamie S Simpson; Peter J Scammells; David K Chalmers
Journal:  J Comput Aided Mol Des       Date:  2012-04-20       Impact factor: 3.686

Review 2.  FLT3-ITD and its current role in acute myeloid leukaemia.

Authors:  Francisco Alejandro Lagunas-Rangel; Venice Chávez-Valencia
Journal:  Med Oncol       Date:  2017-05-03       Impact factor: 3.064

3.  Homology modeling of DFG-in FMS-like tyrosine kinase 3 (FLT3) and structure-based virtual screening for inhibitor identification.

Authors:  Yi-Yu Ke; Vivek Kumar Singh; Mohane Selvaraj Coumar; Yung Chang Hsu; Wen-Chieh Wang; Jen-Shin Song; Chun-Hwa Chen; Wen-Hsing Lin; Szu-Huei Wu; John T A Hsu; Chuan Shih; Hsing-Pang Hsieh
Journal:  Sci Rep       Date:  2015-06-29       Impact factor: 4.379

4.  Structural insights into the polypharmacological activity of quercetin on serine/threonine kinases.

Authors:  Bincy Baby; Priya Antony; Walaa Al Halabi; Zahrah Al Homedi; Ranjit Vijayan
Journal:  Drug Des Devel Ther       Date:  2016-09-27       Impact factor: 4.162

5.  Ligand discrimination between active and inactive activation loop conformations of Aurora-A kinase is unmodified by phosphorylation.

Authors:  James A H Gilburt; Paul Girvan; Julian Blagg; Liming Ying; Charlotte A Dodson
Journal:  Chem Sci       Date:  2019-03-04       Impact factor: 9.825

Review 6.  Mechanisms Underlying Resistance to FLT3 Inhibitors in Acute Myeloid Leukemia.

Authors:  Motoki Eguchi; Yosuke Minami; Ayumi Kuzume; Sunggi Chi
Journal:  Biomedicines       Date:  2020-07-24
  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.