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Kinase selectivity potential for inhibitors targeting the ATP binding site: a network analysis

Bioinformatics, 2010-01, Vol.26 (2), p.198-204

2010

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Optimization of Inhibitors of the Tyrosine Kinase EphB4. 2. Cellular Potency Improvement and Binding Mode Validation by X‑ray Crystallography

Journal of medicinal chemistry, 2013-01, Vol.56 (1), p.84-96

2013

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Pyrrolo[3,2- b ]quinoxaline Derivatives as Types I 1/2 and II Eph Tyrosine Kinase Inhibitors: Structure-Based Design, Synthesis, and in Vivo Validation

Journal of medicinal chemistry, 2014-08, Vol.57 (15), p.6834-6844

2014

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Structure-Based Optimization of Potent and Selective Inhibitors of the Tyrosine Kinase Erythropoietin Producing Human Hepatocellular Carcinoma Receptor B4 (EphB4)

Journal of medicinal chemistry, 2009-10, Vol.52 (20), p.6433-6446

2009

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Pyrrolo[3,2‑b]quinoxaline Derivatives as Types I1/2 and II Eph Tyrosine Kinase Inhibitors: Structure-Based Design, Synthesis, and in Vivo Validation

Journal of medicinal chemistry, 2014-08, Vol.57 (15), p.6834-6844

2014

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Three stories on Eph kinase inhibitors: From in silico discovery to in vivo validation

European journal of medicinal chemistry, 2016-04, Vol.112, p.347-366

2016

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Discovery of a Novel Chemotype of Tyrosine Kinase Inhibitors by Fragment-Based Docking and Molecular Dynamics

ACS medicinal chemistry letters, 2012-10, Vol.3 (10), p.834-838

2012

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Complementing ultrafast shape recognition with an optical isomerism descriptor

Journal of molecular graphics & modelling, 2010-11, Vol.29 (3), p.443-449

2010

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Students' Motivations for Voluntary Remedial Learning in High School

Journal of international education research, 2013-09, Vol.9 (4), p.381-386

2013

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ChemInform Abstract: Three Stories on Eph Kinase Inhibitors: From in silico Discovery to in vivo Validation

ChemInform, 2016-03, Vol.47 (16), p.no-no

2016

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Extractable phenolic yield variation in five cultivars of mature short rotation coppice willow from four plantations in Quebec

Industrial crops and products, 2017-03, Vol.97, p.525-535

2017

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vol. 33/2

Communication, 2015

2015

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Kinase selectivity potential for inhibitors targeting the ATP binding site: a network analysis

Optimization of Inhibitors of the Tyrosine Kinase EphB4. 2. Cellular Potency Improvement and Binding Mode Validation by X‑ray Crystallography

Pyrrolo[3,2- b ]quinoxaline Derivatives as Types I 1/2 and II Eph Tyrosine Kinase Inhibitors: Structure-Based Design, Synthesis, and in Vivo Validation

Structure-Based Optimization of Potent and Selective Inhibitors of the Tyrosine Kinase Erythropoietin Producing Human Hepatocellular Carcinoma Receptor B4 (EphB4)

Pyrrolo[3,2‑b]quinoxaline Derivatives as Types I1/2 and II Eph Tyrosine Kinase Inhibitors: Structure-Based Design, Synthesis, and in Vivo Validation

Three stories on Eph kinase inhibitors: From in silico discovery to in vivo validation

Discovery of a Novel Chemotype of Tyrosine Kinase Inhibitors by Fragment-Based Docking and Molecular Dynamics

Complementing ultrafast shape recognition with an optical isomerism descriptor

Students' Motivations for Voluntary Remedial Learning in High School

ChemInform Abstract: Three Stories on Eph Kinase Inhibitors: From in silico Discovery to in vivo Validation

Extractable phenolic yield variation in five cultivars of mature short rotation coppice willow from four plantations in Quebec

Court métrage : formes, formats, usages

vol. 33/2

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