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2-Aminobenzimidazoles as potent Aurora kinase inhibitors.

artículo científico publicado en 2009

Design and synthesis of 2-amino-pyrazolopyridines as Polo-like kinase 1 inhibitors

artículo científico publicado en 2008

Discovery and Development of Potent LFA-1/ICAM-1 Antagonist SAR 1118 as an Ophthalmic Solution for Treating Dry Eye.

artículo científico publicado en 2012

Discovery and in Vivo Evaluation of the Potent and Selective PI3Kδ Inhibitors 2-((1S)-1-((6-Amino-5-cyano-4-pyrimidinyl)amino)ethyl)-6-fluoro-N-methyl-3-(2-pyridinyl)-4-quinolinecarboxamide (AM-0687) and 2-((1S)-1-((6-Amino-5-cyano-4-pyrimidinyl)ami

artículo científico publicado en 2016

Discovery of Potent, Selective, and Orally Bioavailable Inhibitors of USP7 with In Vivo Anti-Tumor Activity

scientific article published on 17 April 2020

Discovery of a Potent and Selective CCR4 Antagonist That Inhibits Treg Trafficking into the Tumor Microenvironment

scientific article published on 01 July 2019

Discovery of a potent and selective aurora kinase inhibitor

artículo científico publicado en 2008

Discovery of tetrahydroisoquinoline (THIQ) derivatives as potent and orally bioavailable LFA-1/ICAM-1 antagonists

artículo científico publicado en 2010

Optimization of novel reversible Bruton's tyrosine kinase inhibitors identified using Tethering-fragment-based screens

artículo científico publicado en 2019

Structure–activity relationship (SAR) of the α-amino acid residue of potent tetrahydroisoquinoline (THIQ)-derived LFA-1/ICAM-1 antagonists ⬇️

artículo científico publicado el 5 de noviembre de 2010

Synthesis and SAR study of potent and selective PI3Kδ inhibitors

artículo científico publicado en 2015

Water-soluble prodrugs of an Aurora kinase inhibitor

artículo científico publicado en 2009

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