Discovery of 2,3,5-Trisubstituted Pyridine Derivatives as Potent Akt1 and Akt2 Dual Inhibitors.

ChemInform Abstract: Discovery of 5-Pyrr

ChemInform Abstract: Discovery of 5-Pyrrolopyridinyl-2-thiophenecarboxamides as Potent AKT Kinase Inhibitors.

✍ Mark A. Seefeld; et al. et al. 📂 Article 📅 2009 🏛 John Wiley and Sons ⚖ 26 KB 👁 1 views

## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v

Identification of a Novel 3,5-Disubstitu

Identification of a Novel 3,5-Disubstituted Pyridine as a Potent, Selective, and Orally Active Inhibitor of Akt1 Kinase.

✍ Sheela A. Thomas; et al. et al. 📂 Article 📅 2006 🏛 John Wiley and Sons ⚖ 9 KB

## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract, please click on HTML or PDF.

Synthesis and Biological Evaluation of F

Synthesis and Biological Evaluation of Furo[2,3-d]pyrimidines as Akt1 Kinase Inhibitors.

✍ Se Young Kim; Dong Jin Kim; Beom Seok Yang; Kyung Ho Yoo 📂 Article 📅 2007 🏛 John Wiley and Sons ⚖ 18 KB 👁 1 views

## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract, please click on HTML or PDF.

The Discovery of N-(1,3-Thiazol-2-yl)pyr

The Discovery of N-(1,3-Thiazol-2-yl)pyridin-2-amines as Potent Inhibitors of KDR Kinase.

✍ Mark T. Bilodeau; et al. et al. 📂 Article 📅 2004 🏛 John Wiley and Sons ⚖ 87 KB 👁 1 views

Synthesis of 1H-Pyridin-2-one Derivative

Synthesis of 1H-Pyridin-2-one Derivatives as Potent and Selective Farnesyltransferase Inhibitors.

✍ Le Wang; et al. et al. 📂 Article 📅 2004 🏛 John Wiley and Sons ⚖ 28 KB 👁 1 views

Discovery of a Potent, Selective and Ora

Discovery of a Potent, Selective and Orally Active Canine COX-2 Inhibitor, 2-(3-Difluoromethyl-5-phenyl-pyrazol-1-yl)-5-methanesulfonyl-pyridine.

✍ Jin Li; et al. et al. 📂 Article 📅 2004 🏛 John Wiley and Sons ⚖ 104 KB 👁 2 views

## Abstract For Abstract see ChemInform Abstract in Full Text.