Kathryn Bell

SAR studies around a series of triazolopyridines as potent and selective PI3Kγ inhibitors.

G. Neubauer, N. Ramsden, G. Bergamini, 2012, Bioorganic & medicinal chemistry letters.

A Selective Inhibitor Reveals Pi3Kgamma Dependence of T(H)17 Cell Differentiation.

G. Drewes, G. Neubauer, Christina Rau, 2012 .

Discovery of 5-(2-amino-[1,2,4]triazolo[1,5-a]pyridin-7-yl)-N-(tert-butyl)pyridine-3-sulfonamide (CZC24758), as a potent, orally bioavailable and selective inhibitor of PI3K for the treatment of inflammatory disease.

G. Neubauer, N. Ramsden, G. Bergamini, 2012, Bioorganic & medicinal chemistry letters.

Discovery of novel PI3Kγ/δ inhibitors as potential agents for inflammation.

G. Neubauer, N. Ramsden, G. Bergamini, 2012, Bioorganic & medicinal chemistry letters.

A selective inhibitor reveals PI3Kγ dependence of T(H)17 cell differentiation.

G. Drewes, G. Neubauer, M. Bantscheff, 2012, Nature chemical biology.

Corrigendum: A selective inhibitor reveals PI3Kγ dependence of T H 17 cell differentiation

G. Drewes, G. Neubauer, M. Bantscheff, 2012 .