1101119-45-2Relevant academic research and scientific papers
Novel pyrazolo[1,5-a]pyridines with improved aqueous solubility as p110α-selective PI3 kinase inhibitors
Kendall, Jackie D.,Giddens, Anna C.,Tsang, Kit Yee,Marshall, Elaine S.,Lill, Claire L.,Lee, Woo-Jeong,Kolekar, Sharada,Chao, Mindy,Malik, Alisha,Yu, Shuqiao,Chaussade, Claire,Buchanan, Christina,Jamieson, Stephen M.F.,Rewcastle, Gordon W.,Baguley, Bruce C.,Denny, William A.,Shepherd, Peter R.
, p. 187 - 190 (2016/12/27)
As part of our investigation into pyrazolo[1,5-a]pyridines as novel p110α selective PI3 kinase inhibitors, we report a range of analogues with improved aqueous solubility by the addition of a basic amine. The compounds demonstrated comparable p110α potency and selectivity to earlier compounds but with up to 1000× greater aqueous solubility, as the hydrochloride salts. The compounds also displayed good activity in a cellular assay of PI3 kinase activity.
PYRAZOLO[1,5-A]PYRIDINES AND THEIR USE IN CANCER THERAPY
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Page/Page column 93, (2009/03/07)
Pyrazolo[1,5-a]pyridines are described, including methods for their preparation, and their use as agents or drugs for cancer therapy, both alone or in combination with radiation and/or other anticancer drugs.
