Issue 1, 2014

Novel pyrazolo[1,5-a]pyridines as PI3K inhibitors: variation of the central linker group

Abstract

As part of our investigation into the pyrazolo[1,5-a]pyridines as novel PI3K inhibitors, we report a range of analogues where the central linker portion of the molecule was varied while retaining the pyrazolo[1,5-a]pyridine and arylsulfonyl or arylcarbonyl groups. Isostere generating software BROOD was used to assist with producing ideas. The isoform selectivity of the compounds varied from pan-PI3K for compound 41 to p110α-selective for compound 58 or p110δ-selective for compound 57. The latter two compounds varied only in their sulphur oxidation state.

Graphical abstract: Novel pyrazolo[1,5-a]pyridines as PI3K inhibitors: variation of the central linker group

Supplementary files

Article information

Article type
Concise Article
Submitted
30 Jul 2013
Accepted
26 Oct 2013
First published
30 Oct 2013

Med. Chem. Commun., 2014,5, 41-46

Novel pyrazolo[1,5-a]pyridines as PI3K inhibitors: variation of the central linker group

J. D. Kendall, A. J. Marshall, A. C. Giddens, K. Y. Tsang, M. Boyd, R. Frédérick, C. L. Lill, W. Lee, S. Kolekar, M. Chao, A. Malik, S. Yu, C. Chaussade, C. M. Buchanan, G. W. Rewcastle, B. C. Baguley, J. U. Flanagan, W. A. Denny and P. R. Shepherd, Med. Chem. Commun., 2014, 5, 41 DOI: 10.1039/C3MD00221G

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