1093302-70-5Relevant articles and documents
Scaffold oriented synthesis. Part 3: Design, synthesis and biological evaluation of novel 5-substituted indazoles as potent and selective kinase inhibitors employing [2+3] cycloadditions
Akritopoulou-Zanze, Irini,Wakefield, Brian D.,Gasiecki, Alan,Kalvin, Douglas,Johnson, Eric F.,Kovar, Peter,Djuric, Stevan W.
, p. 1476 - 1479 (2011/04/16)
We report the synthesis and biological evaluation of 5-substituted indazoles and amino indazoles as kinase inhibitors. The compounds were synthesized in a parallel synthesis fashion from readily available starting materials employing [2+3] cycloaddition r