Development of dual PLD1/2 and PLD2 selective inhibitors from a common 1,3,8-Triazaspiro[4.5]decane Core: discovery of Ml298 and Ml299 that decrease invasive migration in U87-MG glioblastoma cells

从常见的 1,3,8-三氮杂螺[4.5]癸烷核心开发双重 PLD1/2 和 PLD2 选择性抑制剂:发现 Ml298 和 Ml299 可降低 U87-MG 胶质母细胞瘤细胞的侵袭性迁移

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作者:Matthew C O'Reilly, Sarah A Scott, Kyle A Brown, Thomas H Oguin 3rd, Paul G Thomas, J Scott Daniels, Ryan Morrison, H Alex Brown, Craig W Lindsley

Abstract

An iterative parallel synthesis effort identified a PLD2 selective inhibitor, ML298 (PLD1 IC50 > 20000 nM, PLD2 IC50 = 355 nM) and a dual PLD1/2 inhibitor, ML299 (PLD1 IC50 = 6 nM, PLD2 IC50 = 20 nM). SAR studies revealed that a small structural change (incorporation of a methyl group) increased PLD1 activity within this classically PLD2-preferring core and that the effect was enantiospecific. Both probes decreased invasive migration in U87-MG glioblastoma cells.

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