Recent mouse knockout studies identified adapter protein-2 associated kinase 1 (AAK1) as a viable target for treating neuropathic pain. Potent small-molecule inhibitors of AAK1 have been identified and show efficacy in various rodent pain models. ()-1-((2',6-Bis(difluoromethyl)-[2,4'-bipyridin]-5-yl)oxy)-2,4-dimethylpentan-2-amine (BMS-986176/LX-9211) () was identified as a highly selective, CNS penetrant, potent AAK1 inhibitor from a novel class of bi(hetero)aryl ethers.
View Article and Find Full Text PDFAgOC(CF(3))(3), a soluble source, was found to be a convenient reagent for the one-pot preparation of Ag-NHC and M-NHC complexes starting from imidazoliums (M = Au, Ir, Pd and Ru).
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