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Published on: January 22, 2019
Highly potent aminopyridines as Syk kinase inhibitors
Marcos Castillo1, Pilar Forns, Montse Erra
1Almirall-Barcelona Science Park Unit, Barcelona Science Park, 08028 Barcelona, Spain.
Abstract:
A novel class of potent Syk inhibitors has been developed from rational design. Highly potent aminopyridine derivatives bearing a 4-trifluoromethyl-2-pyridyl motif and represented by compound 13b IC(50): 0.6 nM were identified. Substitution by a 2-pyrazinyl motif and SAR expansion in position 4 of the central core provided diverse potent non-cytotoxic Syk inhibitors showing nanomolar activity inhibiting human mast cell line LAD2 degranulation.
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