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Formula: C21H25N7
ZSTK474 treatment inhibits the production of IFNγ and IL-17 in concanavalin A-activated T cells
3T3 fibroblasts
is a potent and competitive AMPA/kainate receptor antagonist with IC50s of 0
A small molecule modulates Jumonji histone demethylase activity and selectively inhibits cancer growth
NMS-P715 Size:Solid 10 mg Formula: C21H25N7NMS P715 is a selective and orally bioavailable MPS1 inhibitor, which selectively reduces cancer cell proliferation, leaving normal cells almost unaffected. NMS P715 accelerates mitosis and affects kinetochore components localization causing massive aneuploidy and cell death in a variety of tumoral cell lines and inhibits tumor growth in preclinical cancer models. Inhibiting the SAC could represent a promising new approach to selectively target cancer