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A broad-based, cell-permeable, reversible, ATP-competitive serine-threonine kinase inhibitor. Potent inhibitor of myosin light chain kinase (Kᵢ = 97 µM), protein kinase A (Kᵢ = 3.0 µM), protein kinase C (Kᵢ = 6 µM), and protein kinase G (Kᵢ = 5.8 µM). Induces apoptotic DNA fragmentation and cell death in HL-60 human promyelocytic leukemia cells. Also inhibits telomerase activity in quercetin-, H-89-, or herbimycin A-treated NPC-076 cells.,官网链接:https://www.sigmaaldrich.cn/product/mm/371955m
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