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嘌呤衍生物;根据细胞类型诱导分化或去分化;抑制AuroraA、B和C激酶,IC50值为98-876nM;A3受体拮抗剂(Ki=0.66µM);抑制MPS1(其激酶结构域和全长版本的IC50分别为6和2.8nM);诱导WRO人滤泡性甲状腺癌细胞自噬;降低Akt/mTOR信号传导。A purine derivative; induces differentiation or dedifferentiation, depending on cell type; inhibits the Aurora A, B, and C kinases with IC50 values of 98-876 nM; A3 receptor antagonist (Ki = 0.66 µM); inhibits MPS1 (IC50s = 6 and 2.8 nM for its kinase domain and full-length version, respectively); induces autophagy in WRO human follicular thyroid cancer cells; decreases Akt/mTOR signaling.
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