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Entinostat (MS-275) - HDAC Inhibitor. CAS# 209783-80-2 0166 InChiKey: WWONFUQGBVOKOF-UHFFFAOYSA-N

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Entinostat (MS-275) - HDAC Inhibitor. CAS# 209783-80-2 0166 InChiKey: WWONFUQGBVOKOF-UHFFFAOYSA-NEntinostat (MS 275), CAS No. 209783 80 2, is a potent and selective HDAC inhibitor. It inhibits HDAC1 and HDAC3 with IC50 of 0. 51 M and 1. 7 M, but not the other HDACs 4, 6, 8, and 10 (IC50 > 100 M). MS 275 induces accumulation of p21WAF1 CIP1 and gelsolin in K562 cell. It was shown to reduce S phase cells and induce G1 phase cells in A2780 cells. MS 275 shows great inhibition to human leukemia and lymphoma cells, decreases expression of cyclin D1

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InChiKey: WWONFUQGBVOKOF-UHFFFAOYSA-N

Gö 6983: a fast acting protein kinase C inhibitor that attenuates myocardial ischemia/reperfusion injury

NMS-873 provided critical validation of VCP as a cancer target

ITD-1 was used at 5 µM final concentration in vitro and in cellular assays

It was dosed to diabetic ob/ob mice via oral gavage at 3-30 mg/kg once per day for 2 weeks

Entinostat (MS-275) - HDAC Inhibitor. CAS# 209783-80-2 0166 InChiKey: WWONFUQGBVOKOF-UHFFFAOYSA-NEntinostat (MS 275), CAS No. 209783 80 2, is a potent and selective HDAC inhibitor. It inhibits HDAC1 and HDAC3 with IC50 of 0. 51 M and 1. 7 M, but not the other HDACs 4, 6, 8, and 10 (IC50 > 100 M). MS 275 induces accumulation of p21WAF1 CIP1 and gelsolin in K562 cell. It was shown to reduce S phase cells and induce G1 phase cells in A2780 cells. MS 275 shows great inhibition to human leukemia and lymphoma cells, decreases expression of cyclin D1

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