Radiosonde apparatus

NIK SMI1.

InformationWM-8014 WM-8014 is a highly potent inhibitor of histone acetyltransferase KAT6A with an IC50 of 8 nM.TargetsKAT6A (Cell-free assay) 8 nMIn vitroWM-8014 induces cell cycle arrest in embryonic day (E)14.5 mouse embryonic fibroblasts.Cells

InformationWT161 is a potent, selective, and bioavailableHDAC6inhibitor withIC50 valuesof 0.4 nM, 8.35 nM and 15.4 nM for HDAC6, HDAC1 and HDAC2, respectively: shown to have &gt:100-fold selectivity over other HDACs. WT161

InformationWT161 is a potent, selective, and bioavailableHDAC6inhibitor withIC50 valuesof 0.4 nM, 8.35 nM and 15.4 nM for HDAC6, HDAC1 and HDAC2, respectively: shown to have &gt:100-fold selectivity over other HDACs. WT161

InformationWT161 is a potent, selective, and bioavailableHDAC6inhibitor withIC50 valuesof 0.4 nM, 8.35 nM and 15.4 nM for HDAC6, HDAC1 and HDAC2, respectively: shown to have &gt:100-fold selectivity over other HDACs. WT161

InformationWT161 is a potent, selective, and bioavailableHDAC6inhibitor withIC50 valuesof 0.4 nM, 8.35 nM and 15.4 nM for HDAC6, HDAC1 and HDAC2, respectively: shown to have &gt:100-fold selectivity over other HDACs. WT161

InformationWM-8014 WM-8014 is a highly potent inhibitor of histone acetyltransferase KAT6A with an IC50 of 8 nM.TargetsKAT6A (Cell-free assay) 8 nMIn vitroWM-8014 induces cell cycle arrest in embryonic day (E)14.5 mouse embryonic fibroblasts.Cells

InformationWM-8014 WM-8014 is a highly potent inhibitor of histone acetyltransferase KAT6A with an IC50 of 8 nM.TargetsKAT6A (Cell-free assay) 8 nMIn vitroWM-8014 induces cell cycle arrest in embryonic day (E)14.5 mouse embryonic fibroblasts.Cells

InformationWM-8014 WM-8014 is a highly potent inhibitor of histone acetyltransferase KAT6A with an IC50 of 8 nM.TargetsKAT6A (Cell-free assay) 8 nMIn vitroWM-8014 induces cell cycle arrest in embryonic day (E)14.5 mouse embryonic fibroblasts.Cells

InformationWM-8014 WM-8014 is a highly potent inhibitor of histone acetyltransferase KAT6A with an IC50 of 8 nM.TargetsKAT6A (Cell-free assay) 8 nMIn vitroWM-8014 induces cell cycle arrest in embryonic day (E)14.5 mouse embryonic fibroblasts.Cells

InformationWZ4002 is a novel, mutant-selective EGFR inhibitor forEGFR(L858R)/(T790M)withIC50of 2 nM/8 nM in BaF3 cell line: does not inhibit ERBB2 phosphorylation (T798I).In vitroWZ4002 inhibits other EGFR genotypes E746_A750 and E746_A750/T790M

WZ4002 is a novel, mutant-selective EGFR inhibitor for EGFR(L858R)/(T790M) with IC50 of 2 nM/8 nM: does not inhibit ERBB2 phosphorylation (T798I).An EGFR phosphorylation inhibitor.