WebMay 17, 2013 · Biological description. Potent, highly selective aminopyrimidine GSK3 inhibitor (IC 50 values are 6.7 and 10 nM at GSK3β and GSK3α, respectively). Exhibits … WebCHIR-98014 is a potent, cell-permeable GSK-3 inhibitor with IC50 s of 0.65 and 0.58 nM for GSK-3α and GSK-3β, respectively; it shows less potent activities against cdc2 and erk2 . value of 0.87 nM. CHIR 98014 causes GS stimulation in CHO-IR cells and rat hepatocytes, with EC 50 s of 106 nM and 107 nM, respectively [1].
GSK3 inhibitors CHIR99021 and 6-bromoindirubin-3′-oxime inhibit ...
WebJun 1, 2004 · The development of even more potent and specific inhibitors of GSK3 that do not inhibit CDKs, such as CHIR 99021 (Refs 34,35), AR-A014418 (Ref. 36) and bis-7-azaindolylmaleimides 37 , has been an ... WebJan 17, 2024 · GSK3 inhibitors activated Wnt/β-catenin signalling axis in hASCs. To examine whether inhibition of GSK3 would mimic Wnt signalling through direct stabilization of β-catenin in hASCs, the cells ... black band leaders
GSK3 Kinase Inhibitor, CHIR, Suppress Transcription of
WebCHIR-99021 is a GSK-3α/β inhibitor (IC50: 10/6.7 nM). Targets&IC50. GSK-3β:6.7 nM (cell free), GSK-3α:10 nM (cell free) In vitro. CHIR 99021 inhibited human GSK-3β (Ki: 9.8 nmol/L). It exhibited from 500-fold to >10,000-fold selectivity for GSK-3 versus 20 other protein kinases [1]. CHIR99021 can induce the reprogramming of mouse embryonic ... WebMar 19, 2024 · Treatment with BIO or CHIR also affected pY-GSK3 levels, consistent with some auto-regulation by GSK3 itself (Fig. 7c). Finally, we set out to determine whether the excessive levels of pY-GSK3 ... WebProduct Description. Glycogen synthase kinase 3 (GSK3) is a serine/threonine kinase that plays a key inhibitory role in both the insulin and Wnt signaling pathways. 1, 2 CHIR99021 is an aminopyrimidine derivative that inhibits GSK3α and GSK3β with IC 50 values of 10 and 6.7 nM, respectively. 3 When tested against twenty different protein ... gainsborough australian wool blanket