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Cat. No. Product Name Information
PC-73294

MU1787

HIPK inhibitor

MU1787 is a potent, highly selective Homeodomain-interacting protein kinases (HIPKs) inhibitor with IC50 of 285/123/283 nM for HIPK1/2/3, repectively.
PC-73293

BT173

HIPK2 inhibitor

BT173 (BT-173) is a small molecule allosteric inhibitor of HIPK2-Smad3 interaction, specifically inhibits the TGF-β1/Smad3 pathway.
PC-73292

JWD-065

HIPK2 inhibitor

JWD-065 is a potent small molecule HIPK2 kinase inhibitor, blocks HIPK2 phosphorylation on S359/T360 and JNK activation in HEK293 cells and attenuates ER stress-induced cell death with EC50 of 641 nM.
PC-73291

CVM-6-139-1

HIPK2 inhibitor

CVM-6-139-1 (HIPK2 inhibitor A64) is a potent small molecule HIPK2 kinase inhibitor, blocks HIPK2 phosphorylation on S359/T360 and JNK activation in HEK293 cells and attenuates ER stress-induced cell death with EC50 of 401 nM.
PC-72581

CaNDY

CLK/DYRK inhibitor

CaNDY is a highly potent rectifier of the aberrant splicing, potently inhibits DYRK1A, DYRK1B, CLK1/CLK2 with IC50 of 21.6/68.3/116 nM in in vitro kinase assays.
PC-72351

GNF2133

DYRK1A inhibitor

GNF2133 (GNF-2133) is a potent and selective DYRK1A inhibitor with IC50 of 6 nM, without inhibitory effect on GSK3β.
PC-43249

Mirk-IN-1

DYRK1A/1B inhibitor

Mirk-IN-1 is a potent, specific inhibitor of Dyrk1B (Mirk kianse) and Dyrk1A with IC50 of 68 nM and 22 nM respectively, shows SW620 cell IC50 of 1.9 uM.
PC-42939

AZ191

DYRK1B inhibitor

AZ191 is a potent, selective DYRK1B inhibitor with IC50 of 17 nM, displays 10-fold selectivity over DYRK1A and no activity against DYRK2 (IC50=1890 nM).
PC-61025

Leucettine L41

CLK/DYRK inhibitor

Leucettine L41 is a novel potent cdc2-like kinase (CLKs) and DYRKs inhibitor with IC50 of 40, 35 and 15 nM for DYRK1A, DYRK2 and CLK1, respectively.
PC-42167

TBID

HIPK2 inhibitor

tBID is a potent, selective and cell permeable homeodomain-interacting protein kinase 2 (HIPK2) inhibitor with IC50 of 0.33 uM.
PC-27003

DYRK inhibitor FC-3

DYRK1A inhibitor

DYRK inhibitor FC-3 is a potent, selective, reversible, ATP-competitive inhibitor of Dual-specificity tyrosine-regulated kinases (DYRKs) with IC50 of 53 nM (DYRK1A).
PC-27002

DYRK inhibitor FC-2

DYRK1A inhibitor

DYRK inhibitor FC-2 is a potent, selective, reversible, ATP-competitive inhibitor of Dual-specificity tyrosine-regulated kinases (DYRKs) with IC50 of 19 nM (DYRK1A).

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