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Cat. No. Product Name Information
PC-42174

BP-1-102

STAT3 inhibitor

BP-1-102 is an orally bioavailable, small-molecule inhibitor of STAT3 with Kd of 504 nM.
PC-42160

HO-3867

STAT3 inhibitor

HO-3867 is a synthetic curcuminoid that selectively inhibits STAT3 phosphorylation, transcription, and DNA binding without affecting the expression of other active STATs.
PC-42175

SH5-07

STAT3 inhibitor

SH5-07 (SH-5-07, SH 5-07) is a potent, selective small-molecule STAT3 inhibitor with IC50 of 3.9 uM.
PC-45109

SH-4-54

STAT3 inhibitor

SH-4-54 is a potent, BBB permeable, nonphosphorylated STAT3 inhibitor that strongly binds to STAT3 protein with Kd of 300 nM.
PC-43790

Napabucasin

STAT3 inhibitor

Napabucasin (BBI608) is a potent small-molecule inhibitor of STAT3 that has a broad spectrum of activity against stemness-high cancer cells (IC50=0.5-1.5 uM).
PC-42210

AS1517499

STAT6 inhibitor

AS1517499 is a novel potent STAT6 inhibitor with IC50 of 21 nM in STAT6-dependent promoter reporter assay.
PC-25692

STAT6 ligand-1

STAT6 ligand

STAT6 ligand-1 is a specific ligand of STAT6 used for synthesizing STAT6 PROTAC degraders.
PC-25691

STAT6-IN-10

STAT6 inhibitor

STAT6-IN-10 is a potent, selective STAT6 inhibitor with IC50 of 1.2 uM in STAT6 reporter assay using STAT6-HEK293 cells.
PC-25690

STAT6-IN-9

STAT6 inhibitor

STAT6-IN-9 is a potent, selective STAT6 inhibitor with EC50 of 4 nM, efficiently blocks the STAT6 activation process mediated by the IL-13-IL-13 receptor/IL-4 receptor pathway, potently inhibits CCL17 secretion with IC50 of 4.6 nM.
PC-25689

STAT6-IN-7

STAT6 inhibitor

STAT6-IN-7 is a potent, selective STAT6 inhibitor with IC50 of 0.28 uM in STAT6 reporter assay using STAT6-HEK293 cells.
PC-25688

STAT6-IN-8

STAT6 inhibitor

STAT6-IN-8 is a potent, selective STAT6 inhibitor with IC50 of 0.25 uM in STAT6 reporter assay using STAT6-HEK293 cells.
PC-25579

Bt354

STAT3 inhibitor

Bt354 is a specific, small-molecule inhibitor of the STAT3 signalling pathway, prevents STAT3 from entering the nucleus and phosphorylates it at Y705, exhibiting potent anticancer properties.

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