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Cat. No. Product Name Information
PC-60500

HJC0416

STAT3 inhibitor

HJC0416 is an orally bioavailable small-molecule STAT3 inhibitor.
PC-60456

Cucurbitacin I

JAK/STAT3 inhibitor

Cucurbitacin I (JSI-124) is a triterpenoid compound that potently and selectively inhibits JAK/STAT3 pathway, suppresses the levels of phosphotyrosine STAT3 in A549 cell with IC50 of 500 nM.
PC-60417

Debio 0617B

Multi-kinases inhibitor

Debio 0617B is a first-in-class, multi-kinase inhibitor that targets pSTAT3 and/or pSTAT5 in cancer cells through combined inhibition of JAK, SRC, ABL, and class III/V RTKs (Kd<100 nM).
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

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

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 (BBI-608) 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-22095

YY002

STAT3 inhibitor

YY002 is a potent, selective STAT3 inhibitor, selectively binds to the STAT3 Src Homology 2 (SH2) domain (KD=2.24 nM) over other STAT members, inhibits STAT3 Tyr705 and Ser727 phosphorylation.
PC-21893

Stattic

STAT3 inhibitor

Stattic is a potent, selective nonpeptidic STAT3 inhibitor, inhibits the function of the STAT3 SH2 domain (IC50=5.1 uM) regardless of the STAT3 activation state in vitro.
PC-21874

WZ-2-033

STAT3 inhibitor

WZ-2-033 is a potent, selective STAT3 inhibitor, binds to the SH2 domain of the STAT3 protein with KD of 7.4 uM, disrupts STAT3 dimerization and significantly inhibits STAT3 signaling.

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