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Cat. No. Product Name Information
PC-61668

FLLL32

STAT3 inhibitor

FLLL32 is a cell-permeable analog of curcumin that inhibits JAK2-mediated phosphorylation of STAT3 on Tyr705 in cancer cells (IC50=5 uM).
PC-61667

XZH-5

STAT3 inhibitor

XZH-5 is a small moelcule that inhibits constitutive and interleukin-6-induced STAT3 phosphorylation, inhibits STAT3 DNA binding ability and downregulation of STAT3 downstream genes.
PC-61666

SD-1029

STAT3 inhibitor

SD-1029 (NSC 371488) is a potent inhibitor of Stat3 activation, suppresses EGFP-Stat3 nuclear translocation at 10 uM in both BHK-21 and U2-OS cells.
PC-61660

LLL3

STAT3 inhibitor

LLL3 is a structural analogue of STA-21 that acts as a novel STAT3 inhibitor, inhibits STAT3-dependent transcriptional and DNA binding activities.
PC-61629

Capstafin

STAT5b inhibitor

Capstafin is a phosphorylation of capsaicinoid derivative that acts as a highly potent, selective inhibitor of STAT5b with Ki of 0.34 uM.
PC-61628

STAT5b inhibitor 7

STAT5b inhibitor

STAT5b inhibitor 7 (Capstafin prodrug) is the pivaloyloxymethyl ester prodrug of Capstafin, which is a potent, selective STAT5b inhibitor with Ki of 0.34 uM.
PC-61476

SC99

STAT3 inhibitor

SC99 is a novel selective STAT3 inhibitor that inhibits JAK2-STAT3 activation but has no effects on other transcription factors such as NF-κB, and kinases such as AKT, ERK, and c-Src.
PC-61312

IQDMA

STAT5 inhibitor

IQDMA is a cell-permeable, small molecule inhibitor of the transcription factor STAT5, and dual STAT3/5 degrader (IC50=0.54-1.63 μM).
PC-61311

STAT5-IN-1

STAT5 inhibitor

STAT5-IN-1 is a selective, small molecule inhibitor of the transcription factor STAT5 with IC50 of 47±17 uM in FP assays.
PC-61260

BP-5-087

STAT3 inhibitor

BP-5-087 is a potent, selective STAT3 SH2 domain inhibitor (EC50=5.6 uM) that reduces STAT3 phosphorylation and nuclear transactivation.
PC-61235

Indirubin E804

STAT3 inhibitor, Src inhibitor

Indirubin E804 is an indirubin derivative that potently blocks constitutive STAT3 signaling in human breast and prostate cancer cells, directly inhibits Src kinase activity (IC50=0.43 uM) in vitro.
PC-70249

STA-21

STAT3 inhibitor

STA-21 (NSC 628869, Ochromycinone) is a small-molecule inhibitor of STAT3, inhibits Stat3 DNA binding activity, Stat3 dimerization, and Stat3-dependent luciferase activity (20-30 uM).

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