| Cat. No. |
Product Name |
Information |
| PC-24308 |
Hygromycin B
CHI3L1-STAT3 inhibitor
|
Hygromycin B is an aminoglycoside antibiotic active against prokaryotic and eukaryotic cells, also an inhibitor of the STAT3-CCD domain, disrupts the CHI3L1-STAT3 interaction, inhibits glioblastoma both in vitro and in vivo. |
| PC-24234 |
Stafori-1
STAT4 inhibitor
|
Stafori-1 is the first specific small-molecule inhibitor of STAT4, inhibits the protein-protein interaction domain of STAT4, the SH2 domain, with Ki of 1.7 uM, 10-70-fold selectivity over other STAT proteins. |
| PC-24045 |
STAT3 inhibitor NA16
STAT3 inhibitor
|
STAT3 inhibitor NA16 is a nifuroxazide analog and STAT3 inhibitor, downregulates FoxP3 expression with IC50 of 4.7 uM in TCR-stimulated total T cells. |
| PC-23197 |
Scutellarin
STAT3 inhibitor
|
Scutellarin is an active flavone isolated from Scutellaria baicalensis, can down-regulates the STAT3/Girdin/Akt signaling in HCC cells, and inhibits RANKL-mediated MAPK and NF-κB signaling pathway in osteoclasts, also shows anti-HIV-1 activity. |
| PC-23177 |
AK-068
STAT6 inhibitor
|
AK-068 is a highly potent, selective STAT6 ligand / inhibitor with Ki of 6 nM, binds to STAT6 SH2 domain. |
| PC-20633 |
TR120
STAT5 inhibitor
|
TR120 (TR-120) is a potent small molecule STAT5 inhibitor, exhibits antiproliferative in K562 cells with IC50 of 0.12 uM, decreases STAT5 expression in imatinib-sensitive and imatinib-resistant BCR-ABL-expressing leukemia cells. |
| PC-20630 |
SF-1-088
STAT5 inhibitor
|
SF-1-088 is a small molecule STAT5-SH2 domain inhibitor with Ki of 8.3 uM (Stat5b), shows no affinity for Stat1 and Stat3 (Ki>25 uM). |
| PC-20629 |
SF-1-066
STAT3 inhibitor
|
SF-1-066 is an orally bioavailable inhibitor of STAT3 with IC50 of 35 uM for inhibition of STAT3 DNA binding activity in vitro, binds to the STAT3 SH2 domain and inhibits STAT3 dimerization. |
| PC-20628 |
S3I-1757
STAT3 inhibitor
|
S3I-1757 is a small molecule STAT3-STAT3 dimerization inhibitor with IC50 of 13.5 uM in fluorescence polarization (FP) assays, interacts with Y-705 binding site in the SH2 domain. |
| PC-70276 |
OPB-51602
|
A novel small molecule SH2 domain-targeting STAT3 inhibitor with IC50/Kd of 7.3/5 nM. |