STAT3-IN-51 is a STAT3 inhibitor that directly binds to the STAT3 SH2 domain. STAT3-IN-51 induces apoptosis, ferroptosis, and immunogenic cell death (ICD) to potentiate anti-tumor immunity. STAT3-IN-51 inhibits STAT3 activation (phosphorylation, p-STAT3) and its downstream signaling. STAT3-IN-51 induces ROS generation, decreases Bcl-2 expression, disruptes mitochondrial function, suppresses GPX4 activity, and promotes lipid peroxidation. STAT3-IN-51 can be used for the study of colorectal carcinoma, breast adenocarcinoma, non-small cell lung cancer (NSCLC) and Cisplatin (HY-17394)-resistant pulmonary adenocarcinoma[1].
Molekulargewicht:
651.59
Formel:
C36H27F6NO4
Target-Kategorie:
Apoptosis,Bcl-2 Family,Ferroptosis,Glutathione Peroxidase,Reactive Oxygen Species (ROS),STAT
Anwendungsbeschreibung:
MCE Product type: Reference compound
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