ODZ10117 is a STAT3 and NLRP3 inhibitor with a human STAT3 SH2 domain IC 50 of 7.5 μM. ODZ10117 binds to the STAT3 SH2 domain, suppressing tyrosine phosphorylation, dimerization, nuclear translocation, and transcriptional activity. ODZ10117 binds to NLRP3 , impairs NEK7 interaction, prevents inflammasome formation, and inhibits caspase-1 and IL-1β cleavage.ODZ10117 reduces MSU ( HY-B2130A )-induced IL-1β release, lowers LPS ( HY-D1056 )-induced sepsis mortality, and exhibits anti-inflammatory effects. ODZ10117 induces apoptosis , suppresses breast cancer cell migration and invasion, reduces tumor growth and lung metastasis, and extends survival in breast cancer models. ODZ10117 can be used for the research of Monosodium urate ( HY-B2130A )-induced peritonitis, LPS-induced sepsis, breast cancer , glioblastoma, and Alzheimer's disease.
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