CT-1 is a derivative of Cryptotanshinone (HY-N0174). CT-1 is a ferroptosis inducer. CT-1 promotes the interaction between NCOA4 and ferritin by targeting FTH1, triggering ferritinophagy-mediated ferroptosis. CT-1 has anticancer activity against triple-negative breast cancer (TNBC). CT-1 induces ferroptosis in both N2-type tumor-associated neutrophils (TANs) and TNBC cancer cells[1].
Molekulargewicht:
394.42
Reinheit:
99.47
Formel:
C23H22O6
Target-Kategorie:
Ferroptosis
Anwendungsbeschreibung:
MCE Product type: Reference compound
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