Erastin is a ferroptosis inducer. Erastin exhibits the mechanism of ferroptosis induction related to ROS and iron-dependent signaling. Erastin inhibits voltage-dependent anion channels (VDAC2/VDAC3) and accelerates oxidation, leading to the accumulation of endogenous reactive oxygen species. Erastin also disrupts mitochondrial permeability transition pore (mPTP) with anti-tumor activity. Furthermore, Erastin can block the uptake of cystine mediated by SLC7A11 and also spares UMRC6-EV and -C91A cells from disulfidptosis under glucose starvation[1][2][3][4][5][6][7][8][9][10][11][12][13][14].
Molekulargewicht:
547.04
Reinheit:
99.76
CAS Nummer:
[571203-78-6]
Formel:
C30H31ClN4O4
Target-Kategorie:
Disulfidptosis,Ferroptosis,VDAC
Anwendungsbeschreibung:
Reference compound
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