M6766 is a selective endoplasmic reticulum oxidoreductase 1α ( ERO1α ) inhibitor with an IC 50 of 1.4 μM and a K D of 1.1 μM. M6766 also inhibits ERO1β with an IC 50 of 7.2 μM. M6766 binds to the flavin adenine dinucleotide-binding pocket in ERO1α. M6766 inhibits granule secretion, αIIbβ3 integrin activation, Ca 2+ mobilization, and platelet aggregation. M6766 can be used for the research of neurological disease , such as ischemic stroke.
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