SIQ17 is an EGFR inhibitor that inhibits its activity by occupying the ATP-binding site, with IC50 of 0.62 nM. SIQ17 shows more effective EGFR-TK inhibitory activity compared to the known inhibitor Erlotinib (HY-50896) (IC50 of 20 nM). SIQ17 can be used for cancer research[1]
Molekulargewicht:
489.63
CAS Nummer:
[2151881-74-0]
Formel:
C32H27NO2S
Target-Kategorie:
EGFR
Anwendungsbeschreibung:
MCE Product type: Reference compound
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