O-Desmethyl gefitinib is an active metabolite of Gefitinib in human plasma. The formation of O-desmethyl gefitinib is dependent on CYP2D6 activity. O-desmethyl gefitinib inhibits EGFR with an IC50 of 36 nM in subcellular assays[1][2].
Molecular Weight:
432.88
Purity:
99.4
CAS Number:
[847949-49-9]
Formula:
C21H22ClFN4O3
Target:
EGFR
Application Notes:
Reference compound
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