Chemical Name: 4-[(4-Fluoro-2-methyl-1H-indol-5-yl)oxy]-6-methoxy-7-(3-pyrrolidin-1-ylpropoxy)quinazoline. Alternate Names: AZD2171
VEGFR inhibitor
Molekulargewicht:
450.51
Reinheit:
>98% by HPLC NMR (Conforms)
Formulierung:
Beige solid
CAS Nummer:
[288383-20-0]
Formel:
C25H27FN4O3
Anwendungsbeschreibung:
Cediranib is a highly potent (IC50 = <1 nM) inhibitor of VEGFR-2.1 It also inhibits VEGFR-1, VEGFR-3, c-Kit, and PDGFRß (IC50s respectively: 5 nM, 3 nM, 2nM, and 5 nm). It displays broad-spectrum activity in various human tumor models. Cediranib normalized tumor vasculature decreasing permeability, increasing blood perfusion, and allowing better drug delivery in glioblastoma patients.2,3 It enhanced transcription of MHC-I leading to enhanced CD8+ T cell infiltration and improved efficacy of anti-PD-L1 therapy.4
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