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FGFR1/VEGFR2-IN-2

Product Specifications

Target

PDGFR, Necroptosis, Apoptosis, FGFR, VEGFR

Related Pathways

Apoptosis, Angiogenesis, Tyrosine Kinase/Adaptors

Bioactivity

FGFR1/VEGFR2-IN-2 (compound 6) is a dual inhibitor targeting both VEGFR2 and FGFR1 with IC50 values of 0.025 μM and 0.026 μM, respectively. This compound also exhibits inhibitory effects on EGFR and PDGFR-β, with IC50 values of 0.106 μM and 0.077 μM, respectively. FGFR1/VEGFR2-IN-2 demonstrates significant anticancer activity in the NCI-60 cell lines, showing a growth inhibition (GI) of 60.38%. In T-47D cell lines, it achieves an IC50 of 8.51 μM, exhibits anti-migratory properties, induces cell cycle arrest in the G1 phase, and promotes both apoptosis and necrosis. Additionally, while it has an IC50 greater than 100 μM in MCF-7 cell lines, it does so with an IC50 of 69.17 μM in MDA-MB-231 cell lines and shows no toxicity to normal cells.

Molecular Formula

C21H15ClF3NO4S

Molecular Weight

469.86

Shipping Conditions

Ice Packs

Storage Temperature

-20°C

Available Sizes

Frequently Asked Questions

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