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Cayman Chemical JNJ-38158471, Purity: ≥98%, CAS: 951151-97-6, 5 mg
SDP

Catalog No. 502978384
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A VEGFR2 inhibitor (IC50 = 42 nM); selective for VEGFR2 over FMS, PDGFRα, FLT3, and KIT (IC50s = 624, 1,109 nM, 4,810, and 511 nM, respectively) and VEGFR1 and VEGFR3 (IC50s = 4,451 and 1,112 nM, respectively) but does inhibit RET (IC50 = 183 nM); decreases VEGF-induced phosphorylation of VEGFR2 in serum-starved HUVECs at 10, 100, or 500 nM; inhibits VEGF-induced migration in HUVECs at 1 µM; reduces Vegf-induced corneal neovascularization in mice at 100 mg/kg; decreases tumor size in an HCT116 mouse xenograft model at 10-200 mg/kg per day; reduces polyp number in an Apc+/Min-FCCC mouse model of spontaneous colorectal adenoma at 100 mg/kg per day

Catalog No. 50-297-8384 Supplier Cayman Chemical Supplier No. 413615 MG
May include imposed supplier surcharges.
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A VEGFR2 inhibitor (IC50 = 42 nM); selective for VEGFR2 over FMS, PDGFRα, FLT3, and KIT (IC50s = 624, 1,109 nM, 4,810, and 511 nM, respectively) and VEGFR1 and VEGFR3 (IC50s = 4,451 and 1,112 nM, respectively) but does inhibit RET (IC50 = 183 nM); decreases VEGF-induced phosphorylation of VEGFR2 in serum-starved HUVECs at 10, 100, or 500 nM; inhibits VEGF-induced migration in HUVECs at 1 µM; reduces Vegf-induced corneal neovascularization in mice at 100 mg/kg; decreases tumor size in an HCT116 mouse xenograft model at 10-200 mg/kg per day; reduces polyp number in an Apc+/Min-FCCC mouse model of spontaneous colorectal adenoma at 100 mg/kg per day

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