Src tyrosine kinase family cooperates with activated growth factor receptors to regulate growth, invasion and metastasis. The authors examined the influence of a novel c‐Src inhibitor, 1l, derived from 4‐amino‐substituted‐pyrazolo–pyrimidines, on tumor angiogenesis and on the angiogenic output of squamous carcinoma cells, A431 and SCC‐4. The effect of 1l was assessed on growth and microvessel density in A431 tumors and its effect compared with the established c‐Src inhibitor PP‐1. The effects of c‐Src inhibition were investigated on vascular endothelial growth factor (VEGF) expression and activity in tumor cells grown in vivo and in vitro, as well as on VEGF mediated signaling and on endothelial cell functions. Nanomolar concentrations of 1l decreased tumor volume promoted by A431 implanted in nude mice, without affecting in vitro cell tumor survival. This effect was related to 1l inhibition of VEGF production, and secondary to an effect on tumor microvessel density. The rabbit cornea assay confirmed that 1l markedly decreased neovessel growth induced by VEGF. In cultured endothelial cells, 1l inhibited the VEGF‐induced phosphorylation on tyr416 of c‐Src, resulting in a reduced cell proliferation and invasion. Consistently, 1l dowregulated endothelial nitric oxide synthase, MAPK‐extracellular receptor kinase 1–2 (ERK1‐2) activity and matrix metalloproteinases (MMP‐2/MMP‐9), while the tissue inhibitors of metalloproteinases (TIMP2/TIMP‐1) were upregulated. These results demonstrate that nM concentrations of c‐Src kinase inhibitors (1l and PP‐1), by reducing the production of VEGF released by tumor cell and its endothelial cell responses, have a highly selective antiangiogenesis effect, which might be useful in combination therapies.