Molecules · 2008 · 12 citations · 11 references
PharmacyMedicinal ChemistryPharmacologyCancer PharmacologyDrug DesignDrug DiscoveryNatural Product-based Drug DesignOncology PharmacologyStructure-activity Relationship AnalysisAnticancer ActivityAnticancer ChemotherapyAntiproliferative AgentsAntiproliferative Drug ActionAssayBioactive Compound LibrariesMedicinal Chemistry ApplicationsMedicinal Heterocycles
A series of novel substituted 1,2,3-benzotriazines based on the structures of vatalanib succinate (PTK787) and vandetanib (ZD6474) were designed and synthesized. The antiproliferative effects of these compounds were tested on microvascular endothelial cells (MVECs) using the MTT assay. Introduction of a methoxy and a 3-chloropropoxy group into the 1,2,3-benzotriazines increased the antiproliferative effects. 4-(3-Chloro-4- fluoroanilino)-7-(3-chloropropoxy)-6-methoxy-1,2,3-benzotriazine (8m) was the most effective compound. It was 4-10 fold more potent than PTK787 in inhibiting the growth of T47D breast cancer cells, DU145 and PC-3 prostate cancer cells, LL/2 murine Lewis lung cancer cells and B16F0 melanoma cells.
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J M Wood, Guido Bold, Elisabeth Buchdunger et al. · PubMed · 2000 · 847 citations
Medicine, Oncology, Pharmacology +16
Guido Bold, Karl‐Heinz Altmann, J Frei et al. · Journal of Medicinal Chemistry · 2000 · 213 citations · Full text
Kathy D. Miller, José Trigo, Catherine Wheeler et al. · Clinical Cancer Research · 2005 · 197 citations