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1.
Anticancer Agents Med Chem ; 17(1): 67-74, 2017.
Artículo en Inglés | MEDLINE | ID: mdl-27141880

RESUMEN

BACKGROUND: Angiogenesis is physiological process in embryogenesis, organ development, endometrial vasculature in menstrual cycle and wound healing. Angiogenesis has also been associated with several pathological conditions such as cancer, arthritis, atherosclerosis, etc. Out of the many growth factor responsible for angiogenesis, vascular endothelial growth factor (VEGF) is one of the most important and positive regulator of angiogenesis with its distinct specificity for vascular endothelial cells. The current work is the small efforts towards development of newer inhibitor of angiogenesis targeting VEGFR-2. OBJECTIVE: With the view to develop inhibitors of angiogenesis, pharmacophore characteristics were used to design aromatic/ heteroaromatic ring containing compounds. These compounds were then docked in to the active side of VEGFR-2 with the aid of docking. They were then synthesize and spectrally characterized and carry out in-vitro and in-vivo anti-angiogenic evaluation studies to ascertain its angiogenesis inhibition potential. RESULT: 3-substituted-5-(4-pyridin-4yl)-1,3,4-oxadiazole-2-thiones designed as inhibitors of angiogenesis targeting VEGFR2. In docking study, all the molecules showed similar way of binding with VEGFR2 as that of the cocrystallised ligand. Compound 3i and 3j were found to be most active in the series showing good inhibition of angiogenesis in both CAM and in zebrafish embryo assays. The compound 3i was the most active in the series with IC50 of 0.5 µM for VEGR-2. CONCLUSION: To conclude the work we have successfully designed newer inhibitors of angiogenesis targeting VEGFR- 2. These compounds were then screen and found to inhibit angiogenesis of CAM and zebrafish at dose of 1 µM.


Asunto(s)
Inhibidores de la Angiogénesis/química , Inhibidores de la Angiogénesis/farmacología , Oxadiazoles/química , Oxadiazoles/farmacología , Receptor 2 de Factores de Crecimiento Endotelial Vascular/antagonistas & inhibidores , Inhibidores de la Angiogénesis/síntesis química , Animales , Pollos , Membrana Corioalantoides/irrigación sanguínea , Membrana Corioalantoides/efectos de los fármacos , Diseño de Fármacos , Humanos , Simulación del Acoplamiento Molecular , Oxadiazoles/síntesis química , Tionas/síntesis química , Tionas/química , Tionas/farmacología , Receptor 2 de Factores de Crecimiento Endotelial Vascular/metabolismo , Pez Cebra/embriología
2.
Bioorg Chem ; 67: 139-47, 2016 08.
Artículo en Inglés | MEDLINE | ID: mdl-27388635

RESUMEN

A series of novel 5-benzylidene-2,4-thiazolidinediones were designed as inhibitors of angiogenesis targeting VEGFR-2. In docking study, molecules showed similar way of binding with VEGFR-2 as that of the co-crystallized ligand. Compounds were then synthesized, purified and characterized by spectroscopic techniques. Compounds 3f and 3i were found to be most active in the series showing good inhibition of angiogenesis in both CAM and in zebrafish embryo assays. Compound 3i also exhibited IC50 of 0.5µM against VEGFR-2.


Asunto(s)
Compuestos de Bencilideno/farmacología , Diseño de Fármacos , Neovascularización Patológica/tratamiento farmacológico , Inhibidores de Proteínas Quinasas/farmacología , Tiazoles/farmacología , Receptor 2 de Factores de Crecimiento Endotelial Vascular/antagonistas & inhibidores , Animales , Compuestos de Bencilideno/síntesis química , Compuestos de Bencilideno/química , Relación Dosis-Respuesta a Droga , Humanos , Estructura Molecular , Neovascularización Patológica/patología , Inhibidores de Proteínas Quinasas/síntesis química , Inhibidores de Proteínas Quinasas/química , Relación Estructura-Actividad , Tiazoles/síntesis química , Tiazoles/química , Receptor 2 de Factores de Crecimiento Endotelial Vascular/metabolismo , Pez Cebra
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