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Novel pyrazolo[3,4-d]pyrimidines as dual Src-Abl inhibitors active against mutant form of Abl and the leukemia K-562 cell line.

Autori

El-Moghazy SM, George RF, Osman EE, Elbatrawy AA, Kissova M, Colombo A, Crespan E, Maga G.

Riferimenti

EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY 123 1-13, 2016

Autori CNR

CRESPAN, MAGA

Moduli

Abstract

Some novel 6-substituted pyrazolo[3,4-d]pyrimidines 4, 5, 6a-d, 7a-c, 8 and pyrazolo[4,3-e][1,2,4]triazolo[4,3-a]pyrimidines 9a-c, 10a-c, 11, 12a,b, 13a-c and 14 were synthesized and characterized by spectral and elemental analyses. They were screened for their biological activity in vitro against Abl and Src kinases. Compounds 7a and 7b revealed the highest activity against both wild and mutant Abl kinases as well as the Src kinase and the leukemia K-562 cell line. They can be considered as new hits for further structural optimization to obtain better activity.

Link all articolo

http://www.sciencedirect.com/science/article/pii/S0223523416305827

Parole Chiave

Note

10.1016/j.ejmech.2016.07.034

Indietro


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