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Heterocondensed quinazolones: synthesis and protein-tyrosine kinase inhibitory activity of 3,4-dihydro-1H,6H-[1,4] oxazino-[3,4-b]quinazolin-6-one derivatives.

作者信息

Orfi L, Kökösi J, Szász G, Kövesdi I, Mák M, Teplán I, Kéri G

机构信息

Institute for Pharmaceutical Chemistry, Semmelweis Medical School, Budapest, Hungary.

出版信息

Bioorg Med Chem. 1996 Apr;4(4):547-51. doi: 10.1016/0968-0896(96)00040-5.

Abstract

1-Benzylidene (2-14) and 1-phenylhydrazono derivatives (15-29) of 3,4-dihydro-1H,6H-[1,4]oxazino[3,4-b]quinazolin-6-one (1) were obtained from the condensation reactions of 1 with a series of aromatic aldehydes and by direct diazonium coupling with aryl-diazonium chlorides. The substances were tested for their ability to inhibit the tyrosine kinase activity of SW-620 (human colon carcinoma) cells. Compounds 8, 10, 12 and 13 showed remarkable inhibitory activity.

摘要

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