首页> 外文期刊>European Journal of Medicinal Chemistry: Chimie Therapeutique >Synthesis, structural elucidation and DNA-dependant protein kinase and antiplatelet studies of 2-amino-(5, 6, 7, 8-mono and 7, 8-di-substituted)-1,3-benzoxazines.
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Synthesis, structural elucidation and DNA-dependant protein kinase and antiplatelet studies of 2-amino-(5, 6, 7, 8-mono and 7, 8-di-substituted)-1,3-benzoxazines.

机译:合成,结构阐明和DNA依赖性蛋白激酶和抗血小板研究的2-氨基 - (5,6,7,8-单 - 和7,8-二取代的)-1,3-苯并恶嗪。

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摘要

A number of new 2-amino-[5, 6, 7 and 8]-O-substituted 1,3-benzoxazines, and 2-amino 8-methyl-7-O-substituted-1,3-benzoxazines were synthesized. Thirty one new compounds were tested for their effect on collagen induced platelet aggregation and it was found that the most active compounds were 8-methyl-2-morpholin-4-yl-7-(pyridin-3-ylmethoxy)-4H-1,3-benzoxazin-4-one 9f and 8-methyl-2-morpholin-4-yl-7-(pyridin-4-ylmethoxy)-4H-1,3-benzoxazin-4-one 9j with IC(50) = 2 +/- 1.5 and 4 +/- 2 muM respectively. Inhibition of DNA-PK activity at concentrations of 1.6-4 muM were tested for 9 products 5i, 7a-e and 9b, 9f and 9j.
机译:合成了许多新的2-氨基-[5,6,6,7和8] -O-取代的1,3-苯并恶嗪和2-氨基8-甲基-7-O-取代的-1,3-苯并恶嗪。 测试了三十一体的新化合物,对胶原蛋白诱导的血小板聚集进行了影响,发现最活性化合物是8-甲基-2-吗啉-4-基-7-(吡啶-3-基甲氧基)-4H-1, 3-苯并恶化素-4-α-1 9F和8-甲基-2-吗啉-4-基-7-(Pyridin-4-基甲氧基)-4H-1,3-苯并嗪-4-一体化9J,具有IC(50)= 2 +/- 1.5和4 +/- 2妈妈。 测试浓度为1.6-4妈妈的DNA-PK活性的抑制9次产物5i,7a-e和9b,9f和9j。

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