当前位置: X-MOL 学术Bioorg. Med. Chem. Lett. › 论文详情
Our official English website, www.x-mol.net, welcomes your feedback! (Note: you will need to create a separate account there.)
Synthesis and in vitro antiprotozoal activities of 5-phenyliminobenzo[a]phenoxazine derivatives
Bioorganic & Medicinal Chemistry Letters ( IF 2.5 ) Pub Date : 2011-08-05 , DOI: 10.1016/j.bmcl.2011.07.112
Xue-Liang Shi , Jian-Feng Ge , Bao-Qiang Liu , Marcel Kaiser , Sergio Wittlin , Reto Brun , Masataka Ihara

A series of 5-phenyliminobenzo[a]phenoxazine derivatives were synthesized. The in vitro antiprotozoal activities were evaluated against Plasmodium falciparum K1, Trypanosoma cruzi, Leishmania donovani and Trypanosoma brucei rhodesiense. N,N-Diethyl-5-((4-methoxyphenyl)imino)-5H-benzo[a]phenoxazin-9-amine shows IC50 = 0.040 μmol L−1 with a selective index of 1425 against Plasmodium falciparum K1.



中文翻译:

5-苯基亚氨基苯并[ a ]吩恶嗪衍生物的合成及体外抗原生动物活性

合成一系列5-苯基亚氨基苯并[ a ]吩恶嗪衍生物。评价了对恶性疟原虫K1,克鲁斯锥虫,多利什曼原虫杜氏布鲁氏锥虫的体外原生动物活性。NN-二乙基-5-((4-甲氧基苯基)亚氨基)-5 H-苯并[ a ]苯恶嗪-9-胺显示IC 50  = 0.040μmolL -1,对恶性疟原虫K1的选择指数为1425 。

更新日期:2011-08-05
down
wechat
bug