间苯三酚
恶性疟原虫
疟疾
化学
立体化学
预酸化
生药学
生物活性
体外
组合化学
生物
生物化学
有机化学
免疫学
酶
作者
Alexander L. Eaton,Seema Dalal,María B. Cassera,Shuqi Zhao,David G. I. Kingston
标识
DOI:10.1021/acs.jnatprod.6b00347
摘要
The phloroglucinol mallotojaponin C (1) from Mallotus oppositifolius, which was previously shown by us to have both antiplasmodial and cytocidal activities against the malaria parasite Plasmodium falciparum, was synthesized in three steps from 2',4',6'-trihydroxyacetophenone, and various derivatives were synthesized in an attempt to improve the bioactivity of this class of compounds. Two derivatives, the simple prenylated phloroglucinols 12 and 13, were found to have comparable antiplasmodial activities to that of mallotojaponin C.
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