化学
扭结血吸虫
驱虫药
几丁质酶
抗寄生虫药
酶
生物化学
抗寄生虫的
立体化学
蠕虫
药理学
生态学
动物
生物
病理
医学
作者
Satoshi Ōmura,Kazuro Shiomi
标识
DOI:10.1351/pac200779040581
摘要
Abstract Our long-standing and continual screening of microorganisms, especially for antiparasitic agents, has produced a wide variety of compounds of global importance, such as the avermectins. Recent discoveries include nafuredin, atpenins, argifin, and argadin. Nafuredin is a helminth-specific inhibitor of electron-transport enzyme, complex I, which exhibits anthelmintic activity against Haemonchus contortus in sheep. The atpenins are the most potent complex II inhibitors ever reported. Co-crystallization study of atpenin A5 and E. coli complex II indicated the binding mechanism of ubiquinone to complex II. Argifin and argadin are the first cyclic peptides to inhibit chitinase at low concentration. Though structurally similar, their chitinase inhibition mechanisms are quite different.
科研通智能强力驱动
Strongly Powered by AbleSci AI