作者:N. Balu、Jacob V. Thomas、Sujata V. Bhat
DOI:10.1021/jm00113a021
日期:1991.9
Seven analogues of monoterpenic fragment of aplasmomycin were synthesized as targeted antimalarial agents. The potency of the compound 6 was comparable with the sesquiterpene lactone artemisinin and the antibiotic aplasmomycin in vivo against Plasmodium berghei yoelli.