Acton N, Karle J M, Miller R E
Division of Experimental Therapeutics, Walter Reed Army Institute of Research, Washington, D.C. 20307-5100.
J Med Chem. 1993 Aug 20;36(17):2552-7. doi: 10.1021/jm00069a014.
Several 9-substituted derivatives of the antimalarial drug artemisinin have been prepared by functionalizing the double bond of artemisitene and related compounds. Stereochemical assignments for these compounds were made using a combination of NMR experiments, an X-ray diffraction study of one compound, and chemical correlations of several other compounds with this one compound of unambiguous structure and with its epimer. The compounds synthesized show a wide variation in in vitro antimalarial activity.
通过使青蒿烯及相关化合物的双键官能化,已制备出抗疟药物青蒿素的几种9-取代衍生物。这些化合物的立体化学归属是通过结合核磁共振实验、对一种化合物的X射线衍射研究以及其他几种化合物与这种结构明确的化合物及其差向异构体的化学关联来确定的。合成的化合物在体外抗疟活性方面表现出很大差异。