Kuo Ping-Chung, Damu Amooru G, Lee Kuo-Hsiung, Wu Tian-Shung
Department of Chemistry, National Cheng Kung University, Tainan 701, Taiwan, ROC.
Bioorg Med Chem. 2004 Feb 1;12(3):537-44. doi: 10.1016/j.bmc.2003.11.017.
Sixty-five compounds were isolated from the roots of Eurycoma longifolia and characterized by comprehensive analyses of their 1D and 2D NMR, and mass spectral data. Among these isolates, four quassinoid diterpenoids were reported from natural sources for the first time, namely eurycomalide A (1), eurycomalide B (2), 13beta, 21-dihydroxyeurycomanol (3), and 5alpha, 14beta, 15beta-trihydroxyklaineanone (4). Screening of cytotoxicity, anti-HIV and antimalarial activity of these isolated compounds was also furnished by in vitro assays. Compounds 12, 13, 17, 18, 36, 38, 59, and 62 demonstrated strong cytotoxicity toward human lung cancer (A-549) cell lines, however, 12, 13, 17, 38, 57, 58, and 59 exhibited strong cytoxicity toward human breast cancer (MCF-7) cell lines. Compounds 57 and 58 displayed potent antimalarial activity against the resistant Plasmodium falciparum. The thorough studies on the stereochemistry of the different quassinoid diterpenoids provide a clear reference to the scientists who are interested on this field.
从长叶刺蒺藜根中分离出65种化合物,并通过对其一维和二维核磁共振以及质谱数据的综合分析对其进行了表征。在这些分离物中,四种苦木素二萜类化合物首次从天然来源报道,即刺蒺藜内酯A(1)、刺蒺藜内酯B(2)、13β,21-二羟基刺蒺藜醇(3)和5α,14β,15β-三羟基克兰酮(4)。还通过体外试验对这些分离化合物的细胞毒性、抗HIV和抗疟活性进行了筛选。化合物12、13、17、18、36、38、59和62对人肺癌(A-549)细胞系表现出强烈的细胞毒性,然而,12、13、17、38、57、58和59对人乳腺癌(MCF-7)细胞系表现出强烈的细胞毒性。化合物57和58对耐药恶性疟原虫显示出强大的抗疟活性。对不同苦木素二萜类化合物立体化学的深入研究为该领域感兴趣的科学家提供了明确的参考。