Ortet Risoleta, Prado Soizic, Mouray Elisabeth, Thomas Olivier P
Université de Nice-Sophia Antipolis, Laboratoire de Chimie des Molécules Bioactives et des Arômes, UMR 6001 CNRS, Faculté des Sciences, Nice, France.
Phytochemistry. 2008 Dec;69(17):2961-5. doi: 10.1016/j.phytochem.2008.09.022. Epub 2008 Nov 12.
Leaves and flowers of Artemisia gorgonum (Asteraceae) collected in Fogo, Cape Verde islands, were phytochemically investigated and resulted in isolation and characterization of three guaianolides 1, 2, 5, and a secoguainolide 4, in addition to eight known guaianolides 6-11 and two known germacranolides 12, 13. Structures were elucidated by 1D and 2D NMR experiments. Careful examination of the (13)C NMR spectrum led to revision of the structure of a previously described guaianolide from 2 to 3. Most compounds exhibited mild antiplasmodial activities, ridentin (13) being the most interesting with an IC(50) of 3.8+/-0.7microgml(-1) against Plasmodium falciparum FcB1 and weak cytotoxicity in a vero cell line (IC(50) 71.0+/-3.9microgml(-1)).
对采集自佛得角群岛福戈岛的菊科植物高茎蒿的叶和花进行了植物化学研究,除了分离并鉴定出8种已知愈创木内酯6 - 11和2种已知吉马烷型倍半萜内酯12、13外,还得到了3种愈创木内酯1、2、5和1种裂环愈创木内酯4。通过一维和二维核磁共振实验阐明了其结构。对碳-13核磁共振谱的仔细研究导致将先前描述的一种愈创木内酯的结构从2修正为3。大多数化合物表现出温和的抗疟活性,其中瑞登汀(13)最为有趣,对恶性疟原虫FcB1的半数抑制浓度(IC50)为3.8±0.7微克/毫升,在 vero细胞系中具有较弱的细胞毒性(IC50为71.0±3.9微克/毫升)。