Baccelli Chiara, Block Sébastien, Van Holle Benoit, Schanck André, Chapon David, Tinant Bernard, Meervelt Luc Van, Morel Nicole, Quetin-Leclercq Joelle
Laboratoire de Pharmacognosie, Unité d'Analyse Chimique et Physico-Chimique des Médicaments, Université Catholique de Louvain, Bruxelles, Belgium.
Planta Med. 2005 Nov;71(11):1036-9. doi: 10.1055/s-2005-873123.
A mixture of two new diterpenes was isolated from a dichloromethane extract of Croton zambesicus: ent-18-hydroxytrachyloban-3beta-ol (1) and ent-18-hydroxyisopimara-7,15-diene-3beta-ol (2). The two compounds crystallised together and were separated after derivatisation of the pimarane derivative with osmium tetroxide. The structure of 1 was elucidated by 1D- and 2D-NMR analysis and by X-ray diffraction of a crystal containing both compounds while 2 was only identified by crystallographic data. As this plant is widely used in African folk medicine against hypertension, we have analysed the vasorelaxant activity of the isolated molecules. The mixture of the two compounds inhibited the KCl-induced contraction of male Wistar rat aorta (IC (50) = 1 microg/mL), while the purified trachylobane (compound 1) and the hydroxylated pimarane showed a lower activity than the mixture.
对映-18-羟基曲洛巴烷-3β-醇(1)和对映-18-羟基异海松-7,15-二烯-3β-醇(2)。这两种化合物一起结晶,并在用四氧化锇对海松烷衍生物进行衍生化后分离。通过一维和二维核磁共振分析以及对含有这两种化合物的晶体进行X射线衍射阐明了1的结构,而2仅通过晶体学数据鉴定。由于这种植物在非洲民间医学中被广泛用于治疗高血压,我们分析了分离出的分子的血管舒张活性。这两种化合物的混合物抑制了雄性Wistar大鼠主动脉由氯化钾诱导的收缩(IC(50)= 1微克/毫升),而纯化的曲洛巴烷(化合物1)和羟基化海松烷的活性低于该混合物。