Rahman Aziz A, Samoylenko Volodymyr, Jain Surendra K, Tekwani Babu L, Khan Shabana I, Jacob Melissa R, Midiwo Jacob O, Hester John P, Walker Larry A, Muhammad Ilias
National Center for Natural Products Research, Research Institute of Pharmaceutical Sciences, School of Pharmacy, University of Mississippi, Mississippi 38677, USA.
Nat Prod Commun. 2011 Nov;6(11):1645-50.
The EtOH extract of Abrus schimperi (Fabaceae), collected in Kenya, demonstrated significant activity against Leishmania donovani promastigotes with IC50 value of 3.6 microg/mL. Bioassay-guided fractionation of CHCl3 fraction using Centrifugal Preparative TLC afforded two antiparasitic isoflavanquinones, namely amorphaquinone (1) and pendulone (2). They displayed IC50 values of 0.63 microg/mL and 0.43 microg/mL, respectively, against L. donovani promastigotes. Both the compounds were also evaluated against L. donovani axenic amastigotes and amastigotes in THPI macrophage cultures. In addition, compounds 1 and 2 showed antiplasmodial activity against Plasmodium falciparum D6 and W2 strains, while 2 displayed antibacterial activity against Staphylococcus aureus and methicillin-resistant S. aureus (each IC50 1.44 microg/mL). The 1H and 13C data of 1, not fully assigned previously, were unambiguously assigned using 1D and 2D NMR HMBC and HMQC experiments. In addition, the absolute stereochemistry of the isolated compounds 1 and 2 was revised as C-(3S) based on Circular Dichroism experiments. This appears to be the first report of amorphaquinone (1) and pendulone (2) from the genus Abrus.
在肯尼亚采集的豆科植物希氏相思子的乙醇提取物对杜氏利什曼原虫前鞭毛体显示出显著活性,IC50值为3.6微克/毫升。使用离心制备薄层色谱对氯仿部分进行生物测定导向的分离,得到两种抗寄生虫异黄酮醌,即紫穗槐醌(1)和垂丝醌(2)。它们对杜氏利什曼原虫前鞭毛体的IC50值分别为0.63微克/毫升和0.43微克/毫升。这两种化合物还针对杜氏利什曼原虫无菌无鞭毛体和THPI巨噬细胞培养物中的无鞭毛体进行了评估。此外,化合物1和2对恶性疟原虫D6和W2菌株显示出抗疟活性,而化合物2对金黄色葡萄球菌和耐甲氧西林金黄色葡萄球菌具有抗菌活性(每种的IC50为1.44微克/毫升)。之前未完全归属的化合物1的1H和13C数据通过1D和2D NMR HMBC和HMQC实验明确归属。此外,基于圆二色性实验,分离得到的化合物1和2的绝对立体化学被修订为C-(3S)。这似乎是首次从相思子属中报道紫穗槐醌(1)和垂丝醌(2)。