Wangchuk Phurpa, Keller Paul A, Pyne Stephen G, Sastraruji Thanapat, Taweechotipatr Malai, Rattanajak Roonglawan, Tonsomboon Aunchalee, Kamchonwongpaisan Sumalee
School of Chemistry, University of Wollongong, Wollongong, NSW, 2522, Australia.
Nat Prod Commun. 2012 May;7(5):575-80.
The chemical constituents and biological activities of Corydalis crispa (Fumariaceae) were investigated for the first time. The phytochemical study resulted in the isolation of nine known isoquinoline alkaloids: protopine (1), 13-oxoprotopine (2), 13-oxocryptopine (3), stylopine (4), coreximine (5), rheagenine (6), ochrobirine (7), sibiricine (8) and bicuculline (9), with complete NMR data for 2 and 3 provided here for the first time. Crude extracts exhibitedsignificant anti-inflammatory (p < 0.01) activity against TNF-alpha production in LPS activated THP-1 cells. The acetylcholinesterase inhibitory activity of compounds 2, 4 and 7 and the antiplasmodial activity of compound 5 against P. falciparum strains TM4/8.2 and K1CB1 (multidrug resistant strain) are reported here for the first time. Stylopine (4) did not show antimalarial activity against the K1CB1 strain in contrast to a previous report. This study generated a scientific basis for the use of this plant in Bhutanese traditional medicine, either individually or in combination with other medicinal ingredients to treat a broad range of disorders. This study also identified compound 5 as potential new antimalarial lead compound.
首次对皱叶紫堇(紫堇科)的化学成分和生物活性进行了研究。植物化学研究结果分离出9种已知的异喹啉生物碱:原阿片碱(1)、13-氧代原阿片碱(2)、13-氧代隐品碱(3)、斯氏紫堇碱(4)、去氢紫堇碱(5)、紫堇根碱(6)、赭黄碱(7)、西伯利亚紫堇碱(8)和荷包牡丹碱(9),首次在此提供了2和3完整的核磁共振数据。粗提物对脂多糖激活的THP-1细胞中肿瘤坏死因子-α的产生表现出显著的抗炎活性(p < 0.01)。首次在此报道了化合物2、4和7的乙酰胆碱酯酶抑制活性以及化合物5对恶性疟原虫菌株TM4/8.2和K1CB1(多药耐药菌株)的抗疟活性。与之前的报道相反,斯氏紫堇碱(4)对K1CB1菌株未显示抗疟活性。本研究为该植物在不丹传统医学中单独或与其他药用成分联合用于治疗多种疾病奠定了科学基础。本研究还确定化合物5为潜在的新型抗疟先导化合物。