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Phytochemical and Biological Activity Studies of the Bhutanese Medicinal Plant Corydalis crispa

机译:Bhutanese药用植物Corydalis Crispa的植物化学和生物活性研究

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摘要

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 u3c 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.
机译:第一次调查了Corydalis Crispa(FumariCeae)的化学成分和生物活性。植物化学研究导致分离九种已知的异喹啉生物碱:PROTOPINE(1),13-氧丙酮(2),13-氧代夹氨酸(3),风格桥(4),核杂菊(5),rheaGenine(6),核桃柳(7 ),Sibiricine(8)和Biculline(9),具有2和3的完整NMR数据,首次提供。粗提取物在LPS活化的THP-1细胞中表现出针对TNF-α产生的抗炎(P U3C 0.01)活性。本文首次报告了化合物2,4和7的乙酰胆碱酯酶抑制活性和化合物5对P. falciparum菌株Tm4 / 8.2和K1cb1(多药抗性菌株)的抗癌活性。与前一份报告相比,风格滨(4)未显示对k1cb1菌株的抗疟疾活动。本研究为使用这种植物在不丹传统医学中使用这种植物的科学依据,或与其他药用成分组合使用以治疗广泛的病症。该研究还将化合物5鉴定为潜在的新抗疟铅化合物。

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