為期由天然物中開發具臨床價值之抗癌新藥,本論文以初步篩選顯示抗癌活性之植物「姬蕨」,配合活性實驗,進行活性成分分離與結構決定之研究。姬蕨全草鮮品之甲醇萃取物,經以n-Hexane, Ethyl acetate及H2O分配萃取,再藉由各種層析法,共分離出五個化合物,根據其物理數據及光譜儀器分析鑑定,其結構分別確定為Pterosin Z(1), Pterosin I(2), Pterosin A(3), Pterosin D(4)及(+)-pinoresinol-β-D-glucoside(5)。而(+)-pinoresinol-β-D-glucoside則首次於姬蕨中被分離出。另外乙酸乙酯層經管柱層析後,經初步藥理活性篩選,確定對胃癌(NUGC-3)及鼻咽癌(HONE-1)細胞株有明顯細胞毒性作用,而該活性部分分離出Pterosin D(4)。經藥理活性測試結果,首次證實Pterosin Z(1)及Pterosin I(2)對Hep G2肝癌細胞株有細胞毒性,其IC50分別為55.1μg/ml及32.8 μg/ml。
For developing to existed the clinical value using in the new anticancer drugs development. This research is the preliminary step to sieve cytotoxic exhibiter out from Hypolepis punctata (Thunb.) Mett. The fresh full plants of Hypolepis punctata (Thunb.) Mett., were extracted with methanol, to afford crude extracted, which was partitioned between n-Hexane, Ethyl acetate and H2O. These fraction were subject to various chromatography and preliminary screen test cytotoxic activity. Five compounds were isolated and purified. The structures of these compound were determined based on the analysis of their physical property and spectral studies, they are Pterosin Z(1), Pterosin I(2), Pterosin A(3), Pterosin D(4) and(+)-pinoresinol-β-D-glucoside(5). Among them, Fraction 5-1 of Ethyl acetate layer showed cytotoxic effects to NUGC-3 and HONE-1 cells. Moreover, it is note worthy that (+)-pinoresinol-β-D-glucoside(5) was isolated from Hypolepis punctata (Thunb.) Mett. for the first time. Pterosin Z(1) and Pterosin I(2) exhibited cytotoxic effects on the Hep G2 cells, which IC50 are 55.1μg/ml and 32.8μg/ml.