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首页> 外文期刊>Records of Natural Products >Cholinesterase Inhibiting Activity and A New Piperidine Alkaloid from Lobelia laxiflora L. Roots (Campanulaceae)
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Cholinesterase Inhibiting Activity and A New Piperidine Alkaloid from Lobelia laxiflora L. Roots (Campanulaceae)

机译:半边山梗菜根(桔梗)的胆碱酯酶抑制活性和新的哌啶生物碱

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The total alkaloidal fraction of Lobelia laxiflora L. roots was tested for cholinesterase inhibiting activity using spectrophotometric method. The IC 50 value of the alkaloidal fraction recorded was close to that of eserine ( 286.3 μg/mL and 270 μg/mL, respectively) . This biologically active alkaloidal fraction was subjected to a phytochemical study to isolate and identify its major constituents. Two piperidine alkaloids, N-methyl-2(2 ' -methoxybutyl),6(2 '' -hydroxybutyl)- Δ 3 -piperidine (1) and N-methyl- 2(2 ' -hydroxybutyl),6(2 '' -hydroxybutyl)- Δ 3 -piperidine (2), were isolated. The structures of the two compounds were established based on their spectral data, including MS, 1H- and 13C-NMR, COSY, HMQC and HMBC spectral experiments. Compound (1) is a new natural compound while compound (2) was previously isolated from the aerial parts of the same plant.
机译:用分光光度法测定了山梗菜根的总生物碱级分的胆碱酯酶抑制活性。记录的生物碱部分的IC 50值接近于色氨酸(分别为286.3μg/ mL和270μg/ mL)。对该生物活性生物碱部分进行了植物化学研究,以分离并鉴定其主要成分。两个哌啶生物碱,N-甲基-2(2'-甲氧基丁基),6(2''-羟基丁基)-Δ3-哌啶(1)和N-甲基-2(2'-羟基丁基),6(2''分离了(-羟基丁基)-Δ3-哌啶(2)。根据两种化合物的光谱数据(包括MS,1H-和13C-NMR,COSY,HMQC和HMBC光谱实验)建立结构。化合物(1)是一种新的天然化合物,而化合物(2)先前是从同一植物的地上部分中分离出来的。

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