首页> 外文期刊>Saudi Pharmaceutical Journal >A novel monocyclic triterpenoid and a norsesquaterpenol from the aerial parts of Suaeda monoica Forssk. ex J.F. Gmel with cell proliferative potential
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A novel monocyclic triterpenoid and a norsesquaterpenol from the aerial parts of Suaeda monoica Forssk. ex J.F. Gmel with cell proliferative potential

机译:来自Suaeda monoica Forssk地上部分的新型单环三萜和去甲四萜。前J.F. Gmel具有细胞增殖潜能

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Suaeda monoica Forssk. ex J.F. Gmel (Chenopodiaceae), a mangrove herb, is distributed in tropical Africa, Arabian Peninsula, India, Pakistan, Palestine and Jordan. The plant parts are used to treat sore throat, hepatitis, wounds, rheumatism, paralysis, asthma, snakebites, skin disease and ulcer. Two new phytoconstituents characterized as 13,17-octahydropentalene-4,4,10,23-tetramethyl-17,21-diisopropyl-tetradecahydrocyclo-[a]-phenanthrene-(14), 20(23), 21(30)-trien-5@a-ol (SMC-3) and [1,4,4-trimethyl-cyclopent-1(5)-enyl]-9,10,17,21-tetramethyl-9@a-ol-16@a (17@a)-epoxy heptadecan-6,10-dione (SMC-4) belong to the class norsesquaterpenol and monocyclic triterpenoid, respectively, along with two known compounds 3-epi-lupeol (SMC-1) and 4-cyclopentylpyrocatechol (SMC-2) have been isolated from the ethanol extract of aerial parts of S. monoica using normal and reverse phase column as well as planar chromatography. The spectroscopic studies including 1D, 2D NMR (DEPT, COSY, HMBC and HSQC) aided by EIMS mass and IR spectra were used to establish their structures. All the four compounds were tested for cytotoxicity on cultured HepG2 cells and for cell proliferation activities. The results revealed no cytotoxicity even at highest (6.25-50@mg/ml) dose of all the four compounds. The compound SMC-1 showed prominent cell proliferative activity as compared to other SMC compounds.
机译:Suaeda monoica Forssk。前J.F. Gmel(藜科)是一种红树林药草,分布在热带非洲,阿拉伯半岛,印度,巴基斯坦,巴勒斯坦和约旦。植物部位用于治疗喉咙痛,肝炎,伤口,风湿病,瘫痪,哮喘,蛇咬伤,皮肤病和溃疡。两种新的植物成分为13,17-八氢戊烯-4,4,10,23-四甲基-17,21-二异丙基-十四氢环-[a]-菲-(14),20(23),21(30)-三烯-5 @ a-ol(SMC-3)和[1,4,4-三甲基-环戊-1(5)-烯基] -9,10,17,21-四甲基-9 @ a-ol-16 @ a (17 @ a)-环氧庚烷-6,10-二酮(SMC-4)分别属于Norsesquaterpenol和单环三萜类,以及两种已知的化合物3-epi-lupeol(SMC-1)和4-cyclopentylpyrocatechol( SMC-2)已使用正相和反相色谱柱以及平面色谱从S. monoica地上部分的乙醇提取物中分离得到。借助EIMS质谱和IR光谱对包括1D,2D NMR(DEPT,COSY,HMBC和HSQC)的光谱学研究来建立其结构。测试了所有四种化合物对培养的HepG2细胞的细胞毒性和细胞增殖活性。结果显示,即使在所有四种化合物的最高剂量(6.25-50@mg/ml)下也没有细胞毒性。与其他SMC化合物相比,化合物SMC-1表现出突出的细胞增殖活性。

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