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Cytotoxic and anti-HIV-1 constituents from leaves and twigs of Gardenia tubifera

机译:tub子叶和嫩枝的细胞毒性和抗HIV-1成分

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Two new natural cycloartanes, tubiferolide methyl ester (1) and tubiferaoctanolide (2), together with the known coronalolide (3) and coronalolide methyl ester (4) have been isolated from leaves and twigs of Gardenia tubifera. In addition, a new flavone 5,3',5'-trihydroxy-7,4'-dimethoxyflavone (5), five known flavones 6-10 and hexacosyl 4'-hydroxy-trans-cinnamate (11) were also obtained from the same source. The structures were assigned on the basis of spectroscopic methods. Compounds 3, 7, 9, and 10 showed significant cytotoxic activities only in P-388 cell line. Compound 1 was cytotoxic against P-388, KB, Col-2 and Lu-1, while 4 was active in P-388 and BCA-1. Compounds 3 and 4 displayed significant anti-HIV activities in the HIV-IRT assay; compound 7 showed moderate activity in this assay. Compounds 5-10 were also found to be active in the (MC)-M-DeltaTat/Rev 99 syncytium assay. (C) 2003 Elsevier Ltd. All rights reserved. [References: 34]
机译:从Garden子花的叶和嫩枝中分离出了两种新的天然环烷烃,即tubiferolide甲酯(1)和tubiferaoctanolide(2),以及已知的Coronalolide(3)和Coronalolide甲酯(4)。此外,还从中获得了新的黄酮5,3',5'-三羟基-7,4'-二甲氧基黄酮(5),五个已知的黄酮6-10和己基4'-羟基-反式肉桂酸酯(11)。相同的来源。结构是根据光谱方法分配的。化合物3、7、9和10仅在P-388细胞系中显示出明显的细胞毒活性。化合物1对P-388,KB,Col-2和Lu-1具有细胞毒性,而化合物4在P-388和BCA-1中具有活性。化合物3和4在HIV-IRT分析中显示出显着的抗HIV活性。化合物7在该测定中显示中等活性。还发现化合物5-10在(MC)-M-DeltaTat / Rev 99合胞体测定中具有活性。 (C)2003 Elsevier Ltd.保留所有权利。 [参考:34]

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