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首页> 外文期刊>Journal of natural products >Aspidofractinine and Eburnane Alkaloids from a North Borneo Kopsia. Ring-Contracted, Additional Ring-Fused, and Paucidactine-Type Aspidofractinine Alkaloids from K. pauciflora
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Aspidofractinine and Eburnane Alkaloids from a North Borneo Kopsia. Ring-Contracted, Additional Ring-Fused, and Paucidactine-Type Aspidofractinine Alkaloids from K. pauciflora

机译:来自北婆罗洲Kopsia的Aspidofractinine和Eburnane生物碱。拟南芥(K. pauciflora)的环状收缩,额外的环状融合和半胱氨酸型Aspidofractinine生物碱

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摘要

Eleven new indole alkaloids (1-11) comprising seven aspidofractinine and four eburnane alkaloids, were isolated from the stem-bark extract of Kopsia pauciflora occurring in Malaysian Borneo. The aspidofractinine alkaloids include a ring-contracted, an additional ring-fused, a paucidactine regioisomer, two paucidactine, and one kopsine alkaloid. The structures of several of these alkaloids were also confirmed by X-ray diffraction analyses. The bisindole alkaloids isolated, norpleiomutine and kopsoffinol, showed in vitro growth inhibitory activity against human PC-3, HCT-116, MCF-7, and A549 cells and moderate effects in reversing multidrug-resistance in vincristine-resistant human KB cells.
机译:从马来西亚婆罗洲的古朴小花茎皮提取物中分离出11种新的吲哚生物碱(1-11),其中包括7种Aspidofractinine和4种Eburnane生物碱。 Aspidofractinine生物碱包括环缩,附加环稠合,paucidactine区域异构体,两个paucidactine和一个kopsine生物碱。 X射线衍射分析也证实了其中几种生物碱的结构。分离出的双吲哚生物碱,去甲紫杉醇和甲酚四氢萘酚对人PC-3,HCT-116,MCF-7和A549细胞具有体外生长抑制活性,在逆转长春新碱抗性人KB细胞的多药耐药性中具有中等作用。

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