首页> 外文期刊>Journal of natural products >(+/-)-Homocrepidine A, a Pair of Anti-inflammatory Enantiomeric Octahydroindolizine Alkaloid Dimers from Dendrobium crepidatum
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(+/-)-Homocrepidine A, a Pair of Anti-inflammatory Enantiomeric Octahydroindolizine Alkaloid Dimers from Dendrobium crepidatum

机译:(+/-)-高cre啶A,一对来自石cre石end的消炎对映体八氢吲哚嗪生物碱二聚体

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摘要

A pair of racemic indolizidine enantiomers, (+/-)-homocrepidine A (1), and a piperidine derivative, homocrepidine B (2), were isolated from Dendrobium crepidatum along with the known alkaloid crepidine (3). The racemic mixture of 1 was separated into a pair of enantiomers, (+)-1 and (-)-1, by HPLC using a chiral chromatographic substrate, which represents the first successful example of resolving indolizidine racemic mixtures. The absolute configurations of (+)-1 and (-)-1 were assigned from single-crystal X-ray diffraction data. The evaluation of anti-inflammatory activity with LPS-induced RAW 264.7 macrophages revealed that (+)-1 strongly inhibited the production of nitric oxide (IC50, 3.6 mu M) and significantly decreased the expression of inducible nitric oxide synthase, while (-)-1 and (+/-)-1 only had moderate inhibitory effects (IC50, 22.8 and 14.7 mu M). Compound 2 showed moderate anti-inflammatory activity (IC50, 27.6 mu M).
机译:从铁皮石D中分离出一对外消旋吲哚并咪唑对映异构体(+/-)-高氨甲rep啶A(1)和哌啶衍生物高甲idine啶B(2)以及已知的生物碱克雷丁啶(3)。通过使用手性色谱底物的HPLC将1的外消旋混合物分离为一对对映异构体(+)-1和(-)-1,这是拆分吲哚并咪唑外消旋混合物的第一个成功实例。从单晶X射线衍射数据确定(+)-1和(-)-1的绝对构型。用LPS诱导的RAW 264.7巨噬细胞进行的抗炎活性评估表明,(+)-1强烈抑制一氧化氮的产生(IC50,3.6μM),并显着降低了诱导型一氧化氮合酶的表达,而(-) -1和(+/-)-1仅具有中等抑制作用(IC50、22.8和14.7μM)。化合物2显示出中等的抗炎活性(IC50,27.6μM)。

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