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3-hydroxy-3-methylglutaryl flavonol glycosides from Oxytropis falcata.

机译:镰形棘豆(Oxytropis falcata)的3-羟基-3-甲基戊二酮黄酮醇苷

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摘要

Five new 3-hydroxy-3-methylglutaryl (HMG) flavonol 3-O-glycosides, named oxytroflavosides A-E (1-5), and two new rhamnocitrin 3-O-glycosides, oxytroflavosides F and G (6 and 7) were isolated from the n-BuOH-soluble fraction of an EtOH extract of Oxytropis falcata together with seven known kaempferol glycosides (8-14), of which six were isolated from the genus Oxytropis for the first time. The structures of these compounds were elucidated by spectroscopic techniques and chemical methods. The absolute configuration of HMG in compounds 1-5 was determined to be S through spectroscopic analysis of the mevalonamide obtained by amidation and reduction of the HMG moiety. Compounds 1-10 were evaluated for anti-inflammatory activities using lipopolysaccharide-induced RAW 264.7 cells, but none of them showed inhibitory effects on NO production.
机译:从中分离了五个新的3-羟基-3-甲基戊二烯基(HMG)黄酮醇3-O-糖苷,分别称为oxytroflavosides AE(1-5)和两个新的鼠李糖苷3-O-糖苷,oxytroflavosides F和G(6和7)。棘形棘豆EtOH提取物的n-BuOH可溶性级分与七个已知的山ka酚糖苷(8-14)一起,其中六个是首次从棘形棘属中分离出来。通过光谱技术和化学方法阐明了这些化合物的结构。通过光谱分析通过酰胺化和还原HMG部分获得的甲羟戊酰胺,确定化合物1-5中HMG的绝对构型为S。使用脂多糖诱导的RAW 264.7细胞评估了化合物1-10的抗炎活性,但它们均未显示出对NO产生的抑制作用。

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