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首页> 外文期刊>Biological & pharmaceutical bulletin >Peroxisome Proliferator-Activated Receptor gamma Ligands Isolated from Adlay Seed (Coix lacryma-jobi L. var. ma-yuen STAPF.)
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Peroxisome Proliferator-Activated Receptor gamma Ligands Isolated from Adlay Seed (Coix lacryma-jobi L. var. ma-yuen STAPF.)

机译:从Ad仁种子中分离得到的过氧化物酶体增殖物激活的受体γ配体(ix(Coix lacryma-jobi L. var。ma-yuen STAPF)。)

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摘要

Through screening for natural ligands against peroxisome proliferator-activated receptor gamma (PPAR gamma) using the PPAR gamma luciferase reporter assay, 6 hydroxy unsaturated fatty acids were isolated from adlay seed (Coix lacryina-jobi L. var. ma-yuen STAPF.) extracts with acetone and 70% ethanol. The structures of these compounds were determined via spectral analysis as 13-hydroxy-(9E,11E)-octadecadienoic acid (13-E,E-HODE) (1), 9-hydroxy-(10E,12E)-octadecadienoic acid (9-E,E-HODE) (2), 9-hydroxy-(10E)-octadecenoic acid (3), 10-hydroxy-(8E)-octadecenoic acid (4), 8-hydroxy-(9E)-octadecenoic acid (5), 11-hydroxy-(9Z)-octadecenoic acid (6). 9-E,E-HODE (2) exhibited the most potent PPAR gamma agonist activity of the isolated hydroxy unsaturated fatty acids. 9E,E-HODE (2) and 13-E,E-HODE (1) are the respective geometrical isomers of 9-hydroxy-(10E,12Z)-octadecadienoic acid and 13-hydroxy-(9Z,11E)-octadecadienoic acid, both of which are likely to be natural PPAR gamma agonists produced in various mammalian cells, suggesting that 9-E,E-HODE may also act as PPAR gamma agonist.
机译:通过使用PPARγ荧光素酶报告基因检测法筛选抗过氧化物酶体增殖物激活的受体γ(PPARγ)的天然配体,从ad仁种子(Coix lacryina-jobi L. var。ma-yuen STAPF。)提取物中分离出6个羟基不饱和脂肪酸。用丙酮和70%的乙醇。这些化合物的结构通过光谱分析确定为13-羟基-(9E,11E)-十八碳二烯酸(13-E,E-HODE)(1),9-羟基-(10E,12E)-十八碳二烯酸(9 -E,E-HODE)(2),9-羟基-(10E)-十八碳烯酸(3),10-羟基-(8E)-十八碳烯酸(4),8-羟基-(9E)-十八碳烯酸( 5),11-羟基-(9Z)-十八烯酸(6)。 9-E,E-HODE(2)在分离的羟基不饱和脂肪酸中表现出最有效的PPARγ激动剂活性。 9E,E-HODE(2)和13-E,E-HODE(1)分别是9-羟基-(10E,12Z)-十八碳二烯酸和13-羟基-(9Z,11E)-十八碳二烯酸的几何异构体,这两种可能都是在各种哺乳动物细胞中产生的天然PPARγ激动剂,这表明9-E,E-HODE也可以充当PPARγ激动剂。

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