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Isoorientin, a Selective Inhibitor of Cyclooxygenase-2 (COX-2) from the Tubers of Pueraria tuberosa

机译:异东方素,一种来自葛根块茎的环氧合酶-2(COX-2)的选择性抑制剂

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摘要

Bioassay-guided fraction of the methanol extract of the roots of Pueraria tuberose DC yielded puerarin, an isoflavone C-glycoside (PT-1), isoorientin, a flavone C-glycoside (PT-2) and mangiferin, a xanthone C-glycoside (PT-3). The extracts and the isolated compounds were screened for potent anti-inflammatory components inhibiting the cyclooxygenases (COX-1 and COX-2) and 5-lipoxygenase (5-LOX), the target enzymes of inflammation, by employing spectroscopic/polorographic methods. Among these, isoorientin was found to be a potent inhibitorof COX-2with an IC50 value of 39 mu M. Docking studies were carried out to understand the interactions of isorientin (PT-2) with COX-2.The structures of the isolates were determined by mass spectrometry and 2D-NMR techniques including HSQC, HMBC, NOESY and H-1-H-1 COSY experiments. Although isoorientin and mangiferin have been reported from several plant sources, this is the first report of their isolation from a Pueraria species.
机译:葛根DC根部甲醇提取物的生物测定指导馏分可得到葛根素,异黄酮C-糖苷(PT-1),异Orientin,黄酮C-糖苷(PT-2)和芒果苷,x吨C-糖苷( PT-3)。通过采用光谱/层析方法,针对提取物和分离出的化合物筛选抑制炎症的目标酶环氧合酶(COX-1和COX-2)和5-脂氧合酶(5-LOX)的有效抗炎成分。其中,异Orientinin被认为是强效的COX-2抑制剂,IC50值为39​​μM。进行了对接研究以了解isorientin(PT-2)与COX-2的相互作用,并确定了分离物的结构。通过质谱和2D-NMR技术,包括HSQC,HMBC,NOESY和H-1-H-1 COZY实验。尽管从几种植物来源中都报道了异Orientientin和Mangiferin,但这是首次从葛根中分离出异orientin和mangiferin。

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