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Cyclooxygenase inhibitory properties of nor -neolignans from Styrax pohlii

机译:圆叶番荔枝正-新木质素的环氧合酶抑制特性

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摘要

Chemical investigation of the n-hexane and EtOAc fractions of the ethanolic extract from Styrax pohlii (Styracaceae) aerial parts resulted in the isolation of the benzofuran nor-neolignan derivatives egonol (1), homoegonol (2), homoegonol gentiobioside (3), homoegonol glucoside (4) and egonol gentiobioside (5). This is the first report of compounds 1-5 in S. pohlii. Compounds 1-5, the acetyl derivatives 1a and 2a, the ethanolic extract (EE), the n-hexane fraction (HF) and EtOAc fraction (EF) were tested for their inhibitory activities against COX-1 and COX-2. The results showed that EE, HF, EF and compounds 1-5 and 1a-2a shown weak to moderate inhibition of COX-1 and COX-2. Among the assayed nor-neolignans, 4 gave a COX-1 inhibition of 35.7% at 30μM. Compound 5 displayed a COX-2 inhibition of 19.7% at 30μM.
机译:对虎疫菊(Styrax pohlii)(戟科)地上部分乙醇提取物的正己烷和EtOAc馏分进行化学研究,结果分离出苯并呋喃去甲酚,新戊二烯酚衍生物(均一烯酚(2),均草烯醇龙胆苷(3),均草烯酚)葡萄糖苷(4)和烯诺酚龙胆生物苷(5)。这是S. pohlii中化合物1-5的首次报道。测试化合物1-5,乙酰基衍生物1a和2a,乙醇提取物(EE),正己烷馏分(HF)和EtOAc馏分(EF)对COX-1和COX-2的抑制活性。结果表明,EE,HF,EF以及化合物1-5和1a-2a对COX-1和COX-2的抑制作用弱至中度。在测定的去甲酚中,有4种在30μM时对COX-1的抑制率为35.7%。化合物5在30μM时显示出19.7%的COX-2抑制率。

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