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Glaucumolides A and B, Biscembranoids with New Structural Type from a Cultured Soft Coral Sarcophyton glaucum

机译:养殖的软珊瑚中的新结构类型的双萜类青草醚A和B 青草Sarcophyton glaucum

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Glaucumolides A ( 1 ) and B ( 2 ), novel biscembranes composed of an unprecedented α,β-unsaturated ε-lactone, along with the known metabolites ximaolide A ( 3 ) and isosarcophytonolide D ( 4 ), were isolated from the cultured soft coral Sarcophyton glaucum . The structures of the new metabolites were determined by extensive spectroscopic analyses. Compounds 1 and 2 were shown to exhibit cytotoxicity against a limited panel of cancer cell lines. In anti-inflammation assay, compounds 1 and 2 displayed strong inhibition of superoxide anion generation and elastase release in human neutrophils stimulated by fMLP/CB. Furthermore, both 1 and 2 were shown to significantly inhibit the accumulation of the pro-inflammatory inducible nitric oxide synthase protein, and compounds 1 ? 3 were found to effectively reduce the expression of cyclooxygenase-2 protein, in lipopolysaccharide-stimulated RAW264.7 macrophage cells.
机译:从养殖的软珊瑚中分离出了由前所未有的α,β-不饱和ε-内酯组成的新型双萜烯类化合物-青草内酯A(1)和B(2)。蓝藻。新的代谢物的结构通过广泛的光谱分析确定。化合物1和2显示出对有限系列癌细胞系的细胞毒性。在抗炎试验中,化合物1和2在fMLP / CB刺激的人中性粒细胞中显示出对过氧化物阴离子生成和弹性蛋白酶释放的强烈抑制作用。此外,还显示1和2均显着抑制促炎性一氧化氮合酶蛋白和化合物1?在脂多糖刺激的RAW264.7巨噬细胞中,发现3种可有效降低环氧合酶2蛋白的表达。

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