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

机译:Glaucumolides A和B从养殖的软珊瑚青藻中获得新结构类型的双塞类化合物

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摘要

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:新型双癸酸酯,包括前所未有的α,β-不饱和ε-内酯,以及已知的代谢产物希马洛利德A(>),包括青草醚A(> 1 )和B(> 2 )。 > 3 )和异藻藻糖醇内酯D(> 4 )是从培养的软珊瑚绿藻藻中分离得到的。新的代谢产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 对fMLP / CB刺激的人中性粒细胞中的超氧阴离子生成和弹性蛋白酶释放具有强烈的抑制作用。此外,> 1 和> 2 均显示出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,strong> 3 可有效降低环氧合酶2蛋白的表达。

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