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首页> 外文期刊>Bioorganic and Medicinal Chemistry >Symbioimine and neosymbioimine, amphoteric iminium metabolites from the symbiotic marine dinoflagellate Symbiodinium sp.
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Symbioimine and neosymbioimine, amphoteric iminium metabolites from the symbiotic marine dinoflagellate Symbiodinium sp.

机译:共生亚胺和新共生亚胺,来自共生海洋藻鞭毛体Symbiodinium sp。的两性亚胺鎓代谢物。

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摘要

Two amphoteric iminium metabolites, symbioimine (1) and neosymbioimine (2), were isolated from a cultivated symbiotic marine dinoflagellate Symbiodinium sp. Compounds 1 and 2 have a characteristic 6,6,6-tricyclic iminium ring structure and an aryl sulfate moiety. The plausible biogenetic pathway of 1 and 2 can be explained by an intramolecular Diels-Alder reaction followed by imine cyclization. Symbioimine (1) inhibited the differentiation of RAW264 cells into osteoclasts (EC50 = 44 microM), and significantly inhibited cyclooxygenase-2 activity at 10 microM. Thus, symbioimine is a potent anti-resorptive and anti-inflammatory drug.
机译:从培养的共生海洋双鞭毛藻Symbiodinium sp。中分离出两种两性亚胺鎓代谢物,共生亚胺(1)和新共生亚胺(2)。化合物1和2具有特征性的6,6,6-三环亚胺环结构和硫酸芳基部分。 1和2的合理生物遗传途径可以通过分子内Diels-Alder反应然后亚胺环化来解释。共生亚胺(1)抑制RAW264细胞分化为破骨细胞(EC50 = 44 microM),并在10 microM时显着抑制环氧合酶2的活性。因此,共生亚胺是一种有效的抗吸收和抗炎药。

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