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Phomopsichin A–D; Four New Chromone Derivatives from Mangrove Endophytic Fungus Phomopsis sp. 33#

机译:Phomopsichin A–D;红树林内生真菌Phomopsis sp。的四种新色酮衍生物。 33#

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摘要

Four new chromone derivatives, phomopsichins A–D (>1–>4), along with a known compound, phomoxanthone A (>5), were isolated from the fermentation products of mangrove endophytic fungus Phomopsis sp. 33#. Their structures were elucidated based on comprehensive spectroscopic analysis coupled with single-crystal X-ray diffraction or theoretical calculations of electronic circular dichroism (ECD). They feature a tricyclic framework, in which a dihydropyran ring is fused with the chromone ring. Compounds >1–>5 showed weak inhibitory activities on acetylcholinesterase as well as α-glucosidase, weak radical scavenging effects on 1,1-diphenyl-2-picrylhydrazyl (DPPH) as well as OH, and weak antimicrobial activities. Compounds >1–>4 showed no cytotoxic activity against MDA-MB-435 breast cancer cells. Their other bioactivities are worthy of further study, considering their unique molecular structures.
机译:分离了四种新的色酮衍生物,phophopsichins A–D(> 1 – > 4 ),以及已知的化合物苯氧恶蒽酮A(> 5 )。来自红树林内生真菌Phomopsis sp。的发酵产物。 33#。基于全面的光谱分析结合单晶X射线衍射或电子圆二色性(ECD)的理论计算,阐明了它们的结构。它们具有三环骨架,其中二氢吡喃环与色酮环稠合。化合物> 1 – > 5 对乙酰胆碱酯酶和α-葡糖苷酶的抑制作用较弱,对1,1-二苯基-2-吡啶并二肼(DPPH)的自由基清除作用较弱如OH,且抗菌活性弱。化合物> 1 – > 4 对MDA-MB-435乳腺癌细胞没有细胞毒活性。考虑到它们独特的分子结构,它们的其他生物活性值得进一步研究。

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