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从全草中分离得到的新 4',5'-亚甲二氧基黄酮衍生物。

New 4',5'-methylenedioxyflavone derivatives from the whole plant of .

机构信息

State Key Laboratory of Natural Medicines, China Pharmaceutical University, Nanjing, China.

出版信息

Nat Prod Res. 2024 Jan-Feb;38(2):177-185. doi: 10.1080/14786419.2022.2111562. Epub 2022 Aug 12.

Abstract

Two new natural products named 5,7-dihydroxy-3,3',6,8-tetramethoxy-4',5'-methylenedioxyflavone () and 3,3',5,7-tetramethoxy-4',5'-methylenedioxyflavone (), along with thirteen known compounds, β-sitosterol (), desmethoxyyangonin (), hexadecane (), 3,9-bis(2,4-di-tert-butylphenoxy)-2,4,8,10-tetraoxa-3,9-diphosphaspiro [5.5] undecane 3,9-dioxide (), 2'6'-dihydroxy-4'-methoxydihydrochalcone (), cardamonin (), 3,3',5,6,7,8-hexamethoxy-4',5'-methylenedioxyflavone (), isofraxidin (), aniba dimer A (), 3,3',4',5,5',8-hexamethoxy-6,7-methylenedioxyflavone (), quercetin (), quercitrin () and isoquercitrin () were isolated from (Thunb.) Nakai by various chromatographic methods. Compounds , , , , , and were isolated from for the first time. Their chemical structures were identified through the analysis of NMR and HR-MS spectra. The anti-inflammatory and cytotoxic activities of compounds were evaluated in cell assays. The results indicated that compounds , , , , , and significantly inhibited the NO production in LPS-induced RAW 264.7 murine macrophage cells. Moreover, compounds , , , , , , and exhibited a cytotoxic effect on the human HepG2 cell line.

摘要

从(Thunb.)Nakai 中通过各种色谱方法分离得到了两个新的天然产物,分别命名为 5,7-二羟基-3,3',6,8-四甲氧基-4',5'-亚甲二氧基黄酮()和 3,3',5,7-四甲氧基-4',5'-亚甲二氧基黄酮(),以及 13 个已知化合物,β-谷甾醇()、去甲氧基姜黄素()、十六烷()、3,9-双(2,4-二叔丁基苯氧基)-2,4,8,10-四氧杂-3,9-二磷杂螺 [5.5] 十一烷 3,9-二氧化物()、2'6'-二羟基-4'-甲氧基二氢查耳酮()、卡达明()、3,3',5,6,7,8-六甲氧基-4',5'-亚甲二氧基黄酮()、异夫拉定()、阿尼巴二聚体 A()、3,3',4',5,5',8-六甲氧基-6,7-亚甲二氧基黄酮()、槲皮素()、槲皮苷()和异槲皮苷()。化合物、、、、和是首次从中分离得到的。通过对 NMR 和 HR-MS 光谱的分析确定了它们的化学结构。在细胞试验中评价了化合物的抗炎和细胞毒性活性。结果表明,化合物、、、、、和显著抑制了 LPS 诱导的 RAW 264.7 鼠巨噬细胞中 NO 的产生。此外,化合物、、、、、、和对人 HepG2 细胞系表现出细胞毒性作用。

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