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Comparison of antioxidative properties of carbazole alkaloids from Murraya koenigii leaves

机译:茉莉香叶中咔唑生物碱的抗氧化性能比较

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摘要

A new dimeric carbazole alkaloid, 8,10'-[3,3',11,11'-tetrahydro-9,9'-dihydroxy-3,3',5,8'-tetramethyl-3,3'-bi s(4-methyl-3-pentenyl)]bipyrano[3,2-a]carbazole (12), was isolated from the CH2Cl2 extract of Murraya koenigii together with six known carbazole alkaloids, koenimbine (6), O-methylmurrayamine A (7), O-methylmahanine (8), isomahanine (9), bismahanine (10), and bispyrayafoline (11). Their structures were determined on the basis of H-1 and C-13 NMR spectroscopic and mass spectrometric (MS) data. The antioxidative properties of 12 carbazole alkaloids isolated from leaves of M. koenigii were evaluated on the basis of the oil stability index together with their radical scavenging ability against 1, 1-diphenyl-2-picrylhydrazyl (DPPH) radical. On the basis of the lag time to reach a steady state, the 12 carbazoles were classified into three groups. It is suggested that an aryl hydroxyl substituent on the carbazole rings plays a role in stabilizing the thermal oxidation and rate of reaction against DPPH radical.
机译:新的二聚咔唑生物碱8,10'-[3,3',11,11'-四氢-9,9'-二羟基-3,3',5,8'-四甲基-3,3'-bi (4-甲基-3-戊烯基)]双吡喃并[3,2-a]咔唑(12)与六种已知的咔唑生物碱,可宁宁(6),O-甲基墨胺A(7)一起从Murraya koenigii的CH2Cl2提取物中分离得到。 ),O-甲基大黄嘌呤(8),异大黄嘌呤(9),双大黄嘌呤(10)和双吡fo啉(11)。它们的结构是根据H-1和C-13 NMR光谱和质谱(MS)数据确定的。根据油稳定性指数以及它们对1,1-二苯基-2-吡啶并肼基(DPPH)自由基的清除能力,评估了从毛叶锦葵(M. koenigii)叶片中分离出的12种咔唑生物碱的抗氧化性能。根据达到稳定状态的滞后时间,将12种咔唑分为三类。建议咔唑环上的芳基羟基取代基在稳定热氧化和抗DPPH自由基的反应速率方面起作用。

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