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高度取代咔唑生物碱及其相关咔唑的抗氧化作用。

Antioxidant effects of the highly-substituted carbazole alkaloids and their related carbazoles.

作者信息

Hieda Yuhzo, Anraku Makoto, Choshi Tominari, Tomida Hisao, Fujioka Haruto, Hatae Noriyuki, Hori Osamu, Hirose Junzo, Hibino Satoshi

机构信息

Faculty of Pharmacy and Pharmaceutical Sciences, Fukuyama University, Fukuyama, Hiroshima 729-0292, Japan.

Faculty of Pharmaceutical Sciences, Sojo University, Kumamoto 860-0082, Japan.

出版信息

Bioorg Med Chem Lett. 2014 Aug 1;24(15):3530-3. doi: 10.1016/j.bmcl.2014.05.050. Epub 2014 May 27.

Abstract

Antioxidant activities of 3-oxygenated and 3,4-dioxygenated carbazole alkaloids and their related carbazoles were comprehensively evaluated. In all assay systems, the 3,8-dihydroxycarbazoles carbazomadurin A (2) and B (3), and their synthetic precursors 2a and 3a exhibited higher antioxidant activities than the 3-monohydroxycarbazoles carazostatin (1), and the synthetic precursors 4a and 4b of carquinostatin A (4). In particular, 2a and 3a exhibited strong scavenging activities due to the reducing ability of formyl group at the C-5 position of carbazoles. The results suggest that these compounds could serve as useful clues for designing and developing novel antioxidants.

摘要

对3-氧化和3,4-二氧化咔唑生物碱及其相关咔唑的抗氧化活性进行了全面评估。在所有测定系统中,3,8-二羟基咔唑咔唑马杜林A(2)和B(3)及其合成前体2a和3a表现出比3-单羟基咔唑卡拉佐他汀(1)以及卡喹他汀A(4)的合成前体4a和4b更高的抗氧化活性。特别是,由于咔唑C-5位甲酰基的还原能力,2a和3a表现出很强的清除活性。结果表明,这些化合物可为设计和开发新型抗氧化剂提供有用线索。

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