Hieda Yuhzo, Anraku Makoto, Choshi Tominari, Tomida Hisao, Fujioka Haruto, Hatae Noriyuki, Hori Osamu, Hirose Junzo, Hibino Satoshi
Faculty of Pharmacy and Pharmaceutical Sciences, Fukuyama University, Fukuyama, Hiroshima 729-0292, Japan.
Faculty of Pharmaceutical Sciences, Sojo University, Kumamoto 860-0082, Japan.
Bioorg Med Chem Lett. 2014 Aug 1;24(15):3530-3. doi: 10.1016/j.bmcl.2014.05.050. Epub 2014 May 27.
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.
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。