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机构地区:[1]School of Pharmacy, Shanghai University of Traditional Chinese Medicine, Shanghai 201203, China [2]Departmen of Applied Chemistry, East China University of Sciences and Technology, Shanghai 20000, China [3]Basilea Pharmaceutica China Ltd., Haimen, Jiangsu 226100, China
出 处:《Chinese Journal of Chemistry》2012年第7期1405-1409,共5页中国化学(英文版)
摘 要:We reported the first total synthesis of hirtellanine B, using oxidative coupling for the key reactions, which resulted in a high yield. The antiproliferative activities of hirtellanine B against Jurkat cells, Raji cells and K562 cells were also investigated. It was found that hirtellanine B could induce G2/M arrest and apoptosis in human lymphoid/leukemia tumor cells.We reported the first total synthesis of hirtellanine B, using oxidative coupling for the key reactions, which resulted in a high yield. The antiproliferative activities of hirtellanine B against Jurkat cells, Raji cells and K562 cells were also investigated. It was found that hirtellanine B could induce G2/M arrest and apoptosis in human lymphoid/leukemia tumor cells.
关 键 词:hirtellanine B SYNTHESIS ANTIPROLIFERATION G2/M arrest cancer cell
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