Discovery of Structural Diversity Guided N-S Heterocyclic Derivatives Based on Natural Benzothiazole Alkaloids as Potential Cytotoxic Agents
文献类型： 外文期刊
作者： Guo, Lirong 1 ; Wan, Yafei 1 ; Liu, Manli 2 ; Zheng, Fuqiang 2 ; Shi, Yingwu 4 ; Wang, Kaimei 2 ; Cao, Xiufang 1 ; Bao, Longzhu 2 ; Ke, Shaoyong 2 ;
作者机构： 1.Huazhong Agr Univ, Coll Chem, Wuhan, Peoples R China
2.Hubei Acad Agr Sci, Natl Biopesticide Engn Res Ctr, Hubei Biopesticide Engn Res Ctr, Key Lab Microbial Pesticides,Minist Agr & Rural Af, Wuhan, Peoples R China
3.Hubei Univ Technol, Sch Biol Engn & Food, Wuhan, Peoples R China
4.Xinjiang Acad Agr Sci, Inst Microbiol, Urumqi, Xinjiang, Peoples R China
5.Xinjiang Lab Special Environm Microbiol, Urumqi, Xinjiang, Peoples R China
关键词： amino acid conjugates; benzothiazole alkaloids; cytotoxic agents; diacylhydrazine; hydrazone
期刊名称：JOURNAL OF HETEROCYCLIC CHEMISTRY （ 影响因子：2.4； 五年影响因子：2.2 ）
ISSN： 0022-152X
年卷期： 2024 年 61 卷 11 期
页码：
收录情况： SCI
摘要： Benzothiazole alkaloids are a class of rare heterocyclic alkaloids with unique structures and exhibit a wide range of biological activities. So, the aim of this work is to investigate structural diversity-guided N-S heterocyclic derivatives based on natural benzothiazole alkaloids as potential cytotoxic agents. Three series of novel benzothiazole derivatives, including 22 compounds, were designed and synthesized using pharmacophore hybridization, and their in vitro cytotoxic activities against Huh-7 and A875 were fully evaluated. The results indicated that some of these benzothiazole derivatives had significantly good cytotoxic activities against two tested cell lines compared with the positive control 5-fluorouracil, and other compounds 3f-3i displayed good selectivity between A875 and Huh-7 cell lines, which might be used as promising lead molecule for discovery of novel benzothiazole-type cytotoxic agents.
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