有机化学 ›› 2018, Vol. 38 ›› Issue (8): 2167-2173.DOI: 10.6023/cjoc201802010 上一篇    下一篇

研究简报

哌嗪取代3-芳基-5-呋喃基-4,5-二氢吡唑酰胺衍生物的合成及其生物活性评价

毛泽伟a, 刘蓓a, 朱萍a, 张丽君a, 朱加洪a, 伍林泽a, 万春平b   

  1. a 云南中医学院中药学院 昆明 650500;
    b 云南中医学院第一附属医院中心实验室 昆明 650021
  • 收稿日期:2018-02-06 修回日期:2018-03-27 出版日期:2018-08-25 发布日期:2018-04-27
  • 通讯作者: 毛泽伟, 万春平 E-mail:maozw@ynutcm.edu.cn;wanchunping1012@163.com
  • 基金资助:

    国家自然科学基金(No.81460624)和云南省科学技术厅-云南中医学院应用基础研究联合专项(No.2017FF117(-023))资助项目.

Synthesis and Biological Evaluation of Piperazine Substituted 3-Aryl-5-furanyldihydropyrazole Amide Derivatives

Mao Zeweia, Liu Beia, Zhu Pinga, Zhang Lijuna, Zhu Jiahonga, Wu Linzea, Wan Chunpingb   

  1. a College of Pharmaceutical Science, Yunnan University of Traditional Chinese Medicine, Kunming 650500;
    b Central laboratory, The NO.1 Affiliated Hospital of Yunnan University of Traditional Chinese Medicine, Kunming 650021
  • Received:2018-02-06 Revised:2018-03-27 Online:2018-08-25 Published:2018-04-27
  • Contact: 10.6023/cjoc201802010 E-mail:maozw@ynutcm.edu.cn;wanchunping1012@163.com
  • Supported by:

    Project supported by the National Natural Science Foundation of China (No. 81460624) and the Yunnan Provincial Science and Technology Department-Applied Basic Research Joint Special Funds of Yunnan University of Traditional Chinese Medicine (No. 2017FF117(-023)).

吡唑是一类具有优良生物活性的五元杂环化合物.以4-氟苯乙酮和2-呋喃甲醛为原料出发,经Aldol缩合、取代、环化和酰化等反应,合成得到16个未见文献报道的新型哌嗪取代的3-芳基-5-呋喃基-4,5-二氢吡唑酰胺衍生物.采用小鼠巨噬细胞Raw264.7模型和噻唑蓝(MTT)法分别测试了目标化合物的体外抗炎活性和抗肿瘤活性(A549、Hela和SGC7901).研究结果发现,二氢吡唑类化合物能有效抑制炎症因子NO的生成,并对肿瘤细胞株表现出选择性的抑制活性.其中3个化合物与地塞米松活性相当,能有效抑制NO的生成;3个化合物对肿瘤细胞株的体外选择性抑制活性与5-氟尿嘧啶(5-FU)相当,均可做进一步构效关系研究.

关键词: 二氢吡唑, 酰胺, 抗炎活性, 抗肿瘤活性

Pyrazole is a five-membered heterocyclic molecule with a broad range of biological activities. In this study, a series of new 3-aryl-5-furanyl-4,5-dihydropyrazole derivatives have been designed and synthesized by the general principle of molecular hybridization. The structures were characterized by 1H NMR, 13C NMR and HRMS. We screened in vitro anti-inflammatory in lipopolysaccharide (LPS)-stimulated RAW-264.7 macrophages and anticancer activity against 3 strains human tumor cell lines (A549, Hela and SGC7901) by the methyl thiazolyl tetrazolium (MTT) assay. The result indicated that dihydropyrazole compounds showed good inhibitory effect on the generation of NO and selective cytotoxic activity against tumor cell lines, and the acyl moieties of amides had an obvious influence on biological activities. Especially, 3 compounds were found to be similar anti-inflammatory to positive control dexamethasone, and 3 compounds displayed similar selective anti-tumor activity to positive control 5-fluorouracil (5-FU), which were to be lead compounds for further SAR research.

Key words: dihydropyrazole, amide, anti-inflammatory activity, anticancer activity