土槿乙酸C-18醇酯衍生物的合成及其体外免疫抑制活性研究  

Synthesis and immunosuppressive activity of C-18 alcoholic hydroxylesters derivatives of pseudolaric acid B

作　　者：曾宪杰 张猜 陈守强 陈虹[2] ZENG Xian-Jie;ZHAN Cai;CHEN Shou-qiang;CHEN Hong(College of Pharmacy, Tianjin Medical University,Tianjin 300070,China;Logistics College of PAPF Military Pharmacy Teaching Office, Tianjin 300309,China)

机构地区：[1]天津医科大学药学院,天津300070 [2]武警后勤学院军事药学教研室,天津300309

出　　处：《天津医科大学学报》2019年第1期18-23,共6页Journal of Tianjin Medical University

基　　金：国家自然科学基金资助项目(812028431)

摘　　要：目的:将土瑾乙酸C-18位进行结构改造,筛选出具有高效、低毒、水溶性好等优点的新型免疫抑制化合物。方法:将C-18位还原为醇羟基,通过缩合酰化反应引入苯环、呋喃环、吡啶环羧酸,得到土槿乙酸C-18醇酯衍生物。经MTT法对小鼠T、B淋巴细胞的免疫抑制活性和对小鼠正常脾细胞毒性体外细胞实验筛选。结果:合成得到10个未见文献报道的土瑾乙酸C-18醇酯衍生物B1-B10,所合成的目标化合物均经~1H-NMR, ^(13)C-NMR, HR-ESI进行结构确定,并测定了其体外免疫抑制活性,结果显示其中衍生物B2、B6、B7对T淋巴细胞增殖抑制活性强于土槿乙酸,衍生物B6、B7对B淋巴细胞抑制活性明显强于土槿乙酸。尤其是大多数化合物对正常细胞作用很弱,远低于阳性对照药,呈现高效低毒特性。结论:土槿乙酸C-18醇酯衍生物,引入呋喃环,抑制T、B淋巴细胞增殖活性明显增加,引入具有共轭体系的呋喃环时活性更佳,并且毒性降低。Objective: To obtain immunosuppressive compounds with high efficiency, low toxicity and good water solubility by modifying Pseudolaric acid B at the C-18 site. Methods: The carboxylic acid group at the C-18 position of pseudolaric acid B was reduced to the corresponding alcohol. The alcohol which was further converted through condensation acylation reaction into the esters of pseudolaric acid B with the benzene ring,furan ring,and pyridine ring carboxylic acid. The immunosuppressive activity of these compounds in mouse T and B lymphocytes and the normal spleen cytotoxicity were tested by MTT assay in vitro.Results: Ten C-18 alcoholic hydroxylesters derivatives of pseudolaric acid B weresynthesized, which were not reported in the literature.The structures of these compounds were confirmed by spectropic analysis of HR-ESI-MS,^1H-NMR and ^13C-NMR,and the immunocompetence of all the synthesized compounds was tested.The results showed that among the derivatives,the B2, B6and B7 were better than pseudolaric acids B on the immunosuppressive activity in T lymphocyte proliferation while B6 and B7 on B lymphocytes inhibitory activity were significantly stronger thanpseudolaric acids B. Particularly, most compounds had very weak effects on normal cells,which were much lower than the positive control drugs, showing high efficiency and low toxicity.Conclusion: The C-18 alcoholic hydroxylesters derivatives of pseudolaric acid B which were introduced into the furan ring, shows better inhibiting effect in proliferation of T and B lymphocytes,but the activity of the furan ring with conjugated system is higher , and the toxicity could be decreased.

关 键 词：土槿乙酸 免疫抑制活性 高效 低毒 

分 类 号：R914[医药卫生—药物化学]