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作 者:高媛[1] 刘国都[1] 杨健[1] 周乐[1] 孙伟[2]
机构地区:[1]西北农林科技大学理学院,陕西杨凌712100 [2]西北大学化学系,陕西西安710069
出 处:《西北农林科技大学学报(自然科学版)》2008年第5期179-184,共6页Journal of Northwest A&F University(Natural Science Edition)
基 金:国家自然科学基金项目(30571042)
摘 要:【目的】进一步研究新狼毒素B的抑菌活性构效关系。【方法】以新狼毒素B为原料,合成了7″-甲氧基(A2-1)、7,7″-二甲氧基(E3)和7,7,″4-三甲氧基(E1)3个新狼毒素B甲醚化产物及4-亚甲基新狼毒素B(D3),利用ESI-MS1、H NMR和13C NMR对其结构进行了表征。选择金黄色葡萄球菌(S.aureas)、无乳链球菌(S.agalactiae)、大肠杆菌(E.coli)和沙门氏菌(Samonellal)为供试菌,采用药敏纸片法对新狼毒素B及其4种衍生物进行了抑菌活性测定。【结果】4种修饰物对所有供试菌的抑菌活性均小于新狼毒素B;3种甲醚化产物在质量浓度为0.625-5mg/mL时,对沙门氏菌没有抑菌活性;对于其他3种供试菌,各供试物的抑菌活性次序为新狼毒素B≈D3〉A2-1〉E3〉E1。【结论】新狼毒素B分子中,7-OH和7-″OH是其主要抑菌活性基团,4′-OH和4-OH对抑菌活性的贡献较小,4-羰基不是主要抑菌活性基团。[Objective] It further studied the relationship between structure and antibacterial activity of neochamaejasmine B. [Method] Four compounds, 7″-methoxy neochamaejasmine B (A2-1), 7,7″-dimethoxy neochamaejasmine B (E3), 7,7″, 4′″-trimethoxy neochamaejasmine B (El) and 4-methylene neochamaejasmine B (D3) were prepared from neochamaejasmine B. Their structures were confirmed by ESI-MS, l H NMR and ^13C NMR. The antibacterial activity of neochamaejasmine B and its four derivatives were tested with dish diffusion of Neo-Sensitab in vitro against S. aureas, S. agalactiae, E. coli and Samonellal. [Result] The results showed that the antibacterial activity of four derivatives against all bacteria tested was lower than that of neochamaejasmine B. The antibacterial activity of A2-1 ,E3 and El against Samonellal disappeared at 0. 625-5 mg/mL. But the order of the antibacterial activity of all compounds against other bacteria was n-B≈D3〉A2-1〉E3〉E1. [Conclusion] The above mentioned structure-activity relationship studies showed that 7-OH and 7″-OH of neochamaejasmine B were the main active groups,and that 4′-OH and 4′″-OH had less contribution to its antibacterial activity,and that carbonyl group was not the main active group.
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