• 首页期刊简介编委会刊物订阅专栏专刊电子刊广告合作联系我们English
引用本文:唐文健,刘兆明,殷泽法,盛筱,王守信.苯二醛缩氨基硫脲的合成及其酪氨酸酶抑制活性研究[J].中国现代应用药学,2019,36(7):809-815.
TANG Wenjian,LIU Zhaoming,YIN Zefa,SHENG Xiao,WANG Shouxin.Synthesis and Tyrosinase Inhibitory Activities of Phthalaldehyde Thiosemicarbazones[J].Chin J Mod Appl Pharm(中国现代应用药学),2019,36(7):809-815.
【打印本页】   【HTML】   【下载PDF全文】   查看/发表评论  【EndNote】   【RefMan】   【BibTex】
←前一篇|后一篇→ 过刊浏览    高级检索
本文已被:浏览 1770次   下载 1164 本文二维码信息
码上扫一扫!
分享到: 微信 更多
苯二醛缩氨基硫脲的合成及其酪氨酸酶抑制活性研究
唐文健, 刘兆明, 殷泽法, 盛筱, 王守信
济宁医学院药学院, 山东 日照 276826
摘要:
目的 合成苯二醛单缩和二缩氨基硫脲类化合物,并初步研究其抑制酪氨酸酶的活性和作用机制。方法 以5种苯二醛和氨基硫脲为原料,通过缩合反应合成9个目标化合物;采用蘑菇酪氨酸酶多巴速率氧化法和酶抑制动力学实验,测定目标化合物对酪氨酸酶的抑制活性和作用机制;选择化合物3a4a进行抑制机制和抑制动力学研究。结果 目标化合物的结构经1H-NMR、13C-NMR及MS确证;所有化合物抑制酪氨酸酶的活性均优于对照药物曲酸;苯二醛二缩氨基硫脲3a~3d的活性明显强于相应的单缩氨基硫脲4a~4d;化合物3a4a对酪氨酸酶的抑制作用均表现为混合型可逆抑制作用。结论 苯二醛二缩氨基硫脲类化合物具有优异的抑制酪氨酸酶的活性,值得进一步深入研究。
关键词:  酪氨酸酶抑制剂  缩氨基硫脲  合成  机制
DOI:10.13748/j.cnki.issn1007-7693.2019.07.008
分类号:R914.5
基金项目:山东省自然科学基金项目(ZR2015BL008);国家级大学生创新创业训练计划项目(201610443067);济宁医学院大学生创新训练计划项目(cx2015057)
Synthesis and Tyrosinase Inhibitory Activities of Phthalaldehyde Thiosemicarbazones
TANG Wenjian, LIU Zhaoming, YIN Zefa, SHENG Xiao, WANG Shouxin
School of Pharmaceutical Sciences, Jining Medical University, Rizhao 276826, China
Abstract:
OBJECTIVE To synthesize phthalaldehyde mono-and dithiosemicarbazones and evaluate their tyrosinase inhibitory activities and inhibition mechanisms. METHODS Nine target compounds were synthesized through condensation reaction between thiosemicarbazide and 5 phthalaldehydes. The tyrosinase inhibitory activities and mechanisms of the target compounds were determined by measuring the rate of oxidation of L-3-hydroxytyrosine(L-DOPA) and enzyme inhibition kinetics experiment, respectively. The inhibition mechanisms and kinetics of selected compounds 3a and 4a were investigated. RESULTS The structures of the target compounds were confirmed by 1H-NMR, 13C-NMR and MS. The activity test showed that all the obtained compounds displayed potent tyrosinase inhibitory activity more than kojic acid, and the phthalaldehyde dithiosemicarbazones 3a-3d showed significantly stronger activity than the corresponding monothiosemicarbazones 4a-4d. Compounds 3a and 4a were belonged to the reversible and mixed type tyrosinase inhibitors. CONCLUSION The phthalaldehyde dithiosemicarbazones have excellent tyrosinase inhibitory activity, which deserve further study.
Key words:  tyrosinase inhibitor  thiosemicarbazone  synthesis  mechanism
扫一扫关注本刊微信