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新型查尔酮衍生物的合成及酪氨酸酶活性
Synthesis and Activity on Tyrosinase of Novel Chalcone Derivatives

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文摘 合成了8个新型含苯并噻唑环的查尔酮衍生物及8个酰胺查尔酮,并对化合物的结构进行了表征. 生物活性测试结果表明,化合物4d,4h,5d,7b 和7d 表现出一定的酪氨酸酶激动活性,其中化合物7d 对酪氨酸酶的活性最好,其EC_(50) = 9. 6 μmol /L,优于阳性对照药8-MOP(EC_(50) = 14. 8 μmol /L).
其他语种文摘 Ver-nohia anthelmintica L was endemic plant in Xinjiang,which was often used in the treatment of Vitiligo. It was believed that the chalcone compounds of Ver-nohia anthelmintica L played an important role in this treatment. Since it may activate tyrosinase and improve the melanin production,many chalcone compounds and derivatives were described as potential inhibitor on tyrosinase which may act as skin lightening and whitening agents. However,chalcones which showed activator effect were seldom reported. In order to search for chalcones with high activities on tyrosinase,eight novel chalcone derivatives containing benzothiazole and eight amide-derived chalcones were synthesized in this work. All the compounds were identified by ~1H NMR,~(13)C NMR,IR,HRMS and evaluated their activator effect on tyrosinase by measuring the oxidation rate of L-dopa. Compared with the reference drug 8-methoxypsoralen,compounds 4d,4h,5d,7b and 7d showed some activator effect on tyrosinase. Amomg them,compound 7d demonstrated more potent activity with EC_(50) =9. 6 μmol /L than 8-methoxypsoralen,which EC_(50) value was 14. 8 μmol /L. Further structural modification of this novel chalcones containing benzothiazole will be required for improving the solubility of them.
来源 高等学校化学学报 ,2014,35(6):1204-1211 【核心库】
DOI 10.7503/cjcu20131033
关键词 查尔酮 ; 苯并噻唑 ; 酰胺 ; 酪氨酸酶活性
地址

中国科学院新疆理化技术研究所, 中国科学院干旱区植物资源化学重点实验室;;新疆特有药用资源利用新疆省省部共建实验室, 乌鲁木齐, 830011

语种 中文
文献类型 研究性论文
ISSN 0251-0790
学科 化学
基金 中国科学院新疆理化研究所重点支持资助项目 ;  国家973计划 ;  中国科学院西部之光人才培养计划
文献收藏号 CSCD:5166534

参考文献 共 33 共2页

1.  Hu X Y. Inhibition of α/β-K6P2W18O62·10H2O on the Activity of Mushroom Tyrosinase and Its Antimicrobial Effects. Chem. Res. Chinese Universities,2012,28(5):862-865 被引 6    
2.  Khan K M. Bioorg. Med. Chem,2006,14:344-351 被引 4    
3.  Nerya O. Phytochemistry,2004,65:1389-1395 被引 16    
4.  Fenoll L G. Biol. Chem,2000,381(4):313-320 被引 2    
5.  姚莉. 新疆医科大学学报,2010,33(10):1191-1193 被引 1    
6.  邓瑞春. 驱虫斑鸠菊对B-16黑素瘤细胞酪氨酸酶活性及黑素生成影响. 氨基酸和生物资源,2002,24(1):31-32 被引 5    
7.  孙力. 中国现代中药,2006,8(11):10-12 被引 5    
8.  刘铜华. 国外医学中医中药分册,2004,26(2):103-104 被引 8    
9.  尚靖. 紫铆素及其衍生物在制备色素代谢疾病药物的用途,CP 1778294A,2004 被引 1    
10.  闫明. 驱虫斑鸠菊黄酮组分及其制备方法和用途,CP 102526153A,2012 被引 1    
11.  Khatib S. Bioorg. Med. Chem,2005,13:433-441 被引 16    
12.  Thanigaimalai P. Bioorg. Med. Chem. Lett,2011,21:1922-1925 被引 2    
13.  Jun N. Bioorg. Med. Chem,2007,15:2396-2402 被引 9    
14.  Zhang X D. Biol. Pharm. Bull,2009,32(1):86-90 被引 2    
15.  Nixha A R. J. Enzyme. Inhib. Med. Chem,2013,28(4):808-815 被引 2    
16.  Sonmez F. Bioorg. Med. Chem. Lett,2011,21:7479-7482 被引 5    
17.  Rao Y K. Bioorg. Med. Chem,2009,17:7909-7914 被引 4    
18.  Bandgar B P. Eur. J. Med. Chem,2010,45:2629-2633 被引 5    
19.  Chtourou M. Ultrasonics Sonochemistry,2010,17:246-249 被引 3    
20.  Luis F F. Boletim da Escola de Farmacia,Universidade de Coimbra,Edicao Cientifica. 28,1980:49-52 被引 1    
引证文献 1

1 万金林 含1,3,4-噻二唑结构的查尔酮缩氨基脲类化合物的合成及抗细菌活性 高等学校化学学报,2018,39(8):1683-1690
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