期刊文献+

苯基烯丙基硫醚、亚砜和砜类化合物的合成及其抗锥体虫半胱氨酸蛋白酶活性 被引量:3

A Study on the Synthesis and Their Anticruzain Activities of Phenylallylthio ether,Sulfinyl and Sulfonyl Derivatives
下载PDF
导出
摘要 设计合成了 2 1个苯基烯丙基硫醚、亚砜和砜类化合物 ,并对其进行了抗锥体虫半胱氨酸蛋白酶的药理活性筛选 .实验表明化合物 (4) ,(11) ,(15 ) ,(18)和 (2 1)的活性较强 . Twenty one compounds(phenylallylthio ether,sulfinyl and sulfonyl)were synthesized and their activities against Trypanosoma cruzi in vitro were tested.The result showed that compounds (4),(11),(15),(18)and (21) had good anticruzain activity.
出处 《中国药物化学杂志》 CAS CSCD 2000年第1期29-32,共4页 Chinese Journal of Medicinal Chemistry
关键词 砜类化合物 合成 抗锥体虫 半胱氨酸蛋白酶 synthesis Trypanosoma cysteine protease
  • 相关文献

参考文献6

  • 1Li R,J Med Chem,1995年,38卷,26期,5031页
  • 2Li Z,Bioorganic and Medicinal Chemistry,1994年,4卷,9期,1421页
  • 3Li Z,Chem Biol,1994年,1期,31页
  • 4Ring C S,Proc Nat Acad Sci USA,1993年,90期,3583页
  • 5姚风鸣,医药工业杂志,1984年,4期,41页
  • 6抗炎酸的生产工艺,1972年,238页

同被引文献27

  • 1何小芹,曹珍年,俞阳,罗维,宋国胜.亚砜的合成及其含量的确定[J].分析测试学报,2006,25(z1):177-178. 被引量:4
  • 2张海滨.二甲亚砜在农药领域的应用[J].江苏化工,2004,32(5):22-23. 被引量:3
  • 3宋少飞,胡道道,沈淑坤.过氧化氢催化氧化绿色化学研究进展[J].世界科技研究与发展,2006,28(2):20-29. 被引量:11
  • 4Marieke J. van der Werf, Sake J. de Vlas, Simon B. , et al. Quantification of clinical morbidity associated with schistosome infection in sub-Saharan Africa [ J ]. Acta Tropica. , 2003,86 (2-3) : 125-139.
  • 5Charles H, Katherine D, Daniel J, et al. Reassessment of the cost of chronic helminthic infection : a meta-analysis of disability-related outcomes in endemic schistosomiasis [ J ]. The Lancet, 2005,365 (9470) :1561-1569.
  • 6Padraic G, Fallon M, Doenhoff J. Drug-resistant schistosomiasis resistance to praziquantel and oxamniquine induced in Schistosoma Mansoni in mice is drug specific [ J ]. Am. Soc. Trop Med and Hyg. , 1994,51 ( 1 ) ,83-88.
  • 7Norman K, Robert B.. Derivatives of sulfenic acids. XLI- II. The chlorinolysis of certain aryl benzyl sulfides as a route to sulfenyl chlorides [ J ]. J. Org. Chem. , 1963,28 (7) :1903-1905.
  • 8Romano S, Eugenia P, Giorgio S, et al. Heterocycles with a benzothiadiazepine moiety 4. synthesis of novel tetracyclic rings by intramolecular cyclization of 10-bro- moacetyl-10, 11-dihydro-11-ethoxycarbonyl pyrrolo [ 1,2- b ] [ 1 ,2,5 ] benzothiadiazepine 5,5-dioxide and its derivatives [ J]. Synth. commun. , 1994,24 (19) :2685-2695.
  • 9Schmidt U, Langner J, Kirxchbaum B. Synthesis and enantioselective hydrogenation of a-acyloxyacrylates. [ J ]. Synthesis,1994,1994(11) :1138 -1140.
  • 10Marno A, Romano S, Eugenia P, et al. 5H-Pyrrole [ 1,2- b] [ 1,2, 5 ] benzothiadiazepines ( PBTDS ) : A novel class of non-nucleoside reverse transcriptase inhibitors [J]-Bioorg. Med. Chem. ,1996,4(6) ,837-850.

引证文献3

二级引证文献5

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部