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5-苄基-4-叔丁基-2-苄亚氨基噻唑的合成及其对环氧合酶-2的抑制活性

Synthesis,Structure Characterization of 5-Benzyl-4-tert-butyl2-benzyliminothiazoles and their Inhibitory Activity on Cyclooxygenase-2

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【作者】 胡艾希董敏宇林焕冰徐江平马颖绮曹高夏林叶姣

【Author】 HU Ai-xi1,DONG Min-Yu1,LIN Huan-bing2,XU Jiang-ping2,MA Ying-qi3,CAO Gao3,XIA Lin1,YE Jiao1(1.College of Chemistry and Chemical Engineering,Hunan Univ,Changsha,Hunan 410082,China;2.School of Pharmaceutical Sciences,Southern Medical Univ,Guangzhou,Guangdong 510515,China;3.College of Chemistry and Chemical Engineering,South China Univ of Technology,Guangzhou,Guangdong 510640,China)

【机构】 湖南大学化学化工学院南方医科大学药学院华南理工大学化学与化工学院

【摘要】 5-苄基-4-叔丁基-2-氨基噻唑与芳香醛缩合制备了1 1种5-苄基-4-叔丁基-2-苄亚氨基噻唑.结构经1H NMR和元素分析确证,并用单晶X-射线衍射测定了化合物Ⅰc的晶体结构.化合物Ⅰc晶体属单斜晶系,空间群为P21/n,晶胞参数为:a=1.43753(11)nm,b=0.98665(8)nm,c=1.46565(12)nm,β=114.2560(10)°;Z=4,V=1.8953(3)nm3,Dc=1.349 g/cm3,F(000)=808,R1=0.0507,wR2=0.1163,S=1.03.体外筛选结果表明,化合物Ⅰb,Ⅰk在10μmol/L浓度下对COX-2的抑制率超过50%.

【Abstract】 Eleven new 5-benzyl4-tertbutyl-2benzyliminothiazoles were synthesized through the reaction of 5-arylmethyl-4-tert-butylthiazol2-amine and aromatic aldehyde.Their structures were established with 1 H NMR spectra and elemental analysis.The crystal structure of compound Ⅰc has been determined by X-ray diffraction analysis.The compound Ⅰc crystal belonges to monoclinic system with space group P21/n and cell parameters:a=1.437 53(11) nm,b= 0.986 65(8)nm,c=1.465 65(12) nm,β=114.256 0(10)°;Z=4,V=1.895 3(3) nm3,Dc=1.349 g/cm3,F(000)=808,R1=0.050 7,wR2=0.116 3,S=1.03.Biological tests showed that compound Ⅰb,Ⅰk exhibited ≥50% inhibition rate against COX2 in vitro.

【基金】 国家科技支撑计划资助项目(2006BAE01A01-4)
  • 【文献出处】 湖南大学学报(自然科学版) ,Journal of Hunan University(Natural Sciences) , 编辑部邮箱 ,2009年02期
  • 【分类号】O626.2
  • 【被引频次】9
  • 【下载频次】193
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