期刊文献+

PDE-4抑制剂的研究进展 被引量:5

Progress of PDE-4 Inhibitors
暂未订购
导出
摘要 磷酸二酯酶-4(PDE-4)是第二信使环磷酸腺苷(c AMP)的特异性水解酶。近年来,对磷酸二酯酶-4抑制剂的研究为临床上新型抗炎及抗精神失常药物的研发提供了思路。综述了近几年磷酸二酯酶-4抑制剂的研究进展,介绍了磷酸二酯酶-4抑制剂与受体蛋白的结合模式,为进一步寻找磷酸二酯酶-4抑制剂提供参考依据。 Phosphodiesterase-4( PDE-4) is a specific hydrolase of the second messenger cyclic adenosine monophosphate( c AMP). In recent years,the research of phosphodiesterase-4 inhibitors provides an ideal for the development of new anti-inflammatory and clinical antipsychotic drugs. This work covers the recent progress of phospodiesterase-4 inhibitors and binding manner,and provides reference for the further study of phosphodiesterase-4 inhibitors.
出处 《化学试剂》 CAS 北大核心 2015年第9期803-808,共6页 Chemical Reagents
基金 2013年湖南省教育厅资助研究生创新课题(CX2013B337) 湖南省教育厅药学特色专业资助项目
关键词 磷酸二酯酶-4 研究进展 磷酸二酯酶-4抑制剂 phosphodiesterase-4 research progress phosphodiesterase-4 inhibitor
  • 相关文献

参考文献27

  • 1LUGNIER C. Cyclic nucleotide phosphodiesterase (PDE) superfamily:a new target for the development of specific therapeutic agents [J]. Pharmacol. Ther. ,2006,109 ( 3 ) : 366-398.
  • 2GAVALDA A, ROBERTS R S. Phosphodiesterase-4 in- hibitors :a review of current developments ( 2010-2012 ) [J]. Expert Opin. Ther. Patents, 2013, 23 ( 8 ) : 997- 1 016.
  • 3HUAI Qing-huai, WANG Huan-chen, SUN Ying-jie. Three-dimensional structures of PDE-4D in complex with roliprams and implication on inhibitor selectivity [J]. Structure, 2003,11 ( 7 ) : 865-873.
  • 4CARD G L,ENGLAND B P,SUZUKI Y. Structural basis for the activity of drugs that inhibit phosphodiesterases [J]. Structure ,2004,12(12) :2 233-2 247.
  • 5PAGES L, GAVALDA A, LEHNER M D. PDE-4 inhibi- tors : a review of current developments ( 2005-2009 ) [J]. Expert Opin. Ther. Patents,2009 ,19( 11 ) :1 501-1 519.
  • 6GAURAVE A, GAUTAM V, SINGH R. Quantitative structure activity relationship and design of phenyl alkyl ketone derivatives as inhibitors of phosphodiesterase 4 [J]. Curr. Enzyme lnhib. ,2014,10(1) :69-80.
  • 7KUNNERLE A E,SCHMITT M, CARDOZO S V S,et al. Design, synthesis, and pharmacological evaluation of N- acylhydrazones and novel conformationally constrained compounds as selective and potent orally active phos- phodiesterase-4 inhibitors[J].. J. Med. Chem. , 2012,55(17) :7 525-7 545.
  • 8FELDIG J,SORENSEN M D, POULSEN T D, et al. Dis- covery and early clinical development of 2- { 6- [2- ( 3,5- dichloro-4-pyridyl ) acetyl] -2, 3-dimethoxyphenoxy t -N- propylacetamide (LEO29102), a soft-drug inhibitor of phosphodiesterase 4 for topical treatment of atopic derma- titis[J]. J. Med. Chem. ,2014,57(14) :5 893-5 903.
  • 9ARMANI E, AMARI G, RIZZI A, et al. Novel class of benzoic acid ester derivatives as potent PDE-4 inhibitors for inhaled administration in the treatment of respiratory diseases[J]. J. Med. Chem. ,2014,57(3) :793-816.
  • 10KUMAR D,PATEL G,VIJAYAKRISHNAN L,et al. De- sign and synthesis of 3,5-disubstituted-1,2,4-oxadi- azoles as potent inhibitors of phosphodiesterase4B2 [J]. Chem. Biol. Drug. Des. , 2012,79 ( $ ) : 810-818.

同被引文献21

引证文献5

二级引证文献7

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