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Pyrido[1,2-a]pyrimidin-4-ones as antiplasmodial falcipain-2 inhibitors

  • U. R. Mane
  • , H. Li
  • , J. Huang
  • , R. C. Gupta
  • , S. S. Nadkarni
  • , R. Giridhar
  • , P. P. Naik
  • , M. R. Yadav*
  • *此作品的通讯作者
  • M.S. University of Baroda
  • Torrent Research Centre
  • East China University of Science and Technology

科研成果: 期刊稿件文章同行评审

摘要

Plasmodium falciparum cysteine protease falcipain-2 (FP-2) is a promising target for antimalarial chemotherapy and inhibition of this protease affects the growth of parasite adversely. A series of pyrido[1,2-a]pyrimidin-4-ones were synthesized and evaluated for their in vitro FP-2 inhibitory potential. Compounds (14,17) showed excellent FP-2 inhibition and can serve as lead compounds for further development of potent FP-2 inhibitors as potential antimalarial drugs.

源语言英语
页(从-至)6296-6304
页数9
期刊Bioorganic and Medicinal Chemistry
20
21
DOI
出版状态已出版 - 1 11月 2012
已对外发布

联合国可持续发展目标

此成果有助于实现下列可持续发展目标:

  1. 可持续发展目标 3 - 良好健康与福祉
    可持续发展目标 3 良好健康与福祉

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