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 |
| 卷 | 20 |
| 期 | 21 |
| DOI | |
| 出版状态 | 已出版 - 1 11月 2012 |
| 已对外发布 | 是 |
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:
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可持续发展目标 3 良好健康与福祉
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