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Current AQP research:therapeutic approaches to ischemic and hemorrhagic stroke 被引量:1
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作者 Linlin Ma longfei guan +1 位作者 Jessie N.Ding Xiaokun Geng 《Neural Regeneration Research》 SCIE CAS CSCD 2016年第12期1918-1919,共2页
The role of aquaporins(AQPs)in the formation of cerebral edema after stroke:Stroke can be classified into either ischemic or hemorrhagic based on their etiological mechanism.Cerebral edema development often accompa... The role of aquaporins(AQPs)in the formation of cerebral edema after stroke:Stroke can be classified into either ischemic or hemorrhagic based on their etiological mechanism.Cerebral edema development often accompanies both ischemic infarct and intracerebral hemorrhage(ICH).Cerebral edema is differentiated according to their underlying mechanism and time course:cytotoxic and vasogenic. 展开更多
关键词 AQP Current AQP research
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Novel dual inhibitors against FP-2 and PfDHFR as potential antimalarial agents: Design, synthesis and biological evaluation
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作者 Wenhua Chen Xue Yao +8 位作者 Zhenghui Huang Fei Mao longfei guan Yun Tang Hualiang Jiang Jian Li Jin Huang Lubin Jiang Jin Zhu 《Chinese Chemical Letters》 SCIE CAS CSCD 2019年第1期250-254,共5页
Resistance to malaria parasites has quickly developed to almost all used antimalarial drugs. Cysteine protease falcipain-2(FP-2) and Plasmodium falciparum dihydrofolate reductase(PfDHFR) have crucial roles, which are ... Resistance to malaria parasites has quickly developed to almost all used antimalarial drugs. Cysteine protease falcipain-2(FP-2) and Plasmodium falciparum dihydrofolate reductase(PfDHFR) have crucial roles, which are absolutely necessary, in the parasite life cycle. In this study, based on the uniform pharmacophores of reported PfDHFR inhibitors and the first-generation dual inhibitors against FP-2 and PfDHFR, we identified a novel series of dual inhibitors through fragments assembly. Lead optimization led to the identification of 14, which showed potent inhibition against FP-2 and PfDHFR enzyme(IC_(50)= 6.8 + 1.8 mmol/L and IC_(50)= 8.8 + 0.3 mmol/L) and P. falciparum 3D7 strain(IC50= 2.9mmol/L).Additionally, 14 exhibited more potent inhibition to the proliferation of chloroquine-resistant P.falciparum Dd2 strain(IC_(50)= 1.1 mmol/L) than pyrimethamine(IC_(50)>10 mmol/L), and 14 displayed micromolar inhibitory activities against two clinical isolated strains Fab9(IC_(50)= 2.6 mmol/L) and GB4(IC_(50)= 1.0 mmol/L). Collectively, these data demonstrated that 14 might be a good lead compound for the treatment of malaria. 展开更多
关键词 ANTIMALARIAL DRUG PLASMODIUM FALCIPARUM FP-2 PfDHFR Dual INHIBITOR
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