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Design, synthesis, and antiviral properties of 2-aryl-1H- benzimidazole-4-carboxamide derivatives
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作者 Xianjin LUO ZhonglüZHANG +3 位作者 Yutian YANG Fei XUE Naiyun XIU Yuanbin SHE 《Frontiers of Chemical Science and Engineering》 SCIE EI CSCD 2009年第3期305-309,共5页
A series of new benzimidazole derivatives were designed and synthesized.Their chemical structures were testified by 1 H NMR,infrared spectroscopy(IR),mass spectrography(MS),and elemental analysis.Their potent antivira... A series of new benzimidazole derivatives were designed and synthesized.Their chemical structures were testified by 1 H NMR,infrared spectroscopy(IR),mass spectrography(MS),and elemental analysis.Their potent antiviral properties indicated the prospect of new drugs.Compound 13,16,18,19,21,22,and 23 were identified as novel antivirus with much better selective activity and inhibitory activity than the comparable ribavirin against Coxsackie virus B_(3) in VERO cells. 展开更多
关键词 BENZIMIDAZOLE coxsackie virus B_(3) antiviral properties
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Expanding the Therapeutic Spectrum of Artemisinin:Activity Against Infectious Diseases Beyond Malaria and Novel Pharmaceutical Developments 被引量:1
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作者 Thomas Efferth Marta R.Romero +7 位作者 Anna Rita Bilia Ahmed Galal Osman Mahmoud ElSohly Michael Wink Rudolf Bauer Ikhlas Khan Maria Camilla Bergonzi Jose J.G.Marin 《World Journal of Traditional Chinese Medicine》 2016年第2期1-23,共23页
The interest of Western medicine in Traditional Chinese Medicine(TCM) as a source of drug leads/new drugs to treat diseases without available efficient therapies has been dramatically augmented in the last decades by ... The interest of Western medicine in Traditional Chinese Medicine(TCM) as a source of drug leads/new drugs to treat diseases without available efficient therapies has been dramatically augmented in the last decades by the extensive work and the outstanding findings achieved within this kind of medicine. The practice of TCM over thousands of years has equipped scientists with substantial experience with hundreds of plants that led to the discovery of artemisinin(qinghaosu), which is extracted from the medicinal plant Artemisia annua L.(qinghao). The unexpected success of artemisinin in combating malaria has drawn strong attention from the scientific community towards TCM. Artemisinin was discovered by Youyou Tu in 1972. Since then, several novel pharmacological activities based on the well-known properties of the sesquiterpene lactone structure with the oxepane ring and an endoperoxide bridge have been unravelled. Beyond malaria, artemisinin and its derivatives(artemisinins) exert profound activities towards other protozoans(Leishmania, Trypanosoma, amoebas, Neospora caninum, and Eimeria tenella), trematodes(Schistosoma, liver flukes), and viruses(human cytomegalovirus, hepatitis B and C viruses). Less clear is the effect against bacteria and fungi. Based on the promising results of artemisinin and the first generation derivatives(artesunate, artemether, arteether), novel drug development strategies have been pursued.These included the synthesis of acetal-and non-acetal-type artemisinin dimeric molecules as well as developing nanotechnological approaches, e.g.artemisinin-based liposomes, niosomes, micelles, solid lipid nanocarriers, nanostructured lipid carriers, nanoparticles, fullerenes and nanotubes. The current review presents an overview on different aspects of artemisinins, including sources, chemistry, biological/pharmacological properties, types of infectious pathogens that are susceptible to artemisinins in vitro and in vivo, in addition to the advancement in their drug delivery systems utilizing pharmaceutical technology. It would be expected that different therapeutic strategies based on the second and third generation artemisinin derivatives and artemisinin-based drug technologies would be available in the near future to treat specific infectious diseases. 展开更多
关键词 Artemisinin derivatives Artemisia annua Asteraceae Antimalarial drugs Anti-pathogen activity antiviral properties Artemisinin-loaded nanocarriers Traditional Chinese Medicine
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