A series of echinocystic acid (EA) 28-COOH derivatives was synthesized, and their anti-HCV entry activity was evaluated by HCVpp and VSVpp entry assay. It was found that some of them showed moderate anti-HCV entry activity, especially compound 12, and these modifications also removed the undesired hemolytic effect. (C) 2016 Chinese Chemical Society and Institute of Materia Medica, Chinese Academy of Medical Sciences. Published by Elsevier B.V. All rights reserved.supported by the National Natural Science Foundation of China,Open- Fund Program of the State Key Laboratory of Natural and Biomimetic Drugs,Yunnan Basic Research ProjectSCI(E)中国科技核心期刊(ISTIC)中国科学引文数据库(CSCD)ARTICLEfeiyuz8@163.com; deminzhou@bjmu.edu.cn5711-7132
Despite the validation of direct-acting antivirals for hepatitis C treatment, the discovery of new c...
HCMV infection represents a life-threatening condition for immunocompromised patients and newborn in...
AbstractA series of novel N-phenylbenzamide and N-phenylacetophenone compounds were synthesized and ...
A series of triterpene dimers bearing different scaffold were designed and synthesized via CuAAC rea...
To elucidate the pharmacophore of echinocystic acid (EA), an oleanane-type triterpene displaying sub...
AbstractChronic hepatitis C virus (HCV) infection has become a major public health burden worldwide....
The development of entry inhibitors is an emerging approach to the prevention and reduction of HCV i...
In this work, the relationship between cyclophilin A (CypA) and HCV prompted us to screen a series o...
Since the first submission of this article, another report on the antiviral effect of EGCG on HCV en...
从中草药叶下珠中活性追踪、提取出具有体外抑制HCV NS3丝氨酸蛋白酶活性的先导化合物——鞣花酸,进而化学合成鞣花酸的衍生物并用NMR和MS确定结构;采用ELISA法测定了所合成鞣花酸衍生物体外抑制H...
Development of hepatitis C virus (HCV) entry inhibitors represents an emerging approach that satisfi...
Hepatitis C virus (HCV) entry is a key target for the treatment of chronic HCV infection. In our con...
Synthesis and anti-hepatitis C virus (anti-HCV) effects of certain 3-amino-2-hydroxy-propoxy isoflav...
Based on classical drug design theory, a novel series of gentiopicroside derivatives was designed an...
Development of hepatitis C virus (HCV) entry inhibitors represents an emerging approach that satisfi...
Despite the validation of direct-acting antivirals for hepatitis C treatment, the discovery of new c...
HCMV infection represents a life-threatening condition for immunocompromised patients and newborn in...
AbstractA series of novel N-phenylbenzamide and N-phenylacetophenone compounds were synthesized and ...
A series of triterpene dimers bearing different scaffold were designed and synthesized via CuAAC rea...
To elucidate the pharmacophore of echinocystic acid (EA), an oleanane-type triterpene displaying sub...
AbstractChronic hepatitis C virus (HCV) infection has become a major public health burden worldwide....
The development of entry inhibitors is an emerging approach to the prevention and reduction of HCV i...
In this work, the relationship between cyclophilin A (CypA) and HCV prompted us to screen a series o...
Since the first submission of this article, another report on the antiviral effect of EGCG on HCV en...
从中草药叶下珠中活性追踪、提取出具有体外抑制HCV NS3丝氨酸蛋白酶活性的先导化合物——鞣花酸,进而化学合成鞣花酸的衍生物并用NMR和MS确定结构;采用ELISA法测定了所合成鞣花酸衍生物体外抑制H...
Development of hepatitis C virus (HCV) entry inhibitors represents an emerging approach that satisfi...
Hepatitis C virus (HCV) entry is a key target for the treatment of chronic HCV infection. In our con...
Synthesis and anti-hepatitis C virus (anti-HCV) effects of certain 3-amino-2-hydroxy-propoxy isoflav...
Based on classical drug design theory, a novel series of gentiopicroside derivatives was designed an...
Development of hepatitis C virus (HCV) entry inhibitors represents an emerging approach that satisfi...
Despite the validation of direct-acting antivirals for hepatitis C treatment, the discovery of new c...
HCMV infection represents a life-threatening condition for immunocompromised patients and newborn in...
AbstractA series of novel N-phenylbenzamide and N-phenylacetophenone compounds were synthesized and ...