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Recent advances in screening of enzymes inhibitors based on capillary electrophoresis 被引量:5
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作者 Mengxia Cheng Zilin Chen 《Journal of Pharmaceutical Analysis》 SCIE CAS CSCD 2018年第4期226-233,共8页
Capillary electrophoresis with many advantages plays an important role in pharmaceutical analysis and drug screening. This review gives an overview on the recent advances in the developments and applications of capill... Capillary electrophoresis with many advantages plays an important role in pharmaceutical analysis and drug screening. This review gives an overview on the recent advances in the developments and applications of capillary electrophoresis in the field of enzyme inhibitor screening. The period covers 2013 to 2017. Both the pre-capillary enzyme assays and in-capillary enzyme assays which include electrophoretically mediated microanalysis(EMMA) and immobilized enzyme microreactor(IMER) are summarized in this article. 展开更多
关键词 Capillary electrophoresis enzyme inhibitor screening Pre-capillary enzyme assays Electrophoretically mediated microanalysis Immobilized enzyme microreactor
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Crystal Structures of Urokinase-type Plasminogen Activator in Complex with 4-(Aminomethyl) Benzoic Acid and 4-(Aminomethyl-phenyl)-methanol
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作者 江龙光 赵更香 +3 位作者 卞传兵 袁彩 黄子祥 黄明东 《Chinese Journal of Structural Chemistry》 SCIE CAS CSCD 2009年第2期253-259,共7页
Urokinase-type plasminogen activator (uPA) is a trypsin-like serine protease and plays a key role in several biological processes, including tissue remodeling, cell migration, and matrix degradation. The inhibitors ... Urokinase-type plasminogen activator (uPA) is a trypsin-like serine protease and plays a key role in several biological processes, including tissue remodeling, cell migration, and matrix degradation. The inhibitors of uPA have been shown to prevent the spread of metastasis and tumor growth, and accordingly uPA is widely recognized as a target for the treatment of cancer. In this work, we report the crystal structures of the complexes of uPA with its inhibitors: 4- (aminomethyl)-benzoic acid (AMBA) and 4-(aminomethyl-phenyl)-methanol (AMPM), both at a resolution of 2.35 А. The inhibitory constants of these two inhibitors were measured by a chromogenic competitive assay, and it was found that AMBA is a better inhibitor for uPA (Ki = 2.68 mM) than AMPM (Ki = 13.99 mM). The structural study shows that the binding mode of inhibitor AMBA on uPA is similar to that of AMPM on uPA, both docked into the active site S1 pocket of uPA. Structural details of these complexes are provided to explain the difference of inhibitory constants. 展开更多
关键词 urokinase-type plasminogen activator 4-(aminomethyl)benzoic acid (4-aminomethyl-phenyl)-methanol enzyme inhibition assays contact area
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