首页> 外文期刊>The Journal of Antibiotics: An International Journal >F-16438s, Novel Binding Inhibitors of CD44 and Hyaluronic Acid I. Establishment of an Assay Method and Biological Activity
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F-16438s, Novel Binding Inhibitors of CD44 and Hyaluronic Acid I. Establishment of an Assay Method and Biological Activity

机译:F-16438s,CD44和透明质酸的新型结合抑制剂I.测定方法和生物活性的建立

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摘要

In an attempt to obtain inhibitors of hyaluronic acid (HA) binding to its receptor, CD44, we established an efficient assay method to detect and quantify binding using fiuorescein-labeled HA and HEK293 cells stably expressing CD44. As a result of the screening of culture broths of microorganisms, we found fungus strain Gloeoporus dichrous SANK 30502 produced inhibitory activity in this new assay. Five compounds, F-1643 8 A, B, E, F and G, were isolated from the fermentation broths, and their IC_50 values were determined to be 10.3, 13.5, 27.3, 12.0 and 13.0 muM, respectively. F-16438 A, B, E, F and G are the first reported inhibitors of binding HA to CD44. F-16438 A, B, E and F have novel structures.
机译:为了尝试获得透明质酸(HA)与其受体CD44结合的抑制剂,我们建立了一种有效的测定方法,使用荧光素标记的HA和稳定表达CD44的HEK293细胞来检测和定量结合。筛选微生物培养液的结果是,我们发现真菌菌株Gloeoporus dichrous SANK 30502在此新方法中产生了抑制活性。从发酵液中分离出五种化合物F-1643 8 A,B,E,F和G,其IC_50值分别确定为10.3、13.5、27.3、12.0和13.0μM。 F-16438 A,B,E,F和G是最早报道HA结合CD44的抑制剂。 F-16438 A,B,E和F具有新颖的结构。

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