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首页> 外文期刊>ACS medicinal chemistry letters >Epimers Switch Galectin-9 Domain Selectivity: 3N-Aryl Galactosides Bind the C-Terminal and Gulosides Bind the N-Terminal
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Epimers Switch Galectin-9 Domain Selectivity: 3N-Aryl Galactosides Bind the C-Terminal and Gulosides Bind the N-Terminal

机译:缩小率开关Galectin-9结构域选择性:3N-芳基半乳糖叶片结合C末端和谷硼菊酯结合N末端

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A series of 3-deoxy-3-N-arylated-beta-D-galactoside and -guloside derivatives have been synthesized by cesium fluoride/trimetylsilylaryl triflate-mediated benzyne generation and N-arylation of 3-deoxy-3-amino-beta-D-galactosides and -gulosides, respectively. Evaluation as ligands to galectin-1, 2, 3, 4N (N-terminal domain), 4C (C-terminal domain), 7, 8N, 8C, 9C, and 9N revealed that the galactosides selectively bound galectin-9C, whereas the gulosides selectively bound galectin-9N. Hence, the N-aryl group induces galectin-9 selectivity and the ligand 3C-configuration acts as an epimeric selectivity switch between the two domains of galectin-9. Furthermore, MD simulations revealed that galacto derivatives in galectin-9C and gulo derivatives in galectin-9N find stable poses with specific interactions, which proposes a possible explanation to the gal/gulo 9C/9N selectivity.
机译:通过氟化铯/三甲酰甲硅烷基甲酸盐三氟甲酸铯介导的苯并介质产生和3-脱氧-3-氨基 - β - D-半乳糖糖苷和 - 含水皂苷。 评价为加塞锡-1,2,3,4n(n-末端结构域),4℃(C-末端结构域),7,8n,8c,9c和9n的评价显示,半乳糖叶片选择性地结合了Galectin-9c,而是 谷冰苷选择性地结合Galectin-9n。 因此,N-芳基诱导Galectin-9选择性,并且配体3C-构型作为Galectin-9的两个结构域之间的基础选择性开关。 此外,MD仿真显示Galectin-9C和Galectin-9N中Gulo衍生物的吡酰衍生物在具有特异性相互作用的稳定姿势,这提出了对GAL / GULO 9C / 9N选择性的可能解释。

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