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Synthesis of divalent ligands of β-thio- and β-N-galactopyranosides and related lactosides and their evaluation as substrates and inhibitors of Trypanosoma cruzi trans-sialidase

机译：β-硫代和β-N-吡喃半乳糖苷和相关乳糖苷的二价配体的合成及其作为克鲁氏锥虫反唾液酸酶的底物和抑制剂的评价

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期刊名称 Beilstein Journal of Organic Chemistry
作者
María Emilia Cano; Rosalía Agusti; Alejandro J Cagnoni; María Florencia Tesoriero; José Kovensky; María Laura Uhrig; Rosa M de Lederkremer;
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作者单位

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年(卷),期 2014(10),-1
年度 2014
页码 3073–3086
总页数 14
原文格式 PDF
正文语种
中图分类生化遗传学 ; 生化药理学 ;
关键词
β-galactopyranosides multivalent ligands sialic acid sugar scaffolds T. cruzi trans-sialidase;

机译：β-吡喃半乳糖苷;多价配体;唾液酸;糖支架;克鲁维氏锥虫反唾液酸酶;

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专利

1. Synthesis of divalent ligands of β-thio- and β-N-galactopyranosides and related lactosides and their evaluation as substrates and inhibitors of Trypanosoma cruzi trans-sialidase [J] . María Emilia Cano, Rosalía Agusti, Alejandro J. Cagnoni, Beilstein journal of organic chemistry. . 2014 ,第1期

机译：β-硫代和β-N-吡喃半乳糖苷和相关乳糖苷的二价配体的合成及其作为克鲁氏锥虫反唾液酸酶的底物和抑制剂的评价
2. Synthesis of divalent ligands of β-thio- and β-N-galactopyranosides and related lactosides and their evaluation as substrates and inhibitors of Trypanosoma cruzi trans-sialidase [J] . María Emilia Cano, Rosalía Agusti, Alejandro J. Cagnoni, Beilstein journal of organic chemistry. . 2014 ,第1期

机译：β-硫代和β-N-吡喃半乳糖苷和相关乳糖苷的二价配体的合成及其作为克鲁氏锥虫反唾液酸酶的底物和抑制剂的评价
3. Design, synthesis and enzymatic evaluation of 3-O-substituted aryl beta-D-galactopyranosides as inhibitors of Trypanosoma cruzi trans-sialidase [J] . Silva Bruno L., Filho Jose D. S., Andrade Peterson, Bioorganic and Medicinal Chemistry Letters . 2014 ,第18期

机译：设计，合成和酶促评价3-O-取代的芳基β-D-吡喃半乳糖苷作为克氏锥虫转唾液酸酶抑制剂
4. Design, synthesis and the effect of 1,2,3-triazole sialylmimetic neoglycoconjugates on Trypanosoma cruzi and its cell surface trans-sialidase [C] . V. L. Campo, R. Sesti-Costa, Z. A. Carneiro International Carbohydrate Symposium . 2013

机译：1,2,3-三唑丝状新苷杂环物对曲盼瘤Cruzi及其细胞表面反式唾液酸酶的设计，合成及其影响
5. Design, synthesis, and biological evaluation of molecules of medicinal interest: Inhibitors of mammalian and Trypanosoma cruzi protein farnesyltransferase and Trypanosoma cruzi lanosterol-14-alpha-demethylase. [D] . Lockman, Jeffrey William. 2003

机译：设计，合成和具有药用价值的分子的生物学评估：哺乳动物和克鲁斯锥虫蛋白法尼基转移酶和克鲁斯锥虫羊毛甾醇14-α-脱甲基酶的抑制剂。
6. Galactosyl-Lactose Sialylation Using Trypanosoma cruzi trans-Sialidase as the Biocatalyst and Bovine κ-Casein-Derived Glycomacropeptide as the Donor Substrate [O] . Maarten H. Wilbrink, Geert A. ten Kate, Sander S. van Leeuwen, 2014

机译：使用克氏锥虫转唾液酸酶作为生物催化剂和牛κ酪蛋白衍生的糖脂肽作为供体底物进行半乳糖-乳糖唾液酸化
7. Synthesis of divalent ligands of β-thio- and β-N-galactopyranosides and related lactosides and their evaluation as substrates and inhibitors of Trypanosoma cruzi trans-sialidase [O] . María Emilia Cano, Rosalía Agusti, Alejandro J. Cagnoni, 2014

机译：β-硫代-β-β-N-吡喃半乳糖苷和相关乳糖苷的二价配体的合成及其作为克氏锥虫反式唾液酸酶的底物和抑制剂的评价

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Synthesis of divalent ligands of β-thio- and β-N-galactopyranosides and related lactosides and their evaluation as substrates and inhibitors of Trypanosoma cruzi trans-sialidase

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