微波辅助合成氨基酸酯取代苯甲酸酰胺:人类 CD81-受体 HCV-E2 相互作用的潜在抑制剂。

Q2 Pharmacology, Toxicology and Pharmaceutics Open Medicinal Chemistry Journal Pub Date : 2008-04-15 DOI:10.2174/1874104500802010021
Marcel Holzer, Sigrid Ziegler, Bernd Kronenberger, Christian D Klein, Rolf W Hartmann
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引用次数: 0

摘要

我们小组的研究结果表明,水杨酸苄酯是 CD81-LEL-HCV-E2 相互作用的中度抑制剂。为了提高生物活性,我们通过微波辅助 DCC 反应将杂环取代的苯甲酸与氨基酸酯偶联。利用 HUH7.5 细胞,通过荧光标记抗体检测系统测试了所制备化合物的抑制效力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Microwave-Assisted Syntheses of Amino Acid Ester Substituted Benzoic Acid Amides: Potential Inhibitors of Human CD81-Receptor HCV-E2 Interaction.

Results from our group showed benzyl salicylate to be a moderate inhibitor of the CD81-LEL-HCV-E2 interaction. To increase the biological activity, heterocyclic substituted benzoic acids were coupled to amino acid esters via microwave assisted DCC-reaction. The prepared compounds were tested for their inhibitory potency by means of a fluorescence labeled antibody assay system using HUH7.5 cells.

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来源期刊
Open Medicinal Chemistry Journal
Open Medicinal Chemistry Journal Pharmacology, Toxicology and Pharmaceutics-Pharmaceutical Science
CiteScore
4.40
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0.00%
发文量
4
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