受前驱体启发的氟化腺苷A2A受体拮抗剂作为潜在的癌症免疫治疗药物。

International Journal of Medicinal Chemistry Pub Date : 2017-01-01 Epub Date: 2017-10-19 DOI:10.1155/2017/4852537
Gengyang Yuan, Tanner C Jankins, Christopher G Patrick, Phaethon Philbrook, Olivia Sears, Stephen Hatfield, Michail Sitkovsky, Neil Vasdev, Steven H Liang, Mary Jo Ondrechen, Michael P Pollastri, Graham B Jones
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引用次数: 9

摘要

T细胞上腺苷A2A受体的拮抗作用阻断缺氧-腺苷能通路,促进肿瘤排斥反应。利用基于Concanavalin A小鼠模型的体内免疫分析,研究了一系列A2A拮抗剂,并确定了preladenant是一种有效的促进发育的先导化合物。采用分子模型来辅助药物设计和随后的类似物和毒腺剂的合成,包括氟化聚乙二醇聚乙二醇衍生物。使用两种体外功能生物测定法评估了类似物的功效,并确认化合物29 (preladenant的氟化三甘醇衍生物)是一种潜在的免疫治疗剂。
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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Fluorinated Adenosine A2A Receptor Antagonists Inspired by Preladenant as Potential Cancer Immunotherapeutics.

Antagonism of the adenosine A2A receptor on T cells blocks the hypoxia-adenosinergic pathway to promote tumor rejection. Using an in vivo immunoassay based on the Concanavalin A mouse model, a series of A2A antagonists were studied and identified preladenant as a potent lead compound for development. Molecular modeling was employed to assist drug design and subsequent synthesis of analogs and those of tozadenant, including fluorinated polyethylene glycol PEGylated derivatives. The efficacy of the analogs was evaluated using two in vitro functional bioassays, and compound 29, a fluorinated triethylene glycol derivative of preladenant, was confirmed as a potential immunotherapeutic agent.

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期刊介绍: International Journal of Medicinal Chemistry is a peer-reviewed, Open Access journal that publishes original research articles as well as review articles in all areas of chemistry associated with drug discovery, design, and synthesis. International Journal of Medicinal Chemistry is a peer-reviewed, Open Access journal that publishes original research articles as well as review articles in all areas of chemistry associated with drug discovery, design, and synthesis.
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