Yuan Gengyang, Jankins Tanner C, Patrick Christopher G, Philbrook Phaethon, Sears Olivia, Hatfield Stephen, Sitkovsky Michail, Vasdev Neil, Liang Steven H, Ondrechen Mary Jo, Pollastri Michael P, Jones Graham B
Department of Chemistry and Chemical Biology, Northeastern University, 360 Huntington Avenue, Boston, MA 02115, USA.
New England Tissue Protection Institute, Northeastern University, 360 Huntington Avenue, Boston, MA 02115, USA.
Int J Med Chem. 2017;2017:4852537. doi: 10.1155/2017/4852537. Epub 2017 Oct 19.
Antagonism of the adenosine A receptor on T cells blocks the hypoxia-adenosinergic pathway to promote tumor rejection. Using an immunoassay based on the Concanavalin A mouse model, a series of A 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 functional bioassays, and compound , a fluorinated triethylene glycol derivative of preladenant, was confirmed as a potential immunotherapeutic agent.
T细胞上腺苷A受体的拮抗作用可阻断缺氧-腺苷能途径以促进肿瘤排斥。利用基于刀豆蛋白A小鼠模型的免疫测定法,研究了一系列A拮抗剂,并确定普雷拉登特是一种有开发潜力的先导化合物。采用分子建模辅助药物设计以及后续类似物和托扎登特类似物(包括氟化聚乙二醇聚乙二醇化衍生物)的合成。使用两种功能生物测定法评估类似物的疗效,化合物(普雷拉登特的氟化三甘醇衍生物)被确认为一种潜在的免疫治疗剂。