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对WO2017098421的评估:葛兰素史克公司的苯并噻嗪化合物作为CD73抑制剂的申报文件。

Evaluation of WO2017098421: GSK's benzothiazine compounds as CD73 inhibitor filings.

作者信息

Gong Ya-Ping, Wan Ren-Zhong, Liu Zhao-Peng

机构信息

a Institute of Medicinal Chemistry, Key Laboratory of Chemical Biology (Ministry of Education), School of Pharmaceutical Sciences , Shandong University , Jinan PR China.

b College of Animal Science & Veterinary Medicine , Shandong Agricultural University , Taian , PR China.

出版信息

Expert Opin Ther Pat. 2018 Feb;28(2):167-171. doi: 10.1080/13543776.2018.1407756. Epub 2017 Nov 22.

Abstract

There are considerable interests in the development of novel small-molecule CD73 inhibitors for the treatment of cancers, autoimmune diseases, precancerous syndromes, and other diseases associated with CD73 activity. Areas covered: The application claims novel substituted benzothiadiazine derivatives as CD73 inhibitors for the treatment of cancer, precancerous syndromes, AIDS, autoimmune diseases, infections, atherosclerosis, and ischemia-reperfusion injury. Many of the exemplified compounds have pIC50 values between 5 to 8.4 against CD73. Expert Opinion: These benzothiadiazine derivatives provide good leads for the discovery of potent CD73 inhibitors for the treatment of cancer and other diseases mediated by adenosine and its action on adenosine receptors.

摘要

对于开发用于治疗癌症、自身免疫性疾病、癌前综合征以及其他与CD73活性相关疾病的新型小分子CD73抑制剂,人们有着浓厚的兴趣。涵盖领域:该申请要求保护新型取代苯并噻二嗪衍生物作为CD73抑制剂用于治疗癌症、癌前综合征、艾滋病、自身免疫性疾病、感染、动脉粥样硬化和缺血再灌注损伤。许多示例化合物对CD73的pIC50值在5至8.4之间。专家观点:这些苯并噻二嗪衍生物为发现用于治疗癌症和其他由腺苷及其对腺苷受体的作用介导的疾病的强效CD73抑制剂提供了良好的先导化合物。

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