化学
溴尿嘧啶
BRD4
背景(考古学)
小分子
药理学
药物发现
转录因子
计算生物学
作者
Marina Fosso Yatchang,Bini Mathew,Ritesh K. Srivastava,Jasim Khan,Suhail Muzaffar,Sixue Zhang,Mousheng Wu,Ling Zhai,Pedro Ruiz,Anupam Agarwal,James R. Bostwick,Mark J. Suto,Mohammad Athar,Corinne E. Augelli-Szafran
标识
DOI:10.1016/j.bmcl.2022.128696
摘要
Arsenicals belong to the class of chemical warfare agents known as vesicants, which are highly reactive, toxic and cause robust inflammatory response. Cutaneous exposure to arsenicals causes a wide range of systemic organ damage, beginning with cutaneous injuries, and later manifest multi-organ damage and death. Thus, the development of suitable antidotes that can effectively block injury following exposure to these agents is of great importance. Bromodomain 4 (BRD4), a member of the bromodomain and extra terminal domain (BET) family, plays crucial role in regulating transcription of inflammatory, proliferation and cell cycle genes. In this context, the development of potent small molecule inhibitors of BRD4 could serve as potential antidotes for arsenicals. Herein, we describe the synthesis and biological evaluation of a series of compounds.
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