| Literature DB >> 35318165 |
Marina Fosso Yatchang1, Bini Mathew1, Ritesh K Srivastava2, Jasim Khan2, Suhail Muzaffar2, Sixue Zhang1, Mousheng Wu1, Ling Zhai1, Pedro Ruiz1, Anupam Agarwal3, James R Bostwick1, Mark J Suto1, Mohammad Athar4, Corinne E Augelli-Szafran5.
Abstract
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.Entities:
Keywords: Antidotes; Arsenicals; Bromodomain 4; Inflammation
Mesh:
Substances:
Year: 2022 PMID: 35318165 PMCID: PMC9017782 DOI: 10.1016/j.bmcl.2022.128696
Source DB: PubMed Journal: Bioorg Med Chem Lett ISSN: 0960-894X Impact factor: 2.940