| Literature DB >> 27660689 |
Haya Jamali1, Hasan A Khan1, Caroline C Tjin1, Jonathan A Ellman1.
Abstract
The protein arginine deiminases (PADs) catalyze the post-translational deimination of arginine side chains. Multiple PAD isozymes have been characterized, and abnormal PAD activity has been associated with several human disease states. PAD3 has been characterized as a modulator of cell growth via apoptosis inducing factor and has been implicated in the neurodegenerative response to spinal cord injury. Here, we describe the design, synthesis, and evaluation of conformationally constrained versions of the potent and selective PAD3 inhibitor 2. The cell activity of representative inhibitors in this series was also demonstrated for the first time by rescue of thapsigargin-induced cell death in PAD3-expressing HEK293T cells.Entities:
Keywords: Protein arginine deiminases; apoptosis inducing factor; small molecule inhibitor; spinal cord injury
Year: 2016 PMID: 27660689 PMCID: PMC5018872 DOI: 10.1021/acsmedchemlett.6b00215
Source DB: PubMed Journal: ACS Med Chem Lett ISSN: 1948-5875 Impact factor: 4.345