| Literature DB >> 34413956 |
Jennifer Hanisak1, Aileen Soriano2, Gregory C Adam3, Andrea Basso2, David Bauman4, David Bell2, Emily Frank2, Gregory O'Donnell3, Paul Tawa2, Andreas Verras5, Yang Yu1, Lei Zhang6, W Michael Seganish7.
Abstract
PKG1α is a central node in cGMP signaling. Current therapeutics that look to activate this pathway rely on elevation of cGMP levels and subsequent activation of PKG1α. Direct activation of PKG1α could potentially drive additional efficacy without associated side effects of blanket cGMP elevation. We undertook a high-throughput screen to identify novel activators. After triaging through numerous false positive hits, attributed to compound mediated oxidation and activation of PKG1α, a piperidine series of compounds was validated. The hit 1 was a weak activator with EC50 = 47 μM. The activity could be improved to single digit micromolar, as seen in compounds 21 and 25 (7.0 and 3.7 μM, respectively). Several compounds were tested in a pVASP cell-based assay, and for compounds with moderate permeability, good agreement was observed between the biochemical and functional assays. These compounds will function as efficient tools to further interrogate PKG1α biology.Entities:
Year: 2021 PMID: 34413956 PMCID: PMC8365999 DOI: 10.1021/acsmedchemlett.1c00264
Source DB: PubMed Journal: ACS Med Chem Lett ISSN: 1948-5875 Impact factor: 4.632