| Literature DB >> 24466406 |
Eugenia Cifuentes-Pagano1, Jaideep Saha2, Gábor Csányi1, Imad Al Ghouleh1, Sanghamitra Sahoo1, Andrés Rodríguez1, Peter Wipf3, Patrick J Pagano4, Erin M Skoda5.
Abstract
(1SR,4RS)-3,3-Dimethyl-1,2,3,4-tetrahydro-1,4-(epiminomethano)naphthalenes were synthesized in 2-3 steps from commercially available materials and assessed for specificity and effectiveness across a range of Nox isoforms. The N-pentyl and N-methylenethiophene substituted analogs 11g and 11h emerged as selective Nox2 inhibitors with cellular IC50 values of 20 and 32 μM, respectively.Entities:
Year: 2013 PMID: 24466406 PMCID: PMC3897123 DOI: 10.1039/C3MD00061C
Source DB: PubMed Journal: Medchemcomm ISSN: 2040-2503 Impact factor: 3.597