| Literature DB >> 26922229 |
Mei-Lin Tang1, Chen Zhong1, Zheng-Yu Liu1, Peng Peng1, Xin-Hua Liu2, Xun Sun3.
Abstract
To develop novel anti-inflammatory agents with improved pharmaceutical profiles, twenty-eight novel sesquistilbene indanone analogues were synthesized and evaluated for anti-inflammatory activity using RAW264.7 cells. Among these compounds, compound 11k was found to be one of the most potent analogues in inhibiting NO production in LPS-stimulated RAW264.7 cells. Furthermore, it could also significantly suppress LPS-induced iNOS and COX-2 expression and NO production through TLR4/JNK/NF-κB signaling pathway in a concentration dependent manner.Entities:
Keywords: Anti-inflammatory; Indanone; TLR4/JNK/NF-κB
Mesh:
Substances:
Year: 2016 PMID: 26922229 DOI: 10.1016/j.ejmech.2016.02.021
Source DB: PubMed Journal: Eur J Med Chem ISSN: 0223-5234 Impact factor: 6.514