Synthesis and biological evaluation of a novel class of curcumin analogs as anti-inflammatory agents for prevention and treatment of sepsis in mouse model

A novel class of asymmetric mono-carbonyl analogs of curcumin (AMACs) were synthesized and screened for anti-inflammatory activity. These analogs are chemically stable as characterized by UV absorption spectra. In vitro, compounds 3f, 3m, 4b, and 4d markedly inhibited lipopolysaccharide (LPS)-induce...

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Detalles Bibliográficos
Autores principales: Zhao, Chengguang, Zhang, Yali, Zou, Peng, Wang, Jian, He, Wenfei, Shi, Dengjian, Li, Huameng, Liang, Guang, Yang, Shulin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2015
Materias:
Original Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4370917/
https://www.ncbi.nlm.nih.gov/pubmed/25834403
http://dx.doi.org/10.2147/DDDT.S75862

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4370917/
https://www.ncbi.nlm.nih.gov/pubmed/25834403
http://dx.doi.org/10.2147/DDDT.S75862

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