Synthesis and anti-inflammatory evaluation of novel mono-carbonyl analogues of curcumin in LPS-stimulated RAW 264.7 macrophages-Reference-Cited by-同舟云学术

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Synthesis and anti-inflammatory evaluation of novel mono-carbonyl analogues of curcumin in LPS-stimulated RAW 264.7 macrophages

Published:2010-12 Issue:12 Volume:45 Page:5773-5780
ISSN:0223-5234
Container-title:European Journal of Medicinal Chemistry
language:en
Short-container-title:European Journal of Medicinal Chemistry

Author:

Zhao Chengguang,Cai Yuepiao,He Xuzhi,Li Jianling,Zhang Li,Wu Jianzhang,Zhao Yunjie,Yang Shulin,Li Xiaokun,Li Wulan,Liang Guang

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Pharmacology,General Medicine

Reference40 articles.

1. Prevention of nicotine and streptozotocin treatment induced circulatory oxidative stress by bis-1,7-(2-hydroxyphenyl)-hepta-1,6-diene-3,5-dione in diabetic rats

2. Curcumin induces apoptosis-independent death in oesophageal cancer cells

3. Potential protection of curcumin against intracellular amyloid β-induced toxicity in cultured rat prefrontal cortical neurons

4. Curcumin Increases the Pathogenicity of Salmonella enterica Serovar Typhimurium in Murine Model

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