Synthesis and cytotoxicity evaluation of biaryl-based chalcones and their potential in TNFα-induced nuclear factor-κB activation inhibition-Reference-Cited by-同舟云学术

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Synthesis and cytotoxicity evaluation of biaryl-based chalcones and their potential in TNFα-induced nuclear factor-κB activation inhibition

Published:2012-04 Issue: Volume:50 Page:393-404
ISSN:0223-5234
Container-title:European Journal of Medicinal Chemistry
language:en
Short-container-title:European Journal of Medicinal Chemistry

Author:

Zuo Yinglin,Yu Yi,Wang Shuni,Shao Weiyan,Zhou Binhua,Lin Li,Luo Zhuoyu,Huang Ruogu,Du Jun,Bu Xianzhang

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Pharmacology,General Medicine

Reference47 articles.

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2. Natural inhibitors of carcinogenesis;Kinghorn;Planta Med.,2004

3. Isoliquiritigenin, a flavonoid from licorice, reduces prostaglandin E2 and nitric oxide, causes apoptosis, and suppresses aberrant crypt foci development;Takahashi;Cancer Sci.,2004

4. In vivo antitumor activity by 2’,4’-dihydroxy-6’-methoxy-3’,5’-dimethylchalcone in a solid human carcinoma xenograft model;Ye;Cancer Chemother. Pharmacol,2005

5. Flavokawain A, a novel chalcone from kava extract, induces apoptosis in bladder cancer cells by involvement of Bax protein-dependent and mitochondria-dependent apoptotic pathway and suppresses tumor growth in mice;Zi;Cancer Res.,2005

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4. Molecular Docking and DFT Study of Synthesized Oxazine Derivatives;Egyptian Journal of Chemistry;2021-12-26

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