Literature DB >> 17000031

Synthesis and cytotoxic evaluation of a series of resveratrol derivatives modified in C2 position.

Xian-Feng Huang1, Ban-Feng Ruan, Xiao-Ting Wang, Chen Xu, Hui-Ming Ge, Hai-Liang Zhu, Ren-Xiang Tan.   

Abstract

Eleven C2-substituted derivatives of resveratrol (trans-3,4',5-trihydroxystilbene, RES) were prepared by partial synthesis from RES and evaluated for their cytotoxic activities against a human nasopharyngeal epidermoid tumor cell line KB. Among them, compounds 2 and 3 were more active than 5-fluorouracil (5-FU), an anticancer drug, and compound 5f exhibited similar activity to 5-FU. On the basis of the biological results, structure-activity relationships were discussed.

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Year:  2006        PMID: 17000031     DOI: 10.1016/j.ejmech.2006.08.006

Source DB:  PubMed          Journal:  Eur J Med Chem        ISSN: 0223-5234            Impact factor:   6.514


  13 in total

1.  Inhibitory effects of resveratrol and pterostilbene on human colon cancer cells: a side-by-side comparison.

Authors:  Wasamon Nutakul; Hana Shatara Sobers; Peiju Qiu; Ping Dong; Eric Andrew Decker; David Julian McClements; Hang Xiao
Journal:  J Agric Food Chem       Date:  2011-09-29       Impact factor: 5.279

2.  Ethyl 2-(4-chloro-phen-yl)-3-(3,5-dimethoxy-phen-oxy)acrylate.

Authors:  Wu Chen; Yong-Ming Cui; Fei Pan; Dong-Sheng Xia; Qing-Fu Zeng
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2008-11-29

3.  6,6'-oxydichroman.

Authors:  Meng Wang; Yong-Hao Ye
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2007-12-18

4.  Ethyl 3-(2,4-difluoro-phen-oxy)-2-(4-methoxy-phen-yl)acrylate.

Authors:  Wu Chen; Yong-Ming Cui; Fei Pan; Dong-Sheng Xia; Qing-Fu Zeng
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2008-11-20

5.  (E)-2,3-Bis(4-methoxy-phen-yl)acrylic acid.

Authors:  Banfeng Ruan; Ying Yang; Zhenwei Zhu; Pengcheng Lv; Hailiang Zhu
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2009-04-02

6.  Molecular insight into the differential anti-androgenic activity of resveratrol and its natural analogs: in silico approach to understand biological actions.

Authors:  Sandipan Chakraborty; Avinash Kumar; Nasir A Butt; Liangfen Zhang; Raquema Williams; Agnes M Rimando; Pradip K Biswas; Anait S Levenson
Journal:  Mol Biosyst       Date:  2016-05

7.  Resveratrol blocks Akt activation in angiotensin II- or EGF-stimulated vascular smooth muscle cells in a redox-independent manner.

Authors:  Cornelia E Schreiner; Mario Kumerz; Julia Gesslbauer; Daniel Schachner; Helge Joa; Thomas Erker; Atanas G Atanasov; Elke H Heiss; Verena M Dirsch
Journal:  Cardiovasc Res       Date:  2010-11-10       Impact factor: 10.787

8.  New Hybrids Based on Curcumin and Resveratrol: Synthesis, Cytotoxicity and Antiproliferative Activity against Colorectal Cancer Cells.

Authors:  Cristian Hernández; Gustavo Moreno; Angie Herrera-R; Wilson Cardona-G
Journal:  Molecules       Date:  2021-05-01       Impact factor: 4.411

9.  2,4-Dimeth-oxy-6-[(E)-2-(4-meth-oxy-phenyl)ethen-yl]benzaldehyde.

Authors:  Xiao-Lin Ge; Qiu-Xiang Guan; Sheng-Song Deng; Ban-Feng Ruan
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2013-04-05

10.  Crystal structure of (E)-4,6-dimeth-oxy-2-(4-meth-oxy-styr-yl)-3-methyl-benzaldehyde.

Authors:  Seunghyun Ahn; Yoongho Lim; Dongsoo Koh
Journal:  Acta Crystallogr E Crystallogr Commun       Date:  2015-09-26
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