Literature DB >> 15283456

Synthesis and cytotoxicity of 2,5-dihydroxychalcones and related compounds.

Nguyen-Hai Nam1, Dong-Ho Hong, Young-Jae You, Yong Kim, Seong-Cheol Bang, Hwan-Mook Kim, Byung-Zun Ahn.   

Abstract

A series of 2, 5-dihydroxychalcones and related compounds were synthesized, and their cytotoxicities against tumor cell lines and human umbilical venous endothelial cells (HUVEC) evaluated. It was found that chalcones, with electron-withdrawing substituents on an A ring, exhibited significant cytotoxicities. Among the synthesized compounds, 2'-chloro-2, 5-dihydroxychalcone (9) was most potent, with an IC50 value as low as 0.31 microg/mL. This compound also exhibited a significant cytotoxic selectivity toward HUVEC.

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Year:  2004        PMID: 15283456     DOI: 10.1007/BF02980153

Source DB:  PubMed          Journal:  Arch Pharm Res        ISSN: 0253-6269            Impact factor:   4.946


  3 in total

1.  Synthesis of alpha,beta-unsaturated ketones as chalcone analogues via a S(RN)1 mechanism.

Authors:  Christophe Curti; Armand Gellis; Patrice Vanelle
Journal:  Molecules       Date:  2007-04-18       Impact factor: 4.411

2.  Design, synthesis and evaluation of novel 2-oxoindoline-based acetohydrazides as antitumor agents.

Authors:  Do T M Dung; Eun J Park; Duong T Anh; Dung T P Phan; Ik H Na; Joo H Kwon; Jong S Kang; Truong T Tung; Sang-Bae Han; Nguyen-Hai Nam
Journal:  Sci Rep       Date:  2022-02-21       Impact factor: 4.379

3.  Design, synthesis, and evaluation of novel N'-substituted-1-(4-chlorobenzyl)-1H-indol-3-carbohydrazides as antitumor agents.

Authors:  Le Cong Huan; Duong Tien Anh; Pham-The Hai; Lai Duc Anh; Eun Jae Park; A Young Ji; Jong Soon Kang; Do Thi Mai Dung; Dao Thi Kim Oanh; Truong Thanh Tung; Dinh Thi Thanh Hai; Sang-Bae Han; Nguyen-Hai Nam
Journal:  J Enzyme Inhib Med Chem       Date:  2020-12       Impact factor: 5.051

  3 in total

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