Synthesis and Biological Evaluation of 4-Aroyl-6,7,8-Trimethoxyquinolines as a Novel Class of Anticancer Agents

A series of 2-aroyl and 2-aryl-5,6,7-trimethoxyquinoline and 4-aroyl-6,7,8-trimethoxyquinoline combretastatin analogs were synthesized and evaluated for their potential anticancer activity. The 4-aroylquinoline 11 inhibited the growth of the human cancer cells lines KB, HT-29, and MKN45, as well as...

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Main Authors: Jing-Ping Liou, Jang-Yang Chang, Chih-Ying Nien, Cheng-Chih Hsieh, Chi-Yen Chang, Ching-Chuan Kuo, Hsueh-Yun Lee
Format: Article
Language:English
Published: MDPI AG 2011-03-01
Series:Molecules
Subjects:
Online Access:http://www.mdpi.com/1420-3049/16/3/2274/
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author Jing-Ping Liou
Jang-Yang Chang
Chih-Ying Nien
Cheng-Chih Hsieh
Chi-Yen Chang
Ching-Chuan Kuo
Hsueh-Yun Lee
author_facet Jing-Ping Liou
Jang-Yang Chang
Chih-Ying Nien
Cheng-Chih Hsieh
Chi-Yen Chang
Ching-Chuan Kuo
Hsueh-Yun Lee
author_sort Jing-Ping Liou
collection DOAJ
description A series of 2-aroyl and 2-aryl-5,6,7-trimethoxyquinoline and 4-aroyl-6,7,8-trimethoxyquinoline combretastatin analogs were synthesized and evaluated for their potential anticancer activity. The 4-aroylquinoline 11 inhibited the growth of the human cancer cells lines KB, HT-29, and MKN45, as well as the three human resistant cancer cell lines KB-vin10, KB-S15, and KB-7D, with IC50 values of 217, 327, 239, 246, 213, and 252 nM, respectively.
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spelling doaj.art-c5757fd4e4e44640934a2f3f6505fcb82022-12-22T03:26:03ZengMDPI AGMolecules1420-30492011-03-011632274228410.3390/molecules16032274Synthesis and Biological Evaluation of 4-Aroyl-6,7,8-Trimethoxyquinolines as a Novel Class of Anticancer AgentsJing-Ping LiouJang-Yang ChangChih-Ying NienCheng-Chih HsiehChi-Yen ChangChing-Chuan KuoHsueh-Yun LeeA series of 2-aroyl and 2-aryl-5,6,7-trimethoxyquinoline and 4-aroyl-6,7,8-trimethoxyquinoline combretastatin analogs were synthesized and evaluated for their potential anticancer activity. The 4-aroylquinoline 11 inhibited the growth of the human cancer cells lines KB, HT-29, and MKN45, as well as the three human resistant cancer cell lines KB-vin10, KB-S15, and KB-7D, with IC50 values of 217, 327, 239, 246, 213, and 252 nM, respectively.http://www.mdpi.com/1420-3049/16/3/2274/combretastatin analogsmultidrug-resistanttrimethoxyquinolinesantiproliferative activity
spellingShingle Jing-Ping Liou
Jang-Yang Chang
Chih-Ying Nien
Cheng-Chih Hsieh
Chi-Yen Chang
Ching-Chuan Kuo
Hsueh-Yun Lee
Synthesis and Biological Evaluation of 4-Aroyl-6,7,8-Trimethoxyquinolines as a Novel Class of Anticancer Agents
Molecules
combretastatin analogs
multidrug-resistant
trimethoxyquinolines
antiproliferative activity
title Synthesis and Biological Evaluation of 4-Aroyl-6,7,8-Trimethoxyquinolines as a Novel Class of Anticancer Agents
title_full Synthesis and Biological Evaluation of 4-Aroyl-6,7,8-Trimethoxyquinolines as a Novel Class of Anticancer Agents
title_fullStr Synthesis and Biological Evaluation of 4-Aroyl-6,7,8-Trimethoxyquinolines as a Novel Class of Anticancer Agents
title_full_unstemmed Synthesis and Biological Evaluation of 4-Aroyl-6,7,8-Trimethoxyquinolines as a Novel Class of Anticancer Agents
title_short Synthesis and Biological Evaluation of 4-Aroyl-6,7,8-Trimethoxyquinolines as a Novel Class of Anticancer Agents
title_sort synthesis and biological evaluation of 4 aroyl 6 7 8 trimethoxyquinolines as a novel class of anticancer agents
topic combretastatin analogs
multidrug-resistant
trimethoxyquinolines
antiproliferative activity
url http://www.mdpi.com/1420-3049/16/3/2274/
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