Synthesis and biological evaluation of 7-arylindoline-1-benzenesulfonamides as a novel class of potent anticancer agents

Jang-Yang Chang; Mei-Jung Lai; Yi-Ting Chang; Hsueh Yun Lee; Yun-Ching Cheng; Ching-Chuan Kuo; Min-Chieh Su; Chi-Yen Chang; Jing Ping Liou

doi:10.1039/c0md00052c

Synthesis and biological evaluation of 7-arylindoline-1-benzenesulfonamides as a novel class of potent anticancer agents

Jang-Yang Chang, Mei-Jung Lai, Yi-Ting Chang, Hsueh Yun Lee, Yun-Ching Cheng, Ching-Chuan Kuo, Min-Chieh Su, Chi-Yen Chang, Jing Ping Liou

研究成果: 雜誌貢獻 › 文章 › 同行評審

24 引文斯高帕斯（Scopus）

摘要

A series of 7-arylindoline-1-benzenesulfonamides were prepared and evaluated for anticancer activity. 7-(4′-Cyanophenyl)indoline-1- benzenesulfonamide 15 exhibited substantial antiproliferative activity with IC50 values ranging from 17-32 nM against a variety of human cancer cell lines, including MDR resistant line. Compound 15 (IC50 = 1.5 μM) also showed more potent inhibition of tubulin polymerization than 4a (combretastatin A-4, IC50 = 2.0 μM) and displayed strong binding to the colchicine binding site of the tubulin.

原文	英語
頁（從 - 到）	152-155
頁數	4
期刊	MedChemComm
卷	1
發行號	2
DOIs	https://doi.org/10.1039/c0md00052c
出版狀態	已發佈 - 8月 2010

ASJC Scopus subject areas

藥物發現
分子醫學
生物化學
藥理
藥學科學
有機化學

UN SDG

此研究成果有助於以下永續發展目標

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10.1039/c0md00052c

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引用此

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title = "Synthesis and biological evaluation of 7-arylindoline-1-benzenesulfonamides as a novel class of potent anticancer agents",

abstract = "A series of 7-arylindoline-1-benzenesulfonamides were prepared and evaluated for anticancer activity. 7-(4′-Cyanophenyl)indoline-1- benzenesulfonamide 15 exhibited substantial antiproliferative activity with IC50 values ranging from 17-32 nM against a variety of human cancer cell lines, including MDR resistant line. Compound 15 (IC50 = 1.5 μM) also showed more potent inhibition of tubulin polymerization than 4a (combretastatin A-4, IC50 = 2.0 μM) and displayed strong binding to the colchicine binding site of the tubulin.",

author = "Jang-Yang Chang and Mei-Jung Lai and Yi-Ting Chang and Lee, \{Hsueh Yun\} and Yun-Ching Cheng and Ching-Chuan Kuo and Min-Chieh Su and Chi-Yen Chang and Liou, \{Jing Ping\}",

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doi = "10.1039/c0md00052c",

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AU - Chang, Jang-Yang

AU - Lai, Mei-Jung

AU - Chang, Yi-Ting

AU - Lee, Hsueh Yun

AU - Cheng, Yun-Ching

AU - Kuo, Ching-Chuan

AU - Su, Min-Chieh

AU - Chang, Chi-Yen

AU - Liou, Jing Ping

PY - 2010/8

Y1 - 2010/8

N2 - A series of 7-arylindoline-1-benzenesulfonamides were prepared and evaluated for anticancer activity. 7-(4′-Cyanophenyl)indoline-1- benzenesulfonamide 15 exhibited substantial antiproliferative activity with IC50 values ranging from 17-32 nM against a variety of human cancer cell lines, including MDR resistant line. Compound 15 (IC50 = 1.5 μM) also showed more potent inhibition of tubulin polymerization than 4a (combretastatin A-4, IC50 = 2.0 μM) and displayed strong binding to the colchicine binding site of the tubulin.

AB - A series of 7-arylindoline-1-benzenesulfonamides were prepared and evaluated for anticancer activity. 7-(4′-Cyanophenyl)indoline-1- benzenesulfonamide 15 exhibited substantial antiproliferative activity with IC50 values ranging from 17-32 nM against a variety of human cancer cell lines, including MDR resistant line. Compound 15 (IC50 = 1.5 μM) also showed more potent inhibition of tubulin polymerization than 4a (combretastatin A-4, IC50 = 2.0 μM) and displayed strong binding to the colchicine binding site of the tubulin.

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Synthesis and biological evaluation of 7-arylindoline-1-benzenesulfonamides as a novel class of potent anticancer agents

摘要

ASJC Scopus subject areas

UN SDG

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