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Synthesis and Biological Evaluation of Novel 4-(4-Formamidophenylamino)-N-methylpicolinamide Derivatives as Potential Antitumor Agents

A novel series of 4-(4-formamidophenylamino)-N-methylpicolinamide derivatives were synthesized and evaluated against different tumor cell lines. Experiments in vitro showed that these derivatives could inhibit the proliferation of two kinds of human cancer cell lines (HepG2, HCT116) at low micromola...

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Detalles Bibliográficos
Autores principales: Meng, Nana, Zhou, Shuyan, Hu, Min, Xu, Youzhi, Xia, Yong, Zeng, Xiuxiu, Yu, Luoting
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7926825/
https://www.ncbi.nlm.nih.gov/pubmed/33670007
http://dx.doi.org/10.3390/molecules26041150
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author Meng, Nana
Zhou, Shuyan
Hu, Min
Xu, Youzhi
Xia, Yong
Zeng, Xiuxiu
Yu, Luoting
author_facet Meng, Nana
Zhou, Shuyan
Hu, Min
Xu, Youzhi
Xia, Yong
Zeng, Xiuxiu
Yu, Luoting
author_sort Meng, Nana
collection PubMed
description A novel series of 4-(4-formamidophenylamino)-N-methylpicolinamide derivatives were synthesized and evaluated against different tumor cell lines. Experiments in vitro showed that these derivatives could inhibit the proliferation of two kinds of human cancer cell lines (HepG2, HCT116) at low micromolar concentrations and the most potent analog 5q possessed broad-spectrum antiproliferative activity. Experiments in vivo demonstrated that 5q could effectively prolong the longevity of colon carcinoma-burdened mice and slow down the progression of cancer cells by suppression of angiogenesis and the induction of apoptosis and necrosis.
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spelling pubmed-79268252021-03-04 Synthesis and Biological Evaluation of Novel 4-(4-Formamidophenylamino)-N-methylpicolinamide Derivatives as Potential Antitumor Agents Meng, Nana Zhou, Shuyan Hu, Min Xu, Youzhi Xia, Yong Zeng, Xiuxiu Yu, Luoting Molecules Article A novel series of 4-(4-formamidophenylamino)-N-methylpicolinamide derivatives were synthesized and evaluated against different tumor cell lines. Experiments in vitro showed that these derivatives could inhibit the proliferation of two kinds of human cancer cell lines (HepG2, HCT116) at low micromolar concentrations and the most potent analog 5q possessed broad-spectrum antiproliferative activity. Experiments in vivo demonstrated that 5q could effectively prolong the longevity of colon carcinoma-burdened mice and slow down the progression of cancer cells by suppression of angiogenesis and the induction of apoptosis and necrosis. MDPI 2021-02-21 /pmc/articles/PMC7926825/ /pubmed/33670007 http://dx.doi.org/10.3390/molecules26041150 Text en © 2021 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Meng, Nana
Zhou, Shuyan
Hu, Min
Xu, Youzhi
Xia, Yong
Zeng, Xiuxiu
Yu, Luoting
Synthesis and Biological Evaluation of Novel 4-(4-Formamidophenylamino)-N-methylpicolinamide Derivatives as Potential Antitumor Agents
title Synthesis and Biological Evaluation of Novel 4-(4-Formamidophenylamino)-N-methylpicolinamide Derivatives as Potential Antitumor Agents
title_full Synthesis and Biological Evaluation of Novel 4-(4-Formamidophenylamino)-N-methylpicolinamide Derivatives as Potential Antitumor Agents
title_fullStr Synthesis and Biological Evaluation of Novel 4-(4-Formamidophenylamino)-N-methylpicolinamide Derivatives as Potential Antitumor Agents
title_full_unstemmed Synthesis and Biological Evaluation of Novel 4-(4-Formamidophenylamino)-N-methylpicolinamide Derivatives as Potential Antitumor Agents
title_short Synthesis and Biological Evaluation of Novel 4-(4-Formamidophenylamino)-N-methylpicolinamide Derivatives as Potential Antitumor Agents
title_sort synthesis and biological evaluation of novel 4-(4-formamidophenylamino)-n-methylpicolinamide derivatives as potential antitumor agents
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7926825/
https://www.ncbi.nlm.nih.gov/pubmed/33670007
http://dx.doi.org/10.3390/molecules26041150
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