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Development of 3-methyl/3-(morpholinomethyl)benzofuran derivatives as novel antitumor agents towards non-small cell lung cancer cells

As one of the most lethal malignancies, lung cancer is considered to account for approximately one-fifth of all malignant tumours-related deaths worldwide. This study reports the synthesis and in vitro biological assessment of two sets of 3-methylbenzofurans (4a–d, 6a–c, 8a–c and 11) and 3-(morpholi...

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Autores principales: Al-Sanea, Mohammad M., Al-Ansary, Ghada H., Elsayed, Zainab M., Maklad, Raed M., Elkaeed, Eslam B., Abdelgawad, Mohamed A., Bukhari, Syed Nasir Abbas, Abdel-Aziz, Marwa M., Suliman, Howayda, Eldehna, Wagdy M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8128204/
https://www.ncbi.nlm.nih.gov/pubmed/33985397
http://dx.doi.org/10.1080/14756366.2021.1915302
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author Al-Sanea, Mohammad M.
Al-Ansary, Ghada H.
Elsayed, Zainab M.
Maklad, Raed M.
Elkaeed, Eslam B.
Abdelgawad, Mohamed A.
Bukhari, Syed Nasir Abbas
Abdel-Aziz, Marwa M.
Suliman, Howayda
Eldehna, Wagdy M.
author_facet Al-Sanea, Mohammad M.
Al-Ansary, Ghada H.
Elsayed, Zainab M.
Maklad, Raed M.
Elkaeed, Eslam B.
Abdelgawad, Mohamed A.
Bukhari, Syed Nasir Abbas
Abdel-Aziz, Marwa M.
Suliman, Howayda
Eldehna, Wagdy M.
author_sort Al-Sanea, Mohammad M.
collection PubMed
description As one of the most lethal malignancies, lung cancer is considered to account for approximately one-fifth of all malignant tumours-related deaths worldwide. This study reports the synthesis and in vitro biological assessment of two sets of 3-methylbenzofurans (4a–d, 6a–c, 8a–c and 11) and 3-(morpholinomethyl)benzofurans (15a–c, 16a–b, 17a–b and 18) as potential anticancer agents towards non-small cell lung carcinoma A549 and NCI-H23 cell lines, with VEGFR-2 inhibitory activity. The target benzofuran-based derivatives efficiently inhibited the growth of both A549 and NCI-H23 cell lines with IC(50) spanning in ranges 1.48–47.02 and 0.49–68.9 µM, respectively. The three most active benzofurans (4b, 15a and 16a) were further investigated for their effects on the cell cycle progression and apoptosis in A549 (for 4b) and NCI-H23 (for 15a and 16a) cell lines. Furthermore, benzofurans 4b, 15a and 16a displayed good VEGFR-2 inhibitory activity with IC(50) equal 77.97, 132.5 and 45.4 nM, respectively.
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spelling pubmed-81282042021-05-21 Development of 3-methyl/3-(morpholinomethyl)benzofuran derivatives as novel antitumor agents towards non-small cell lung cancer cells Al-Sanea, Mohammad M. Al-Ansary, Ghada H. Elsayed, Zainab M. Maklad, Raed M. Elkaeed, Eslam B. Abdelgawad, Mohamed A. Bukhari, Syed Nasir Abbas Abdel-Aziz, Marwa M. Suliman, Howayda Eldehna, Wagdy M. J Enzyme Inhib Med Chem Research Paper As one of the most lethal malignancies, lung cancer is considered to account for approximately one-fifth of all malignant tumours-related deaths worldwide. This study reports the synthesis and in vitro biological assessment of two sets of 3-methylbenzofurans (4a–d, 6a–c, 8a–c and 11) and 3-(morpholinomethyl)benzofurans (15a–c, 16a–b, 17a–b and 18) as potential anticancer agents towards non-small cell lung carcinoma A549 and NCI-H23 cell lines, with VEGFR-2 inhibitory activity. The target benzofuran-based derivatives efficiently inhibited the growth of both A549 and NCI-H23 cell lines with IC(50) spanning in ranges 1.48–47.02 and 0.49–68.9 µM, respectively. The three most active benzofurans (4b, 15a and 16a) were further investigated for their effects on the cell cycle progression and apoptosis in A549 (for 4b) and NCI-H23 (for 15a and 16a) cell lines. Furthermore, benzofurans 4b, 15a and 16a displayed good VEGFR-2 inhibitory activity with IC(50) equal 77.97, 132.5 and 45.4 nM, respectively. Taylor & Francis 2021-05-13 /pmc/articles/PMC8128204/ /pubmed/33985397 http://dx.doi.org/10.1080/14756366.2021.1915302 Text en © 2021 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Paper
Al-Sanea, Mohammad M.
Al-Ansary, Ghada H.
Elsayed, Zainab M.
Maklad, Raed M.
Elkaeed, Eslam B.
Abdelgawad, Mohamed A.
Bukhari, Syed Nasir Abbas
Abdel-Aziz, Marwa M.
Suliman, Howayda
Eldehna, Wagdy M.
Development of 3-methyl/3-(morpholinomethyl)benzofuran derivatives as novel antitumor agents towards non-small cell lung cancer cells
title Development of 3-methyl/3-(morpholinomethyl)benzofuran derivatives as novel antitumor agents towards non-small cell lung cancer cells
title_full Development of 3-methyl/3-(morpholinomethyl)benzofuran derivatives as novel antitumor agents towards non-small cell lung cancer cells
title_fullStr Development of 3-methyl/3-(morpholinomethyl)benzofuran derivatives as novel antitumor agents towards non-small cell lung cancer cells
title_full_unstemmed Development of 3-methyl/3-(morpholinomethyl)benzofuran derivatives as novel antitumor agents towards non-small cell lung cancer cells
title_short Development of 3-methyl/3-(morpholinomethyl)benzofuran derivatives as novel antitumor agents towards non-small cell lung cancer cells
title_sort development of 3-methyl/3-(morpholinomethyl)benzofuran derivatives as novel antitumor agents towards non-small cell lung cancer cells
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8128204/
https://www.ncbi.nlm.nih.gov/pubmed/33985397
http://dx.doi.org/10.1080/14756366.2021.1915302
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