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Synthesis and Anticancer Evaluation of Some New 3-Benzyl-4,8-Dimethylbenzopyrone Derivatives

INTRODUCTION: New benzopyrone derivatives such as Schiff’s like compounds, acetohydrazides or substituted with oxadiazole or pyrazole heterocycles were synthesized from parent acid hydrazide compound 3. METHODS AND MATERIALS: Structures of the synthesized compounds were elucidated using IR, NMR and...

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Autores principales: El-Ansary, Sohair L., Abdel Rahman, Doaa E., Abdel Ghany, Lina M. A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Bentham Open 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5676012/
https://www.ncbi.nlm.nih.gov/pubmed/29151985
http://dx.doi.org/10.2174/1874104501711010081
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author El-Ansary, Sohair L.
Abdel Rahman, Doaa E.
Abdel Ghany, Lina M. A.
author_facet El-Ansary, Sohair L.
Abdel Rahman, Doaa E.
Abdel Ghany, Lina M. A.
author_sort El-Ansary, Sohair L.
collection PubMed
description INTRODUCTION: New benzopyrone derivatives such as Schiff’s like compounds, acetohydrazides or substituted with oxadiazole or pyrazole heterocycles were synthesized from parent acid hydrazide compound 3. METHODS AND MATERIALS: Structures of the synthesized compounds were elucidated using IR, NMR and mass spectroscopy. All the synthesized derivatives were selected by National Cancer Institute (NCI), Bethesda, and evaluated for their in vitro anticancer activity in the full NCI 60 cell lines panel assay. RESULTS AND CONCLUSION: Schiffs like compounds 4a, b and c were found to have good growth inhibition % against numerous cell lines that belong mainly to leukemia, non-small cell lung, CNS and breast Cancer subpanels.
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spelling pubmed-56760122017-11-17 Synthesis and Anticancer Evaluation of Some New 3-Benzyl-4,8-Dimethylbenzopyrone Derivatives El-Ansary, Sohair L. Abdel Rahman, Doaa E. Abdel Ghany, Lina M. A. Open Med Chem J Article INTRODUCTION: New benzopyrone derivatives such as Schiff’s like compounds, acetohydrazides or substituted with oxadiazole or pyrazole heterocycles were synthesized from parent acid hydrazide compound 3. METHODS AND MATERIALS: Structures of the synthesized compounds were elucidated using IR, NMR and mass spectroscopy. All the synthesized derivatives were selected by National Cancer Institute (NCI), Bethesda, and evaluated for their in vitro anticancer activity in the full NCI 60 cell lines panel assay. RESULTS AND CONCLUSION: Schiffs like compounds 4a, b and c were found to have good growth inhibition % against numerous cell lines that belong mainly to leukemia, non-small cell lung, CNS and breast Cancer subpanels. Bentham Open 2017-09-21 /pmc/articles/PMC5676012/ /pubmed/29151985 http://dx.doi.org/10.2174/1874104501711010081 Text en © 2017 El-Ansary et al. https://creativecommons.org/licenses/by/4.0/legalcode This is an open access article distributed under the terms of the Creative Commons Attribution 4.0 International Public License (CC-BY 4.0), a copy of which is available at: https://creativecommons.org/licenses/by/4.0/legalcode. This license permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Article
El-Ansary, Sohair L.
Abdel Rahman, Doaa E.
Abdel Ghany, Lina M. A.
Synthesis and Anticancer Evaluation of Some New 3-Benzyl-4,8-Dimethylbenzopyrone Derivatives
title Synthesis and Anticancer Evaluation of Some New 3-Benzyl-4,8-Dimethylbenzopyrone Derivatives
title_full Synthesis and Anticancer Evaluation of Some New 3-Benzyl-4,8-Dimethylbenzopyrone Derivatives
title_fullStr Synthesis and Anticancer Evaluation of Some New 3-Benzyl-4,8-Dimethylbenzopyrone Derivatives
title_full_unstemmed Synthesis and Anticancer Evaluation of Some New 3-Benzyl-4,8-Dimethylbenzopyrone Derivatives
title_short Synthesis and Anticancer Evaluation of Some New 3-Benzyl-4,8-Dimethylbenzopyrone Derivatives
title_sort synthesis and anticancer evaluation of some new 3-benzyl-4,8-dimethylbenzopyrone derivatives
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5676012/
https://www.ncbi.nlm.nih.gov/pubmed/29151985
http://dx.doi.org/10.2174/1874104501711010081
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