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Synthesis and evaluation of novel spiro derivatives for pyrrolopyrimidines as anti-hyperglycemia promising compounds

Pyrrolopyrimidin-4-ylidene-malononitriles IIa–d were prepared as important intermediates for preparation of a new series of spiro-pyrrolopyrimidines. These intermediates undergo cyclisation via reaction with acetylacetone, guanidine hydrochloride or hydrazine hydrate. Elemental and spectroscopic evi...

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Autores principales: Fatahala, Samar Said, Mahgub, Shahenda, Taha, Heba, Abd-El Hameed, Rania Helmy
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6009929/
https://www.ncbi.nlm.nih.gov/pubmed/29708461
http://dx.doi.org/10.1080/14756366.2018.1461854
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author Fatahala, Samar Said
Mahgub, Shahenda
Taha, Heba
Abd-El Hameed, Rania Helmy
author_facet Fatahala, Samar Said
Mahgub, Shahenda
Taha, Heba
Abd-El Hameed, Rania Helmy
author_sort Fatahala, Samar Said
collection PubMed
description Pyrrolopyrimidin-4-ylidene-malononitriles IIa–d were prepared as important intermediates for preparation of a new series of spiro-pyrrolopyrimidines. These intermediates undergo cyclisation via reaction with acetylacetone, guanidine hydrochloride or hydrazine hydrate. Elemental and spectroscopic evidences for the structures of these compounds are presented. The final compounds have been monitored for in vivo anti-hyperglycemic activity, compared with Amaryl as standard drug. Among 12 tested compounds, both spiro (pyrano IIIb and pyrazlo Va) derivatives exhibit promising anti-hyperglycemic activity.
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spelling pubmed-60099292018-07-11 Synthesis and evaluation of novel spiro derivatives for pyrrolopyrimidines as anti-hyperglycemia promising compounds Fatahala, Samar Said Mahgub, Shahenda Taha, Heba Abd-El Hameed, Rania Helmy J Enzyme Inhib Med Chem Research Paper Pyrrolopyrimidin-4-ylidene-malononitriles IIa–d were prepared as important intermediates for preparation of a new series of spiro-pyrrolopyrimidines. These intermediates undergo cyclisation via reaction with acetylacetone, guanidine hydrochloride or hydrazine hydrate. Elemental and spectroscopic evidences for the structures of these compounds are presented. The final compounds have been monitored for in vivo anti-hyperglycemic activity, compared with Amaryl as standard drug. Among 12 tested compounds, both spiro (pyrano IIIb and pyrazlo Va) derivatives exhibit promising anti-hyperglycemic activity. Taylor & Francis 2018-04-30 /pmc/articles/PMC6009929/ /pubmed/29708461 http://dx.doi.org/10.1080/14756366.2018.1461854 Text en © 2018 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. http://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/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Paper
Fatahala, Samar Said
Mahgub, Shahenda
Taha, Heba
Abd-El Hameed, Rania Helmy
Synthesis and evaluation of novel spiro derivatives for pyrrolopyrimidines as anti-hyperglycemia promising compounds
title Synthesis and evaluation of novel spiro derivatives for pyrrolopyrimidines as anti-hyperglycemia promising compounds
title_full Synthesis and evaluation of novel spiro derivatives for pyrrolopyrimidines as anti-hyperglycemia promising compounds
title_fullStr Synthesis and evaluation of novel spiro derivatives for pyrrolopyrimidines as anti-hyperglycemia promising compounds
title_full_unstemmed Synthesis and evaluation of novel spiro derivatives for pyrrolopyrimidines as anti-hyperglycemia promising compounds
title_short Synthesis and evaluation of novel spiro derivatives for pyrrolopyrimidines as anti-hyperglycemia promising compounds
title_sort synthesis and evaluation of novel spiro derivatives for pyrrolopyrimidines as anti-hyperglycemia promising compounds
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6009929/
https://www.ncbi.nlm.nih.gov/pubmed/29708461
http://dx.doi.org/10.1080/14756366.2018.1461854
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