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Synthesis and Pharmacological Activities of Some New Triazolo- and Tetrazolopyrimidine Derivatives

A new series of fused triazolo- and tetrazolopyrimidine derivatives 2–14 were synthesized and their anti-inflammatory and ulcerogenic activities were evaluated. The pharmacological screening showed that many of these obtained compounds have good anti-inflammatory activities, comparable to the refere...

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Autores principales: Bahashwan, Saleh A., Fayed, Ahmed A., Amr, Abd El-Galil E., Flefel, Eman M., Kalmouch, Atef
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6269734/
https://www.ncbi.nlm.nih.gov/pubmed/24322490
http://dx.doi.org/10.3390/molecules181215051
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author Bahashwan, Saleh A.
Fayed, Ahmed A.
Amr, Abd El-Galil E.
Flefel, Eman M.
Kalmouch, Atef
author_facet Bahashwan, Saleh A.
Fayed, Ahmed A.
Amr, Abd El-Galil E.
Flefel, Eman M.
Kalmouch, Atef
author_sort Bahashwan, Saleh A.
collection PubMed
description A new series of fused triazolo- and tetrazolopyrimidine derivatives 2–14 were synthesized and their anti-inflammatory and ulcerogenic activities were evaluated. The pharmacological screening showed that many of these obtained compounds have good anti-inflammatory activities, comparable to the reference drug. The toxicity of the compounds was also assayed via the determination of their LD(50) values. The structures of newly synthesized compounds were confirmed by IR, (1)H-NMR, MS spectral data and elemental analysis.
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spelling pubmed-62697342018-12-20 Synthesis and Pharmacological Activities of Some New Triazolo- and Tetrazolopyrimidine Derivatives Bahashwan, Saleh A. Fayed, Ahmed A. Amr, Abd El-Galil E. Flefel, Eman M. Kalmouch, Atef Molecules Article A new series of fused triazolo- and tetrazolopyrimidine derivatives 2–14 were synthesized and their anti-inflammatory and ulcerogenic activities were evaluated. The pharmacological screening showed that many of these obtained compounds have good anti-inflammatory activities, comparable to the reference drug. The toxicity of the compounds was also assayed via the determination of their LD(50) values. The structures of newly synthesized compounds were confirmed by IR, (1)H-NMR, MS spectral data and elemental analysis. MDPI 2013-12-06 /pmc/articles/PMC6269734/ /pubmed/24322490 http://dx.doi.org/10.3390/molecules181215051 Text en © 2013 by the authors; licensee MDPI, Basel, Switzerland. http://creativecommons.org/licenses/by/3.0/ This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Article
Bahashwan, Saleh A.
Fayed, Ahmed A.
Amr, Abd El-Galil E.
Flefel, Eman M.
Kalmouch, Atef
Synthesis and Pharmacological Activities of Some New Triazolo- and Tetrazolopyrimidine Derivatives
title Synthesis and Pharmacological Activities of Some New Triazolo- and Tetrazolopyrimidine Derivatives
title_full Synthesis and Pharmacological Activities of Some New Triazolo- and Tetrazolopyrimidine Derivatives
title_fullStr Synthesis and Pharmacological Activities of Some New Triazolo- and Tetrazolopyrimidine Derivatives
title_full_unstemmed Synthesis and Pharmacological Activities of Some New Triazolo- and Tetrazolopyrimidine Derivatives
title_short Synthesis and Pharmacological Activities of Some New Triazolo- and Tetrazolopyrimidine Derivatives
title_sort synthesis and pharmacological activities of some new triazolo- and tetrazolopyrimidine derivatives
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6269734/
https://www.ncbi.nlm.nih.gov/pubmed/24322490
http://dx.doi.org/10.3390/molecules181215051
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