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Pyrido[2,3-d]pyrimidin-7(8H)-ones: Synthesis and Biomedical Applications

Pyrido[2,3-d]pyrimidines (1) are a type of privileged heterocyclic scaffolds capable of providing ligands for several receptors in the body. Among such structures, our group and others have been particularly interested in pyrido[2,3-d]pyrimidine-7(8H)-ones (2) due to the similitude with nitrogen bas...

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Autores principales: Jubete, Guillem, Puig de la Bellacasa, Raimon, Estrada-Tejedor, Roger, Teixidó, Jordi, Borrell, José I.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6891647/
https://www.ncbi.nlm.nih.gov/pubmed/31744155
http://dx.doi.org/10.3390/molecules24224161
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author Jubete, Guillem
Puig de la Bellacasa, Raimon
Estrada-Tejedor, Roger
Teixidó, Jordi
Borrell, José I.
author_facet Jubete, Guillem
Puig de la Bellacasa, Raimon
Estrada-Tejedor, Roger
Teixidó, Jordi
Borrell, José I.
author_sort Jubete, Guillem
collection PubMed
description Pyrido[2,3-d]pyrimidines (1) are a type of privileged heterocyclic scaffolds capable of providing ligands for several receptors in the body. Among such structures, our group and others have been particularly interested in pyrido[2,3-d]pyrimidine-7(8H)-ones (2) due to the similitude with nitrogen bases present in DNA and RNA. Currently there are more than 20,000 structures 2 described which correspond to around 2900 references (half of them being patents). Furthermore, the number of references containing compounds of general structure 2 have increased almost exponentially in the last 10 years. The present review covers the synthetic methods used for the synthesis of pyrido[2,3-d]pyrimidine-7(8H)-ones (2), both starting from a preformed pyrimidine ring or a pyridine ring, and the biomedical applications of such compounds.
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spelling pubmed-68916472019-12-12 Pyrido[2,3-d]pyrimidin-7(8H)-ones: Synthesis and Biomedical Applications Jubete, Guillem Puig de la Bellacasa, Raimon Estrada-Tejedor, Roger Teixidó, Jordi Borrell, José I. Molecules Review Pyrido[2,3-d]pyrimidines (1) are a type of privileged heterocyclic scaffolds capable of providing ligands for several receptors in the body. Among such structures, our group and others have been particularly interested in pyrido[2,3-d]pyrimidine-7(8H)-ones (2) due to the similitude with nitrogen bases present in DNA and RNA. Currently there are more than 20,000 structures 2 described which correspond to around 2900 references (half of them being patents). Furthermore, the number of references containing compounds of general structure 2 have increased almost exponentially in the last 10 years. The present review covers the synthetic methods used for the synthesis of pyrido[2,3-d]pyrimidine-7(8H)-ones (2), both starting from a preformed pyrimidine ring or a pyridine ring, and the biomedical applications of such compounds. MDPI 2019-11-16 /pmc/articles/PMC6891647/ /pubmed/31744155 http://dx.doi.org/10.3390/molecules24224161 Text en © 2019 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 Review
Jubete, Guillem
Puig de la Bellacasa, Raimon
Estrada-Tejedor, Roger
Teixidó, Jordi
Borrell, José I.
Pyrido[2,3-d]pyrimidin-7(8H)-ones: Synthesis and Biomedical Applications
title Pyrido[2,3-d]pyrimidin-7(8H)-ones: Synthesis and Biomedical Applications
title_full Pyrido[2,3-d]pyrimidin-7(8H)-ones: Synthesis and Biomedical Applications
title_fullStr Pyrido[2,3-d]pyrimidin-7(8H)-ones: Synthesis and Biomedical Applications
title_full_unstemmed Pyrido[2,3-d]pyrimidin-7(8H)-ones: Synthesis and Biomedical Applications
title_short Pyrido[2,3-d]pyrimidin-7(8H)-ones: Synthesis and Biomedical Applications
title_sort pyrido[2,3-d]pyrimidin-7(8h)-ones: synthesis and biomedical applications
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6891647/
https://www.ncbi.nlm.nih.gov/pubmed/31744155
http://dx.doi.org/10.3390/molecules24224161
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