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Synthesis and Anti-Inflammatory Activities of Phloroglucinol-Based Derivatives

The natural product phloroglucinol-based derivatives representing monoacyl-, diacyl-, dimeric acyl-, alkylated monoacyl-, and the nitrogen-containing alkylated monoacylphloro- glucinols were synthesized and evaluated for inhibitory activities against the inflammatory mediators such as inducible nitr...

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Detalles Bibliográficos
Autores principales: Li, Ning, Khan, Shabana I., Qiu, Shi, Li, Xing-Cong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6321231/
https://www.ncbi.nlm.nih.gov/pubmed/30544542
http://dx.doi.org/10.3390/molecules23123232
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author Li, Ning
Khan, Shabana I.
Qiu, Shi
Li, Xing-Cong
author_facet Li, Ning
Khan, Shabana I.
Qiu, Shi
Li, Xing-Cong
author_sort Li, Ning
collection PubMed
description The natural product phloroglucinol-based derivatives representing monoacyl-, diacyl-, dimeric acyl-, alkylated monoacyl-, and the nitrogen-containing alkylated monoacylphloro- glucinols were synthesized and evaluated for inhibitory activities against the inflammatory mediators such as inducible nitric oxide synthase (iNOS) and nuclear factor kappaB (NF-κB). The diacylphloroglucinol compound 2 and the alkylated acylphloroglucinol compound 4 inhibited iNOS with IC(50) values of 19.0 and 19.5 µM, respectively, and NF-κB with IC(50) values of 34.0 and 37.5 µM, respectively. These compounds may serve as leads for the synthesis of more potent anti-inflammatory compounds for future drug discovery.
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spelling pubmed-63212312019-01-14 Synthesis and Anti-Inflammatory Activities of Phloroglucinol-Based Derivatives Li, Ning Khan, Shabana I. Qiu, Shi Li, Xing-Cong Molecules Article The natural product phloroglucinol-based derivatives representing monoacyl-, diacyl-, dimeric acyl-, alkylated monoacyl-, and the nitrogen-containing alkylated monoacylphloro- glucinols were synthesized and evaluated for inhibitory activities against the inflammatory mediators such as inducible nitric oxide synthase (iNOS) and nuclear factor kappaB (NF-κB). The diacylphloroglucinol compound 2 and the alkylated acylphloroglucinol compound 4 inhibited iNOS with IC(50) values of 19.0 and 19.5 µM, respectively, and NF-κB with IC(50) values of 34.0 and 37.5 µM, respectively. These compounds may serve as leads for the synthesis of more potent anti-inflammatory compounds for future drug discovery. MDPI 2018-12-07 /pmc/articles/PMC6321231/ /pubmed/30544542 http://dx.doi.org/10.3390/molecules23123232 Text en © 2018 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 Article
Li, Ning
Khan, Shabana I.
Qiu, Shi
Li, Xing-Cong
Synthesis and Anti-Inflammatory Activities of Phloroglucinol-Based Derivatives
title Synthesis and Anti-Inflammatory Activities of Phloroglucinol-Based Derivatives
title_full Synthesis and Anti-Inflammatory Activities of Phloroglucinol-Based Derivatives
title_fullStr Synthesis and Anti-Inflammatory Activities of Phloroglucinol-Based Derivatives
title_full_unstemmed Synthesis and Anti-Inflammatory Activities of Phloroglucinol-Based Derivatives
title_short Synthesis and Anti-Inflammatory Activities of Phloroglucinol-Based Derivatives
title_sort synthesis and anti-inflammatory activities of phloroglucinol-based derivatives
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6321231/
https://www.ncbi.nlm.nih.gov/pubmed/30544542
http://dx.doi.org/10.3390/molecules23123232
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