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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...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2018
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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. |
format | Online Article Text |
id | pubmed-6321231 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
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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