Cargando…

Synthesis and Biological Evaluation of Novel Curcuminoid Derivatives

Curcuminoids have been reported to possess multiple bioactivities, such as antioxidant, anticancer and anti-inflammatory properties. Three novel series of curcuminoid derivatives (11a–h, 15a–h and 19a–d) with enhanced bioactivity have been synthesized. Among the synthesized compounds, 11b exhibited...

Descripción completa

Detalles Bibliográficos
Autores principales: Cao, Ya-Kun, Li, Hui-Jing, Song, Zhi-Fang, Li, Yang, Huai, Qi-Yong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6271059/
https://www.ncbi.nlm.nih.gov/pubmed/25314599
http://dx.doi.org/10.3390/molecules191016349
_version_ 1783376841436823552
author Cao, Ya-Kun
Li, Hui-Jing
Song, Zhi-Fang
Li, Yang
Huai, Qi-Yong
author_facet Cao, Ya-Kun
Li, Hui-Jing
Song, Zhi-Fang
Li, Yang
Huai, Qi-Yong
author_sort Cao, Ya-Kun
collection PubMed
description Curcuminoids have been reported to possess multiple bioactivities, such as antioxidant, anticancer and anti-inflammatory properties. Three novel series of curcuminoid derivatives (11a–h, 15a–h and 19a–d) with enhanced bioactivity have been synthesized. Among the synthesized compounds, 11b exhibited the most significant activity with an MIC of 0.5 µM /mL against selected medically important Gram-positive cocci (S. aureus and S. viridans) and Gram-negative bacilli (E. coli and E. cloacae). The derivatives exhibited remarkable results in an antioxidant test with an IC(50) 2.4- to 9.3-folder smaller than curcuminoids. With respect to antiproliferative activity against Hep-G2, LX-2, SMMC7221 and MDA-MB-231, the derivatives exhibited an effect stronger than curcuminoids with an IC(50) ranging from 0.18 to 4.25 µM.
format Online
Article
Text
id pubmed-6271059
institution National Center for Biotechnology Information
language English
publishDate 2014
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-62710592018-12-27 Synthesis and Biological Evaluation of Novel Curcuminoid Derivatives Cao, Ya-Kun Li, Hui-Jing Song, Zhi-Fang Li, Yang Huai, Qi-Yong Molecules Article Curcuminoids have been reported to possess multiple bioactivities, such as antioxidant, anticancer and anti-inflammatory properties. Three novel series of curcuminoid derivatives (11a–h, 15a–h and 19a–d) with enhanced bioactivity have been synthesized. Among the synthesized compounds, 11b exhibited the most significant activity with an MIC of 0.5 µM /mL against selected medically important Gram-positive cocci (S. aureus and S. viridans) and Gram-negative bacilli (E. coli and E. cloacae). The derivatives exhibited remarkable results in an antioxidant test with an IC(50) 2.4- to 9.3-folder smaller than curcuminoids. With respect to antiproliferative activity against Hep-G2, LX-2, SMMC7221 and MDA-MB-231, the derivatives exhibited an effect stronger than curcuminoids with an IC(50) ranging from 0.18 to 4.25 µM. MDPI 2014-10-13 /pmc/articles/PMC6271059/ /pubmed/25314599 http://dx.doi.org/10.3390/molecules191016349 Text en © 2014 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 license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Cao, Ya-Kun
Li, Hui-Jing
Song, Zhi-Fang
Li, Yang
Huai, Qi-Yong
Synthesis and Biological Evaluation of Novel Curcuminoid Derivatives
title Synthesis and Biological Evaluation of Novel Curcuminoid Derivatives
title_full Synthesis and Biological Evaluation of Novel Curcuminoid Derivatives
title_fullStr Synthesis and Biological Evaluation of Novel Curcuminoid Derivatives
title_full_unstemmed Synthesis and Biological Evaluation of Novel Curcuminoid Derivatives
title_short Synthesis and Biological Evaluation of Novel Curcuminoid Derivatives
title_sort synthesis and biological evaluation of novel curcuminoid derivatives
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6271059/
https://www.ncbi.nlm.nih.gov/pubmed/25314599
http://dx.doi.org/10.3390/molecules191016349
work_keys_str_mv AT caoyakun synthesisandbiologicalevaluationofnovelcurcuminoidderivatives
AT lihuijing synthesisandbiologicalevaluationofnovelcurcuminoidderivatives
AT songzhifang synthesisandbiologicalevaluationofnovelcurcuminoidderivatives
AT liyang synthesisandbiologicalevaluationofnovelcurcuminoidderivatives
AT huaiqiyong synthesisandbiologicalevaluationofnovelcurcuminoidderivatives