Cargando…

Synthesis of Scutellarein Derivatives with a Long Aliphatic Chain and Their Biological Evaluation against Human Cancer Cells

Scutellarin is the major active flavonoid extracted from the traditional Chinese herbal medicine Erigeron breviscapus (Vant.) Hand-Mazz., which is widely used in China. Recently, accumulating evidence has highlighted the potential role of scutellarin and its main metabolite scutellarein in the treat...

Descripción completa

Detalles Bibliográficos
Autores principales: Ni, Guanghui, Tang, Yanling, Li, Minxin, He, Yuefeng, Rao, Gaoxiong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6017256/
https://www.ncbi.nlm.nih.gov/pubmed/29389889
http://dx.doi.org/10.3390/molecules23020310
_version_ 1783334707541311488
author Ni, Guanghui
Tang, Yanling
Li, Minxin
He, Yuefeng
Rao, Gaoxiong
author_facet Ni, Guanghui
Tang, Yanling
Li, Minxin
He, Yuefeng
Rao, Gaoxiong
author_sort Ni, Guanghui
collection PubMed
description Scutellarin is the major active flavonoid extracted from the traditional Chinese herbal medicine Erigeron breviscapus (Vant.) Hand-Mazz., which is widely used in China. Recently, accumulating evidence has highlighted the potential role of scutellarin and its main metabolite scutellarein in the treatment of cancer. To explore novel anticancer agents with high efficiency, a series of new scutellarein derivatives with a long aliphatic chain were synthesized, and the antiproliferative activities against Jurkat, HCT-116 and MDA-MB-231 cancer cell lines were assessed. Among them, compound 6a exhibited the strongest antiproliferative effects on Jurkat (IC(50) = 1.80 μM), HCT-116 (IC(50) = 11.50 μM) and MDA-MB-231 (IC(50) = 53.91 μM). In particular, 6a even showed stronger antiproliferative effects than the positive control NaAsO(2) on Jurkat and HCT-116 cell lines. The results showed that a proper long aliphatic chain enhanced the antiproliferative activity of scutellarein.
format Online
Article
Text
id pubmed-6017256
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-60172562018-11-13 Synthesis of Scutellarein Derivatives with a Long Aliphatic Chain and Their Biological Evaluation against Human Cancer Cells Ni, Guanghui Tang, Yanling Li, Minxin He, Yuefeng Rao, Gaoxiong Molecules Article Scutellarin is the major active flavonoid extracted from the traditional Chinese herbal medicine Erigeron breviscapus (Vant.) Hand-Mazz., which is widely used in China. Recently, accumulating evidence has highlighted the potential role of scutellarin and its main metabolite scutellarein in the treatment of cancer. To explore novel anticancer agents with high efficiency, a series of new scutellarein derivatives with a long aliphatic chain were synthesized, and the antiproliferative activities against Jurkat, HCT-116 and MDA-MB-231 cancer cell lines were assessed. Among them, compound 6a exhibited the strongest antiproliferative effects on Jurkat (IC(50) = 1.80 μM), HCT-116 (IC(50) = 11.50 μM) and MDA-MB-231 (IC(50) = 53.91 μM). In particular, 6a even showed stronger antiproliferative effects than the positive control NaAsO(2) on Jurkat and HCT-116 cell lines. The results showed that a proper long aliphatic chain enhanced the antiproliferative activity of scutellarein. MDPI 2018-02-01 /pmc/articles/PMC6017256/ /pubmed/29389889 http://dx.doi.org/10.3390/molecules23020310 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
Ni, Guanghui
Tang, Yanling
Li, Minxin
He, Yuefeng
Rao, Gaoxiong
Synthesis of Scutellarein Derivatives with a Long Aliphatic Chain and Their Biological Evaluation against Human Cancer Cells
title Synthesis of Scutellarein Derivatives with a Long Aliphatic Chain and Their Biological Evaluation against Human Cancer Cells
title_full Synthesis of Scutellarein Derivatives with a Long Aliphatic Chain and Their Biological Evaluation against Human Cancer Cells
title_fullStr Synthesis of Scutellarein Derivatives with a Long Aliphatic Chain and Their Biological Evaluation against Human Cancer Cells
title_full_unstemmed Synthesis of Scutellarein Derivatives with a Long Aliphatic Chain and Their Biological Evaluation against Human Cancer Cells
title_short Synthesis of Scutellarein Derivatives with a Long Aliphatic Chain and Their Biological Evaluation against Human Cancer Cells
title_sort synthesis of scutellarein derivatives with a long aliphatic chain and their biological evaluation against human cancer cells
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6017256/
https://www.ncbi.nlm.nih.gov/pubmed/29389889
http://dx.doi.org/10.3390/molecules23020310
work_keys_str_mv AT niguanghui synthesisofscutellareinderivativeswithalongaliphaticchainandtheirbiologicalevaluationagainsthumancancercells
AT tangyanling synthesisofscutellareinderivativeswithalongaliphaticchainandtheirbiologicalevaluationagainsthumancancercells
AT liminxin synthesisofscutellareinderivativeswithalongaliphaticchainandtheirbiologicalevaluationagainsthumancancercells
AT heyuefeng synthesisofscutellareinderivativeswithalongaliphaticchainandtheirbiologicalevaluationagainsthumancancercells
AT raogaoxiong synthesisofscutellareinderivativeswithalongaliphaticchainandtheirbiologicalevaluationagainsthumancancercells