Synthesis and anti-inflammatory activities of 1- O -acetylbritannilactone analogues-Reference-Cited by-同舟云学术

Synthesis and anti-inflammatory activities of 1- O -acetylbritannilactone analogues

Published:2017-03 Issue: Volume:19 Page:248-253
ISSN:1874-3900
Container-title:Phytochemistry Letters
language:en
Short-container-title:Phytochemistry Letters

Author:

Wei Xiao-Peng,Chen Yu-Fen,Zhu Hong,Wu Xiao-Ran,Yu Yang,Kong De-Xin,Duan Hong-Quan,Jin Mei-Hua,Qin Nan

Funder

National Natural Science Foundation of China (NSFC)

Tianjin Research Program of Applied Basic and Cutting-edge Technologies

Publisher

Elsevier BV

Subject

Plant Science,Agronomy and Crop Science,Biochemistry,Biotechnology

Reference13 articles.

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2. IVSE, isolated from Inula japonica, suppresses LPS-induced NO production via NF-κB and MAPK inactivation in RAW264.7 cells;Chen;Life Sci.,2015

3. Semisynthesis and in vitro cytotoxic evaluation of new analogues of 1-O-acetylbritannilactone, a sesquiterpene from Inula britannica;Dong;Eur. J. Med. Chem.,2014

4. Acetylbritannilactone suppresses growth via upregulation of krüppel-like transcription factor 4 expression in HT-29 colorectal cancer cells;Fang;Oncol. Rep.,2011

5. A new semisynthetic 1-O-acetyl-6-O-lauroylbritannilactone induces apoptosis of human laryngocarcinoma cells through p53-dependent pathway;Han;Toxicol. In Vitro,2016

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