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Triterpenoids from Ainsliaea yunnanensis Franch. and their biological activities    

文献类型:期刊文献

英文题名:Triterpenoids from Ainsliaea yunnanensis Franch. and their biological activities

作者:Li, Jinjie[1,2];Zhang, Bo[3];Liu, Hailing[4];Zhang, Xuan[5];Shang, Xiaoya[6];Zhao, Changqi[7]

第一作者:李金杰;Li, Jinjie

机构:[1]Key Laboratory of Cell Proliferation and Regulation Biology, Ministry of Education, College of Life Science, Beijing Normal University, Beijing, 100875, China;[2]Beijing Key Laboratory of Bioactive Substances and Functional Foods, Beijing Union University, Beijing, 100191, China

第一机构:Key Laboratory of Cell Proliferation and Regulation Biology, Ministry of Education, College of Life Science, Beijing Normal University, Beijing, 100875, China

通讯机构:[2]Beijing Key Laboratory of Bioactive Substances and Functional Foods, Beijing Union University, Beijing, 100191, China|[1141726]北京联合大学生物化学工程学院;[11417]北京联合大学;[114172]北京联合大学应用文理学院;

年份:2016

卷号:21

期号:11

外文期刊名:Molecules

收录:MEDLINE(收录号:27827998);;Scopus(收录号:2-s2.0-84997605075);PubMed

语种:英文

外文关键词:Activity; Ainsliaea yunnanensis; NMR; Structures; Triterpenoids

摘要:One new pentacyclic triterpenoid, 3β-carboxylicfilic-4(23)-ene (1), and three known pentacyclic triterpenoids, adian-5-en-3α-ol (2), fernenol (3), and fern-7-en-3β-ol (4) were isolated from the petroleum ether phase of the ethanolic extract of Ainsliaea yunnanensis Franch. Their structures were established by spectroscopic methods including 1-D and 2-D NMR, and MS experiments. Compounds 1, 2, 3, and 4 showed significant selective cytotoxicity against human acute monocytic leukemia cell line (THP-1) with IC50 values of 5.12 μM, 1.78 μM, 1.74 μM, and 1.75 μM, respectively. Compound 1 also showed an anti-inflammatory effect through the inhibition of the activity of NF-κB by blocking the nuclear translocation of p65. ? 2016 by the authors; licensee MDPI.

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