Identification of benzisoquinolinone derivatives with cytotoxicities from the leaves of Portulaca oleracea

Author:

Wei Rong-Rui1,Ma Qin-Ge2,Zhong Guo-Yue1,Yang Ming2,Sang Zhi-Pei3

Affiliation:

1. State Key Laboratory of Innovative Drugs and High Efficiency Energy Saving and Consumption Reduction Pharmaceutical Equipment, Research Center of Natural Resources of Chinese Medicinal Materials and Ethnic Medicine , Jiangxi University of Traditional Chinese Medicine , Nanchang 330004 , China

2. State Key Laboratory of Innovative Drugs and High Efficiency Energy Saving and Consumption Reduction Pharmaceutical Equipment, Key Laboratory of Modern Preparation of TCM of Ministry of Education , Jiangxi University of Traditional Chinese Medicine , Nanchang 330004 , China

3. College of Chemistry and Pharmaceutical Engineering , Nanyang Normal University , Nanyang 473061 , China

Abstract

Abstract Three new benzisoquinolinones (1–3), together with seven known benzisoquinolinone derivatives (4–10), were isolated from Portulaca oleracea for the first time. The structures of the isolated compounds (1–10) had been elucidated on the basis of extensive spectroscopic methods including ultraviolet, infrared, mass spectrometry, and nuclear magnetic resonance techniques and by comparison with data reported in the references. All isolated compounds were assayed for cytotoxicities against selected human lines in vitro by 3-(4,5-dimethyl-2-thiazolyl)-2,5-diphenyl-2-H-tetrazolium bromide assay. Compounds 1, 2, 4, and 7 showed important cytotoxicities against HCT116, MCF-7, U87, and A549 cell lines with IC50 values in the range of 11.62–84.45 μM, which compared with positive control doxorubicin.

Funder

National Natural Science Foundation of China

Publisher

Walter de Gruyter GmbH

Subject

General Biochemistry, Genetics and Molecular Biology

Reference27 articles.

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