中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
In vitro antitumor activity and synthesis of the key intermediate of bakuchiol

文献类型:期刊论文

作者CHEN Hong-li; FENG Hui-jin; LI Yuan-chao
刊名Acta Pharmaceutica Sinica
出版日期2010
卷号45期号:4页码:467-470
关键词bakuchiol antitumor activity Ireland-Claisen rearrangement synthesis
ISSN号0513-4870
其他题名补骨脂酚的体外抗肿瘤活性及其关键中间体的合成研究
文献子类Article
英文摘要The in vitro antitumor activity of bakuchiol was exploited.compared with tamoxifen.The result of biological activities showed that bakuchiol could inhibit human breast cancer and the IC_(50) values were 2.89*10~(-5)mol·L~(-1)and 8.29*10~(-3) mol·L~(-1) against the cells line T-47D and MDA-MB-231 respectively. On the other hand.the key intermediate to synthesize bakuchiol was obtained by the method of Ireland-Claisen rearrangement.Comparing with traditional Claisen rearrangement,the reaction conditions are milder and the reaction reagents are safer.
WOS研究方向Pharmacology & Pharmacy (provided by Clarivate Analytics)
语种中文
CSCD记录号CSCD:3863665
源URL[http://119.78.100.183/handle/2S10ELR8/267965]  
专题中国科学院上海药物研究所
作者单位Shanghai lnstitute of Materia Medica,Chinese Academy of Sciences, Shanghai 201203, China.
推荐引用方式
GB/T 7714
CHEN Hong-li,FENG Hui-jin,LI Yuan-chao. In vitro antitumor activity and synthesis of the key intermediate of bakuchiol[J]. Acta Pharmaceutica Sinica,2010,45(4):467-470.
APA CHEN Hong-li,FENG Hui-jin,&LI Yuan-chao.(2010).In vitro antitumor activity and synthesis of the key intermediate of bakuchiol.Acta Pharmaceutica Sinica,45(4),467-470.
MLA CHEN Hong-li,et al."In vitro antitumor activity and synthesis of the key intermediate of bakuchiol".Acta Pharmaceutica Sinica 45.4(2010):467-470.

入库方式: OAI收割

来源:上海药物研究所

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