中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Semisynthesis and antitumor activities of new styryl-lactone derivatives

文献类型:期刊论文

作者Zhou, FS; Tang, WD; Mu, Q; Yang, GX; Wang, Y; Liang, GL; Lou, LG
刊名CHEMICAL & PHARMACEUTICAL BULLETIN
出版日期2005-11
卷号53期号:11页码:1387-1391
关键词styryl-lactone semisynthesis goniothalamin antitumor activity
ISSN号0009-2363
DOI10.1248/cpb.53.1387
文献子类Article
英文摘要Nineteen new derivatives (2-20) of the naturally occurring compound, goniothalamin (1), were prepared by chemical modification and semi-synthetic methods. The antitumor activities of these derivatives and goniothalamin were evaluated in vitro against human tumor cell lines, and most of them showed an inhibitory effect against HL-60 cancer cells. The derivatives 10-nitro-goniothalamin (2) and 10-amino-goniothalamin (4) gave selective inhibition concentration (IC50) of 1.10 and 1.14 mu g/ml, respectively, against human stomach cancer SGC-7901 cells, while that of etoposide (vp-16) as the positive control was 6.07 mu g/ml. Finally, the partition coefficients, logP (pi values), of these derivative molecules, were evaluated by calculating the additive approximate organic fragment logP value.
WOS关键词GONIOTHALAMIN ; ANNONACEAE
WOS研究方向Pharmacology & Pharmacy ; Chemistry
语种英语
WOS记录号WOS:000233350600002
出版者PHARMACEUTICAL SOC JAPAN
源URL[http://119.78.100.183/handle/2S10ELR8/273779]  
专题中国科学院上海药物研究所
通讯作者Mu, Q
作者单位1.Fudan Univ, Sch Pharm, Shanghai 200032, Peoples R China
2.Shanghai Inst Mat Med, Shanghai Inst Biol Sci, Shanghai 200032, Peoples R China
推荐引用方式
GB/T 7714
Zhou, FS,Tang, WD,Mu, Q,et al. Semisynthesis and antitumor activities of new styryl-lactone derivatives[J]. CHEMICAL & PHARMACEUTICAL BULLETIN,2005,53(11):1387-1391.
APA Zhou, FS.,Tang, WD.,Mu, Q.,Yang, GX.,Wang, Y.,...&Lou, LG.(2005).Semisynthesis and antitumor activities of new styryl-lactone derivatives.CHEMICAL & PHARMACEUTICAL BULLETIN,53(11),1387-1391.
MLA Zhou, FS,et al."Semisynthesis and antitumor activities of new styryl-lactone derivatives".CHEMICAL & PHARMACEUTICAL BULLETIN 53.11(2005):1387-1391.

入库方式: OAI收割

来源:上海药物研究所

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