Search for Anticancer Drugs of Taxol Analogue
Search for Anticancer Drugs of Taxol Analogue
批准号:
06558092
负责人:
FUJI Kaoru
金额:
$6.66万
依托单位:
依托单位国家:
日本
项目类别:
Grant-in-Aid for Developmental Scientific Research (B)
财政年份:
1994
资助国家:
日本
项目状态:
已结题
起止时间:
1994 至 1995
中文摘要
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英文摘要
Taxol, a highly functional diterpene isolated in 1971 from the Pacific yew tree, Taxus brevifolia (Taxaceae), is currently considered the most exciting lead in cancer chemotherapy, hence called as the anticancer drug of '90s. Some aspects of taxoids, such as their promising antitumor activity, unique structural features, novel mode of action and unusual biogenesis, stimulated the search for new related diterpenoids having similar activity from the widely distributed species of the family Taxaceae as well as natural products. In this project, three Taxaceaes which grow at Yunnan in China, Taxus chinensis, Taxus Yunnansis and Taxus chinensis var. mairei, were chosen as a plant source for a lead compound. From these plants, more than twenty new diterpenes have been isolated in a pure form together with sixteen known taxoids including taxol and 10-deacetyl baccatin III.Among the new diterpenoids, the structures of totally sixteen compounds could be elucidated, in which twelve diterpenoids … More possesses novel 5/7/6/carbon framework and the four an ordinary taxoid skeleton. For structural determination, some 2D NMR techniques, such as Long Range ^<13>C-^1H COSY,ROESY,NOESY,were found to be extremely effective. The final proof on the structures of some new diterpenoids was afforded by X-ray crystallographic analyzes. Particular interest is that the diterpenoids of the former exist as a mixture of conformational isomers in a solution at an ambient temperature. The ratio depends upon the substitution pattern on the B and C ring. Unfortunately, no significant inhibitory activity of the new diterpenoids isolated against tublin depolymerization has been recognized so far. Introduction of the phenyl isoserine moiety, which is known as an essential structural unit for antitumor activity in taxol, into C13 position of the newly isolated 5/7/6 compounds as well as the synthesis of artificially designed compounds based on conformational analysis of active compounds and computationary chemistry, are currently in progress. Less
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K.FUJI,K.TANAKA,B.LI,T.SHINGU,T.YOKOI,H.SUN,T.TAGA: "Structures of Nine New Diterpenoids from Taxus Chinensis" Tetrahedron. 51(37). 10175-10188 (1995)
K.FUJI,K.TANAKA,B.LI,T.Shingu,T.YOKOI,H.SUN,T.TAGA:“红豆杉九种新二萜的结构”四面体。
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通讯作者:
冨士薫,田中圭, 他: "On the Structures of Six New Diterpenoids,Taxchinin E,H,I,J,K and Taxchin B" Chemical & Pharmaceutical Bulletin. 42. 1539-1541 (1994)
Kaoru Fuji、Kei Tanaka 等人:“关于六种新二萜类化合物、Taxchinin E、H、I、J、K 和 Taxchinin B 的结构”《化学与制药公报》42. 1539-1541 (1994)。
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冨士 薫、田中 圭、他: "Structures of Taxchinins L and M, Two New Diterpenoids from Taxus Chinensis var. mairei" Chemical and Pharmaceutical Bulletin. 44(発表予定). (1996)
Kaoru Fuji、Kei Tanaka 等人:“Taxchinins L 和 M 的结构,Taxus Chinensis var. mairei 中的两种新二萜”,《化学与制药通报》44(待出版)。
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通讯作者:
冨士 薫、田中 圭、他: "Structures of Nine New Diterpenoids from Taxus Chinensis" Tetrahedron. 51. 10175-10188 (1995)
Kaoru Fuji、Kei Tanaka 等人:“红豆杉中九种新二萜的结构”四面体 51。10175-10188 (1995)
DOI:
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发表时间:
期刊:
影响因子:
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作者:
[]
通讯作者:
冨士 薫、田中 圭、他: "Structures of Nine New Diterpenoids from Taxus Chinensis" Tetrahedron. 51(37). 10175-10188 (1995)
Kaoru Fuji、Kei Tanaka 等人:“红豆杉中的九种新二萜的结构”Tetrahedron 51(37) (1995)。
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共 8 条
Construction of Asymmetric Field Utilizing Atropisomers
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批准号:10470467
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项目类别:Grant-in-Aid for Scientific Research (B).
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资助金额:$7.81万
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负责人:FUJI Kaoru
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依托单位:
Creation of Novel Axially-Chiral Compounds : Developments toward Asymmetric Synthesis
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负责人:FUJI Kaoru
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Basic Studies and Synthetic Application of Enzyme Functions
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财政年份:1991
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负责人:FUJI Kaoru
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依托单位:
Construction of Chiral Building Blocks through Enantioselective Protonation
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批准号:63430024
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项目类别:Grant-in-Aid for General Scientific Research (A)
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资助金额:$1.98万
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财政年份:1988
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负责人:FUJI Kaoru
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依托单位:
国内基金
海外基金
Taxol抗UUO模型肾间质纤维化的机制研究
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批准号:81100507
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项目类别:青年科学基金项目
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资助金额:23.0万元
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批准年份:2011
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负责人:张东山
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依托单位: