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題名:大豆素衍生物的合成
書刊名:師大學報
作者:曾德煌許順吉
出版日期:1985
卷期:30
頁次:頁537-545
主題關鍵詞:大豆素合成衍生物
原始連結:連回原系統網址new window
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大豆素為葛根的主要藥效,其相關化合物亦多具藥理活性。本研究以-羥基或-甲氧基苯乙酸為起始物進行環化及烷化反應,合成個化合物(包括4個新化合物),發現取代基大小及羥基的存在似與若干藥理活性有關連
Daidzein is the most important active component in Pueraria root. Many com-pounds related to it are also found to have special biological activities. In order to find the relationship between the structure and the biological activities, daidzein, l, and its 6 derivatives, 2-7, have been synthesized from 4-hydroxy or 4-methoxyphenyl ethanoic acid via cyclization and alkylation reaction. The pharmacological test showed that the factor of the size of substituents and the presence of hydroxyl group on the benzene ring could not be ignored.
期刊論文
1.Miura, K.、Takeda, R.、Nakamoto, H.、Saito, H.(1971)。The chemical and pharmacological study of Puerariae radix (Pueraria hirsuta Matsumura)。Oyo Yakuri,5,247-254。  new window
2.Shibata, S.、Murakami, T.、Nishikawa, Y.、Harada, M.(1959)。The Constituents of Pueraria Root。Chemical and Pharmaceutical Bulletin,7。  new window
3.Kagal, S. A.、Madhavan Nair, P.、Venkataraman, K.(1962)。A synthesis of isoflavones by a modified vilsmeier-haack reaction。Tetrahedron Letters,3(14),593-597。  new window
4.Shibata, S.、Harada, M.、Murakami, T.(1959)。Studies on the Constituents of Japanese and Chinese Crude Drugs. II: Antispasmodic Action of the Constituents of Pueraria Root。Yakugaku Zasshi,79,863-866。  new window
5.Dorofeenko, G. N.、Shinkarenko, A. L.、Lisevitskaia, L. I.、Mezheritskiĭ, V. V.、Kazakov, A. L.(1975)。Effect of isoflavones on lipid metabolism in experimental hypercholesterinemia。Biologicheskie nauki,18(3),35-38。  new window
6.Ravisé, A.、Kirkiacharian, B. S.(1976)。Influence de la structure de composés phénoliques sur l'inhibition du Phytophthora parasitica et d'enzymes participant aux processus parasitaires I. Isoflavonoïdes et coumestanes。Phytopathol. Z.,85,74-85。  new window
7.Farkas, L.、Várady, J.(1959)。A Soja hispida flavonoidjai。Magyar Kémiai Folyóirat,65,94-96。  new window
圖書
1.Pelter, S.(1975)。Synthesis。  new window
2.Miura, K.、Takeda, R.、Nakamoto, H.、Saito, H.(1972)。Chemical Abstracts。  new window
3.Ravisé, A.、Kirkiacharian, B. S.(1976)。Chemical Abstracts。  new window
4.Ravise, A.、Khatib, A. E.、Kiriacharia, B. S.(1976)。Poljor. Znan. Smotra。  new window
5.Ravise, A.、Khatib, A. E.、Kiriacharia, B. S.(1977)。Chemical Abstracts。  new window
6.Palamarchuk, A. S.、Bundarenko, V. E.(1976)。Kastit. Resur.。  new window
7.Palamarchuk, A. S.、Bundarenko, V. E.(1976)。Chemical Abstracts。  new window
8.Farkas, L.、Várady, J.(1960)。Chemical Abstracts。  new window
9.Allen, C. F. H.、Barker, W. E.(1955)。Organic Synthesis Col.。New York:John Wley & Sons Inc。  new window
10.Vasilenko, Y. K.、Durofeenko, G. N.、Kazakov, A. L.、Lisevitskaya, L. I.、Lenoteva, T. P.、Shinkarenko, V. V.(1979)。Chemical Abstracts。  new window
11.Vasilenko, Y. K.、Durofeenko, G. N.、Kazakov, A. L.、Lisevitskaya, L. I.、Lenoteva, T. P.、Shinkarenko, V. V.(1978)。Izv. Sev. Kavk. Nauchr. Tsentra Vyssh. Skh. Estestv. Nauki。  new window
 
 
 
 
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