{"title":"来自褐藻马尾藻的具有细胞毒性的双环二萜。","authors":"S E Ayyad, M O Slama, A H MoKhtar, A F Anter","doi":"","DOIUrl":null,"url":null,"abstract":"<p><p>Study of the brown alga Sargassum crispum collected from Red Sea resulted in the isolation of new diterpene with hydroazulene skeleton, Sargassinone (6), some fatty acids ethyl ester andsome fatty acids. The identification of the isolated metabolites was established mainly by spectral methods and chemical transformation of sargassinone (6) to its acetate (7). The two diterpens (6, 7) exhibited substantial cytotoxic activities, as indicated by their IC50 values at the dose of 10 micrograms/ml or less.</p>","PeriodicalId":502097,"journal":{"name":"Bollettino chimico farmaceutico","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2001-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Cytotoxic bicyclic diterpene from the brown alga Sargassum crispum.\",\"authors\":\"S E Ayyad, M O Slama, A H MoKhtar, A F Anter\",\"doi\":\"\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Study of the brown alga Sargassum crispum collected from Red Sea resulted in the isolation of new diterpene with hydroazulene skeleton, Sargassinone (6), some fatty acids ethyl ester andsome fatty acids. The identification of the isolated metabolites was established mainly by spectral methods and chemical transformation of sargassinone (6) to its acetate (7). The two diterpens (6, 7) exhibited substantial cytotoxic activities, as indicated by their IC50 values at the dose of 10 micrograms/ml or less.</p>\",\"PeriodicalId\":502097,\"journal\":{\"name\":\"Bollettino chimico farmaceutico\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2001-05-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Bollettino chimico farmaceutico\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Bollettino chimico farmaceutico","FirstCategoryId":"1085","ListUrlMain":"","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Cytotoxic bicyclic diterpene from the brown alga Sargassum crispum.
Study of the brown alga Sargassum crispum collected from Red Sea resulted in the isolation of new diterpene with hydroazulene skeleton, Sargassinone (6), some fatty acids ethyl ester andsome fatty acids. The identification of the isolated metabolites was established mainly by spectral methods and chemical transformation of sargassinone (6) to its acetate (7). The two diterpens (6, 7) exhibited substantial cytotoxic activities, as indicated by their IC50 values at the dose of 10 micrograms/ml or less.
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