A. Dawidar, M. Abou-Elzahab, M. Berghot, K. H. AI-Maah
{"title":"β-谷甾醇和豆甾醇的光氧化作用及其过氧化氢产物的dna损伤特性","authors":"A. Dawidar, M. Abou-Elzahab, M. Berghot, K. H. AI-Maah","doi":"10.7019/CPJ.200212.0471","DOIUrl":null,"url":null,"abstract":"The phytosterol β-sitosterol (1), its acetate derivative (3) and stigmasterol (2) were photo-oxygenated using tetraphenyl porphorin (TPP) or rose Bengal (RB) and sensitizer in different solvents to give hydroperoxides 4,8 and dihydroperoxide 7, respectively. Structures 4,8 and 7 were elucidated on the basis of spectral data from their 1H NMR, MS and IR spectra. Product 7 produced moderate DNA degradation, but 4 did not.","PeriodicalId":22409,"journal":{"name":"The Chinese Pharmaceutical Journal","volume":"34 1","pages":"471-476"},"PeriodicalIF":0.0000,"publicationDate":"2002-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":"{\"title\":\"Photooxygenation of β-sitosterol and stigmasterol and DNA-damaging properties of their hydroperoxide products\",\"authors\":\"A. Dawidar, M. Abou-Elzahab, M. Berghot, K. H. AI-Maah\",\"doi\":\"10.7019/CPJ.200212.0471\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"The phytosterol β-sitosterol (1), its acetate derivative (3) and stigmasterol (2) were photo-oxygenated using tetraphenyl porphorin (TPP) or rose Bengal (RB) and sensitizer in different solvents to give hydroperoxides 4,8 and dihydroperoxide 7, respectively. Structures 4,8 and 7 were elucidated on the basis of spectral data from their 1H NMR, MS and IR spectra. Product 7 produced moderate DNA degradation, but 4 did not.\",\"PeriodicalId\":22409,\"journal\":{\"name\":\"The Chinese Pharmaceutical Journal\",\"volume\":\"34 1\",\"pages\":\"471-476\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2002-12-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"1\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"The Chinese Pharmaceutical Journal\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.7019/CPJ.200212.0471\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"The Chinese Pharmaceutical Journal","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.7019/CPJ.200212.0471","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Photooxygenation of β-sitosterol and stigmasterol and DNA-damaging properties of their hydroperoxide products
The phytosterol β-sitosterol (1), its acetate derivative (3) and stigmasterol (2) were photo-oxygenated using tetraphenyl porphorin (TPP) or rose Bengal (RB) and sensitizer in different solvents to give hydroperoxides 4,8 and dihydroperoxide 7, respectively. Structures 4,8 and 7 were elucidated on the basis of spectral data from their 1H NMR, MS and IR spectra. Product 7 produced moderate DNA degradation, but 4 did not.