Dang Dinh Kim, Vu Thi Nguyet, Ha Xuan Anh, N. Trang, Nguyen Hong Chuyen, L. Huong, Tran Thị Hong Ha, D. H. Ho, N. Dat
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{"title":"黑藤叶的细胞毒性酚类成分","authors":"Dang Dinh Kim, Vu Thi Nguyet, Ha Xuan Anh, N. Trang, Nguyen Hong Chuyen, L. Huong, Tran Thị Hong Ha, D. H. Ho, N. Dat","doi":"10.3329/bjp.v14i4.42414","DOIUrl":null,"url":null,"abstract":"Compound 1: 4-hydroxy-3-[4-(2-hydroxyethyl)-phenoxy]-benzaldehyde HR-ESI-MS: m/z 259.0975 [M+H]+ (calcld. 259.0970 for C15H15O4). 1H-NMR (500 MHz, CD3OD): δH 9.71 (1H, s, H-7), 7.34 (1H, dd, J = 8.0, 2.0 Hz, H-6), 7.32 (1H, d, J = 2.0 Hz, H-2), 7.15 (2H, d, J = 8.0 Hz, H-3′, 5′), 7.04 (1H, d, J = 8.0 Hz, H-5), 6.84 (2H, d, J = 8.0 Hz, H-2′, 6′), 3.71 (2H, t, J = 7.0 Hz, H-8′), 2.73 (2H, t, J = 7.0 Hz, H-7′). 13C-NMR (125 MHz. CD3OD): δC 131.1 (C, C-1), 118.3 (CH, C-2), 147.2 (C, C-3), 151.8 (C, C-4), 116.1 (CH, C5), 128.8 (CH, C-6), 158.5 (C, C-1′), 119.5 (CH, C-2′, 6′), 131.0 (CH, C-3′, 5′), 133.7 (C, C4′), 193.1 (CH, C-7), 39.4 (CH2, C-7′), 64.0 (CH2, C-8′).","PeriodicalId":8719,"journal":{"name":"Bangladesh Journal of Pharmacology","volume":"14 1","pages":"196-197"},"PeriodicalIF":0.9000,"publicationDate":"2019-12-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.3329/bjp.v14i4.42414","citationCount":"2","resultStr":"{\"title\":\"Cytotoxic phenolic constituents from the leaves of Ehretia asperula\",\"authors\":\"Dang Dinh Kim, Vu Thi Nguyet, Ha Xuan Anh, N. Trang, Nguyen Hong Chuyen, L. Huong, Tran Thị Hong Ha, D. H. Ho, N. Dat\",\"doi\":\"10.3329/bjp.v14i4.42414\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Compound 1: 4-hydroxy-3-[4-(2-hydroxyethyl)-phenoxy]-benzaldehyde HR-ESI-MS: m/z 259.0975 [M+H]+ (calcld. 259.0970 for C15H15O4). 1H-NMR (500 MHz, CD3OD): δH 9.71 (1H, s, H-7), 7.34 (1H, dd, J = 8.0, 2.0 Hz, H-6), 7.32 (1H, d, J = 2.0 Hz, H-2), 7.15 (2H, d, J = 8.0 Hz, H-3′, 5′), 7.04 (1H, d, J = 8.0 Hz, H-5), 6.84 (2H, d, J = 8.0 Hz, H-2′, 6′), 3.71 (2H, t, J = 7.0 Hz, H-8′), 2.73 (2H, t, J = 7.0 Hz, H-7′). 13C-NMR (125 MHz. CD3OD): δC 131.1 (C, C-1), 118.3 (CH, C-2), 147.2 (C, C-3), 151.8 (C, C-4), 116.1 (CH, C5), 128.8 (CH, C-6), 158.5 (C, C-1′), 119.5 (CH, C-2′, 6′), 131.0 (CH, C-3′, 5′), 133.7 (C, C4′), 193.1 (CH, C-7), 39.4 (CH2, C-7′), 64.0 (CH2, C-8′).\",\"PeriodicalId\":8719,\"journal\":{\"name\":\"Bangladesh Journal of Pharmacology\",\"volume\":\"14 1\",\"pages\":\"196-197\"},\"PeriodicalIF\":0.9000,\"publicationDate\":\"2019-12-15\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.3329/bjp.v14i4.42414\",\"citationCount\":\"2\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Bangladesh Journal of Pharmacology\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.3329/bjp.v14i4.42414\",\"RegionNum\":4,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"PHARMACOLOGY & PHARMACY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Bangladesh Journal of Pharmacology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.3329/bjp.v14i4.42414","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"PHARMACOLOGY & PHARMACY","Score":null,"Total":0}
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Cytotoxic phenolic constituents from the leaves of Ehretia asperula
Compound 1: 4-hydroxy-3-[4-(2-hydroxyethyl)-phenoxy]-benzaldehyde HR-ESI-MS: m/z 259.0975 [M+H]+ (calcld. 259.0970 for C15H15O4). 1H-NMR (500 MHz, CD3OD): δH 9.71 (1H, s, H-7), 7.34 (1H, dd, J = 8.0, 2.0 Hz, H-6), 7.32 (1H, d, J = 2.0 Hz, H-2), 7.15 (2H, d, J = 8.0 Hz, H-3′, 5′), 7.04 (1H, d, J = 8.0 Hz, H-5), 6.84 (2H, d, J = 8.0 Hz, H-2′, 6′), 3.71 (2H, t, J = 7.0 Hz, H-8′), 2.73 (2H, t, J = 7.0 Hz, H-7′). 13C-NMR (125 MHz. CD3OD): δC 131.1 (C, C-1), 118.3 (CH, C-2), 147.2 (C, C-3), 151.8 (C, C-4), 116.1 (CH, C5), 128.8 (CH, C-6), 158.5 (C, C-1′), 119.5 (CH, C-2′, 6′), 131.0 (CH, C-3′, 5′), 133.7 (C, C4′), 193.1 (CH, C-7), 39.4 (CH2, C-7′), 64.0 (CH2, C-8′).