{"title":"龙血龙属植物中甾体皂苷类成分及其化学分类意义","authors":"Mbiesset Mouzié Cédric, Kemvoufo Ponou Beaudelaire, Tematio Fouedjou Romuald, B. Rémy, Azefack Tapondjou Léon","doi":"10.20307/nps.2021.27.2.122","DOIUrl":null,"url":null,"abstract":" A new steroidal saponin, (23 S ,24 S )-spirosta-5,25(27)-diene-1 β ,3 β ,23,24-tetrol 1- O-((2,3-diacetyl-α-L-rhamnopyranosyl)-(1→2)-[ β -D-xylopyranosyl-(1→3)]- α -L-arabinopyranoside)-24- O - β -D-glucopyranoside (humilisoside) together with the known β -sitosterol 3-O -glucopyranoside, adenosine, dioscin, and methylprotodioscin were isolated from the leaves of Dracaena humilis . Their structures were elucidated by spectral techniques including mass spectrometry (ESIMS, HRESIMS, tandem MS-MS), 1D NMR ( 1 H, 13 C NMR), 2D NMR (HSQC, 1 H-1 H COSY, HMBC, NOESY), chemical method as well as by comparison with spectroscopic data reported in the literature. The chemotaxonomic significance of the isolation of these compounds is discussed. This is the first report on the phytochemical investigation of D. humilis .","PeriodicalId":19080,"journal":{"name":"Natural product sciences","volume":" ","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2021-06-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":"{\"title\":\"Steroidal Saponins from Dracaena humilis (Dracaenaceae) and their Chemotaxonomic Significance\",\"authors\":\"Mbiesset Mouzié Cédric, Kemvoufo Ponou Beaudelaire, Tematio Fouedjou Romuald, B. Rémy, Azefack Tapondjou Léon\",\"doi\":\"10.20307/nps.2021.27.2.122\",\"DOIUrl\":null,\"url\":null,\"abstract\":\" A new steroidal saponin, (23 S ,24 S )-spirosta-5,25(27)-diene-1 β ,3 β ,23,24-tetrol 1- O-((2,3-diacetyl-α-L-rhamnopyranosyl)-(1→2)-[ β -D-xylopyranosyl-(1→3)]- α -L-arabinopyranoside)-24- O - β -D-glucopyranoside (humilisoside) together with the known β -sitosterol 3-O -glucopyranoside, adenosine, dioscin, and methylprotodioscin were isolated from the leaves of Dracaena humilis . Their structures were elucidated by spectral techniques including mass spectrometry (ESIMS, HRESIMS, tandem MS-MS), 1D NMR ( 1 H, 13 C NMR), 2D NMR (HSQC, 1 H-1 H COSY, HMBC, NOESY), chemical method as well as by comparison with spectroscopic data reported in the literature. The chemotaxonomic significance of the isolation of these compounds is discussed. This is the first report on the phytochemical investigation of D. humilis .\",\"PeriodicalId\":19080,\"journal\":{\"name\":\"Natural product sciences\",\"volume\":\" \",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2021-06-30\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"1\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Natural product sciences\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.20307/nps.2021.27.2.122\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"Chemistry\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Natural product sciences","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.20307/nps.2021.27.2.122","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"Chemistry","Score":null,"Total":0}
Steroidal Saponins from Dracaena humilis (Dracaenaceae) and their Chemotaxonomic Significance
A new steroidal saponin, (23 S ,24 S )-spirosta-5,25(27)-diene-1 β ,3 β ,23,24-tetrol 1- O-((2,3-diacetyl-α-L-rhamnopyranosyl)-(1→2)-[ β -D-xylopyranosyl-(1→3)]- α -L-arabinopyranoside)-24- O - β -D-glucopyranoside (humilisoside) together with the known β -sitosterol 3-O -glucopyranoside, adenosine, dioscin, and methylprotodioscin were isolated from the leaves of Dracaena humilis . Their structures were elucidated by spectral techniques including mass spectrometry (ESIMS, HRESIMS, tandem MS-MS), 1D NMR ( 1 H, 13 C NMR), 2D NMR (HSQC, 1 H-1 H COSY, HMBC, NOESY), chemical method as well as by comparison with spectroscopic data reported in the literature. The chemotaxonomic significance of the isolation of these compounds is discussed. This is the first report on the phytochemical investigation of D. humilis .
期刊介绍:
Natural Product Sciences is the official publication of the Korean Society of Pharmacognosy which was launched in 1995. The journal is published quarterly at the end of March, June, September, and December each year and the official title of the journal is abbreviated title as "Nat. Prod. Sci." The research papers on original work, either experimental or theoretical, that advance our understanding of natural product sciences, including important questions of phytochemistry, chemistry, and bio-chemistry of natural resources will be published. Timely reviews and commentaries on recent progress in active areas of natural products research will be also published.