A new dammarane type triterpene glucoside from the aerial parts of Gouania longipetala (Rhamnaceae).
3-O-β-D-glucopyranosyl gouanogenin A (1), a new naturally occurring dammarane class of triterpene glucoside, has been isolated from the aerial parts of Gouania longipetala along with six known secondary metabolites 2–7. Their structure was elucidated through spectroscopic data including 1 D- and 2 D...
| Publicado en: | Natural Product Research Vol. 35; no. 19; pp. 3192 - 3204 |
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| Autores principales: | , , , , , , , , |
| Formato: | Journal Article |
| Publicado: |
Taylor & Francis Ltd
Oct2021
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| Acceso en línea: | Ver este registro en EBSCOhost |
| fields | @attributes: recordID: 1 pdfLink: plink: https://search.ebscohost.com/login.aspx?direct=true&db=ccm&AN=152760061&site=ehost-live header: @attributes: shortDbName: ccm uiTerm: 152760061 longDbName: CINAHL Complete uiTag: AN controlInfo: bkinfo: dissinfo: jinfo: jid: 14786419 RFT jtl: Natural Product Research issn: 14786419 maglogo: Y pubinfo: dt: Oct2021 vid: 35 iid: 19 pid: 377 pub: Taylor & Francis Ltd place: Philadelphia, Pennsylvania artinfo: ui: 152760061 10.1080/14786419.2019.1690483 152760061 ppf: 3192 ppct: 12 formats: tig: atl: A new dammarane type triterpene glucoside from the aerial parts of Gouania longipetala (Rhamnaceae). aug: au: Désiré, Soh Ernestine, Nkwengoua Bruno, Tchebemou Bakang Lazare, Sidjui Sidjui Ulrich, Dzo Defokou Lateef, Mehreen Schneider, Bernd Ali, Muhammad Shaiq Barthélemy, Nyassé affil: Department of Chemistry, Higher Teacher Training College, TWAS Research Unit (TRU), University of Bamenda, Bamenda, Cameroon sug: ab: 3-O-β-D-glucopyranosyl gouanogenin A (1), a new naturally occurring dammarane class of triterpene glucoside, has been isolated from the aerial parts of Gouania longipetala along with six known secondary metabolites 2–7. Their structure was elucidated through spectroscopic data including 1 D- and 2 D-NMR. The compounds 1 and 6 showed significant antioxidant potential in DPPH radical scavenging assay. On the other hand, the compound 4 revealed potent inhibitory potential against the enzyme urease, while 1 and 3 were significantly active. pubtype: Academic Journal doctype: Journal Article ougenre: Article language: English refInfo: holdings: @attributes: islocal: N |
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