Natural Product Research · 2018 · 14 citations · 12 references
PharmacyBiochemistryMedicinal ChemistryCarbohydrate ChemistryDrug DiscoveryStructure-activity RelationshipsMarine Bioactive CompoundsMarine Natural ProductsMedicinal Plant KnowledgeMedicinal PlantsMetabolite ExtractionStructure-activity Relationship AnalysisActive Compound IsolationActivitiesBioactive Compounds From Marine CoralsBioactive Compounds From Marine EchinodermsBioactive ConstituentsBioassay-guided FractionationBioassay-guided Isolation
Three new compounds (1–3) and seven known compounds (4–10) have been isolated from the ethanolic extract of Viburnum macrocephalum f. keteleeri using bioactivity-guided fractionation and identified as methyl (2-α-L-rhamnopyranosyloxy)acetate (1), methyl (2R-3-α-L-rhamnopyranosyloxy)glycerate (2), methyl (3R-4-α-L-rhamnopyranosyloxy-3-hydroxy)butanoate (3), bridelionoside B (4), (6S,7E,9R)-roseoside (5), linarionoside A (6), 3,7,11-trimethyl-1,6-dodecadien-3,10,11-triol (7), (+)-8-hydroxylinalool (8), β-sitosterol (9) and daucosterol (10). The structures of 1–3, including absolute configurations, were determined by spectroscopic data (1H and 13C NMR, HSQC, HMBC and ORD) and chemical methods. In addition, compounds 1–8 were assayed for their insecticidal and antimicrobial activities. Compounds 7 and 8 exhibited moderately insecticidal effects against Mythimna separata with LD50 values of 180 and 230 μg g−1, respectively. Compounds 2, 3, 7 and 8 showed varying antimicrobial activities with IC50 values ranging from 125 to 529 μM.
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13C nmr study of α- and β-anomeric pairs of d-mannopyranosides and l-rhamnopyranosides
R. Kasai, Miho Okihara, J. Asakawa et al. · Tetrahedron · 1979 · 401 citations
Chemotaxonomical investigation in the genus Viburnum
Annelise Lobstein, Gisèle Haan-Archipoff, Jürgen Englert et al. · Phytochemistry · 1999 · 53 citations