Journal of Natural Products · 2002 · 57 citations · 8 references
Life SciencesBotanyPlant SciencesMycologyPlant BiochemistryStructure-activity RelationshipsAntifungal AgentsAntifungal PharmacologyFungal BiochemistryFungal Secondary MetabolitesMedicinal PlantsPlant Natural Product BiosynthesisActive Compound IsolationBioactive Fungal MetabolitesBioactive Plant CompoundsBotanical BioassaysCandida Albicans InfectionFungal Bioactive CompoundsNatural Antifungal CompoundsSpectroscopic Characterization
Using bioactivity-directed isolation procedures, five new spirostan saponins and two sterol glycosides have been isolated from Solanum chrysotrichum leaves. The structure of these compounds was established based upon spectroscopic measurements, especially 1D and 2D NMR data of their peracetate derivatives. These compounds showed antimycotic activity. The most active compound is 6alpha-O-beta-d-xylopyranosyl-(1-->3)-beta-d-quinovopyranosyl-(25R)-5alpha-spirostan-3beta,23alpha-ol (2) (MIC =12.5, 12.5, 100, and 200 microg/mL against Trichophyton mentagrophytes, T. rubrum, Aspergillis niger, and Candida albicans, respectively).
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Carbon-13 NMR spectroscopy of steroidal sapogenins and steroidal saponins
Pawan K. Agrawal, D. C. Jain, Rajesh Gupta et al. · Phytochemistry · 1985 · 575 citations
New sources of steroid sapogenins—XIV
Antonio González, Raimundo Freire, M. G. García-Estrada et al. · Tetrahedron · 1972 · 44 citations