Chemical and Pharmaceutical Bulletin · 2005 · 43 citations · 8 references
PharmacyMedicinal ChemistryPharmacologyDrug DiscoveryMycologyStructure-activity RelationshipsAntifungal AgentsAntifungal PharmacologyFungal BiochemistryFungal Secondary MetabolitesStructure-activity Relationship AnalysisMinimum Inhibitory Concentration DeterminationNatural Antifungal CompoundsNew Antifungal Agents
Two new C-3/C-3'' biflavanones, chamaejasmenin D (1) and isochamaejasmenin B (2), were isolated from the roots of Stellera chamaejasme, together with five known biflavanones, chamaejasmenin A (3), chamaejasmenin B (4), neochamaejasmin A (5), sikokianin A (6), and chamaejasmenin C (7). Their structures were elucidated by spectroscopic methods, including 2D NMR techniques. Among these compounds, 1-3 demonstrated potent antimitotic and antifungal activity with minimum inhibitory concentration (MIC) values of 6.25, 6.25, and 3.12 microg/ml, respectively.
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Hisayoshi Kobayashi, Michio Namikoshi, Takeshi Yoshimoto et al. · The Journal of Antibiotics · 1996 · 98 citations · Full text
Life Sciences, Botany, Microbiology +17
Novel C-3/C-3"-biflavanones from Stellera chamaejasme L.
Guoquan Liu, Hiroshi Tatematsu, MIKIO KUROKAWA et al. · Chemical and Pharmaceutical Bulletin · 1984 · 50 citations · Full text