Journal of Natural Products · 2000 · 141 citations · 4 references
PharmacyMedicinal ChemistryPharmacologyCancer PharmacologyDrug DiscoveryStructure-activity RelationshipsMedicinal PlantsOncology PharmacologyStructure-activity Relationship AnalysisAnticancer ActivityChemical ModificationChemical Structure-activity RelationshipsToxicity Of Medicinal Plants
Four new biflavonoids-robustaflavone 4'-methyl ether (1), robustaflavone 7,4'-dimethyl ether (2), 2",3" -dihydrorobustaflavone 7,4', -dimethyl ether (3), and 2",3" '-dihydrorobustaflavone 7,4', 7"-trimethyl ether (4)-as well as two known biflavonoids, robustaflavone and amentoflavone, and three caffeoylquinic acids, 3,5-di-O-caffeoylquinic acid, 3, 4-di-O-caffeoylquinic acid, and 4,5-di-O-caffeoylquinic acid, were isolated from Selaginella delicatula. The structures of the new compounds were established by spectroscopic analysis and chemical modification. The cytotoxic activity of these compounds on various tumor cell lines was evaluated, and both compounds 1 and 3 significantly suppressed the growth of Raji and Calu-1 tumor cell lines.
4
Cytotoxic biflavonoids from Selaginella willdenowii
Gloria L. Silva, Heebyung Chai, Mahabir P. Gupta et al. · Phytochemistry · 1995 · 125 citations
Biflavones in Selaginella species
Masayoshi Okigawa, Chiang Wu Hwa, Nobusuke Kawano et al. · Phytochemistry · 1971 · 51 citations