Natural Product Research · 2014 · 19 citations · 15 references
PharmacyMedicinal ChemistryPharmacologyCancer PharmacologyDrug DiscoveryStructure-activity RelationshipsMedicinal PlantsSteroid StructureCytotoxicity AssaysSpectroscopic Identification
In our continuing effort to discover more new cytotoxic sesquiterpenoids from Solanum lyratum, one new eudesmane-type sesquiterpenoid (1, 3-keto-eudesm-9β,11-diol, named lyratol G), together with one known eudesmane-type sesquiterpenoid (2, 1β-hydroxy-1,2-dihydro-α-santonin), was obtained. The structure of the new sesquiterpenoid was elucidated on the basis of integrated spectroscopic techniques, mainly HR-FAB-MS, 1D and 2D NMR ((1)H-(1)H COSY, HMQC, HMBC and ROESY). In vitro, two sesquiterpenoids were found to exhibit significant cytotoxicity against three cancer cell lines (P-388, HONE-1 and HT-29), and gave IC50 values in the range of 3.1-6.9 μM.
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Steroidal Saponins from <i>Solanum nigrum</i>
Xin-Lan Zhou, Xiangjiu He, Guanghui Wang et al. · Journal of Natural Products · 2006 · 97 citations
Two New Sesquiterpenoids from Solanum lyratum with Cytotoxic Activities
Yan Ren, Shen Li, Dewu Zhang et al. · Chemical and Pharmaceutical Bulletin · 2009 · 46 citations · Full text
Lx2-32c, a novel taxane and its antitumor activities in vitro and in vivo
Hongbo Wang, Hongyan Li, Minxin Zuo et al. · Cancer Letters · 2008 · 45 citations
Medicine, Oncology, Pharmacology +14