Helvetica Chimica Acta · 2012 · 33 citations · 10 references
PharmacyBiochemistryPharmacologyDrug DiscoveryHepatotoxicologyStructure-activity RelationshipsMetabolite IdentificationOrganic AcidsPhenolic Compound AnalysisStructure-activity Relationship AnalysisHepatoprotective Agents
Abstract Fractionation directed by hepatoprotective activity of Inula crithmoides L. root resulted in the isolation of two new quinic acid derivatives, 3,5‐di‐ O ‐caffeoylquinic acid 1‐methyl ether ( I ; caffeoyl=( E )‐3‐(3,4‐dihydroxyphenyl)prop‐2‐enoyl; quinic acid=1,3,4,5‐tetrahydroxycyclohexanecarboxylic acid) and 4,5‐di‐ O ‐caffeoylquinic acid 1‐methyl ether ( II ), in addition to the well‐known hepatoprotective compound, 1,5‐di‐ O ‐caffeoylquinic acid ( III ). The hepatoprotective effect was indicated by the significant decrease in the level of four measured serum biochemical parameters (SGOT, SGPT, ALP, and bilirubin) in experimental rats. The structures of the isolated compounds were determined by analyses of 1D‐ and 2D‐NMR spectroscopic data.
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Caffeoyl conjugates from Echinacea species: Structures and biological activity
Annie Cheminat, Rainer Zawatzky, Hans Becker et al. · Phytochemistry · 1988 · 199 citations
Efficacy of different Cynara scolymus preparations on liver complaints
Ester Speroni, Rinaldo Cervellati, Paolo Govoni et al. · Journal of Ethnopharmacology · 2003 · 125 citations
Medicine, Pathology, Hepatology +5