Antifungal Quinoline Alkaloids from Waltheria indica
journal contributionposted on 05.02.2016, 00:00 by Sylvian Cretton, Stéphane Dorsaz, Antonio Azzollini, Quentin Favre-Godal, Laurence Marcourt, Samad Nejad Ebrahimi, Francine Voinesco, Emilie Michellod, Dominique Sanglard, Katia Gindro, Jean-Luc Wolfender, Muriel Cuendet, Philippe Christen
Chemical investigation of a dichloromethane extract of the aerial parts of Waltheria indica led to the isolation and characterization of five polyhydroxymethoxyflavonoids, namely, oxyanin A (1), vitexicarpin (3), chrysosplenol E (4), flindulatin (5), 5-hydroxy-3,7,4′-trimethoxyflavone (6), and six quinolone alkaloids, waltheriones M–Q (2, 7, 8, 10, 11) and 5(R)-vanessine (9). Among these, compounds 2, 7, 8, 10, and 11 have not yet been described in the literature. Their chemical structures were established by means of spectroscopic data interpretation including 1H and 13C, HSQC, HMBC, COSY, and NOESY NMR experiments and UV, IR, and HRESIMS. The absolute configurations of the compounds were established by ECD. The isolated constituents and 10 additional quinoline alkaloids previously isolated from the roots of the plant were evaluated for their in vitro antifungal activity against the human fungal pathogen Candida albicans, and 10 compounds (7, 9, 11–16, 18, 21) showed growth inhibitory activity on both planktonic cells and biofilms (MIC ≤ 32 μg/mL). Their spectrum of activity against other pathogenic Candida species and their cytotoxicity against human HeLa cells were also determined. In addition, the cytological effect of the antifungal isolated compounds on the ultrastructure of C. albicans was evaluated by transmission electron microscopy.
Read the peer-reviewed publication
MICWaltheria indicaChemical investigation13 CcompoundNOESY NMR experimentsCandida speciesHSQCUVHeLa cellsantifungal activityAntifungal Quinoline AlkaloidsCOSYECDchemical structuresHMBCcytological effect1 Htransmission electron microscopyquinoline alkaloidsWaltheria indicapathogen Candida albicansspectroscopic data interpretationquinolone alkaloidsplanktonic cellsIRHRESIMS