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A Comprehensive View on (−)‐7‐Oxo‐ent‐kaur‐16‐en‐19‐oic Acid,the Major Constituent of Xylopia sericea Leaves Extract: Complete NMR Assignments,X‐Ray Crystallographic Structure,in Vitro Antimalarial Activity and Cytotoxicity
Authors:Douglas Costa&#x  Gontijo,Maria Fernanda&#x  Alves&#x  do&#x  Nascimento,Tatiane Freitas Borgati,Nivaldo Lú  cio Speziali,Jos   Dias&#x  de&#x  Souza&#x  Filho,Alaí  de Braga&#x  de&#x  Oliveira
Affiliation:Douglas Costa Gontijo,Maria Fernanda Alves do Nascimento,Tatiane Freitas Borgati,Nivaldo Lúcio Speziali,José Dias de Souza Filho,Alaíde Braga de Oliveira
Abstract:Bioguided fractionation of Xylopia sericea antiplasmodial dichloromethane leaves extract led to the isolation of (?)‐7‐oxo‐ent‐kaur‐16‐en‐19‐oic acid (C20H28O3) that was identified by a combination of 1D and 2D NMR experiments (COSY, HMBC, HSQC, HSQC‐TOCSY, HSQC‐NOESY and NOESY) and by X‐ray crystallography. A feature to be pointed out is its (4R) configuration that was inferred from the NOE experiments (HSQC‐NOESY and NOESY) and X‐ray crystallography. In vitro evaluation of this rare diterpene acid against the chloroquine‐resistant strain Plasmodium falciparum W2 by the PfLDH method showed it disclosed a low antiplasmodial activity and was not cytotoxic to HepG2 cells (CC50 862.6±6.7 μm ) by the MTT assay. The unequivocal NMR signals assignments, the X‐ray crystallographic structure, the assessment to the bioactivities and the occurrence this diterpene in X. sericea are reported here for the first time.
Keywords:Diterpene  X-ray crystallography  LC–  DAD-MS  antiplasmodial activity  biological activity
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