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Chem Biodivers ; 16(7): e1900141, 2019 Jul.
Article in English | MEDLINE | ID: mdl-31087758

ABSTRACT

Bioguided fractionation of Xylopia sericea antiplasmodial dichloromethane leaves extract led to the isolation of (-)-7-oxo-ent-kaur-16-en-19-oic acid (C20 H28 O3 ) 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.


Subject(s)
Antimalarials/pharmacology , Antineoplastic Agents, Phytogenic/pharmacology , Diterpenes, Kaurane/pharmacology , Diterpenes/pharmacology , Plant Extracts/pharmacology , Plant Leaves/chemistry , Plasmodium falciparum/drug effects , Xylopia/chemistry , Antimalarials/chemistry , Antimalarials/isolation & purification , Antineoplastic Agents, Phytogenic/chemistry , Antineoplastic Agents, Phytogenic/isolation & purification , Cell Line, Tumor , Cell Proliferation/drug effects , Crystallography, X-Ray , Diterpenes/chemistry , Diterpenes/isolation & purification , Diterpenes, Kaurane/chemistry , Diterpenes, Kaurane/isolation & purification , Dose-Response Relationship, Drug , Drug Screening Assays, Antitumor , Humans , Magnetic Resonance Spectroscopy , Models, Molecular , Molecular Conformation , Plant Extracts/chemistry , Plant Extracts/isolation & purification , Structure-Activity Relationship
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