Identification of oleamide in Guatteria recurvisepala by LC/MS-Based Plasmodium falciparum thioredoxin reductase ligand binding method

Our current research on applications of mass spectrometry to natural product drug discovery against malaria aims to screen plant extracts for new ligands to PLASMODIUM FALCIPARUM thioredoxin reductase ( PFTrxR) followed by their identification and structure elucidation. PFTrxR is involved in the antioxidant defense and redox regulation of the parasite and is validated as a promising target for therapeutic intervention against malaria. In the present study, detannified methanol extracts from GUATTERIA RECURVISEPALA, LICANIA KALLUNKIAE, and TOPOBEA WATSONII were screened for ligands to PFTrxR using ultrafiltration and liquid chromatography/mass spectrometry-based binding experiments. The PFTrxR ligand identified in the extract of GUATTERIA RECURVISEPALA displayed a relative binding affinity of 3.5-fold when incubated with 1 microM PFTrxR. The ligand corresponding to the protonated molecule M/Z 282.2792 [M + H] (+) was eluted at a retention time of 17.95 min in a 20-min gradient of 95 % B consisting of (A) 0.1 % formic acid in 95 % H (2)O-5 % ACN, and (B) 0.1 % formic acid in 95 % ACN-5% H (2)O in an LC-QTOF-MS. Tandem MS of the protonated molecule M/Z 282.2792 [M + H] (+), C (18)H (36)NO (DBE: 2; error: 1.13 ppm) resulted in two daughter ions M/Z 265.2516 [M + H-NH (3)] (+) (DBE: 3; error: 0.35 ppm) and M/Z 247.2405 [M + H-NH (3)-H (2)O] (+), (DBE: 4; error: 2.26 ppm). The PFTrxR ligand was identified as oleamide and confirmed by comparison of the retention time, molecular formula, accurate mass, and double bond equivalence with the standard oleamide. This is the first report on the identification of oleamide as a PFTrxR ligand from GUATTERIA RECURVISEPALA R. E. Fr. and the corresponding IN VITRO activity against P. FALCIPARUM strain K1 (IC (50) 4.29 microg/mL)