Phytochemical, metabolic profiling and antiparasitic potential from Inga semialata leaves (Fabaceae).

Natural Products phytochemical provide a rich source for therapeutic discovery and has led to the development of many drugs. Thus, the aim of this study was to obtaining a metabolic profiling from ethanol extract of Inga semialata leaves (EEIS) selected by bioassay antimalarial and nematostatic and identify metabolites in mixture by co-injection experiments and NMR spectroscopy. The chemical composition of this species indicated a wide variety of aromatic acids (vanillic acid, 3,4,5-trimethoxy benzoic acid, gallic acid, methyl gallate, p-coumaric acid and ferulic acid), flavonoids (quercetin, myricetin-3-O-rhamnoside and myricetin-3-O-(2"-O-galloyl)-α-rhamnopyranoside), triterpenes (lupeol, α-amyrin, friedelin and oleanolic acid) and the 2-hydroxyethyl-dodecanoate. The antimalarial assay showed that the I. semialata n-hexane fraction presented higher inhibition percentage than the Chloroquine standard and may be considered a potential source of compounds with antimalarial activity while the EEIS and its fractions showed nematostatic potential below 17% in the assay of nematostatic evaluation against the parasite Meloidogyne incognita.

Nematicidal activity of leaf extracts from Lantana camara L. against Meloidogyne incognita (kofoid and white) chitwood and its use to manage roots infection of Solanum melongena L

Various concentrations of aqueous leaf extract of Lantana camara were assessed in vitro conditions against second stage juveniles (J2) of Meloidogyne incognita. The standard concentration 'S' of leaf extract was found to be highly nematostatic, where nematodes were completely paralyzed after 12 h and after 48 h of exposure, 96 percent of juveniles were killed at same concentration. However, the mortality of juveniles was 75 percent in S/2 dilution at 48 h. The degree of effectiveness and dilutions of extract were directly proportional. The percentage of paralyzed juveniles was decreased, when J2 transferred in distilled water after 48 h incubation in standard aqueous leaf extract. Addition of freeze-dried aqueous extract to sterile sandy substrate at S/2 dilution significantly decreased the root-knot infection to susceptible eggplants whereas second stage juveniles (J2) that penetrated roots of eggplant were able to complete development in sterile sandy substrate without treatment of freeze-dried aqueous extract.