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Gastrointestinal nematode infections significantly impact small ruminant production, causing substantial economic losses worldwide. The rising resistance to anthelmintics has led to the search for alternative treatments, including phytotherapeutic approaches. This study investigates the chemical composition and anthelmintic activity of crude extracts and fractions from Simarouba berteroana, an endemic plant from Hispaniola, against a multidrug-resistant isolate of Haemonchus contortus. Chemical analyses revealed high contents of phenolic compounds, tannins, and flavonoids and confirmed the presence of 22 quassinoids, 5 phytosterol lipids, 3 terpenoid quinones, 3 alkaloids, and 1 naphthoquinone. The hydroalcoholic and iso-butanol fractions showed the strongest egg hatching inhibition (IC50 = 0.93 and 1.21 mg/mL, respectively), while hexane fractions were less effective (p < 0.05). Fluorescence microscopy showed that the extracts and fractions adhered to eggshells, causing evisceration and cuticle detachment in hatched larvae. All extracts, except for hexane fractions, inhibited larval exsheathment at 0.3 mg/mL, with phenolic compounds being responsible for this effect. These results provide the first evidence of the ovicidal and larval exsheathment inhibition activities of S. berteroana extracts and fractions against H. contortus, highlighting their potential in managing gastrointestinal nematodes in small ruminants. Further in vivo studies are needed to confirm these findings.

We have developed a dual enzymatic system assay involving liquid chromatography-mass spectrometry (LC–MS) to screen AChE and BACE1 ligands. A fused silica capillary (30 cm × 0.1 mm i.d. × 0.362 mm e.d.) was used as solid support. The co-immobilization procedure encompassed two steps and random immobilization. The resulting huAChE+BACE1-ICER/MS was characterized by using acetylcholine (ACh) and JMV2236 as substrates. The best conditions for the dual enzymatic system assay were evaluated and compared to the conditions of the individual enzymatic system assays. Analysis was performed in series for each enzyme. The kinetic parameters (KMapp) and inhibition assays were evaluated. To validate the system, galantamine and a β-secretase inhibitor were employed as standard inhibitors, which confirmed that the developed screening assay was able to identify reference ligands and to provide quantitative parameters. The combination of these two enzymes in a single on-line system allowed possible multi-target inhibitors to be screened and identified. The innovative huAChE+BACE1-ICER/MS dual enzymatic system reported herein proved to be a reliable tool to identify and to characterize hit ligands for AChE and BACE1 in an enzymatic competitive environment. This innovative system assay involved lower costs; measured the product from enzymatic hydrolysis directly by MS; enabled immediate recovery of the enzymatic activity; showed specificity, selectivity, and sensitivity; and mimicked the cellular process.