BackgroundAnti-malarial drug resistance threatens to undermine efforts to eliminate this deadly disease. The resulting omnipresent requirement for drugs with novel modes of action prompted a national consortium initiative to discover new anti-plasmodial agents from South African medicinal plants. One of the plants selected for investigation was Dicoma anomala subsp. gerrardii, based on its ethnomedicinal profile.MethodsStandard phytochemical analysis techniques, including solvent-solvent extraction, thin-layer- and column chromatography, were used to isolate the main active constituent of Dicoma anomala subsp. gerrardii. The crystallized pure compound was identified using nuclear magnetic resonance spectroscopy, mass spectrometry and X-ray crystallography. The compound was tested in vitro on Plasmodium falciparum cultures using the parasite lactate dehydrogenase (pLDH) assay and was found to have anti-malarial activity. To determine the functional groups responsible for the activity, a small collection of synthetic analogues was generated - the aim being to vary features proposed as likely to be related to the anti-malarial activity and to quantify the effect of the modifications in vitro using the pLDH assay. The effects of the pure compound on the P. falciparum transcriptome were subsequently investigated by treating ring-stage parasites (alongside untreated controls), followed by oligonucleotide microarray- and data analysis.ResultsThe main active constituent was identified as dehydrobrachylaenolide, a eudesmanolide-type sesquiterpene lactone. The compound demonstrated an in vitro IC50 of 1.865 μM against a chloroquine-sensitive strain (D10) of P. falciparum. Synthetic analogues of the compound confirmed an absolute requirement that the α-methylene lactone be present in the eudesmanolide before significant anti-malarial activity was observed. This feature is absent in the artemisinins and suggests a different mode of action. Microarray data analysis identified 572 unique genes that were differentially expressed as a result of the treatment and gene ontology analysis identified various biological processes and molecular functions that were significantly affected. Comparison of the dehydrobrachylaenolide treatment transcriptional dataset with a published artesunate (also a sesquiterpene lactone) dataset revealed little overlap. These results strengthen the notion that the isolated compound and the artemisinins have differentiated modes of action.ConclusionsThe novel mode of action of dehydrobrachylaenolide, detected during these studies, will play an ongoing role in advancing anti-plasmodial drug discovery efforts.
The three-ring eudesmanolide, C15H16O3, is a natural product isolated from Dicoma anomala Sond. (Asteraceae). The compound contains an endo–exo cross conjugated methylenecyclohexenone ring with an envelope conformation trans-fused with cyclohexane and trans-annelated with an α-methylene γ-lactone. The absolute structure was assigned by optical rotation measurements compared to those from the synthetic compound with known stereochemistry. The crystal packing is consolidated by C—H⋯O interactions.
Concentration of the surface active agents in industrial products is a common source of error. In order to compare the efficiency of a number of polyisobutylene succinic anhydride (PIBSA) based surfactants, their concentration needs to be determined with a fair degree of accuracy. Industrial samples of the monoethanolamine adduct of PIBSA (PIBSA-MEA) concentrate were used for chromatographic separation of the functionalized surfactant from the sample matrix. Complete spectroscopic assignments were based on detailed analysis of all the precursors and of the purified mixture of structural isomers. The structures of the double bond isomers were consistent with the expected addition products of the classic Alderene reaction-derived PIBSA. The carbon-carbon connectivity of the succinamide head group to the bulky polymer tail of PIBSA-MEA was more complicated than previously thought, pointing towards regioselectivity in the nucleophilic substitution of PIBSA. By analogy, further structural assignments of two other surfactants, branded as PIBSA-IMIDE and PIBSA-UREA were made from the spectroscopic data recorded on crude industrial samples. Detailed nuclear magnetic resonance (NMR) assignments for all three surfactants reported here were utilized to develop a semi-quantitative 13 C-NMR based method for the estimation of the amount of the functionalized surfactant relative to the total PIB content in the industrial concentrates. The results highlight common sources of structure-and concentration-dependent errors in high internal phase emulsion formulations.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.
hi@scite.ai
10624 S. Eastern Ave., Ste. A-614
Henderson, NV 89052, USA
Copyright © 2024 scite LLC. All rights reserved.
Made with 💙 for researchers
Part of the Research Solutions Family.