Two new limonoids, named rubescins D-E (1-2) along with eight known compounds, including five havanensin type limonoids, TS1 (3), TS3 (4), rubescins A-C (5-7) and three known phytosterols, β-sitosterol, stigmasterol and its 3β-O-glucopyranoside derivative were isolated from the roots and stem bark of Trichilia rubescens, collected from Cameroon. The structures of the new compounds were determined by detailed analyses of 1D and 2D NMR spectra, in combination with high-resolution mass spectrometry data and by comparison with related data from literature. Anti-plasmodial activities of some of the isolated limonoids 1, 2, 4, 6 and 7 were evaluated against erythrocytic stages of strain 3D7 Plasmodium falciparum. Compounds 2 and 4 exhibited significant anti-plasmodial in vitro activity with IC50 values of 1.13 and 0.79 μM, respectively.
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http://dx.doi.org/10.2174/1573406412666160106154357 | DOI Listing |
Molecules
January 2024
School of Pharmaceutical Sciences, College of Medical, Pharmaceutical and Health Sciences, Kanazawa University, Kanazawa 920-1192, Japan.
Eight vilasinin-class limonoids, including the unusually chlorinated rubescins K-M (-), the 2,3-epoxylated rubescin N (), and rubescins O-R (-), were newly isolated from . The structures of the isolated compounds were determined through spectroscopic and spectrometric analyses, as well as ECD calculations. The natural occurrence of chlorinated limonoids - was confirmed by chemical methods and HPLC analysis of a roughly fractionated portion of the plant extract.
View Article and Find Full Text PDFJ Basic Clin Physiol Pharmacol
April 2020
Laboratory of Applied Biochemistry, Department of Biological Sciences, Faculty of Science, University of Ngaoundere, Ngaoundere, Cameroon.
Background Alcoholic liver disease (ALD) is regarded as a global health problem with limited therapeutic options. Previous studies highlighted some anticancer, antiviral, and hepatoprotective activities of limonoids, but the effects of these compounds on ALD remain unknown. The present study aimed to evaluate the effect of some natural limonoids on ethanol-induced liver injury.
View Article and Find Full Text PDFZ Naturforsch C J Biosci
July 2019
Department of Organic Chemistry, Faculty of Science, University of Yaoundé I, P.O. Box 812, Yaoundé, Cameroon.
Three new limonoids, designated as rubescins F (1), G (2), and H (3), together with two known compounds of this type, TS1 (4) and trichirubine A (5), were isolated from methylene chloride/methanol extracts of Trichilia rubescens leaves. The structures of these compounds were elucidated based on 1D and 2D nuclear magnetic resonance (NMR) analysis and complemented by electrospray ionization high-resolution mass spectrometry results and by comparison to data of related compounds described in the literature and ab initio calculations. Rubescin F (1) is the first limonoid from Trichilia spp.
View Article and Find Full Text PDFActa Crystallogr E Crystallogr Commun
August 2018
Chemistry Department, University of Dschang, PO Box 67, Dschang, Cameroon.
The title limonoid compound, CHO·0.5HO () [systematic name: (3a,3b,4a,5a,6,7a,8a,8b,11a)-6-(furan-3-yl)-3a,5a,8b,11a-tetra-methyl-3a,4a,5,5a,6,7,7a,8b,11,11a-deca-hydro-oxireno[2',3':4b,5]oxireno[2'',3'':2',3']cyclo-penta-[1',2':7,8]phenanthro[10,1-]furan-3(3a)-one hemihydrate], crystallizes with two independent mol-ecules (1 and 2) in the asymmetric unit and one water mol-ecule. is composed of three six-membered rings (, and ), three five-membered rings (, and ) and two epoxide rings.
View Article and Find Full Text PDFNat Prod Res
January 2019
a Faculty of Science, Department of Organic Chemistry , University of Yaounde I, Yaounde , Cameroon.
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