Introduction: Several taccalonolides with various bioactivities have been isolated from Tacca species but no studies to isolate taccalonolides with anti-trypanosomal activity from Tacca leontopetaloides have been reported.
Objectives: To analyse extracts of the roots of Tacca leontopetaloides, purify the extracts by column chromatography and identify isolated compounds by spectroscopic methods. The compounds and fractions will be tested for antitrypanosomal activity in vitro against Trypanosoma brucei brucei.
Material And Methods: Dried roots or tubers of Tacca leontopetaloides, chromatographic separation and spectroscopic identification.
Results: A novel taccalonolide A propanoate and some known taccalonolides were isolated and their structures were determined by NMR and mass spectrometry
Conclusion: Several taccalonolides were isolated from Tacca leontopetaloides and were found to have in vitro antitrypanosomal activity against Trypanosoma brucei brucei and EC50 values for the isolated compounds were from 0.79 µg/mL. Copyright © 2016 John Wiley & Sons, Ltd.
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http://dx.doi.org/10.1002/pca.2619 | DOI Listing |
Molecules
December 2022
Faculty of Agriculture, Soil Science Department, Universitas Syiah Kuala, Banda Aceh 23111, Indonesia.
() contain a number of active compounds such as flavonoids, tannins, phenolics, steroids, and alkaloids. The active compounds from plants have been shown to reduce the risk of cardiovascular disease by lowering cholesterol levels by inhibiting the enzyme 3-hydroxy-3-methylglutaryl-coenzym A (HMG-CoA) reductase activity. This study aims to investigate the potential active compounds in the ethanolic extract of Tacca tubers () from the Banyak Islands, Aceh Singkil Regency, Aceh Province both in vitro and in silico.
View Article and Find Full Text PDFInt J Biol Macromol
October 2018
Division of Pharmaceutical Technology, Faculty of Pharmaceutical Sciences, Khon Kaen University, Khon Kaen 40002, Thailand. Electronic address:
Arrowroot (Tacca leontopetaloides L. Kuntze) starch in gelatinized and ungelatinized forms was used to modify the characteristics of calcium alginate (CA) beads containing diclofenac sodium (DS). Sodium alginate (SA) was able to molecularly interact with ungelatinized starch (UGS) granules and gelatinized starch (GS) gel via hydrogen bonding mechanisms in the dispersions, leading to viscosity synergism before cross-linking.
View Article and Find Full Text PDFPhytochem Anal
May 2016
Strathclyde Institute of Pharmacy and Biomedical Sciences, University of Strathclyde, 27 Taylor Street, Glasgow, G4 0NR, UK.
Introduction: Several taccalonolides with various bioactivities have been isolated from Tacca species but no studies to isolate taccalonolides with anti-trypanosomal activity from Tacca leontopetaloides have been reported.
Objectives: To analyse extracts of the roots of Tacca leontopetaloides, purify the extracts by column chromatography and identify isolated compounds by spectroscopic methods. The compounds and fractions will be tested for antitrypanosomal activity in vitro against Trypanosoma brucei brucei.
Planta Med
April 1990
Welsh School of Pharmacy, UWCC, PO Box 13, Cardiff CF1 3XF, U.K.
Diosgenin and its ring-F-hydroxylated derivatives isonarthogenin {spirost-5-ene-3,27-diol {3beta, 22 R, 25 S)} and isonuatigenin {spirost-5-ene-3,25-diol (3beta, 22 R, 25 S)}, together with the 22,25-epoxyfurost-5-ene isomer nuatigenin {furost-5-ene-3,26-diol-22,25-epoxy (3beta, 22 R, 25 S)}, were identified as the major steroidal sapogenins of the acid hydrolysate of an extract of leaves of TACCA LEONTOPETALOIDES by IR, (1)H-NMR, (13)C-NMR, and mass spectroscopy. A diosgenin ester was isolated which apparently arose by ring closure of a glycosylated furostene during hydrolysis.
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