Speed of action and stage specificity of Bencha-loga-wichian, a Thai traditional antipyretic formulation, against Plasmodium falciparum and the chloroquine-potentiating activity of its active compounds, tiliacorinine and yanangcorinine

2020 ◽  
Vol 258 ◽  
pp. 112909
Author(s):  
Thanutchaporn Nutmakul ◽  
Kovit Pattanapanyasat ◽  
Noppamas Soonthornchareonnon ◽  
Kazuro Shiomi ◽  
Mihoko Mori ◽  
...  
PLoS ONE ◽  
2016 ◽  
Vol 11 (3) ◽  
pp. e0149996 ◽  
Author(s):  
Gregory J. Crowther ◽  
Heidi K. Hillesland ◽  
Katelyn R. Keyloun ◽  
Molly C. Reid ◽  
Maria Jose Lafuente-Monasterio ◽  
...  

2004 ◽  
Vol 48 (9) ◽  
pp. 3241-3245 ◽  
Author(s):  
Mei-Lin Go ◽  
Mei Liu ◽  
Prapon Wilairat ◽  
Philip J. Rosenthal ◽  
Kevin J. Saliba ◽  
...  

ABSTRACT A series of alkoxylated and hydroxylated chalcones previously reported to have antiplasmodial activities in vitro were investigated for their effects on the new permeation pathways induced by the malaria parasite in the host erythrocyte membrane. Of 21 compounds with good antiplasmodial activities (50% inhibitory concentrations [IC50s], ≤20 μM), 8 members were found to inhibit sorbitol-induced lysis of parasitized erythrocytes to a significant extent (≤40% of control values) at a concentration (10 μM) that was close to their antiplasmodial IC50s. Qualitative structure-activity analysis suggested that activity was governed to a greater extent by a substitution on ring B than on ring A of the chalcone template. Most of the active compounds had methoxy or dimethoxy groups on ring B. Considerable variety was permitted on ring A in terms of the electron-donating or -withdrawing property. Lipophilicity did not appear to be an important determinant for activity. Although they are not exceptionally potent as inhibitors (lowest IC50, 1.9 μM), the chalcones compare favorably with other more potent inhibitors in terms of their selective toxicities against plasmodia and their neutral character.


Author(s):  
I Made Prasetya Kurniawan ◽  
Prawesty Diah Utami ◽  
Risma Risma

Indonesia is a country that has abundant natural resources; one of them is the Baru laut plant which is the latest breakthrough because it has an active substance that can be used as an anti-malaria medicine. It is very beneficial because there has been a case of resistance of artemisinin derivatives in Indonesia. The purpose of this study was to determine the potential of active compounds in Baru laut plants (Thespesia populnea (L.) Soland ex. Correa) against the Plasmodium falciparum enoyl acyl carrier protein reductase receptor in P. falciparum through in silico studies. This research is purely experimental using the One-Shot Experimental Study research design method. Observations were only made once between the variables studied through three analyzes, namely prediction analysis of active compound content, prediction analysis of the mechanism of action of active compound content, and prediction analysis of ADME active compound. The study results show that there are three active compounds in Baru laut plants that have antimalarial potential. The three compounds include gossypol, linoleic acid, and beta-sitosterol, have their respective potential in becoming a malaria drug. This study concludes that Baru laut plants have potential as anti-malaria drugs.


2013 ◽  
Vol 12 (1) ◽  
pp. 424 ◽  
Author(s):  
Claire Le Manach ◽  
Christian Scheurer ◽  
Sibylle Sax ◽  
Sarah Schleiferböck ◽  
Diego Cabrera ◽  
...  

2016 ◽  
Vol 15 (1) ◽  
Author(s):  
Whitney A. Kite ◽  
Viviana A. Melendez-Muniz ◽  
Roberto R. Moraes Barros ◽  
Thomas E. Wellems ◽  
Juliana M. Sá

Planta Medica ◽  
2012 ◽  
Vol 78 (11) ◽  
Author(s):  
J Guizado ◽  
T Hoffman ◽  
M Piepenbring ◽  
L Cubilla-Rios

2016 ◽  
Vol 11 (1) ◽  
pp. 1-7
Author(s):  
Eti Nurwening Sholikhah ◽  
Mahardika Agus Wijayanti ◽  
Ratna Asmah Susidarti ◽  
Indah Purwantini ◽  
Rani Afifah Nur Hestiyani ◽  
...  

2012 ◽  
Vol 84 (4) ◽  
pp. 899-910 ◽  
Author(s):  
Maria Fâni Dolabela ◽  
Salma G. Oliveira ◽  
José M. Peres ◽  
José M.S. Nascimento ◽  
Marinete M. Póvoa ◽  
...  

Ethnomedicinal informations point to some Aspidosperma species (Apocynaceae) as antimalarial plants in Brazil and have motivated the evaluation of six species which were collected in the state of Minas Gerais: A. cylindrocarpon Müll. Arg., A. parvifolium A. DC., A. olivaceum Müll. Arg., A. ramiflorum Müll. Arg., A. spruceanum Benth. ex Müll. Arg. and A. tomentosum Mart.. A total of 23 extracts of different plant parts in different solvents were assayed in vitro against chloroquine-resistant (W2) and chloroquine-sensitive (3D7) strains of Plasmodium falciparum. All the extracts were shown to be active with IC50 values in the range of 5.0 ± 0 2.8 µg/mL to 65.0 ± 4.2 µg/mL. TLC profile of the extracts revealed the presence of alkaloids in the six species assayed. These results seem to confirm the popular use of Aspidosperma species to treat human malaria in Brazil and seem point to alkaloids as the putative active compounds of the assayed species.


2021 ◽  
Vol 28 ◽  
Author(s):  
Gilles Degotte ◽  
Bernard Pirotte ◽  
Pierre Francotte ◽  
Michel Frédérich

Background: Despite the major advances in the fight against this parasitic disease, malaria remains a major cause of concerns in 2020. This infection, mainly due to Plasmodium falciparum, causes every year more than 200 million of cases and hundreds of thousands of deaths in developing regions, mostly in Africa. The last statistics show an increase of cases for the third consecutive year, from 211 million in 2015, it has reached 229 million in 2019. This trend could be partially explained by the appearance of resistances to all the used antimalarials, even to artemisinin. Thus, the design of new anti-Plasmodium compounds is an urgent need. For thousands of years, nature has offered to humans the medicines to cure their diseases or the inspiration for development of new active principles. It seems then logical to explore the natural sources to find new molecules to treat this parasitosis. Method: Therefore, this review reports and analyzes the extracts (plants, bacteria, sponges, fungi) and the corresponding isolated compounds showing antiplasmodial properties between 2013 and 2019. Results & Conclusion: Nature remains a major source of active compounds. Indeed, 648 molecules from various origins, mostly plants, have been reported for their inhibitory effect on Plasmodium falciparum. Among them, 188 scaffolds were defined as highly active with IC50 ≤ 5 µM and have been reported here in details. Moreover, the most active compounds showed a large variety of structures: flavonoids, triterpenes, alkaloids... Therefore, these compounds could be an interesting source of inspiration for medicinal chemists. May-be several of these molecules should become the next leads for malaria treatment.


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