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1.
Molecules ; 19(5): 6070-9, 2014 May 14.
Article in English | MEDLINE | ID: mdl-24830711

ABSTRACT

Natural compounds represent a rich and promising source of novel, biologically active chemical entities for treating leishmaniasis. Sesquiterpene lactones are a recognized class of terpenoids with a wide spectrum of biological activities, including activity against Leishmania spp. In this work, a sesquiterpene lactone-rich preparation-a leaf rinse extract (LRE) from Tithonia diversifolia-was tested against promastigote forms of L. braziliensis. The results revealed that the LRE is a rich source of potent leishmanicidal compounds, with an LD50 value 1.5 ± 0.50 µg·mL-1. Therefore, eight sesquiterpene lactones from the LRE were initially investigated against promastigote forms of L. braziliensis. One of them did not present any significant leishmanicidal effect (LD50 > 50 µg·mL-1). Another had a cytotoxic effect against macrophages (4.5 µg·mL-1). The five leishmanicidal compounds with the highest level of selectivity were further evaluated against intracellular parasites (amastigotes) using peritoneal macrophages. Tirotundin 3-O-methyl ether, tagitinin F, and a guaianolide reduced the internalization of parasites after 48 h, in comparison with the negative control. This is the first report on sesquiterpene lactones that have potent leishmanicidal effects on both developmental stages of L. braziliensis.


Subject(s)
Lactones/administration & dosage , Leishmaniasis, Cutaneous/drug therapy , Plant Extracts/administration & dosage , Sesquiterpenes/administration & dosage , Animals , Asteraceae/chemistry , Humans , In Vitro Techniques , Lactones/isolation & purification , Leishmania braziliensis/drug effects , Leishmaniasis, Cutaneous/parasitology , Parasitic Sensitivity Tests , Plant Extracts/chemistry , Plant Leaves/chemistry , Sesquiterpenes/isolation & purification
2.
J Nat Prod ; 77(1): 70-8, 2014 Jan 24.
Article in English | MEDLINE | ID: mdl-24387625

ABSTRACT

Three new azaphilones with an unusual methylene bridge, named mycoleptones A, B, and C (2, 4, and 5), were isolated from cultures of Mycoleptodiscus indicus, a fungus associated with the South American medicinal plant Borreria verticillata. Additionally, four known polyketides, austdiol (1), eugenitin (3), 6-methoxyeugenin (6), and 9-hydroxyeugenin (7), were also isolated. The structural characterization of compounds was carried out by nuclear magnetic resonance spectroscopy, high-resolution mass spectrometry, electronic circular dichroism spectroscopy, time-dependent density functional theory calculations, and X-ray crystallography. Compounds 1-9 were weakly active when tested in antileishmanial and cytotoxicity assays.


Subject(s)
Benzofurans/isolation & purification , Endophytes/chemistry , Polyketides/isolation & purification , Benzofurans/chemistry , Benzofurans/pharmacology , Brazil , Crystallography, X-Ray , Drug Screening Assays, Antitumor , HL-60 Cells , Humans , Leishmania/drug effects , Lymphocytes/drug effects , Molecular Structure , Nuclear Magnetic Resonance, Biomolecular , Polyketides/chemistry , Polyketides/pharmacology , Rubiaceae/microbiology
3.
Chem Biol Drug Des ; 81(6): 749-56, 2013 Jun.
Article in English | MEDLINE | ID: mdl-23421616

ABSTRACT

The leishmaniasis is a spectral disease caused by the protozoan Leishmania spp., which threatens millions of people worldwide. Current treatments exhibit high toxicity, and there is no vaccine available. The need for new lead compounds with leishmanicidal activity is urgent. Considering that many lead leishmanicidal compounds contain a quinoidal scaffold and the thiazole heterocyclic ring is found in a number of antimicrobial drugs, we proposed a hybridization approach to generate a diverse set of semi-synthetic heterocycles with antileishmanial activity. We found that almost all synthesized compounds demonstrated potent activity against promastigotes of Leishmania (Viannia) braziliensis and reduced the survival index of Leishmania amastigotes in mammalian macrophages. Furthermore, the compounds were not cytotoxic to macrophages at fivefold higher concentrations than the EC50 for promastigotes. All molecules fulfilled Lipinski's Rule of Five, which predicts efficient orally absorption and permeation through biological membranes, the in silico pharmacokinetic profile confirmed these characteristics. The potent and selective activity of semi-synthetic naphthothiazoles against promastigotes and amastigotes reveals that the 2-amino-naphthothiazole ring may represent a scaffold for the design of compounds with leishmanicidal properties and encourage the development of drug formulation and new compounds for further studies in vivo.


Subject(s)
Antiprotozoal Agents/chemical synthesis , Thiazoles/chemistry , Administration, Oral , Animals , Antiprotozoal Agents/pharmacokinetics , Antiprotozoal Agents/toxicity , Biological Availability , Blood Proteins/metabolism , Cell Survival/drug effects , Half-Life , Humans , Leishmania braziliensis/drug effects , Macrophages/cytology , Mice , Mice, Inbred BALB C , Protein Binding , Thiazoles/pharmacokinetics , Thiazoles/toxicity
4.
Rev. bras. farmacogn ; 22(6): 1276-1281, Nov.-Dec. 2012. ilus, tab
Article in English | LILACS | ID: lil-659045

ABSTRACT

Ethyl acetate extracts of cultures grown in liquid Czapek and on solid rice media of the fungal endophyte Fusarium oxysporum SS46 isolated from the medicinal plant Smallanthus sonchifolius (Poepp.) H. Rob., Asteraceae, exhibited considerable cytotoxic activity when tested in vitro against human cancer cells. Chromatographic separation yielded anhydrofusarubin (1) and beauvericin (2) that were identified based on their ¹H and 13C NMR data. Compounds 1 and 2 showed the strongest cytotoxic activity against different cancer cell lines. Compound 2 also showed promising activity against Leishmania braziliensis. Hexanic extract of F. oxysporum SS50 grown on solid rice media also afforded a mixture of compounds that displayed cytotoxic activity against different cancer cell lines. Chemical analysis of the mixture of compounds, investigated by gas chromatography-mass spectrometry (GC-MS), showed that there was a predominance of methyl esters of fatty acids and alkanes.

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