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1.
Chemosphere ; 104: 51-6, 2014 Jun.
Article in English | MEDLINE | ID: mdl-24268343

ABSTRACT

In search of environmentally-friendly ionic liquids (ILs), 14 were prepared based on the imidazolium, pyridinium and choline cations, with bromide and several amino acids as anions. Good yields were obtained in the synthesis of pyridinium ILs and those prepared from choline and amino acids. Four of the ILs synthesized from choline and the amino acids arginine, glutamine, glutamic acid and cystine are described here for the first time. The toxicity of the synthesized ILs was checked against organisms of various levels of organization: the crustacean Artemia salina; Human cell HeLa (cervical carcinoma); and bacteria with different types of cell wall, Bacillus subtilis and Escherichia coli. The toxicity was observed to depend on both the cation and anion. Choline-amino acid ILs showed a remarkable low toxicity to A. salina and HeLa cell culture, ten times less than imidazolium and pyridinium ILs. None of ionic liquids exhibited marked toxicity to bacteria, and the effect was 2-3 orders of magnitude smaller than that of the antibiotic chloramphenicol.


Subject(s)
Amino Acids/toxicity , Biocompatible Materials/toxicity , Bromides/toxicity , Ionic Liquids/toxicity , Amino Acids/chemistry , Animals , Anions/chemistry , Anions/toxicity , Artemia/drug effects , Bacillus subtilis/drug effects , Biocompatible Materials/chemistry , Bromides/chemistry , Cations/chemistry , Cations/toxicity , Escherichia coli/drug effects , HeLa Cells , Humans , Ionic Liquids/chemistry
2.
Carbohydr Res ; 347(1): 47-54, 2012 Jan 10.
Article in English | MEDLINE | ID: mdl-22153708

ABSTRACT

Microwave-assisted synthesis of oxo-/thioxopyrimidines and tetrazoles linked to furanoses with D-xylo and D-ribo configuration, and to a D-galacto pyranose is reported and compared to conventional methods. Reaction of dialdofuranoses and dialdopyranoses with a ß-keto ester and urea or thiourea under microwave irradiation at 300 W gave in 10 min the target molecules containing the 2-oxo- or 2-thioxo-pyrimidine ring in high yield. The tetrazole-derived compounds were obtained in two steps by reaction of the formyl group with hydroxylamine hydrochloride, copper sulfate, triethylamine and dicyclohexylcarbodiimide to give an intermediate nitrile, which was then treated with sodium azide. The use of microwave irradiation in the latter step also resulted in a considerably shorter reaction time (10 min) compared to hours under conventional heating to obtain a complete starting materials conversion. Acetylcholinesterase inhibition ranged from 20% to 80% for compounds concentration of 100 µg/mL, demonstrating the potential of this family of compounds for the control of Alzheimer's disease symptoms. Most of the compounds showed antioxidant activity in the ß-carotene/linoleic acid assay, some of them exhibiting IC(50) values in the same order of magnitude as those of gallic acid. The bioactive compounds did not show cytotoxic effects to human lymphocytes using the MTT method adapted for non-adherent cells, nor genotoxicity determined by the short-term in vitro chromosomal aberration assay.


Subject(s)
Antioxidants/chemical synthesis , Carbohydrates/chemical synthesis , Carbohydrates/pharmacology , Chemistry Techniques, Synthetic/methods , Cholinesterase Inhibitors/chemical synthesis , Pyrimidines/chemistry , Tetrazoles/chemistry , Acetylcholinesterase/metabolism , Animals , Antioxidants/chemistry , Antioxidants/pharmacology , Antioxidants/toxicity , Carbohydrates/chemistry , Carbohydrates/toxicity , Cattle , Cell Line , Cell Survival/drug effects , Cholinesterase Inhibitors/chemistry , Cholinesterase Inhibitors/pharmacology , Cholinesterase Inhibitors/toxicity , Humans , Linoleic Acid/chemistry , beta Carotene/chemistry
3.
J Ethnopharmacol ; 108(1): 31-7, 2006 Nov 03.
Article in English | MEDLINE | ID: mdl-16737790

ABSTRACT

Essential oil, ethanolic extract and decoction of 10 plant species from interior Portugal were analyzed for their activity towards acetylcholinesterase (AChE) enzyme and their antioxidant activity. Of these, Melissa officinalis, Paronychia argentea, Sanguisorba minor, Hypericum undulatum and Malva silvestris are used in herbal medicine, Laurus nobilis and Mentha suaveolens as condiments, and Salvia officinalis, Lavandula angustifolia and Lavandula pedunculata also as aromatics. Melissa officinalis and Mentha suaveolens showed AChE inhibitory capacity higher then 50% in the essential oil fraction. Laurus nobilis, Hypericum undulatum, and Sanguisorba minor showed a high inhibition value of AChE in the ethanolic fraction, 64% (1 mg ml(-1)) 68% (0.5 mg ml(-1)), and 78% (1 mg ml(-1)), respectively. Higher values of AChE inhibitory activity were found using decoctions of Lavandula pedunculata, Mentha suaveolens and Hypericum undulatum, 68, 69 and 82% (at a concentration of 5mg dry plant ml(-1) of assay), respectively. The free radical scavenger activity was higher for the polar extracts. In the water extracts most of the plants showed values around 90%. When antioxidant activity was measured with the beta-carotene-linoleic acid assay high activity (65-95%) was also found in the water extracts. Hypericum undulatum, Melissa officinalis and Laurus nobilis showed both high AChE inhibitory capacity and antioxidant activity.


Subject(s)
Antioxidants/chemistry , Antioxidants/pharmacology , Cholinesterase Inhibitors/chemistry , Cholinesterase Inhibitors/pharmacology , Plant Preparations/pharmacology , Plants, Medicinal/chemistry , Drug Evaluation, Preclinical , Plant Oils/chemistry , Plant Oils/pharmacology , Plant Preparations/chemistry , Portugal
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