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Palm fatty acid distillate PFAD is an example of potential low-cost palm biofuel second generation feedstock, most used as a source of fatty acid for non-food applications in industry. Catalytic application of Oxone® salt was used in the present study for the esterification reaction of PFAD for biodiesel production for the first time. After optimizing the conversion rate, was possible to observe that, among the process variables studied [Oxone® concentration (%), temperature (°C) and reaction time (h)], Oxone® concentration was the only significant variable for the fatty acid ethyl esters (FAEEs) generation response variable. A > 90% conversion rate was reached with 15% Oxone® at 42 °C, using a PFAD:ethanol molar ratio of 1:5 at 12 h reaction time. The reaction system has a series of advantages, such as mild conditions, simple operation, green and high conversion. As alternative for make the biodiesel production as sustainable as possible.

The Aedes aegypti mosquito is a vector of several diseases, such as dengue, malaria and the Zika virus. Synthetic insecticides such as chlorpyrifos and chlorothalonil have been used for plague control, despite causing damage to the environment and to humans. It is therefore important to study natural active compounds with a low environmental impact. The present paper developed an environmentally friendly formulation of silk fibroin (SF) associated with fatty acid esters [ethyl (FAEE-SF), propyl (FAPE-SF) and butyl (FABE-SF)] from Astrocaryum murumuru Mart. fat, which was effective against Aedes aegypti 3th instar larvae. The FABE-SF nanoemulsion induced a higher mortality rate in the larvae of the A. aegypti after 48 h (LC50 = 18.92 µg / mL). The stabilities of the nanoemulsions were monitored for 21 days, and FABE-SF exhibited greater stability throughout the monitored period, with average particle, zeta and PDI values of around 217 ± 0.85 nm, -25.6 ± 3.24 mV and 0.338 ± 0.01, respectively. This paper reported the first effective action of fatty acid esters from A. murumuru Mart. associated with silk fibroin against A. aegypti. The FABE-SF solution also had a low hemolytic index, suggesting that treatment may be safe for animal and human use.

Fatty amides (N-alkylamides) are a group of bioactive lipids widely distributed in microorganisms, animals, and plants. The low yield in the extraction process of spilantol, a grease amide, which has been related mainly to diverse biological effects, compromises its application on a large scale. Thus, this study proposed an alternative to the synthesis of fatty amides from Bertholletia excelsa (AGBe) oil, with a chemical structure similar to that of spilantol. In vivo models induced by carrageenan were used in Zebrafish (Danio rerio). In in vivo studies, oral AGBe produced no signs of toxicity. In the histopathological study, AGBe did not cause significant changes in the main metabolizing organs (liver, kidneys, and intestines). In the anti-inflammatory evaluation, all doses (45 mg/kg, 500 mg/kg, and 1000 mg/kg) were effective, significantly reducing edema and producing a dose-response effect when compared to spilantol. In the in silico study, with the use of molecular docking, he showed that among the AGBe, the molecules 18:1, ω-7-ethanolamine and 18:1, ω-9-ethanolamine stood out, which had 21 interactions for COX-2 and 20 interactions for PLA2, respectively, surpassing the spilantol standard with 15 interactions for COX-2 and PLA2. The hypothesis of anti-inflammatory action was confirmed in the in silico study, demonstrating the involvement of AGBe in the process of inhibiting the enzymes COX-2 and PLA2. Therefore, based on all the results obtained and the fact that until the dose of 1000 mg/kg, orally, in zebrafish, it was not possible to determine the LD50, it can be said that AGBe is effective and safe for the activity anti-inflammatory.

The distillate from the deodorization of palm oil (DDPO) is an agro-industrial residue, approximately 84% of which consists of free fatty acids (FFAs), which can be used for the production of fatty acid ethyl esters (FAEE). A catalyst (10HPMo/AlSiM) obtained from a waste material, Amazon flint kaolin, was applied in the esterification of the DDPO, reaching a conversion index of 94%, capable of maintaining satisfactory activity (>75%) after four consecutive cycles. Flint kaolin is therefore proven to be an efficient option in the search for new heterogeneous low-cost catalysts obtained from industrial by-products, contributing to the reduction of environmental impact and adding value to widely available wastes that would otherwise be discarded directly into the environment. Based on the catalytic results, esterification of DDPO using 10HPMo/AlSiM can be a cheaper alternative for the production of sustainable fuels.

The amidation of fatty acid is an important reaction for synthesis of fatty alkolamines with a variety of pharmacological activities. The objective of this paper was to demonstrate the aminolysis direct and solvent of the triglycerides from the patawa oil by heterogeneous catalysis. The results of the amidation direct free solvents were favorable using 5% Al2O3 as catalyst, with a conversion of 94% at 24 h of reaction. After spectroscopic characterization, we decided explore the antimicrobial tests of the fatty amides (FAA) against the Staphylococcus aureus strain (ATCC 33591), showing a MIC activity of 1.9612 mg/mL and the fatty ethyl esters (FAEE) a 3.4125 mg/mL MIC. Therefore, the synthesis direct free solvents of FAA by Al2O3 from patawa oil was viable and innovative.

This study reports the synthesis of fatty acid amides (FAA), analogous to anandamide, prepared from Brazil nut oil (BNO), using Amano lipase from Pseudomonas fluorescens as a catalyst of direct aminolysis, with a good yield (95-68%). The anti-inflammatory effects of BNO and FAA were evaluated by the carrageenan-induced paw edema method. Analysis of the formation of edema showed that these FAA, at all dose used, significantly reduced the development of edema.

Universidade Federal do Amap?. Departamento de Ci?ncias Biol?gicas e da Sa?de. Macap?, AP, Brasil. Universidade Federal do Amap?. Departamento de Ci?ncias Biol?gicas e da Sa?de. Macap?, AP, Brasil. Universidade Federal do Amap?. Departamento de Ci?ncias Biol?gicas e da Sa?de. Macap?, AP, Brasil. Universidade Federal do Amap?. Departamento de Ci?ncias Biol?gicas e da Sa?de. Macap?, AP, Brasil. Universidade de S?o Paulo. Faculdade de Ci?ncias Farmac?uticas de Ribeir?o Preto. Ribeir?o Preto, SP, Brasil. Universidade de S?o Paulo. Faculdade de Ci?ncias Farmac?uticas de Ribeir?o Preto. Ribeir?o Preto, SP, Brasil. Minist?rio da Sa?de. Secretaria de Vigil?ncia em Sa?de. Instituto Evandro Chagas. Ananindeua, PA, Brasil. Minist?rio da Sa?de. Secretaria de Vigil?ncia em Sa?de. Instituto Evandro Chagas. Ananindeua, PA, Brasil. Universidade Federal do Amap?. Colegiado de Qu?mica. Macap?, AP, Brasil. Centro Brasileiro de Pesquisas F?sicas. Urca, RJ, Brasil. Universidade Federal do Amap?. Colegiado de Qu?mica. Macap?, AP, Brasil. Universidade Federal do Amap?. Departamento de Ci?ncias Biol?gicas e da Sa?de. Macap?, AP, Brasil. Glioblastoma is an aggressive primary tumor of the central nervous system (CNS). Is the most aggressive among infiltrative gliomas arising from the CNS. This tumor has low patient survival rate and several studies aiming at developing new drugs have increased. Patients with this cancer type face significant morbidity and mortality. This study evaluated the antineoplastic activity of synthetic chalcones (3a-3f) using in vitro glioblastoma models and molecular modeling. Cytotoxicity assay showed that Astrocitoma Hospital Ofir Loyola No 1 (AHOL1) and Uppsala 87 neoplastic glioblastoma lines (U87) cellular viability were significantly reduced compared to Healthy human fibroblasts cell lines (AN27) when exposed to chalcones. Interaction with the serine amino acid was present in the most promising and the reference binder docking, suggesting its importance inhibiting cell growth. Comparative analysis between the reference ligands and the molecules showed that the amino acid LYS352 present in all fittings, suggesting that this is the main amino acid for interaction with tubulin and are consistent with those in cytotoxicity assay, suggesting antineoplastic potential in glioblastoma. Long trajectory molecular dynamics studies were also carried out in order to investigate stability and conformations amongst the chalcones bound tubulin as well, in comparison to doxorubicin (here used as control), however future studies are needed to further assess the mechanism of inhibition of chalcones used in this investigation.

The chemoselective bioreduction of α,β-unsaturated compounds is an important synthetic tool that can have applications in the synthesis of many fine chemicals and pharmaceutical molecules. The synthesis of aromatic malononitrile derivatives through Knoevenagel condensation by microwave radiation under green chemistry conditions using methanol like solvent, free base and free catalyst is here reported. In addiction the biocatalytic reduction of the C–C double bond of aromatic malononitrile derivatives by whole cells of the marine-derived fungal Penicillium citrinum CBMAI 1186 was also tested. The products catalyzed by the fungus ene-reductase were obtained in very good yields (up to >98%).

This paper report the use of Carapa guianensis Abul. (Meliaceae) oil and derivates [fatty acid ethyl ester (FAEE’s) and free fatty acid (FFA’s)] associate with silk fibroin (SF), and its activity against the larvae of the vector Aedes aegypti. The emulsions FFA2-SF derived from AO2, that mostly contained unsaturated fatty acids, presented the best results against the larvae of Ae. aegypti after a 48 h period (LC50 = 16.79 mg.mL−1), causing structural alterations to the vector. It is suggested that the biopolymeric matrix of silk fibroin increases the biodistribution and bioavailability of active in medium aqueous. This is the first work of its type which has pointed larvicidal activity of the free fatty acid from C. guianensis, associate with silk fibroin against Aedes aegypti.

Microalgae are an indispensable food source for the various growth stages of mollusks, crustaceans, and several fish species. Using a microalgae biomass present in the Amazonian ecosystem (Macapá-AP), we study extraction methods for fatty acid such as solvent extraction (magnetic stirring and/or Soxhlet) and/or hydrolysis (acid and/or enzymatic catalysis) followed by esterification and/or direct transesterification. Extraction of crude triacylglycerides by mechanical stirring at room temperature was more efficient than continuous reflux (Soxhlet). Subsequently, the lipid extract was subject to transesterification with ethanol and CAL-B as a biocatalyst, leading to production of fatty acid ethyl esters (FAEE). Additionally, FAEEs were prepared by hydrolysis of crude triacylglycerides followed by acid-mediated esterification or enzymatic catalysis (lipase). In this case, the type of catalyst did not significantly influence FAEE yields. In the lipid extract, we identified palmitic, linoleic, oleic, and stearic acids with palmitic acid being the most abundant. Our results suggest that enzymatic catalysis is a viable method for the extraction of lipids in the microalga, Scenedesmus ecornis.

The Amano AK lipase from Pseudomonas fluorescens was immobilized in fibroin-alginate spheres (FA-LPf) and used to catalyze the transesterification reaction of soybean oil under different conditions (solvents, time, amounts of immobilized lipase, and temperature) for the production of biodiesel (fatty acid ethyl esters, FAEE). The FAEE was quantified by GC-FID analysis, and tricaprin was used as an internal standard. The maximum FAEE yield (63%) was attained after 96 h at 32 °C and 400 rpm in 30% (v/v) n-hexane, which used 20% (w/w) of the immobilized lipase. However, it is noteworthy that with a period of 96 h, the spheres of FA-LPf were partially destroyed by friction from the magnetic stirring, and the long time for the transesterification reactions is impractical in these conditions. For this reason, the reaction time was reduced to 48 h, which resulted in 42% FAEE and assures better reuse conditions for four consecutive cycles. This study shows the efficacy of an enzyme immobilized in a biodegradable FA-LPf support.

To broaden the range of applicability of a reduction reaction mediated by the marine fungal strain Penicillium citrinum CBMAI 1186 to organic chemical processes, the ability of whole mycelia to grow in biphasic mixtures with organic solvents was tested with acetone, ethyl acetate, n-butanol, dichloromethane, n-hexane and toluene. n-Hexane was the least toxic solvent according to the amount of mycelial mass grown in an artificial sea water medium mixed with each solvent. Therefore, whole hyphae of P. citrinum CBMAI 1186 were used as biocatalysts in the chemoselective biotransformation of the carbon–carbon double bond in α,β-, di-α,β-, and mono-α,β,γ,δ-unsaturated ketones (3a, 3c–f) in a biphasic system of phosphate buffer and n-hexane (9:1). Only the di-α,β,γ,δ-unsaturated ketone (3b) was not biocatalyzed under these conditions. In general, there were good conversions of saturated ketones by the enoate reductase enzymes of P. citrinum CBMAI 1186.

1,2,3-Triazole derivatives have gained attention as an attractive heterocyclic compound with antifungal, antibacterial, anti-HIV, anticonvulsants and antiallergic activities. 1 The copper-catalyzed azidealkyne cycloaddition reaction (CuAAC) is an example of click reaction, since is a simple method for synthesized triazoles with an wide scope, high yields in mild conditions. Combining with concept of green chemistry, the CuAAC click reaction has been improved by immobilization of copper species onto various supports. 2 In this work, it was studied the recovery and reuse of copper in CuAAC reaction by immobilizing it in alginate spheres (Alg-CuSO4).