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1

Ni, Ruidong, Suzeeta Bhandari, Perry R. Mitchell, et al. "Synthesis, Quantification, and Characterization of Fatty Acid Amides from In Vitro and In Vivo Sources." Molecules 26, no. 9 (2021): 2543. http://dx.doi.org/10.3390/molecules26092543.

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Fatty acid amides are a diverse family of underappreciated, biologically occurring lipids. Herein, the methods for the chemical synthesis and subsequent characterization of specific members of the fatty acid amide family are described. The synthetically prepared fatty acid amides and those obtained commercially are used as standards for the characterization and quantification of the fatty acid amides produced by biological systems, a fatty acid amidome. The fatty acid amidomes from mouse N18TG2 cells, sheep choroid plexus cells, Drosophila melanogaster, Bombyx mori, Apis mellifera, and Triboli
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2

Nolsøe, Jens, Silje Johansson, Tonje Johannessen, et al. "A Convenient Protocol for the Synthesis of Fatty Acid Amides." Synlett 30, no. 02 (2018): 213–17. http://dx.doi.org/10.1055/s-0037-1611939.

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Several classes of biologically occurring fatty acid amides have been reported from mammalian and plant sources. Many amides conjugated with fatty acids of mammalian origin exhibit specific activation of individual receptors. Their potential as pharmacological tools or as lead compounds towards the development of novel therapeutics is of great interest. Hence, access to such amides by a practical, high-yielding and scalable protocol without affecting the geometry or position of sensitive functionalities is needed. A protocol that meets all these requirements involves activation of the correspo
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3

Boshoff, Helena I., Valerie Mizrahi, and Clifton E. Barry. "Effects of Pyrazinamide on Fatty Acid Synthesis by Whole Mycobacterial Cells and Purified Fatty Acid Synthase I." Journal of Bacteriology 184, no. 8 (2002): 2167–72. http://dx.doi.org/10.1128/jb.184.8.2167-2172.2002.

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ABSTRACT The effects of low extracellular pH and intracellular accumulation of weak organic acids were compared with respect to fatty acid synthesis by whole cells of Mycobacterium tuberculosis and Mycobacterium smegmatis. The profile of fatty acids synthesized during exposure to benzoic, nicotinic, or pyrazinoic acids, as well as that observed during intracellular hydrolysis of the corresponding amides, was not a direct consequence of modulation of fatty acid synthesis by these compounds but reflected the response to inorganic acid stress. Analysis of fatty acid synthesis in crude mycobacteri
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4

Dahan, Wasmia Mohammed, Faruq Mohammad, AbdelRahman O. Ezzat, Ayman M. Atta, Hissah Hamad Al-Tilasi, and Hamad A. Al-Lohedan. "Enhanced Delivery of Insulin through Acrylamide-Modified Chitosan Containing Smart Carrier System." Gels 8, no. 11 (2022): 701. http://dx.doi.org/10.3390/gels8110701.

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The present study develops on insulin-release studies from the chitosan-amide-modified stimuli-responsive polymers formed from various fatty acids including stearic acid, oleic acid, linoleic acid, and linolenic acid. This is the continuation of an earlier reported study that investigates the insulin-release profiles of chitosan-modified fatty acid amides (without stimuli responsive polymers). Following the synthesis and characterization of many different fatty acid amides with a varying amount of unsaturation, the insulin drug loading and release effects were compared among N-isopropylacrylam
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5

Dembitsky, Valery M. "Microbiological Aspects of Unique, Rare, and Unusual Fatty Acids Derived from Natural Amides and Their Pharmacological Profile." Microbiology Research 13, no. 3 (2022): 377–417. http://dx.doi.org/10.3390/microbiolres13030030.

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In the proposed review, the pharmacological profile of unique, rare, and unusual fatty acids derived from natural amides is considered. These amides are produced by various microorganisms, lichens, and fungi. The biological activity of some natural fatty acid amides has been determined by their isolation from natural sources, but the biological activity of fatty acids has not been practically studied. According to QSAR data, the biological activity of fatty acids is shown, which demonstrated strong antifungal, antibacterial, antiviral, antineoplastic, anti-inflammatory activities. Moreover, so
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6

Zeimaran, Ehsan, Sobhan Bahraeian, Taravat Ghanbari, Sara Pourshahrestani, and Hussin Mohd Nor. "Synthesis and Characterization of Supramolecular Elastomers from Polyacids Composed of Vegetable Oils." Advanced Materials Research 747 (August 2013): 505–8. http://dx.doi.org/10.4028/www.scientific.net/amr.747.505.

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Supramolecular elastomers were synthesized using vegetable oil materials namely palm acid oil (PAO) and sunflower oil (SFO). The oils were first epoxidized using formic acid and hydrogen peroxide. The epoxidized oils and adipic acid were then reacted to make polyacids, mainly triacid. Finally, diethylenetriamine (DETA) was added to polyacid to yield fatty amide and a polycondensation with urea performed to achieve the desired elastomers. The synthesized materials were characterized by using Fourier Transform Infrared (FTIR), Nuclear Magnetic Resonance (NMR) and Thermogravimetric Analyzer (TGA)
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7

D’Oca, Caroline Da Ros Montes, Tatiane Coelho, Tamara Germani Marinho, et al. "Synthesis and antituberculosis activity of new fatty acid amides." Bioorganic & Medicinal Chemistry Letters 20, no. 17 (2010): 5255–57. http://dx.doi.org/10.1016/j.bmcl.2010.06.149.

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8

Gerogianni, Velisaria-Eleni, Giorgos S. Koutoulogenis, Dimitrios Triantafyllos Gerokonstantis, and George Kokotos. "Synthesis of Amino-Acid-Based Nitroalkenes." Organics 3, no. 2 (2022): 137–49. http://dx.doi.org/10.3390/org3020011.

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Fatty-acid-based nitroalkenes have recently received great attention because of their bioactivities. On the contrary, peptide- or amino-acid-based nitroalkenes have been scarcely explored so far, although they may exhibit interesting biological properties, for example, as enzyme inhibitors. In this work, we study protocols for the efficient synthesis of nitroalkenes based on natural amino acids. A variety of N-protected amino alcohols and Weinreb amides, derived from α-amino acids, were converted to the corresponding N-protected amino aldehydes, and, through a Henry reaction with nitroalkanes,
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9

Lambruschini, Chiara, Ilaria Demori, Zeinab El Rashed, et al. "Synthesis, Photoisomerization, Antioxidant Activity, and Lipid-Lowering Effect of Ferulic Acid and Feruloyl Amides." Molecules 26, no. 1 (2020): 89. http://dx.doi.org/10.3390/molecules26010089.

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The Ugi four-component reaction employing naturally occurred ferulic acid (FA) is proposed as a convenient method to synthesize feruloyl tertiary amides. Applying this strategy, a peptoid-like derivative of ferulic acid (FEF77) containing 2 additional hydroxy-substituted aryl groups, has been synthesized. The influence of the configuration of the double bond of ferulic acid and feruloyl amide on the antioxidant activity has been investigated thanks to light-mediated isomerization studies. At the cellular level, both FA, trans and cis isomers of FEF77 were able to protect human endothelial cord
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10

Srivastava, Vandana, Hari Om Saxena, Karuna Shanker, et al. "Synthesis of gallic acid based naphthophenone fatty acid amides as cathepsin D inhibitors." Bioorganic & Medicinal Chemistry Letters 16, no. 17 (2006): 4603–8. http://dx.doi.org/10.1016/j.bmcl.2006.06.010.

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11

Liñares, Guadalupe García, Paula G. Quintana, Santiago N. Chanquía, and Alicia Baldessari. "Enzymatic synthesis of N-hydroxyalkyl-fatty acid amides analogs of anandamide." New Biotechnology 29 (September 2012): S53. http://dx.doi.org/10.1016/j.nbt.2012.08.146.

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12

Hosseini-Sarvari, Mona, Esmat Sodagar, and Mohammad Mahdi Doroodmand. "Nano Sulfated Titania as Solid Acid Catalyst in Direct Synthesis of Fatty Acid Amides." Journal of Organic Chemistry 76, no. 8 (2011): 2853–59. http://dx.doi.org/10.1021/jo2002769.

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13

Oben, J., L. Morgan, J. Fletcher, and V. Marks. "Effect of the entero-pancreatic hormones, gastric inhibitory polypeptide and glucagon-like polypeptide-1(7–36) amide, on fatty acid synthesis in explants of rat adipose tissue." Journal of Endocrinology 130, no. 2 (1991): 267–72. http://dx.doi.org/10.1677/joe.0.1300267.

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ABSTRACT The effect of gastric inhibitory polypeptide (GIP), glucagon-like peptide-1(7–36) amide, (GLP-1(7–36) amide), glucagon-like peptide-2 (GLP-2), glucagon and insulin on fatty acid synthesis in explants of rat adipose tissue from various sites was investigated. GIP, GLP-1(7–36) amide and insulin stimulated fatty acid synthesis, as determined by measuring the incorporation of [14C]acetate into saponifiable fat, in a dose-dependent manner, over the concentration range 5–15 ng/ml (0·87–2·61 nmol/l) for insulin and 0·5–7·5 ng/ml for GIP (0·10–1·50 nmol/l) and GLP-1(7–36) amide (0·15–2·27 nmo
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14

Tremblay, Hugo, Catherine St-Georges, Marc-André Legault, Caroline Morin, Samuel Fortin, and Eric Marsault. "One-pot synthesis of polyunsaturated fatty acid amides with anti-proliferative properties." Bioorganic & Medicinal Chemistry Letters 24, no. 24 (2014): 5635–38. http://dx.doi.org/10.1016/j.bmcl.2014.10.084.

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15

de Zoete, M. C., A. C. Kock-van Dalen, F. van Rantwijk, and R. A. Sheldon. "Lipase-catalysed ammoniolysis of lipids. A facile synthesis of fatty acid amides." Journal of Molecular Catalysis B: Enzymatic 1, no. 3-6 (1996): 109–13. http://dx.doi.org/10.1016/1381-1177(95)00012-7.

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16

Almeida, Bruno, Jesús Joglar, María Jesús Luque Rojas, et al. "Synthesis of Fatty Acid Amides of Catechol Metabolites that Exhibit Antiobesity Properties." ChemMedChem 5, no. 10 (2010): 1781–87. http://dx.doi.org/10.1002/cmdc.201000161.

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17

Moazami, Yasamin, Travis V. Gulledge, Scott M. Laster, and Joshua G. Pierce. "Synthesis and biological evaluation of a series of fatty acid amides from Echinacea." Bioorganic & Medicinal Chemistry Letters 25, no. 16 (2015): 3091–94. http://dx.doi.org/10.1016/j.bmcl.2015.06.024.

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18

Rostron, Paul, and Sonia Kasshanna. "Novel Synthesis of Vegetable Oil Derived Corrosion Inhibitors." International Journal of Corrosion 2015 (2015): 1–7. http://dx.doi.org/10.1155/2015/851698.

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Two different naturally occurring vegetable oils, Cress seed oil, and Linseed oil were chemically modified via novel one pot synthesis to produce fatty acid derived amides. These were characterized by their ability to prevent corrosion of carbon steel in vigorously stirred, aerated seawater, one of the most corrosive naturally occurring environments. Corrosion inhibitor efficiencies of up to 99.6% or a corrosion rate reduction factor of 250 in this medium is reported. The one pot synthetic strategy means that the corrosion inhibitors can be made at very low cost.
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19

Awasthi, Neeraj Praphulla, and R. P. Singh. "Lipase-catalyzed Synthesis of Fatty Acid Amide (Erucamide) Using Fatty Acid and Urea." Journal of Oleo Science 56, no. 10 (2007): 507–9. http://dx.doi.org/10.5650/jos.56.507.

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20

Khalkar, Sharmishtha, DiptiNarayan Bhowmick, and Amit Pratap. "Synthesis and Effect of Fatty Acid Amides as Friction Modifiers in Petroleum Base Stock." Journal of Oleo Science 62, no. 11 (2013): 901–4. http://dx.doi.org/10.5650/jos.62.901.

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21

Hosseini-Sarvari, Mona, Esmat Sodagar, and Mohammad Mahdi Doroodmand. "ChemInform Abstract: Nano Sulfated Titania as Solid Acid Catalyst in the Direct Synthesis of Fatty Acid Amides." ChemInform 42, no. 28 (2011): no. http://dx.doi.org/10.1002/chin.201128045.

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22

Vulfovich, S. L., N. A. Sergeeva, V. V. Ragulin, A. G. Telin, and V. A. Dokichev. "OBTAINING AN EMULSIFIER OF INVERSE EMULSIONS WITH A CORROSION INHIBITOR PROPERTIES." Problems of Gathering Treatment and Transportation of Oil and Oil Products, no. 2 (May 16, 2023): 20–30. http://dx.doi.org/10.17122/ntj-oil-2023-2-20-30.

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Reverse emulsions are widely used in oil production processes; moreover, due to a number of unique properties, they are used both in drilling and in killing wells, and for leveling the injectivity profile, as well as in repair and isolation works as a liquid packer. Most industrial emulsifiers belong to the class of fatty acid amides derived from natural and synthetic carboxylic acids and amines (primary and secondary) or amino alcohols. Given that many technological operations, such as killing with concentrated salt solutions (reverse emulsions are used as blocking fluids), treatment of the b
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23

Fetisov, L. N., A. E. Svyatogorova, K. N. Kononenko, V. V. Chekrysheva, and A. A. Zubenko. "Development issue of antiprotozoal agents to treat and prevent protozoal infections of fish, and theoretical and practical approaches to its solution." Russian Journal of Parasitology 16, no. 3 (2022): 367–76. http://dx.doi.org/10.31016/1998-8435-2022-16-3-367-376.

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The purpose of the research is to determine safe parameters for the use of certain fatty acid amides against protozoal diseases of fish.Materials and methods. The synthesis and biological activity determination of new compounds were studied in laboratory conditions of the chemical synthesis creative team of the North Caucasus Zonal Research Veterinary Institute. The protistocidal activity of the new substances was determined in a liquid nutritional medium by serial dilution according to our technique. The ciliate Colpoda steinii was used as a test culture. The solution toxicity was determined
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24

Matthes, Bernd, Jochen Schmalfuß, and Peter Böger. "Chloroacetamide Mode of Action, II: Inhibition of Very Long Chain Fatty Acid Synthesis in Higher Plants." Zeitschrift für Naturforschung C 53, no. 11-12 (1998): 1004–11. http://dx.doi.org/10.1515/znc-1998-11-1211.

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Abstract In short-term -experiments [14C]-labelled malonic acid, stearic acid and acetate have been incorporated into leaf fatty acids of seedlings of Cucumis sativus, Hordeum vulgare and Zea mays. The pattern of labelled fatty acids changed markedly by treatment with the chloroacetamide herbicides metazachlor, metolachlor or butachlor. During a 2-h incubation time, 1 μᴍ chloroacetamide specifically inhibited up to 100% the formation of the saturated very long chain fatty acids (V LCFAs) with a carbon number of 20, 22 and 24. In cucumber and barley a 50% inhibition of VLCFA formation is achiev
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25

Chruma, Jason J., Douglas J. Cullen, Lydia Bowman, and Patrick H. Toy. "Polyunsaturated fatty acid amides from the Zanthoxylum genus – from culinary curiosities to probes for chemical biology." Natural Product Reports 35, no. 1 (2018): 54–74. http://dx.doi.org/10.1039/c7np00044h.

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26

Alvarado, Mario, Pilar Goya, Manuel Macías-González, et al. "Antiobesity designed multiple ligands: Synthesis of pyrazole fatty acid amides and evaluation as hypophagic agents." Bioorganic & Medicinal Chemistry 16, no. 23 (2008): 10098–105. http://dx.doi.org/10.1016/j.bmc.2008.10.023.

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27

Nichols, Frank, and Baliram Maraj. "Relationship between Hydroxy Fatty Acids and Prostaglandin E2 in Gingival Tissue." Infection and Immunity 66, no. 12 (1998): 5805–11. http://dx.doi.org/10.1128/iai.66.12.5805-5811.1998.

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ABSTRACT Bacterial hydroxy fatty acids and alpha-hydroxy fatty acids have been demonstrated in complex lipid extracts of subgingival plaque and gingival tissue. However, little is known about the relationship between these hydroxy fatty acids in plaque and gingival tissues or the significance of these complex lipids in promoting inflammatory periodontal disease. The present study determined the percentages of ester-linked and amide-linked hydroxy fatty acids in complex lipids recovered from plaque and gingival tissue samples and the relationship between bacterial hydroxy fatty acids and alpha-
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28

Ginting, B. S., A. Ginting, E. K. Sitepu, and J. Br Tarigan. "NON-CATALYTIC SYNTHESIS OF FATTY ACID ALKANOLAMIDES FROM PALM FATTY ACID DISTILLATE AND MONOETHANOLAMINE UNDER MICROWAVE IRRADIATION." RASAYAN Journal of Chemistry 16, no. 01 (2023): 391–97. http://dx.doi.org/10.31788/rjc.2023.1618188.

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The non-catalytic synthesis of fatty acid alkanol amide (FAA) from the amidation of palm fatty acid distillate (PFAD) and monoethanolamine (MEA) under microwave irradiation has been investigated. Parameters of the molar ratio of PFAD to MEA, reaction time, and microwave power were determined using the response surface method and the Box-Behnken experimental design. The optimum conversion of FAA of 98.89% was obtained under reaction conditions of ratio molar PFAD to MEA of 1:1, a reaction time of 18.5 minutes, and a microwave power of 100%. The formation of FAA compounds was confirmed with FT-I
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29

Betancourt-Jimenez, Daniela, Jeffrey P. Youngblood, and Carlos J. Martinez. "Synthesis and Characterization of Fatty Acid Amides from Commercial Vegetable Oils and Primary Alkyl Amines for Phase Change Material Applications." ACS Sustainable Chemistry & Engineering 8, no. 36 (2020): 13683–91. http://dx.doi.org/10.1021/acssuschemeng.0c03626.

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30

Canela-Xandri, Anna, Gemma Villorbina, Mercè Balcells, Xavier Fernández-Francos, Luisa F. Cabeza, and Ramon Canela-Garayoa. "Synthesis and Thermophysical Characterization of Fatty Amides for Thermal Energy Storage." Molecules 24, no. 20 (2019): 3777. http://dx.doi.org/10.3390/molecules24203777.

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Nine monoamides were synthesized from carboxylic acids (C8–C18) and crude glycerol. The final monoamides were the result of a rearrangement of the acyl chain during the final hydrogenation process. The purity of the final compounds was determined by spectroscopic and mass spectrometry (MS) techniques. The thermophysical properties of solid monoamides were investigated to determine their capability to act as phase change materials (PCM) in thermal energy storage. Thermophysical properties were determined with a differential scanning calorimeter (DSC). The melting temperatures of the analyzed ma
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31

GRUDININ, A. L., I. M. KOSHKINA, and I. N. DOMNIN. "ChemInform Abstract: Synthesis of Novel Amphiphilic Diacetylene Amides of High Fatty Acids." ChemInform 25, no. 4 (2010): no. http://dx.doi.org/10.1002/chin.199404103.

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32

P. More, Aarti, Ravindra Abhimanyu Kute, and Shashank T. Mhaske. "Polyesteramide resin from PET waste and fatty amide." Pigment & Resin Technology 43, no. 5 (2014): 285–92. http://dx.doi.org/10.1108/prt-05-2013-0033.

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Purpose – The purpose of this paper is synthesis of polyesteramide resin from jatropha oil and monomer from recycling of poly(ethylene terephthalate) (PET) to get the excellent benefit of individual structure. Along with the synthesis of polyesteramide resin, this research work will also help in recycling of PET waste and help for the conversion of monomer obtained from recycling of PET to value-added application. Design/methodology/approach – Polyesteramide resin was synthesized by conventional method, i.e. by converting jatropha oil to corresponding fatty amide, i.e. hydroxyl ethyl jatropha
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33

Ikyenge, Barnabas Aloo, Terungwa Iorkaha, and Ishwah Benjamin. "Synthesis and Characterization of Fatty Polyamide from Dimer Acid Prepared from Afzelia Africana seed oil." American Journal of Innovation in Science and Engineering 1, no. 1 (2022): 13–17. http://dx.doi.org/10.54536/ajise.v1i1.709.

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Afzelia africana seed oil was extracted from its oil-bearing seeds via soxhlet extraction with n-hexane as the solvent. The oil was characterized and the percentage yield, specific gravity, refractive index, iodine value, acid value and saponification value were; 24.6%, 0.9184, 1.4708, 105.75 (Wij’s), 5.61 (mg KOH/g) and 199.155 (mg/KOH/g) respectively. Dimer acids were synthesized by heating 50g of the oil at 3400C in nitrogen inert atmosphere using iodine crystals as catalyst. Characterization of the dimer acid indicated that refractive index, iodine value, acid value and saponification valu
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34

Bezuglov, Vladimir, Mikhail Bobrov, Natalia Gretskaya, et al. "Synthesis and biological evaluation of novel amides of polyunsaturated fatty acids with dopamine." Bioorganic & Medicinal Chemistry Letters 11, no. 4 (2001): 447–49. http://dx.doi.org/10.1016/s0960-894x(00)00689-2.

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35

Umerzakova, M. B., B. K. Donenov, R. B. Sarieva, and Zh N. Kainarbaeva. "PREPARATION OF SULPHATED FATTY ACID DERIVATIVES OF SPIRULINA OIL." Chemical Journal of Kazakhstan 73, no. 1 (2021): 34–42. http://dx.doi.org/10.51580/2021-1/2710-1185.03.

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A new sulfonated derivative of Spirulina oil fatty acids was obtained in the work.This derivative is obtained from dry biomass of microalgae in several stages: extraction of lipids from dry biomass, lipid methylation, amination of the formed methyl esters of Spirulina fatty acids, modification of amide with maleic anhydrideand subsequent reaction of the synthesized monoester with sodium bisulfate. The conditions for all stages of the synthesis of the sulfonated derivative were optimized.The initial compounds and reaction products were identified by IR spectroscopy.
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de Oliveira, Fábio Rodrigues, Nágila Monteiro da Silva, Moisés Hamoy, et al. "The GABAergic System and Endocannabinoids in Epilepsy and Seizures: What Can We Expect from Plant Oils?" Molecules 27, no. 11 (2022): 3595. http://dx.doi.org/10.3390/molecules27113595.

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Seizures and epilepsy are some of the most common serious neurological disorders, with approximately 80% of patients living in developing/underdeveloped countries. However, about one in three patients do not respond to currently available pharmacological treatments, indicating the need for research into new anticonvulsant drugs (ACDs). The GABAergic system is the main inhibitory system of the brain and has a central role in seizures and the screening of new ACD candidates. It has been demonstrated that the action of agents on endocannabinoid receptors modulates the balance between excitatory a
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37

Qiu, Yan, Jie Ren, Hongwei Ke, et al. "Design and synthesis of uracil urea derivatives as potent and selective fatty acid amide hydrolase inhibitors." RSC Advances 7, no. 37 (2017): 22699–705. http://dx.doi.org/10.1039/c7ra02237a.

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38

Zhou, Pan, Lei Xiang, Dongsheng Zhao, Jie Ren, Yan Qiu, and Yuhang Li. "Synthesis, biological evaluation, and structure activity relationship (SAR) study of pyrrolidine amide derivatives as N-acylethanolamine acid amidase (NAAA) inhibitors." MedChemComm 10, no. 2 (2019): 252–62. http://dx.doi.org/10.1039/c8md00432c.

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39

Bezuglov, Vladimir, and et al et al. "ChemInform Abstract: Synthesis and Biological Evaluation of Novel Amides of Polyunsaturated Fatty Acids with Dopamine." ChemInform 32, no. 22 (2010): no. http://dx.doi.org/10.1002/chin.200122161.

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40

Zerkowski, Jonathan A., and Daniel K. Y. Solaiman. "Synthesis of polyfunctional fatty amines from sophorolipid-derived 17-hydroxy oleic acid." Journal of the American Oil Chemists' Society 83, no. 7 (2006): 621–28. http://dx.doi.org/10.1007/s11746-006-1248-1.

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41

de Zoete, M. C., A. C. Kock-van Dalen, F. van Rantwijk, and R. A. Sheldon. "Lipase-catalysed ammoniolysis of lipids. A facile synthesis of fatty acid amides [J. Mol. Catal. B, 1 (1996) 109–113]." Journal of Molecular Catalysis B: Enzymatic 2, no. 2-3 (1996): 141–45. http://dx.doi.org/10.1016/s1381-1177(96)00025-2.

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42

Ianni, Luca, Martino, et al. "Dietary Supplementation of Dried Grape Pomace Increases the Amount of Linoleic Acid in Beef, Reduces the Lipid Oxidation and Modifies the Volatile Profile." Animals 9, no. 8 (2019): 578. http://dx.doi.org/10.3390/ani9080578.

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The aim of this study was to evaluate the effect of dietary supplementation with dried grape pomace on beef quality. Ten Friesian calves were divided into two groups, a control group that received a standard diet, and an experimental group that was administered the dietary supplementation. At the end of the 75 days of the trial, animals were slaughtered, and meat samples analyzed for physical and chemical properties, fatty acids composition, lipid oxidation, volatile compounds, and biogenic amines. The fatty acid profile resulted affected by dietary supplementation, since an increase in concen
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43

Vergara, John H., Yunze Tian, John J. La Scala, Joshua M. Sadler, and Giuseppe R. Palmese. "Synthesis and characterization of fatty acid modified amines with improved water barrier properties." European Polymer Journal 97 (December 2017): 112–19. http://dx.doi.org/10.1016/j.eurpolymj.2017.09.035.

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44

Takao, Koichi, Kaori Noguchi, Yosuke Hashimoto, Akira Shirahata та Yoshiaki Sugita. "Synthesis and Evaluation of Fatty Acid Amides on the N-Oleoylethanolamide-Like Activation of Peroxisome Proliferator Activated Receptor α". Chemical and Pharmaceutical Bulletin 63, № 4 (2015): 278–85. http://dx.doi.org/10.1248/cpb.c14-00881.

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Deplano, Alessandro, Jessica Karlsson, Federica Moraca, et al. "Design, synthesis and in vitro and in vivo biological evaluation of flurbiprofen amides as new fatty acid amide hydrolase/cyclooxygenase-2 dual inhibitory potential analgesic agents." Journal of Enzyme Inhibition and Medicinal Chemistry 36, no. 1 (2021): 940–53. http://dx.doi.org/10.1080/14756366.2021.1875459.

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Onnis, Valentina, Cenzo Congiu, Emmelie Björklund, Franziska Hempel, Emma Söderström, and Christopher J. Fowler. "Synthesis and Evaluation of Paracetamol Esters As Novel Fatty Acid Amide Hydrolase Inhibitors." Journal of Medicinal Chemistry 53, no. 5 (2010): 2286–98. http://dx.doi.org/10.1021/jm901891p.

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Faure, Lionel, Subbiah Nagarajan, Hyeondo Hwang, et al. "Synthesis of Phenoxyacyl-Ethanolamides and Their Effects on Fatty Acid Amide Hydrolase Activity." Journal of Biological Chemistry 289, no. 13 (2014): 9340–51. http://dx.doi.org/10.1074/jbc.m113.533315.

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Maisonneuve, Lise, Arvind S. More, Stéphanie Foltran, et al. "Novel green fatty acid-based bis-cyclic carbonates for the synthesis of isocyanate-free poly(hydroxyurethane amide)s." RSC Adv. 4, no. 49 (2014): 25795–803. http://dx.doi.org/10.1039/c4ra03675a.

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Shoup, Timothy M., Ali A. Bonab, Alan A. Wilson, and Neil Vasdev. "Synthesis and Preclinical Evaluation of [18F]FCHC for Neuroimaging of Fatty Acid Amide Hydrolase." Molecular Imaging and Biology 17, no. 2 (2014): 257–63. http://dx.doi.org/10.1007/s11307-014-0789-1.

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Kurahashi, Yuko, Natsuo Ueda, Hiroshi Suzuki, Mitsujiro Suzuki, and Shozo Yamamoto. "Reversible Hydrolysis and Synthesis of Anandamide Demonstrated by Recombinant Rat Fatty-Acid Amide Hydrolase." Biochemical and Biophysical Research Communications 237, no. 3 (1997): 512–15. http://dx.doi.org/10.1006/bbrc.1997.7180.

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