Works matching AU Deplano, Alessandro
Results: 8
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.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2021, v. 36, n. 1, p. 940, doi. 10.1080/14756366.2021.1875459
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Exploring the fatty acid amide hydrolase and cyclooxygenase inhibitory properties of novel amide derivatives of ibuprofen.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2020, v. 35, n. 1, p. 815, doi. 10.1080/14756366.2020.1743283
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Benzylamides and piperazinoarylamides of ibuprofen as fatty acid amide hydrolase inhibitors.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2019, v. 34, n. 1, p. 562, doi. 10.1080/14756366.2018.1532418
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Interaction of the N-(3-Methylpyridin-2-yl)amide Derivatives of Flurbiprofen and Ibuprofen with FAAH: Enantiomeric Selectivity and Binding Mode.
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- PLoS ONE, 2015, v. 10, n. 10, p. 1, doi. 10.1371/journal.pone.0142711
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Characterisation of (R)-2-(2-Fluorobiphenyl-4-yl)-N-(3-Methylpyridin-2-yl)Propanamide as a Dual Fatty Acid Amide Hydrolase: Cyclooxygenase Inhibitor.
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- PLoS ONE, 2015, v. 10, n. 9, p. 1, doi. 10.1371/journal.pone.0139212
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- Article
Molecular Basis for Non-Covalent, Non-Competitive FAAH Inhibition.
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- International Journal of Molecular Sciences, 2022, v. 23, n. 24, p. 15502, doi. 10.3390/ijms232415502
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Synthesis of Sulfonamides Incorporating Piperidinyl-Hydrazidoureido and Piperidinyl-Hydrazidothioureido Moieties and Their Carbonic Anhydrase I, II, IX and XII Inhibitory Activity.
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- Molecules, 2022, v. 27, n. 17, p. 5370, doi. 10.3390/molecules27175370
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- Article
Design, Synthesis and Evaluation of Antiproliferative Activity of New Benzimidazolehydrazones.
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- Molecules, 2016, v. 21, n. 5, p. 579, doi. 10.3390/molecules21050579
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- Article