Zobrazeno 1 - 10 of 18 pro vyhledávání: '"F, Ducrey"'
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A reversible monoamine oxidase inhibitor, Toloxatone: comparison of its physicochemical properties with those of other inhibitors including Brofaromine, Harmine, R40519 and Moclobemide
Autor: F. Ducrey, M Depas, Johan Wouters, J. J. Koenig, F. Moureau, Daniel P. Vercauteren, François Durant, F.X. Jarreau
Publikováno v: European Journal of Medicinal Chemistry. 30:823-837
Summary Reversible, competitive and selective monoamine oxidase A inhibitors (MAO A Is) are an exciting new type of anti-depressants with a safe profile. The mechanism for reversible inhibition of MAO A at the molecular level is still unknown. The pl
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::49e6f29bbc1e233ebda473549e51be71
https://doi.org/10.1016/0223-5234(96)88302-4
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A reversible monoamine oxidase inhibitor, toloxatone: Structural and electronic properties
Autor: Guy Evrard, François Durant, Johan Wouters, J. J. Koenig, F. Moureau, Sonia Collin, F. Ducrey, Daniel P. Vercauteren, F.X. Jarreau
Publikováno v: European Journal of Medicinal Chemistry. 27:939-948
Toloxatone is a reversible MAOA-inhibitor, marketed as antidepressant (Humoryl®), with an original chemical structure. It differs from first generation irreversible MAOIs, known to induce covalent bonds with the enzyme active site. In order to under
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::2624bcf563af34f0e819e7f29f4f855d
https://doi.org/10.1016/0223-5234(92)90026-w
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5
Experimental and theoretical study of reversible monoamine oxidase inhibitors: structural approach of the active site of the enzyme
Autor: F. Ducrey, François Durant, F. Moureau, J. J. Koenig, F.X. Jarreau, Johan Wouters, Daniel P. Vercauteren, Guy Evrard
Publikováno v: Amine Oxidases: Function and Dysfunction ISBN: 9783211825211
Experimental and theoretical physico-chemical methods were used to investigate the interaction between aryl-oxazolidinones and monoamine oxidase (MAO). Several arguments suggest that these compounds interact with the flavin adenine dinucleotide (FAD)
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::6b31946704800574cfc61e1dde436dd7
https://doi.org/10.1007/978-3-7091-9324-2_41
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6
Experimental and theoretical study of reversible monoamine oxidase inhibitors: structural approach of the active site of the enzyme
Autor: J, Wouters, F, Moureau, D P, Vercauteren, G, Evrard, F, Durant, J J, Koenig, F, Ducrey, F X, Jarreau
Publikováno v: Journal of neural transmission. Supplementum. 41
Experimental and theoretical physico-chemical methods were used to investigate the interaction between aryl-oxazolidinones and monoamine oxidase (MAO). Several arguments suggest that these compounds interact with the flavin adenine dinucleotide (FAD)
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::c8c33509ee3be0b1a2c4dae95493b488
https://pubmed.ncbi.nlm.nih.gov/7931244
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