Zobrazeno 1 - 10 of 34 pro vyhledávání: '"F.X. Jarreau"'
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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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2
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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3
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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7
Further confirmation of the presence of indolylacrylic acid in lentil seedlings and identification of hypaphorine as its precursor
Autor: X. Monseur, M. Pais, F.X. Jarreau, M. Hofinger
Publikováno v: Phytochemistry. 14:475-477
The physiologically active indolylacrylic acid previously found in the lentil seedlings was further identified. Its natural formation in the same plant was demonstrated and the identification of its precursor was found to be hypaphorine, N -trimethyl
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::9f925587da30fc5eb3a64a069bee8183
https://doi.org/10.1016/0031-9422(75)85112-0
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8
Comparative hemodynamic study of a new aminosteroid: LND-623 with its 20 alpha-isomer: LND-369, and with digoxin and digoxigenin-rhamnoside in the anesthetized dog
Autor: G. Cheymol, Patrice Jaillon, Heckle J, M. Biour, F.X. Jarreau, Weissenburger J, J.M. Poirier
Publikováno v: Fundamentalclinical pharmacology. 3(1)
Summary— Hemodynamic effects of LND-623, a new aminosteroid lacking the C17 lactone ring and the C14 hydroxyl group common to the natural glycosides, were studied in the pentobarbital-anesthetized dog and compared to those of its 20α-isomer LND-36
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b566086bdb1bc145c539fce00e9c5b15
https://pubmed.ncbi.nlm.nih.gov/2653992
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10
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