Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Janssens Frans Eduard"'
Norpiperidine Imidazoazepines as a New Class of Potent, Selective, and Nonsedative H1 Antihistamines
Autor:
Marcel Borgers, Jos Leenaerts, Janssens Frans Eduard, Xavier Langlois, Johan Beetens, Koen van Rossem, Gaston Stanislas Marcell Diels, Benoit Christian Albert Ghislain De Boeck, Anton Megens
Publikováno v:
Journal of Medicinal Chemistry. 48:2154-2166
Clinical doses of available H(1) antihistamines are limited mainly by sedative side effects. However, higher doses are often required to obtain optimal therapeutic activity, especially in dermatology. We report the synthesis of three norpiperidine im
Autor:
Philippe Muller, Pieter Van Remoortere, Rudy Edmond Willebrords, Fortin Jerome Michel Claude, Tom Valerius Josepha Gevers, Koen Andries, Christophe Meyer, Piet Wigerinck, Heidi Szel, Jean-François Bonfanti, Janssens Frans Eduard, Philip Timmerman, Frederic Marc Maurice Doublet, Peggy Janssens, Koen Wuyts, Laurence Queguiner
Publikováno v:
Journal of medicinal chemistry
A preceding paper (Bonfanti et al. J. Med Chem. 2007, 50, 4572−4584) reported the optimization of the pharmacokinetic profile of substituted benzimidazoles by reducing their tissue retention. However, the modifications that were necessary to achiev
Autor:
Jerome Emile Georges Guillemont, Koen Wuyts, Heidi Szel, Peggy Janssens, Laurence Queguiner, Fortin Jerome Michel Claude, Eric Arnoult, Philippe Muller, Jean Fernand Armand Lacrampe, Frederic Marc Maurice Doublet, Cois Sommen, Rudy Edmond Willebrords, Jean-François Bonfanti, Philip Timmerman, Tom Valerius Josepha Gevers, Koen Andries, Piet Wigerinck, Janssens Frans Eduard
Publikováno v:
Journal of medicinal chemistry
We previously reported the discovery of substituted benzimidazole fusion inhibitors with nanomolar activity against respiratory syncytial virus (Andries, K.; et al. Antiviral Res. 2003, 60, 209−219). A lead compound of the series was selected for p
Autor:
Xavier Langlois, Janssens Frans Eduard, C.G.M. Janssen, Albert D. Windhorst, Josée E. Leysen, F.M. Sommen, B. Verreet, Mirek Jurzak, Jacobus D. M. Herscheid, M. Van der Mey
Publikováno v:
Van Der Mey, M, Janssen, C G M, Janssens, F E, Jurzak, M, Langlois, X, Sommen, F M, Verreet, B, Windhorst, A D, Leysen, J E & Herscheid, J D M 2005, ' Synthesis and biodistribution of [ 11 C]R116301, a promising PET ligand for central NK 1 receptors ', Bioorganic and Medicinal Chemistry, vol. 13, no. 5, pp. 1579-1586 . https://doi.org/10.1016/j.bmc.2004.12.019
Bioorganic and Medicinal Chemistry, 13(5), 1579-1586. Elsevier Limited
Bioorganic and Medicinal Chemistry, 13(5), 1579-1586. Elsevier Limited
N1-(2,6-Dimethylphenyl)-2-(4-{(2R,4S)-2-benzyl-1-[3,5-di(trifluoromethyl) [carbonyl-11C]benzoyl]hexahydro-4-pyridinyl}piperazino)acetamide ([11C]R116301) was prepared and evaluated as a potential positron emission tomography (PET) ligand for investig
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ebae1ade440e4079848c9bff21099622
https://research.vumc.nl/en/publications/491f21c4-da78-43a9-a940-de27e3a89995
https://research.vumc.nl/en/publications/491f21c4-da78-43a9-a940-de27e3a89995
Autor:
Marc Moeremans, Koen Andries, Philip R. Wyde, Rudy Edmond Willebrords, Janssens Frans Eduard, Cois Sommen, Tom Valerius Josepha Gevers, Jean Fernand Armand Lacrampe
Publikováno v:
Antiviral research
A cell-based assay was used to discover compounds inhibiting respiratory syncytial virus (RSV)-induced fusion in HeLa/M cells. A lead compound was identified and subsequent synthesis of >300 analogues led to the identification of JNJ 2408068 (R170591
Publikováno v:
Journal of Medicinal Chemistry. 48:1685-1685
Publikováno v:
Journal of Medicinal Chemistry. 48:1686-1686
Autor:
Janssens Frans Eduard, Marcel Gerebernus Maria Luyckx, Marcel Janssen, Raymond Antoine Stokbroekx, Paul A. J. Janssen, Joseph Leo Ghislanus Torremans
Publikováno v:
Journal of Medicinal Chemistry. 28:1934-1943
The synthesis of a series of 1-[(4-fluorophenyl)methyl]-N-(4-piperidinyl)-1H-benzimidazol-2-ami nes and the preliminary evaluation of their in vivo antihistamine activity are described. The title compounds were obtained starting from either 1, 4, 10,
Autor:
Raymond Antoine Stokbroekx, Janssens Frans Eduard, Marcel Gerebernus Maria Luyckx, Marcel Janssen, Joseph Leo Ghislanus Torremans, Paul A. J. Janssen
Publikováno v:
Journal of Medicinal Chemistry. 28:1925-1933
The synthesis of a series N-(4-piperidinyl)-1H-benzimidazol-2-amines and the preliminary evaluation of their in vitro and in vivo antihistaminic activity are described. Cyclodesulfurization of (2-aminophenyl)thioureas with mercury(II) oxide resulted
Publikováno v:
ChemInform. 18
The synthesis of a series of N-1,4-disubstituted-1,4-dihydro-5H-tetrazol-5-one piperidinyl derivatives of fentanyl, carfentanil, and sufentanil is described. The 1-substituted tetrazolinones 2 were essentially prepared via the addition reaction of al