Zobrazeno 1 - 10
of 25
pro vyhledávání: '"Markus Zollinger"'
Autor:
Kenichi Umehara, Veit J. Erpenbeck, Markus Zollinger, H. Markus Weiss, Meredith Cain, Walid Elbast, Janardhana Vemula
Publikováno v:
Drug metabolism and disposition: the biological fate of chemicals. 48(10)
This drug-drug interaction (DDI) study determined the effect of cyclosporine, an inhibitor of OATP1B3 and P-gp, on the pharmacokinetics (PK) of fevipiprant, an oral, highly selective, competitive antagonist of the prostaglandin D2 receptor 2 and a su
Publikováno v:
Metabolite Safety in Drug Development
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4089cd6006b81bec27e5ce237eaadced
https://doi.org/10.1002/9781118949689.ch10
https://doi.org/10.1002/9781118949689.ch10
Autor:
Elizabeth Kigondu, Felix Huth, Markus Zollinger, Gian Camenisch, Claire Juif, Marc Witschi, Hilmar Schiller, Kelly Chibale, Kenichi Umehara
Publikováno v:
Xenobiotica; the fate of foreign compounds in biological systems. 46(10)
1. Esterases may play a major role in the clearance of drugs with functional groups amenable to hydrolysis, particularly in the case of ester prodrugs. To understand the processes involved in the elimination of such drugs, it is necessary to determin
Autor:
Piet Swart, Frédéric Lozac'h, Felix Waldmeier, Kevin R. Kelly, Yanfeng Wang, Patrick Urban, Suraj Anand, Eugene Tan, Chris H. Takimoto, Alain C. Mita, Markus Zollinger, Monica M. Mita
Publikováno v:
Investigational New Drugs. 31:605-615
A phase 1, open-label, non-randomized, single center study was conducted to determine the pharmacokinetics, distribution, metabolism, elimination, and mass balance of patupilone in patients with advanced solid tumors. Five patients with advanced soli
Autor:
Yi Jin, Markus Zollinger, Stefan Hartmann, Frédéric Zecri, Claudia Sayer, Hans-Peter Gschwind
Publikováno v:
Drug Metabolism and Disposition. 39:199-207
Fingolimod [(FTY720), Gilenya; 2-amino-2-[2-(4-octylphenyl)ethyl]-1,3-propanediol], a new drug for the treatment of relapsing multiple sclerosis, acts through its phosphate metabolite, which modulates sphingosine 1-phosphate receptors. This represent
Autor:
Markus Zollinger, Gerard Bruin, Felix Waldmeier, Gerhard Gross, K. Olaf Boernsen, Ulrike Pfaar
Publikováno v:
Journal of Chromatography A. 1133:184-194
Sensitive radioactivity detection following high performance liquid chromatography (HPLC) separation remains a challenge in many drug metabolism studies with radiolabeled compounds. In this work, solid scintillation counting (SSC) after fraction coll
Autor:
Markus Zollinger, Gerhard Zenke, Alfred Zimmerlin, Thomas Moenius, Stefan Hartmann, Maximilian Grassberger, Felix Waldmeier, Ulrike Glaenzel, Alain Schweitzer, Jean-Pierre Baldeck, Stephane Berthier
Publikováno v:
Drug Metabolism and Disposition. 34:765-774
The absorption and disposition of pimecrolimus, a calcineurin inhibitor developed for the treatment of inflammatory skin diseases, was investigated in four healthy volunteers after a single oral dose of 15 mg of [(3)H]pimecrolimus. Supplementary info
Autor:
Eric Francotte, Danilo Guerini, Markus Streiff, Markus Zollinger, Karl Welzenbach, Rainer Albert, Klaus Hinterding, Trixie Wagner, Helmut Knecht, Nigel Graham Cooke, Frédéric Zecri, Corinne Simeon, Constanze Müller-Hartwieg, Volker Brinkmann
Publikováno v:
Journal of Medicinal Chemistry. 48:5373-5377
In vivo phosphorylation of FTY720 (1) in rats and humans resulted exclusively in the biologically active (S)-configured enantiomer, which was proven by an ex vivo o-phthaldialdehyde derivatization protocol especially elaborated for phosphates of 1. S
Autor:
Monique Ben-Am, Felix Waldmeier, Hans-Peter Gschwind, Rolf Pokorny, Michael Hayes, Ulrike Pfaar, Bin Peng, Peter Zbinden, Markus Zollinger, Gerhard Gross, Michael Seiberling, Claudia Sayer
Publikováno v:
Drug Metabolism and Disposition. 33:1503-1512
Imatinib mesylate (GLEEVEC, GLIVEC, formerly STI571) has demonstrated unprecedented efficacy as first-line therapy for treatment for all phases of chronic myelogenous leukemia and metastatic and unresectable malignant gastrointestinal stromal tumors.
Autor:
Kim Q. Do, Michel Cuenod, Peter Streit, Ursula Gutteck-Amsler, Markus Zollinger, J. Brauchli‐Theotokis
Publikováno v:
Journal of Neurochemistry. 63:1133-1142
The release of endogenous N-acetylaspartylglutamate (NAAG) from slices of rat cerebellum, striatum, and spinal cord upon depolarization with 50 mM K+ was investigated. NAAG in superfusates was prepurified using an ion exchanger, esterified, and then