نتایج جستجو برای: terfenadine

تعداد نتایج: 282  

2013
Cho-Ming Loi Dennis A. Smith Deepak Dalvie

Characterization of the circulating metabolites for a new chemical entity in humans is essential for safety assessment, an understanding of their contributions to pharmacologic activities, and their potential involvement in drug-drug interactions. This review examines the abundance of metabolites relative to the total parent drug [metabolite-to-parent (M/P) ratio] from 125 drugs in relation to ...

2011
Haretsugu Hishigaki Satoru Kuhara

Drug-induced QT interval prolongation is one of the most common reasons for the withdrawal of drugs from the market. In the past decade, at least nine drugs, i.e. terfenadine, astemizole, grepafloxacin, terodiline, droperidol, lidoflazine, sertindole, levomethadyl and cisapride, have been removed from the market or their use has been severely restricted because of drug-induced QT interval prolo...

2014
Hyoung-Goo Park Young-Ran Lim Songhee Han Donghak Kim

The human cytochrome P450 2J2 catalyzes an epoxygenase reaction to oxidize various fatty acids including arachidonic acid. In this study, three recombinant enzyme constructs of P450 2J2 were heterologously expressed in Escherichia coli and their P450 proteins were successfully purified using a Ni(2+)-NTA affinity column. Deletion of 34 amino acid residues in N-terminus of P450 2J2 enzyme (2J2-D...

2009
Muthukrishnan Renganathan Serguei Sidach Andrew R Blight

INTRODUCTION: Non-clinical evaluation of a medication's potential to induce cardiac toxicity is recommended by regulatory agencies. 4-Aminopyridine (fampridine) is a potassium channel blocker with the demonstrated ability to improve walking ability in patients with multiple sclerosis. We evaluated the in vitro effects of 4-aminopyridine on the human ether-à-go-go-related gene (hERG) channel cur...

Journal: :Blood 2006
Karl J Aichberger Matthias Mayerhofer Anja Vales Maria-Theresa Krauth Karoline V Gleixner Martin Bilban Harald Esterbauer Karoline Sonneck Stefan Florian Sophia Derdak Winfried F Pickl Hermine Agis Andras Falus Christian Sillaber Peter Valent

Basophil numbers are typically elevated in chronic myeloid leukemia (CML) and increase during disease progression. Histamine is an essential mediator and marker of basophils and is highly up-regulated in CML. We examined the biochemical basis of histamine synthesis in CML cells. The CML-specific oncoprotein BCR/ABL was found to promote expression of histidine decarboxylase (HDC) and synthesis o...

2017
Lawrence Vernetti Albert Gough Nicholas Baetz Sarah Blutt James R. Broughman Jacquelyn A. Brown Jennifer Foulke-Abel Nesrin Hasan Julie In Edward Kelly Olga Kovbasnjuk Jonathan Repper Nina Senutovitch Janet Stabb Catherine Yeung Nick C. Zachos Mark Donowitz Mary Estes Jonathan Himmelfarb George Truskey John P. Wikswo D. Lansing Taylor

Organ interactions resulting from drug, metabolite or xenobiotic transport between organs are key components of human metabolism that impact therapeutic action and toxic side effects. Preclinical animal testing often fails to predict adverse outcomes arising from sequential, multi-organ metabolism of drugs and xenobiotics. Human microphysiological systems (MPS) can model these interactions and ...

Journal: :Journal of pharmacological sciences 2005
Shigeki Toyoshima Akihiro Kanno Tetsuya Kitayama Koji Sekiya Keiko Nakai Masao Haruna Terumasa Mino Hiroyasu Miyazaki Koji Yano Keiji Yamamoto

The goal of the present study was to examine the utility of the conscious dog model by assessing the QT-interval-prolonging potential of ten positive compounds that have been reported to induce QT interval prolongation in clinical use and seven negative compounds considered not to have such an effect. Three doses of test compounds or vehicle were administered orally to male beagle dogs (n=4), a...

Journal: :Drug metabolism and disposition: the biological fate of chemicals 2004
J Andrew Williams Ruth Hyland Barry C Jones Dennis A Smith Susan Hurst Theunis C Goosen Vincent Peterkin Jeffrey R Koup Simon E Ball

Glucuronidation is a listed clearance mechanism for 1 in 10 of the top 200 prescribed drugs. The objective of this article is to encourage those studying ligand interactions with UDP-glucuronosyltransferases (UGTs) to adequately consider the potential consequences of in vitro UGT inhibition in humans. Spurred on by interest in developing potent and selective inhibitors for improved confidence a...

Journal: :The Analyst 2010
Justin M Wiseman Christopher A Evans Chester L Bowen Joseph H Kennedy

A novel approach to the quantitative determination of xenobiotics in whole blood samples without sample preparation or chromatography is described. This method is based on direct analysis of microlitre volumes of blood which are spotted onto specialized paper cards and dried, with the resulting dried blood spots (DBS) analyzed directly via desorption electrospray ionization (DESI) mass spectrom...

Journal: :The Journal of the American Board of Family Practice 1992
J Nuovo A J Ellsworth E B Larson

BACKGROUND Single-patient randomized clinical trials (RCTs) can be utilized to maintain methodologic precision in the analysis of treatment effect in individual patients. We describe the results of a single-patient RCT in a patient with atopic dermatitis and review practical considerations regarding the use of antihistamines. METHODS Using double-blind, crossover techniques, the patient was r...

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