نتایج جستجو برای: gp iibiiia inhibitor

تعداد نتایج: 228902  

2005
David J. Cohen

More than 1.2 million percutaneous coronary intervention (PCI) procedures are performed each year in the United States, with average hospital costs of more than $10 000 per procedure. Balloon inflation and stent placement rupture atherosclerotic plaque and damage the vascular endothelium, both of which stimulate platelet activation and thrombus formation within the target vessel. Antiplatelet a...

2016
Ryohei Katayama Takuya Sakashita Noriko Yanagitani Hironori Ninomiya Atsushi Horiike Luc Friboulet Justin F. Gainor Noriko Motoi Akito Dobashi Seiji Sakata Yuichi Tambo Satoru Kitazono Shigeo Sato Sumie Koike A. John Iafrate Mari Mino-Kenudson Yuichi Ishikawa Alice T. Shaw Jeffrey A. Engelman Kengo Takeuchi Makoto Nishio Naoya Fujita

The anaplastic lymphoma kinase (ALK) fusion oncogene is observed in 3%-5% of non-small cell lung cancer (NSCLC). Crizotinib and ceritinib, a next-generation ALK tyrosine kinase inhibitor (TKI) active against crizotinib-refractory patients, are clinically available for the treatment of ALK-rearranged NSCLC patients, and multiple next-generation ALK-TKIs are currently under clinical evaluation. T...

2016
Elodie Jouan Marc Le Vée Abdullah Mayati Claire Denizot Yannick Parmentier Olivier Fardel

In vitro evaluation of P-glycoprotein (P-gp) inhibitory potential is now a regulatory issue during drug development, in order to predict clinical inhibition of P-gp and subsequent drug-drug interactions. Assays for this purpose, commonly based on P-gp-expressing cell lines and digoxin as a reference P-gp substrate probe, unfortunately exhibit high variability, raising thus the question of devel...

Journal: :Molecular pharmacology 2012
Jurjen S Lagas Carola W N Damen Robert A B van Waterschoot Dilek Iusuf Jos H Beijnen Alfred H Schinkel

We investigated the interactions of the anticancer drug vinorelbine with drug efflux transporters and cytochrome P450 3A drug-metabolizing enzymes. Vinorelbine was transported by human multidrug-resistance associated protein (MRP) 2, and Mrp2 knockout mice displayed increased vinorelbine plasma exposure after oral administration, suggesting that Mrp2 limits the intestinal uptake of vinorelbine....

Journal: :Drug metabolism and disposition: the biological fate of chemicals 2000
C Wandel R B Kim F P Guengerich A J Wood

Mibefradil, a calcium T- and L-channel blocker developed for use in hypertension, was recently removed from the market after reports of severe drug-drug interactions. Mibefradil is known to inhibit various cytochrome P450 enzymes involved in drug metabolism, particularly CYP3A. However, the extent and the severity of the observed drug interactions in humans suggest that inhibition of additional...

Journal: :Bioorganic & medicinal chemistry 2008
Nicola Antonio Colabufo Francesco Berardi Mariangela Cantore Maria Grazia Perrone Marialessandra Contino Carmela Inglese Mauro Niso Roberto Perrone Amalia Azzariti Grazia Maria Simone Letizia Porcelli Angelo Paradiso

The development of small molecules as P-gp modulating agents and SAR studies on these ligands represented the aim of the present work. A series of 6,7-dimethoxytetrahydroisoquinoline derivatives was prepared and their ability to inhibit P-gp activity has been evaluated. The basic nucleus of these compounds, common to the best P-gp inhibitors such as Tariquidar and Elacridar, has been functional...

2013
Naoki Ishiguro Wataru Kishimoto Astrid Volz Eva Ludwig-Schwellinger Thomas Ebner Olaf Schaefer

Dabigatran etexilate, a double prodrug of dabigatran, is a reversible, competitive, direct thrombin inhibitor that has been approved for use in many countries. A recent guideline from the European Medicines Agency on drug-drug interactions proposed dabigatran etexilate as a sensitive in vivo and in vitro probe substrate for intestinal P-glycoprotein (P-gp) inhibition. We therefore performed a s...

2016
Ruben M. Markosyan Chunhui Miao Yi-Min Zheng Gregory B. Melikyan Shan-Lu Liu Fredric S. Cohen Christopher F. Basler

Ebola virus (EBOV) is a highly pathogenic filovirus that causes hemorrhagic fever in humans and animals. Currently, how EBOV fuses its envelope membrane within an endosomal membrane to cause infection is poorly understood. We successfully measure cell-cell fusion mediated by the EBOV fusion protein, GP, assayed by the transfer of both cytoplasmic and membrane dyes. A small molecule fusion inhib...

Journal: :The Journal of pharmacology and experimental therapeutics 2004
Patrick J Sinko Jeevan R Kunta Helen H Usansky Barbara A Perry

The current study was performed in intestinal and vascular access ported rabbits to quantify and differentiate the components of intestinal and hepatic first pass extraction (i.e., metabolism and secretion) of saquinavir (SQV) mediated by P-glycoprotein (P-gp) and CYP3A. SQV was administered i.v. (1-5 mg/kg) or into the upper small intestine (USI) (5 mg/kg). The roles of intestinal and hepatic ...

2013
Donglu Zhang Kan He John J. Herbst Janet Kolb Wilson Shou Lifei Wang Praveen V. Balimane Yong-Hae Han Jinping Gan Charles E. Frost W. Griffith Humphreys

The studies reported here were conducted to investigate the transport characteristics of apixaban (1-(4-methoxyphenyl)-7-oxo6-(4-(2-oxopiperidin-1-yl)phenyl)-4,5,6,7-tetrahydro-1H-pyrazolo [3,4-c]pyridine-3-carboxamide) and to understand the impact of transporters on apixaban distribution and disposition. In human permeability glycoprotein (P-gp)and breast cancer resistance protein (BCRP)-cDNA–...

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