Consensus and future directions on the definition of high on-treatment platelet reactivity to adenosine diphosphate
L Bonello, US Tantry, R Marcucci, R Blindt… - Journal of the American …, 2010 - jacc.org
The addition of clopidogrel to aspirin treatment reduces ischemic events in a wide range of
patients with cardiovascular disease. However, recurrent ischemic event occurrence during …
patients with cardiovascular disease. However, recurrent ischemic event occurrence during …
Pharmacogenetics, pharmacogenomics, and individualized medicine
Q Ma, AYH Lu - Pharmacological reviews, 2011 - ASPET
Individual variability in drug efficacy and drug safety is a major challenge in current clinical
practice, drug development, and drug regulation. For more than 5 decades, studies of …
practice, drug development, and drug regulation. For more than 5 decades, studies of …
Evaluation of six proton pump inhibitors as inhibitors of various human cytochromes P450: focus on cytochrome P450 2C19
T Zvyaga, SY Chang, C Chen, Z Yang… - Drug Metabolism and …, 2012 - ASPET
Six proton pump inhibitors (PPIs), omeprazole, lansoprazole, esomeprazole,
dexlansoprazole, pantoprazole, and rabeprazole, were shown to be weak inhibitors of …
dexlansoprazole, pantoprazole, and rabeprazole, were shown to be weak inhibitors of …
Carboxylesterase 1 as a determinant of clopidogrel metabolism and activation
Clopidogrel pharmacotherapy is associated with substantial interindividual variability in
clinical response, which can translate into an increased risk of adverse outcomes …
clinical response, which can translate into an increased risk of adverse outcomes …
Clopidogrel increases dasabuvir exposure with or without ritonavir, and ritonavir inhibits the bioactivation of clopidogrel
MK Itkonen, A Tornio… - Clinical …, 2019 - Wiley Online Library
Dasabuvir is mainly metabolized by cytochrome P450 (CYP) 2C8 and is predominantly used
in a regimen containing ritonavir. Ritonavir and clopidogrel are inhibitors of CYP3A4 and …
in a regimen containing ritonavir. Ritonavir and clopidogrel are inhibitors of CYP3A4 and …
P2Y nucleotide receptors: promise of therapeutic applications
KA Jacobson, JM Boeynaems - Drug discovery today, 2010 - Elsevier
Extracellular nucleotides, such as ATP and UTP, have distinct signaling roles through a
class of G-protein-coupled receptors, termed P2Y. The receptor ligands are typically …
class of G-protein-coupled receptors, termed P2Y. The receptor ligands are typically …
Pharmacokinetics and pharmacodynamics of approved and investigational P2Y12 receptor antagonists
U Schilling, J Dingemanse, M Ufer - Clinical Pharmacokinetics, 2020 - Springer
Coronary artery disease remains the major cause of mortality worldwide. Antiplatelet drugs
such as acetylsalicylic acid and P2Y12 receptor antagonists are cornerstone treatments for …
such as acetylsalicylic acid and P2Y12 receptor antagonists are cornerstone treatments for …
Clopidogrel Loading Dose Adjustment According to Platelet Reactivity Monitoring in Patients Carrying the 2C19*2Loss of Function Polymorphism
L Bonello, S Armero, O Ait Mokhtar, J Mancini… - Journal of the American …, 2010 - jacc.org
Objectives: We aimed to investigate the biological impact of a tailored clopidogrel loading
dose (LD) according to platelet reactivity monitoring in carriers of the cytochrome (CYP) …
dose (LD) according to platelet reactivity monitoring in carriers of the cytochrome (CYP) …
Evaluation of a new molecular entity as a victim of metabolic drug-drug interactions—an industry perspective
T Bohnert, A Patel, I Templeton, Y Chen, C Lu… - Drug Metabolism and …, 2016 - ASPET
Under the guidance of the International Consortium for Innovation and Quality in
Pharmaceutical Development (IQ), scientists from 20 pharmaceutical companies formed a …
Pharmaceutical Development (IQ), scientists from 20 pharmaceutical companies formed a …
Comparison of substrate specificity among human arylacetamide deacetylase and carboxylesterases
T Fukami, M Kariya, T Kurokawa, A Iida… - European Journal of …, 2015 - Elsevier
Human arylacetamide deacetylase (AADAC) is an esterase responsible for the hydrolysis of
some drugs, including flutamide, indiplon, phenacetin, and rifamycins. AADAC is highly …
some drugs, including flutamide, indiplon, phenacetin, and rifamycins. AADAC is highly …