A systematic comparison of the properties of clinically used angiotensin II type 1 receptor antagonists
MC Michel, C Foster, HR Brunner, L Liu - Pharmacological reviews, 2013 - ASPET
Angiotensin II type 1 receptor antagonists (ARBs) have become an important drug class in
the treatment of hypertension and heart failure and the protection from diabetic nephropathy …
the treatment of hypertension and heart failure and the protection from diabetic nephropathy …
Clinical pharmacokinetics of angiotensin II (AT1) receptor blockers in hypertension
ZH Israili - Journal of human hypertension, 2000 - nature.com
Angiotensin II receptor blockers (ARBs) represent a new class of effective and well tolerated
orally active antihypertensive agents. Recent clinical trials have shown the added benefits of …
orally active antihypertensive agents. Recent clinical trials have shown the added benefits of …
Substrates, inducers, inhibitors and structure-activity relationships of human Cytochrome P450 2C9 and implications in drug development
SF Zhou, ZW Zhou, LP Yang… - Current medicinal …, 2009 - ingentaconnect.com
Cytochrome P450 2C9 (CYP2C9) is one of the most abundant CYP enzymes in the human
liver. CYP2C9 metabolizes more than 100 therapeutic drugs, including tolbutamide …
liver. CYP2C9 metabolizes more than 100 therapeutic drugs, including tolbutamide …
Effects of organic anion transporting polypeptide 1B1 haplotype on pharmacokinetics of pravastatin, valsartan, and temocapril
K Maeda, I Ieiri, K Yasuda, A Fujino… - Clinical …, 2006 - Wiley Online Library
Objective Recent reports have shown that genetic polymorphisms in organic anion
transporting polypeptide (OATP) 1B1 have an effect on the pharmacokinetics of drugs …
transporting polypeptide (OATP) 1B1 have an effect on the pharmacokinetics of drugs …
A multicompartment human kidney proximal tubule-on-a-chip replicates cell polarization–dependent cisplatin toxicity
TTG Nieskens, M Persson, EJ Kelly… - Drug Metabolism and …, 2020 - ASPET
Drug-induced kidney injury is a major clinical problem and causes drug attrition in the
pharmaceutical industry. To better predict drug-induced kidney injury, kidney in vitro cultures …
pharmaceutical industry. To better predict drug-induced kidney injury, kidney in vitro cultures …
Implications of cytochrome P450 interactions when prescribing medication for hypertension
DA Flockhart, JE Tanus-Santos - Archives of internal medicine, 2002 - jamanetwork.com
Many of the estimated 50 million Americans with high blood pressure receive medications
for hypertension and for other conditions, placing them at risk for adverse drug interactions …
for hypertension and for other conditions, placing them at risk for adverse drug interactions …
Rapid determination of valsartan in human plasma by protein precipitation and high-performance liquid chromatography
J Macek, J Klima, P Ptáček - Journal of Chromatography B, 2006 - Elsevier
A high-performance liquid chromatographic (HPLC) method for the determination of
valsartan in human plasma is reported. The assay is based on protein precipitation with …
valsartan in human plasma is reported. The assay is based on protein precipitation with …
Clinically important drug interactions with zopiclone, zolpidem and zaleplon
LM Hesse, LL von Moltke, DJ Greenblatt - CNS drugs, 2003 - Springer
Insomnia, an inability to initiate or maintain sleep, affects approximately one-third of the
American population. Conventional benzodiazepines, such as triazolam and midazolam …
American population. Conventional benzodiazepines, such as triazolam and midazolam …
[PDF][PDF] Bioavailability file: valsartan
M Saydam, S Takka - FABAD Journal of Pharmaceutical Sciences, 2007 - academia.edu
Valsartan is a new potent, highly selective and orally active antihypertensive drug belonging
to the family of angiotensin II type 1 receptor antagonists. Valsartan has much greater affinity …
to the family of angiotensin II type 1 receptor antagonists. Valsartan has much greater affinity …
Identification of cytochrome P450 forms involved in the 4-hydroxylation of valsartan, a potent and specific angiotensin II receptor antagonist, in human liver …
A Nakashima, H Kawashita, N Masuda, C Saxer… - Xenobiotica, 2005 - Taylor & Francis
Valsartan is known to be excreted largely as unchanged compound and is minimally
metabolized in man. Although the only notable metabolite is 4-hydroxyvaleryl metabolite (4 …
metabolized in man. Although the only notable metabolite is 4-hydroxyvaleryl metabolite (4 …