ANIMAL EXPERIMENT;
ANIMAL MODEL;
AREA UNDER THE CURVE;
ARTICLE;
BODY WEIGHT;
CONTROLLED STUDY;
DOSE RESPONSE;
DRUG BIOAVAILABILITY;
DRUG BLOOD LEVEL;
DRUG HALF LIFE;
DRUG POTENCY;
DRUG STRUCTURE;
HEART RATE;
HYPERTENSION;
INTRAVENOUS DRUG ADMINISTRATION;
LONG TERM CARE;
MALE;
NONHUMAN;
ORAL DRUG ADMINISTRATION;
PRESSOR RESPONSE;
PRIORITY JOURNAL;
RAT;
RENOVASCULAR HYPERTENSION;
SPONTANEOUSLY HYPERTENSIVE RAT;
SYSTOLIC BLOOD PRESSURE;
Clinical experience with angiotensin II receptor antagonists
Brunner HR, Christen Y, Munafo A, Lee RJ, Waeber B, Nussberger J. Clinical experience with angiotensin II receptor antagonists. Am J Hypertens 1992;12:243-6S.
Identification of a highly specific chymase as the major angiotensin II forming enzyme in the human heart
Urata H, Kinoshita A, Misono KS, Bumpus FM, Hussain A. Identification of a highly specific chymase as the major angiotensin II forming enzyme in the human heart. J Biol Chem 1990;265:22348-57.
Expression cloning of type 2 angiotensin II receptor reveals a unique class of seven-transmembrane receptors
Mukoyama M, Nakajima M, Horiuchi M, Sasamura H, Pratt RE, Dzau VJ. Expression cloning of type 2 angiotensin II receptor reveals a unique class of seven-transmembrane receptors. J Biol Chem 1993;268:24539-42.
Nonpeptide angiotensin II receptor antagonists. IX. Antihypertensive activity in rats of Dup 753, an orally active antihypertensive agent
Wong PC, Price WA, Chiu AT, et al. Nonpeptide angiotensin II receptor antagonists. IX. Antihypertensive activity in rats of Dup 753, an orally active antihypertensive agent. J Pharmacol Exp Ther 1990;252:726-32.
Nonpeptide angiotensin II receptor antagonists. XI. Pharmacology of EXP3174: An active metabolite of DuP 753, an orally active antihypertensive agent
Wong PC, Price WA, Chiu AT, et al. Nonpeptide angiotensin II receptor antagonists. XI. Pharmacology of EXP3174: an active metabolite of DuP 753, an orally active antihypertensive agent. J Pharmacol Exp Ther 1990;255:211-7.
Pharmacological profile of 606A, a novel angiotensin II receptor antagonist
Hashimoto Y, Harada Y, Narita H, Naito K, Murata S. Pharmacological profile of 606A, a novel angiotensin II receptor antagonist. J Cardiovasc Pharmacol 1997;29:284-90.
A novel angiotensin II-receptor antagonist, 606A, induces regression of cardiac hypertrophy, augments endothelium-dependent relaxation and improves renal function in stroke-prone spontaneously hypertensive rats
Hashimoto Y, Harada Y, Minami K, Fushimi K, Narita H. A novel angiotensin II-receptor antagonist, 606A, induces regression of cardiac hypertrophy, augments endothelium-dependent relaxation and improves renal function in stroke-prone spontaneously hypertensive rats. Jpn J Pharmacol 1998;76:185-92.
DuP 532, an angiotensin II receptor antagonist: First administration and comparison with losartan
Goldberg M, Lo MW, Christ DD, et al. DuP 532, an angiotensin II receptor antagonist: first administration and comparison with losartan. Clin Pharmacol Ther 1997;61:59-69.
Clinical usefulness of imidapril hydrochloride (ACE/TA-6366) on essential hypertension: A double-blind comparative study with enalapril maleate
Saruta T, Omae T, Kuramochi M, et al. Clinical usefulness of imidapril hydrochloride (ACE/TA-6366) on essential hypertension: a double-blind comparative study with enalapril maleate. Rinsho lyaku 1992;8:661-97.