A new class of AT1 antagonists has been synthesized, replacing the imidazole of Losartan with an imidazo[1,2-a]pyridine moiety, the tetrazole ring with a carboxylic group, while the biphenyl group is linked by an amidic bond. The effects of the new synthesized angiotensin AT1 antagonists have been evaluated in vivo on the hypertensive response, caused by intravenous (i.v.) administration of ANGII , and compared with Losartan. Synthesized compounds have also been tested in vitro for the antagonism of ANGII-induced contraction of rat aortic ring, to demonstrate the ability to counteract the effects of the agonist in a physiologically relevant system. Affinity for AT1 receptor has been evaluated with an Angiotensin II Receptor binding assay ...
This study aimed to evaluate 2-(N-((2′-(2H-tetrazole-5-yl)-[1,1′-biphenyl]-4yl)-methyl)-pentanamido)...
A far-reaching understanding of the molecular action mechanism of AT1-receptor antagonists (AIIAs) w...
As a continuing effort to establish the structure-activity relationships (SARs) within the series of...
A new class of AT1 antagonists has been synthesized, replacing the imidazole of Losartan with an imi...
The synthesis and antihypertensive activity of a group of imidazo[1,2-a]pyridine is described. New s...
In the present work, a facile and efficient route for the synthesis of a series of N-substituted im...
Novel AT1 receptor antagonists bearing substituted 4-phenylquinoline moieties instead of theclassica...
A series of benzimidazole derivatives bearing a heterocyclic ring imidazole (1), 5-chloroimidazole (...
Objective(s) Four novel losartan analogues 5a-d were synthesized by connecting a dihydropyridine nuc...
A new series of non peptide angiotensin(A-II) receptor antagonist has been prepared. This N-(bipheny...
Extensive molecular modelling studies, including conformational analysis and the comparison of molec...
A new series of non peptide angiotensin(A-II) receptor antagonist has been prepared. This N-(bipheny...
A series of new angiotensin II receptor 1 antagonists were prepared. They displayed nanomolar affini...
In the present work, a facile and efficient route for the synthesis of a series of N-substituted imi...
Antagonists of various components of the renin-angiotensin system have been the subject of many stud...
This study aimed to evaluate 2-(N-((2′-(2H-tetrazole-5-yl)-[1,1′-biphenyl]-4yl)-methyl)-pentanamido)...
A far-reaching understanding of the molecular action mechanism of AT1-receptor antagonists (AIIAs) w...
As a continuing effort to establish the structure-activity relationships (SARs) within the series of...
A new class of AT1 antagonists has been synthesized, replacing the imidazole of Losartan with an imi...
The synthesis and antihypertensive activity of a group of imidazo[1,2-a]pyridine is described. New s...
In the present work, a facile and efficient route for the synthesis of a series of N-substituted im...
Novel AT1 receptor antagonists bearing substituted 4-phenylquinoline moieties instead of theclassica...
A series of benzimidazole derivatives bearing a heterocyclic ring imidazole (1), 5-chloroimidazole (...
Objective(s) Four novel losartan analogues 5a-d were synthesized by connecting a dihydropyridine nuc...
A new series of non peptide angiotensin(A-II) receptor antagonist has been prepared. This N-(bipheny...
Extensive molecular modelling studies, including conformational analysis and the comparison of molec...
A new series of non peptide angiotensin(A-II) receptor antagonist has been prepared. This N-(bipheny...
A series of new angiotensin II receptor 1 antagonists were prepared. They displayed nanomolar affini...
In the present work, a facile and efficient route for the synthesis of a series of N-substituted imi...
Antagonists of various components of the renin-angiotensin system have been the subject of many stud...
This study aimed to evaluate 2-(N-((2′-(2H-tetrazole-5-yl)-[1,1′-biphenyl]-4yl)-methyl)-pentanamido)...
A far-reaching understanding of the molecular action mechanism of AT1-receptor antagonists (AIIAs) w...
As a continuing effort to establish the structure-activity relationships (SARs) within the series of...