Home > Compound List > Product Information
Olmesartan medoxomil_Molecular_structure_CAS_144689-63-4)
Click picture or here to close

Olmesartan medoxomil

Catalog No. S1604 Name Selleck Chemicals
CAS Number 144689-63-4 Website http://www.selleckchem.com
M. F. C29H30N6O6 Telephone (877) 796-6397
M. W. 558.5851 Fax (832) 582-8590
Purity Email sales@selleckchem.com
Storage -20°C Chembase ID: 160

SYNONYMS

IUPAC name
(5-methyl-2-oxo-2H-1,3-dioxol-4-yl)methyl 4-(2-hydroxypropan-2-yl)-2-propyl-1-({4-[2-(2H-1,2,3,4-tetrazol-5-yl)phenyl]phenyl}methyl)-1H-imidazole-5-carboxylate
IUPAC Traditional name
(5-methyl-2-oxo-1,3-dioxol-4-yl)methyl 5-(2-hydroxypropan-2-yl)-2-propyl-3-({4-[2-(2H-1,2,3,4-tetrazol-5-yl)phenyl]phenyl}methyl)imidazole-4-carboxylate

DATABASE IDS

CAS Number 144689-63-4

PROPERTIES

Target RAAS
Salt Data Free Base
Storage Condition -20°C

DETAILS

Description (English)
Research Area: Cancer
Biological Activity:
Olmesartan medoxomil (Benicar) is a compound which is hydrolyzed to olmesartan that is a selective AT1 subtype angiotensin II receptor antagonist.Olmesartan medoxomil (Benicar) was converted to olmesartan  during absorption from the gastrointestinal tract. Olmesartan is indicated for the treatment of hypertension. It may be used alone or in combination with other antihypertensive agents. Olmesartan medoxomil (Benicar) exerts its pharmacological functions via blocking the binding of angiotensin II to the AT1 receptors in vascular muscle; it is therefore independent of angiotensin II synthesis pathways, unlike ACE inhibitors. By blocking the binding rather than the synthesis of angiotensin II, olmesartan prevents the negative regulatory feedback on renin secretion. As a result of this blockage, olmesartan attenuates vasoconstriction and the secretion of aldosterone. Olmesartan lowers blood pressure by producing vasodilation, and decreasing peripheral resistance.

REFERENCES