Weight | 446.511 g/mol |
---|---|
Formula | C24H26N6O3 |
Hydrogen Acceptors | 7 |
Hydrogen Donors | 3 |
Aromatic Rings | 4 |
Rotatable Bonds | 8 |
Olmesartan (144689-63-4, 144689-24-7)
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#240 in Neuroscience
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#302 in Biochemistry
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#1111 in Biology
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#1252 in Chemistry
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- Sigma-Aldrich - Olmesartan105.00 USD
- Fisher Scientific - Search for Olmesartan
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- Olmesartan for the delay or prevention of microalbuminuria in type 2 diabetes (The New England Journal of Medicine, 2011)
- Rationale, study design and implementation of the COLM study : the combination of OLMesartan and calcium channel blocker or diuretic in high-risk elderly hypertensive patients (Hypertension Research, 2009)
- The combination of olmesartan medoxomil and amlodipine besylate in controlling high blood pressure: COACH, a randomized, double-blind, placebo-controlled, 8-week factorial efficacy and safety study. (Clinical Therapeutics, 2008)
- Comparative efficacy of olmesartan, losartan, valsartan, and irbesartan in the control of essential hypertension. (Journal of Clinical Hypertension, 2001)
- Severe Spruelike Enteropathy Associated With Olmesartan (2012)
- Evaluation of antihypertensive therapy with the combination of olmesartan medoxomil and hydrochlorothiazide (American Journal of Hypertension, 2004)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCCCC1=NC(=C(N1CC2=CC=C(C=C2)C3=CC=CC=C3C4=NNN=N4)C(=O)O)C(C)(C)O
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InChIKeyVTRAEEWXHOVJFV-UHFFFAOYSA-N
- Pubchem - Olmesartan
- Wikipedia - olmesartan
Olmesartan medoxomil is an angiotensin II receptor antagonist which is used for the treatment of high blood pressure. It was developed by Sankyo in 1995, and is sold under the trade name Benicar, among others. An ester prodrug, it is completely and rapidly hydrolyzed to the active acid form, olmesartan (RNH-6270).
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