| Weight | 428.54 g/mol |
|---|---|
| Formula | C25H28N6O |
| Hydrogen Acceptors | 5 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 3 |
| Rotatable Bonds | 7 |
irbesartan (138402-11-6)
Avapro · SR 47436 · BMS 186295
Score:
#286 in Biochemistry
,
#1217 in Chemistry
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- Renoprotective effect of the angiotensin-receptor antagonist irbesartan in patients with nephropathy due to type 2 diabetes. (The New England Journal of Medicine, 2001)
- THE EFFECT OF IRBESARTAN ON THE DEVELOPMENT OF DIABETIC NEPHROPATHY IN PATIENTS WITH TYPE 2 DIABETES (The New England Journal of Medicine, 2001)
- Clopidogrel plus aspirin versus oral anticoagulation for atrial fi brillation in the Atrial fi brillation Clopidogrel Trial with Irbesartan for prevention of Vascular Events (ACTIVE W): a randomised controlled trial (The Lancet, 2006)
- Irbesartan in Patients with Heart Failure and Preserved Ejection Fraction (The New England Journal of Medicine, 2008)
- Use of Irbesartan to Maintain Sinus Rhythm in Patients With Long-Lasting Persistent Atrial Fibrillation A Prospective and Randomized Study (Circulation, 2002)
- Use of Irbesartan to Maintain Sinus Rhythm in Patients With Long-Lasting Persistent Atrial Fibrillation (Circulation, 2002)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - Avapro
- SR 47436
- BMS 186295
- 2-n-butyl-3-((2'-(1H-tetrazol-5-yl)biphenyl-4-yl)methyl)-1,3-diazaspiro(4,4)non-1-en-4-one
- Karvea
- SR-47436
- Aprovel
- BMS-186295
-
SMILESCCCCC1=NC2(CCCC2)C(=O)N1CC3=CC=C(C=C3)C4=CC=CC=C4C5=NNN=N5
-
InChIKeyYOSHYTLCDANDAN-UHFFFAOYSA-N
- Pubchem - irbesartan
- Wikipedia - irbesartan
Irbesartan (INN) is an angiotensin II receptor antagonist used mainly for the treatment of hypertension. It was developed by Sanofi Research (now part of Sanofi-Aventis). It is jointly marketed by Sanofi-Aventis and Bristol-Myers Squibb under the trade names Aprovel, Karvea, and Avapro.
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