| Weight | 514.629 g/mol |
|---|---|
| Formula | C33H30N4O2 |
| Hydrogen Acceptors | 5 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 6 |
| Rotatable Bonds | 7 |
Telmisartan (144701-48-4)
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#204 in Neuroscience
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#251 in Biochemistry
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#954 in Biology
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#1057 in Chemistry
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- Telmisartan, Ramipril, or Both in Patients at High Risk for Vascular Events (The New England Journal of Medicine, 2008)
- Renal outcomes with telmisartan, ramipril, or both, in people at high vascular risk (the ONTARGET study): a multicentre, randomised, double-blind, controlled trial (The Lancet, 2008)
- Identification of Telmisartan as a Unique Angiotensin II Receptor Antagonist With Selective PPARModulating Activity (Hypertension, 2004)
- Effects of the angiotensin-receptor blocker telmisartan on cardiovascular events in high-risk patients intolerant to angiotensin-converting enzyme inhibitors: a randomised controlled trial (The Lancet, 2008)
- Telmisartan to Prevent Recurrent Stroke and Cardiovascular Events (The New England Journal of Medicine, 2008)
- Rationale, design, and baseline characteristics of 2 large, simple, randomized trials evaluating telmisartan, ramipril, and their combination in high-risk patients: the Ongoing Telmisartan Alone and in Combination with Ramipril Global Endpoint Trial/Telmisartan Randomized Assessment Study in ACE Intolerant Subjects with Cardiovascular Disease (ONTARGET/TRANSCEND) trials. (American Heart Journal, 2004)
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SMILESCCCC1=NC2=C(C=C(C=C2N1CC3=CC=C(C=C3)C4=CC=CC=C4C(=O)O)C5=NC6=CC=CC=C6N5C)C
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- Pubchem - Telmisartan
- Wikipedia - telmisartan
Telmisartan (INN) is an angiotensin II receptor antagonist (angiotensin receptor blocker, ARB) used in the management of hypertension. It was discovered by Boehringer Ingelheim and launched in 1999 as Micardis. In January 2014, Actavis as generic version of Micardis got appoval from FDA.
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