Weight | 326.44 g/mol |
---|---|
Formula | C20H26N2O2 |
Hydrogen Acceptors | 4 |
Hydrogen Donors | 2 |
Aromatic Rings | 1 |
Rotatable Bonds | 1 |
Ajmaline (4360-12-7)
Wolfina · Ajmaline Hydrochloride · Aritmina
Score:
#4297 in Chemistry
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- Effect of Procaine Amide, Quinidine, and Ajmaline in the Wolff-Parkinson-White Syndrome (Circulation, 1974)
- The ajmaline challenge in Brugada syndrome: Diagnostic impact, safety, and recommended protocol (European Heart Journal, 2003)
- Intravenous drug challenge using flecainide and ajmaline in patients with Brugada syndrome (Heart Rhythm, 2005)
- Value of electrocardiographic parameters and ajmaline test in the diagnosis of Brugada syndrome caused by SCN5A mutations. (Circulation, 2004)
- Use of ajmaline in patients with the Wolff-Parkinson-White syndrome to disclose short refractory period of the accessory pathway (American Journal of Cardiology, 1980)
- Local depolarization abnormalities are the dominant pathophysiologic mechanism for type 1 electrocardiogram in brugada syndrome a study of electrocardiograms, vectorcardiograms, and body surface potential maps during ajmaline provocation. (Journal of the American College of Cardiology, 2010)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - Wolfina
- Ajmaline Hydrochloride
- Aritmina
- Serenol
- Rauverid
- Cardiorythmine
- Tachmalin
- Gilurtymal
-
SMILESCCC1C2CC3C4C5(CC(C2C5O)N3C1O)C6=CC=CC=C6N4C
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InChIKeyCJDRUOGAGYHKKD-UHFFFAOYSA-N
- Pubchem - Ajmaline
- Wikipedia - Ajmaline
Ajmaline (also known by trade names Gilurytmal, Ritmos, and Aritmina) is an alkaloid that is class Ia antiarrhythmic agent. It is often used to bring out typical findings of ST elevations in patients suspected of having Brugada syndrome. The compound was first isolated by Salimuzzaman Siddiqui in 1931 from the roots of Rauwolfia serpentina.
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