| Weight | 239.315 g/mol |
|---|---|
| Formula | C13H21NO3 |
| Hydrogen Acceptors | 4 |
| Hydrogen Donors | 4 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 4 |
Levalbuterol (18559-94-9, 34391-04-3)
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- Improved bronchodilation with levalbuterol compared with racemic albuterol in patients with asthma (The Journal of Allergy and Clinical Immunology, 1998)
- The safety and efficacy of nebulized levalbuterol compared with racemic albuterol and placebo in the treatment of asthma in pediatric patients. (The Journal of Allergy and Clinical Immunology, 1999)
- Comparison of racemic albuterol and levalbuterol for treatment of acute asthma (The Journal of Pediatrics, 2003)
- Low-dose levalbuterol in children with asthma: Safety and efficacy in comparison with placebo and racemic albuterol (The Journal of Allergy and Clinical Immunology, 2001)
- Clinical Efficacy of Racemic Albuterol Versus Levalbuterol for the Treatment of Acute Pediatric Asthma (Annals of Emergency Medicine, 2005)
- Levalbuterol Compared to Racemic Albuterol: Efficacy and Outcomes in Patients Hospitalized With COPD or Asthma (Chest, 2003)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCC(C)(C)NCC(C1=CC(=C(C=C1)O)CO)O
-
InChIKeyNDAUXUAQIAJITI-UHFFFAOYSA-N
- Pubchem - Levalbuterol
- Wikipedia - levalbuterol
Levosalbutamol, also known as levalbuterol, is a short-acting 2 adrenergic receptor agonist used in the treatment of asthma and chronic obstructive pulmonary disease (COPD). Evidence does not show that levosalbutamol works better than salbutamol, thus there may not be sufficient justification for prescribing it. The drug is the (R)-()-enantiomer of its prototype drug salbutamol.
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Levalbuterol
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