- Mechanism of Action & Protocol. (1R)-2-[(1,1-Dimetyletyl)amino)-1-[4-hydroxy-3-(hydroxymetyl)phenyl]etanol (R)-alpha-(((1,1-dimetyletyl)amino)metyl)-4-hydroxy-1,3-benzenedimetanol (R)-alpha-[(tert-Butylamino)metyl]-4-hydroxy-3-(hydroxymetyl)benzylalkohol (IUPAC) (R)-alpha-[tert-butylamino)metyl]-4-hydroxy-m-xylene-alpha,alpha'-diol (WHO) Parent Compound: CID 123600 (Levalbuterol) Component Compounds: CID 123600 (Levalbuterol) CID 1118 (Sulfuric acid) Date s: Modify: Generally, levosalbutamol is well tolerated. It is not intended as a substitute for the expertise and judgement of your physician, pharmacist or other healthcare professional.
C4H6O6. Available for Android and iOS devices. Molecular Weight: The sum of the weights of the atoms that make up the compound. The salt form has different physical and chemical properties from the base form while retaining the same pharmacological properties. This means it is still under development and may contain inaccuracies. (1R)-2-[(1,1-Dimetyletyl)amino)-1-[4-hydroxy-3-(hydroxymetyl)phenyl]etanol(R)-alpha-(((1,1-dimetyletyl)amino)metyl)-4-hydroxy-1,3-benzenedimetanol(R)-alpha-[(tert-Butylamino)metyl]-4-hydroxy-3-(hydroxymetyl)benzylalkohol (IUPAC)(R)-alpha-[tert-butylamino)metyl]-4-hydroxy-m-xylene-alpha,alpha'-diol (WHO)Important Notice: The Drugs.com international database is in BETA release. It should not be construed to indicate that the use of any medication in any country is safe, appropriate or effective for you. Levalbuterol is a short-acting sympathomimetic beta-2 adrenergic receptor agonist with bronchodilator activity. It is a white to light-yellow solid, freely soluble in water and very slightly soluble in ethanol. Levalbuterol is a more potent bronchodilator than Salbutamol and has the potential for the treatment of COPD. Salt: The product of a reaction of an acidic substance and an alkaline substance. Common mild side-effects include an elevated heart rate, muscle cramps, and gastric upset (including heartburn and diarrhea).Symptoms of overdose in particular include: collapse into a Rarer side effects may indicate a dangerous allergic reaction. Synonyms Levalbuterol HCl / Levalbuterol hydrochloride / Levosalbutamol HCl / Levosalbutamol hydrochloride UNII WDQ1526QJM CAS Number 50293-90-8 Weight Average: 275.77 Monoisotopic: 275.1288213 Chemical Formula C 13 H 22 ClNO 3 InChI Key OWNWYCOLFIFTLK-YDALLXLXSA-N Aurobindo Pharma USA, United States; Cipla, United States; IMPAX Laboratories, United States; Mylan, United States; Ritedose, United States; Teva, United StatesWe comply with the HONcode standard for trustworthy health information -
Levalbuterol binds to beta-2 adrenergic receptors in bronchial smooth muscle and activates intracellular adenyl cyclase, an enzyme that catalyzes the conversion of adenosine triphosphate to cyclic-3',5'-adenosine monophosphate (). These include: paradoxical Levosalbutamol relaxes the smooth muscles of all airways, from the Levalbuterol was approved in the United States as a solution to be used with a InChI=1S/C13H21NO3/c1-13(2,3)14-7-12(17)9-4-5-11(16)10(6-9)8-15/h4-6,12,14-17H,7-8H2,1-3H3/t12-/m0/s1 Evidence does not show that levosalbutamol works better than salbutamol; thus there may not be sufficient justification for prescribing it.. Levosalbutamol, also known as levalbuterol, is a short-acting β 2 adrenergic receptor agonist used in the treatment of asthma and chronic obstructive pulmonary disease (COPD).
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Levalbuterol inhalation solution is indicated for the treatment or prevention of bronchospasm in adults, adolescents, and children 6 years of age and older with reversible obstructive airway disease. Molecular Weight: 576.7 g/mol. Levalbuterol ((R)-Albuterol; (R)-Salbutamol) is a short-acting β2-adrenergic receptor agonist and the active (R)-enantiomer of Salbutamol. The drug is the (R)-(−)-enantiomer of its prototype drug … Select one or more newsletters to continue.