Isoproterenol Sulfate
This sulfate salt of isoproterenol has been used as an inhaled bronchodilator for acute asthma attacks and as an intravenous agent for cardiac emergencies. It stimulates both cardiac and pulmonary beta receptors non-selectively. It has been largely replaced by more selective beta-2 agonists for asthma management.
Peso Molecular
556,6000 g/mol
TPSA
230,00 Ų
Áreas Terapêuticas
Mecanismo de Ação
Activates beta-2 adrenergic receptors on bronchial smooth muscle, stimulating adenylyl cyclase and increasing intracellular cAMP. This relaxes airway smooth muscle and produces bronchodilation.
Pharmacokinetics (PK)
Pharmacodynamics (PD)
Activates beta-2 adrenergic receptors on bronchial smooth muscle, stimulating adenylyl cyclase and increasing intracellular cAMP. This relaxes airway smooth muscle and produces bronchodilation.
Estrutura 2D
Cite this structure
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SMILES
CC(C)NCC(O)c1ccc(O)c(O)c1.CC(C)NCC(O)c1ccc(O)c(O)c1.O.O.O=S(=O)(O)O
InChI
InChI=1S/2C11H17NO3.H2O4S.2H2O/c2*1-7(2)12-6-11(15)8-3-4-9(13)10(14)5-8;1-5(2,3)4;;/h2*3-5,7,11-15H,6H2,1-2H3;(H2,1,2,3,4);2*1H2
Molecular Formula
C22H40N2O12S
HBD / HBA
12 / 14
Ligações Rotacionáveis
8
Átomos Pesados
37
No targets recorded
Target interaction data is not yet available for this drug.
No interactions recorded
Drug interaction data is not yet available for this compound.
No side effects recorded
Side effect data is not yet available for this drug.
Perguntas frequentes
This sulfate salt of isoproterenol has been used as an inhaled bronchodilator for acute asthma attacks and as an intravenous agent for cardiac emergencies. It stimulates both cardiac and pulmonary beta receptors non-selectively. It has been largely replaced by more selective beta-2 agonists for asthma management.
Activates beta-2 adrenergic receptors on bronchial smooth muscle, stimulating adenylyl cyclase and increasing intracellular cAMP. This relaxes airway smooth muscle and produces bronchodilation.
Yes, Isoproterenol Sulfate is an approved drug. It has reached clinical phase 4. It is classified as a Small molecule.
References & Data Sources
- ChEMBL — European Bioinformatics Institute (EBI). CHEMBL3989521. Open-access bioactivity database.
- PubChem — National Center for Biotechnology Information (NCBI). CID 656677. Chemical information database.
Data aggregated from publicly available pharmacological databases. Last updated 2026-03-04.
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