Substance

ID:939

Names and Identifiers
Brand Name
AleudrinAleudrineAsiprenolBronkephrineIsonoreneIsoreninAsmalarAssiprenolIsuprel MistometerNovodrinNeo-EpinineProternolRespifralSaventrineVapo-IsoEuspiranIsadrineIsonorinIsuprelAeroloneAludrinAludrineBellasthmanIsuprenMedihaler-IsoNeodrenalNorisodrineNorisodrine Aerotrol
Synonyms
Isoproterenol HClIsopropydrinIsopropyladrenalineIsopropylnorepinephrineIsoprenalineIsoproterenolIPAIsopropylnoradrenalineIsoproterenol ChlorideL-IsoproterenolN-IsopropylnoradrenalineIsoprenalinIsopropylarterenolL-IsopropylnoradrenalineN-IsopropylnorepinephrineEpinephrine Isopropyl Homolog
IUPAC name
4-{1-hydroxy-2-[(propan-2-yl)amino]ethyl}benzene-1,2-diol
IUPAC Traditional name
(+-)-isoproterenol
Registration numbers
PubChem CID
CAS Number
PubChem SID
Properties
Physical Property
Hydrophobicity(logP)
1.4
Molecule Details
Drug Groups
approved
Description
Isopropyl analog of epinephrine; beta-sympathomimetic that acts on the heart, bronchi, skeletal muscle, alimentary tract, etc. It is used mainly as bronchodilator and heart stimulant. [PubChem]
Indication
For the treatment of mild or transient episodes of heart block that do not require electric shock or pacemaker therapy also used in management of asthma and chronic bronchitis
Pharmacology
Isoproterenol is a relatively selective beta2-adrenergic bronchodilator. Isoproterenol is indicated for the relief of bronchospasm associated with chronic obstructive pulmonary disease. The pharmacologic effects of beta adrenergic agonist drugs, including Isoproterenol, are at least in part attributable to stimulation through beta adrenergic receptors of intracellular adenyl cyclase, the enzyme which catalyzes the conversion of adenosine triphosphate (ATP) to cyclic- 3',5'- adenosine monophosphate (c-AMP). Increased c-AMP levels are associated with relaxation of bronchial smooth muscle and inhibition of release of mediators of immediate hypersensitivity from cells, especially from mast cells.
Affected Organisms
Humans and other mammals
Elimination
Excretion following inhalation administration is primarily renal and the major metabolite is the sulfate conjugate of isoproterenol.
External Links
Molecular Spectra
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References
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