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ISOPROTERENOL

FDA-approved approved Small molecule Verified Quality 80/100

Isoproterenol activates beta-adrenergic receptors without affecting alpha-adrenergic receptors.

Isoproterenol, a non-selective beta-adrenergic receptor agonist, is currently marketed for improving hemodynamic status in shock patients. Its key strength lies in its ability to activate beta-adrenergic receptors without affecting alpha-adrenergic receptors, which can be advantageous in certain clinical scenarios. The primary risk is the competition from epinephrine and albuterol, both of which offer additional benefits such as vasoconstriction and selective bronchodilation, respectively.

At a glance

Generic nameISOPROTERENOL
Also known asisoprenaline
Drug classBeta-adrenergic agonist
Targetbeta-adrenergic receptors
ModalitySmall molecule
Therapeutic areaCardiovascular
PhaseFDA-approved
First approval1956

Mechanism of action

Isoproterenol is designed to strongly bind to and activate beta-adrenergic receptors, which are involved in various physiological responses such as heart rate and bronchodilation. It has minimal interaction with alpha-adrenergic receptors, making it more selective for beta-adrenergic effects.

Approved indications

Common side effects

Drug interactions

Key clinical trials

Primary sources

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SourceUsed for
FDA labelMechanism, indications, dosing, boxed warnings, drug interactions
ClinicalTrials.govTrial enrolment, design, endpoints, results

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