Isoproterenol

CHEMBL434 Phase 4 Approuvé Small molecule

Half-Life

—

Bioavailability

—

Protein Binding

—

Molecular Weight

211.3 g/mol

LogP

-0.6

Phase

4

This synthetic catecholamine acts as a non-selective beta-adrenergic agonist, stimulating both beta-1 receptors in the heart (increasing heart rate and contractility) and beta-2 receptors in the lungs (causing bronchodilation). It is used in emergency settings for heart block, bradycardia, and bronchospasm. Its cardiac-stimulating effects limit its use compared to more selective agents.

Masse moléculaire

211,2600 g/mol

LogP

-0,60

TPSA

72,70 Å²

Règle des 5 de Lipinski

Conforme

Aires thérapeutiques

Generalized Anxiety Disorder Obesity Lymphoma Hypertension Major Depressive Disorder Heart Failure Atrial Fibrillation Cardiovascular Disease Leukemia

Pharmacokinetics (PK)

Pharmacodynamics (PD)

Structure 2D

SVG PNG

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SMILES

CC(C)NCC(O)c1ccc(O)c(O)c1

InChI

InChI=1S/C11H17NO3/c1-7(2)12-6-11(15)8-3-4-9(13)10(14)5-8/h3-5,7,11-15H,6H2,1-2H3

Molecular Formula

C11H17NO3

HBD / HBA

4 / 4

Liaisons Rotatives

4

Atomes Lourds

15

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.

Foire aux questions

This synthetic catecholamine acts as a non-selective beta-adrenergic agonist, stimulating both beta-1 receptors in the heart (increasing heart rate and contractility) and beta-2 receptors in the lungs (causing bronchodilation). It is used in emergency settings for heart block, bradycardia, and bronchospasm. Its cardiac-stimulating effects limit its use compared to more selective agents.

Yes, Isoproterenol is an approved drug. It has reached clinical phase 4. It is classified as a Small molecule.

{# References & Data Sources section for drug detail pages. Renders standard pharmacological database links plus the drug's data_sources field. #}

References & Data Sources

ChEMBL — European Bioinformatics Institute (EBI). CHEMBL434. Open-access bioactivity database.
PubChem — National Center for Biotechnology Information (NCBI). CID 3779. Chemical information database.

Data aggregated from publicly available pharmacological databases. Last updated 2026-03-04.

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Structure

Données Clés

Formule: C11H17NO3
Synonymes: 1

Liens externes

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Avertissement médical

This content is for educational and informational purposes only. It is not a substitute for professional medical advice, diagnosis, or treatment. Always consult a qualified healthcare provider before making medication decisions.

Data sources: ChEMBL, PubChem, DailyMed.