Arbutamine Hydrochloride

CHEMBL1200385 Phase 4 Approuvé Small molecule
Half-Life
Bioavailability
Protein Binding
Molecular Weight
353.8 g/mol
LogP
Phase
4

The hydrochloride salt of arbutamine, used as a pharmacological stress agent during cardiac imaging tests. It stimulates beta-adrenergic receptors to mimic the cardiovascular demands of exercise.

Masse moléculaire

353,8000 g/mol

TPSA

93,00 Ų

Mécanisme d'action

Selectively blocks angiotensin II type 1 (AT1) receptors, preventing the vasoconstrictive and aldosterone-secreting effects of angiotensin II. This results in vasodilation, reduced sodium retention, and decreased blood pressure.

Pharmacokinetics (PK)

Pharmacodynamics (PD)

Mécanisme

Selectively blocks angiotensin II type 1 (AT1) receptors, preventing the vasoconstrictive and aldosterone-secreting effects of angiotensin II. This results in vasodilation, reduced sodium retention, and decreased blood pressure.

Structure 2D

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SMILES

Cl.Oc1ccc(CCCCNC[C@H](O)c2ccc(O)c(O)c2)cc1

InChI

InChI=1S/C18H23NO4.ClH/c20-15-7-4-13(5-8-15)3-1-2-10-19-12-18(23)14-6-9-16(21)17(22)11-14;/h4-9,11,18-23H,1-3,10,12H2;1H/t18-;/m0./s1

Molecular Formula

C18H24ClNO4

HBD / HBA

6 / 5

Liaisons Rotatives

8

Atomes Lourds

24

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

The hydrochloride salt of arbutamine, used as a pharmacological stress agent during cardiac imaging tests. It stimulates beta-adrenergic receptors to mimic the cardiovascular demands of exercise.

Selectively blocks angiotensin II type 1 (AT1) receptors, preventing the vasoconstrictive and aldosterone-secreting effects of angiotensin II. This results in vasodilation, reduced sodium retention, and decreased blood pressure.

Yes, Arbutamine Hydrochloride 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). CHEMBL1200385. Open-access bioactivity database.
  • PubChem — National Center for Biotechnology Information (NCBI). CID 166551. Chemical information database.

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

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.