Anodyne

Collapse all
Toggle theme
Ibopamine
Generated by the Chemistry Development Kit (http://github.com/cdk)
Salts
[]
Ibopamine hydrochloride
Generated by the Chemistry Development Kit (http://github.com/cdk)
Molecular structure via molpic
Enable javascript to view conformer structure via 3Dmol.js
Physical properties
[]
Molecular mass307.4 g/mol [1]
Predicted LogP2.9 [1]
Structural Identifiers
[]
Molecular formulaC17H25NO4 [1]
IUPAC name[4-[2-(methylamino)ethyl]-2-(2-methylpropanoyloxy)phenyl] 2-methylpropanoate [1]
SMILESCC(C)C(=O)OC1=C(C=C(C=C1)CCNC)OC(=O)C(C)C [1]
InChIInChI=1S/C17H25NO4/c1-11(2)16(19)21-14-7-6-13(8-9-18-5)10-15(14)22-17(20)12(3)4/h6-7,10-12,18H,8-9H2,1-5H3 [1]
InChIKeyWDKXLLJDNUBYCY-UHFFFAOYSA-N [1]
Dosing

Ibopamine

Ibopamine (also known as Ibopaminum, Ibopamina, SB 7505, SB-7505, Propanoic acid, 2-methyl-, 4-(2-(methylamino)ethyl)-1,2-phenylene ester, N-methyldopamine diisobutyrate, (4-(2-(methylamino)ethyl)-2-(2-methylpropanoyloxy)phenyl) 2-methylpropanoate, 5-(2-(methylamino)ethyl)-2-((2-methylpropanoyl)oxy)phenyl 2-methylpropanoate, 5-[2-(methylamino)ethyl]-2-[(2-methylpropanoyl)oxy]phenyl 2-methylpropanoate or C01CA16) is a prodrug substance of the carboxylic acid class.

Chemistry

Salts []

Ibopamine is typically found in the form of its hydrochloride salt.

Pharmacology

Ibopamine acts as a for:

Active metabolites
 []
Epinine Generated by the Chemistry Development Kit (http://github.com/cdk)

Subjective effects
 []

See also []

  • Substituted carboxylic acids
  • Substituted catecholamines
  • Anodyne

    • External links []

    References []

    1. National Center for Biotechnology Information. PubChem Compound Summary for CID 68555, Ibopamine. Accessed July 19, 2025. https://pubchem.ncbi.nlm.nih.gov/compound/68555

    2. U.S. Food and Drug Administration; National Center for Advancing Translational Sciences. Ibopamine. UNII: 8ZCA2I2L11. Global Substance Registration System. Accessed July 19, 2025. https://gsrs.ncats.nih.gov/ginas/app/beta/substances/8ZCA2I2L11