Prenylamine
Prenylamine is a calcium channel antagonist and monoamine depleting agent that was used for the treatment of angina pectoris by reducing myocardial oxygen demand through vasodilation and negative inotropic effects. It was withdrawn from many markets due to its propensity to cause QT prolongation and potentially fatal ventricular arrhythmias, particularly torsades de pointes.
분자량
329.5000 g/mol
LogP
6.00
TPSA
12.00 Ų
리핀스키 5의 법칙
통과
Pharmacokinetics (PK)
Pharmacodynamics (PD)
2D 구조
Cite this structure
Embed this structure
SMILES
CC(Cc1ccccc1)NCCC(c1ccccc1)c1ccccc1
InChI
InChI=1S/C24H27N/c1-20(19-21-11-5-2-6-12-21)25-18-17-24(22-13-7-3-8-14-22)23-15-9-4-10-16-23/h2-16,20,24-25H,17-19H2,1H3
Molecular Formula
C24H27N
HBD / HBA
1 / 1
회전 가능 결합
8
무거운 원자
25
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.
자주 묻는 질문
Prenylamine is a calcium channel antagonist and monoamine depleting agent that was used for the treatment of angina pectoris by reducing myocardial oxygen demand through vasodilation and negative inotropic effects. It was withdrawn from many markets due to its propensity to cause QT prolongation and potentially fatal ventricular arrhythmias, particularly torsades de pointes.
Yes, Prenylamine is an approved drug. It has reached clinical phase 4. It is classified as a Small molecule.
References & Data Sources
- ChEMBL — European Bioinformatics Institute (EBI). CHEMBL24072. Open-access bioactivity database.
- PubChem — National Center for Biotechnology Information (NCBI). CID 9801. Chemical information database.
Data aggregated from publicly available pharmacological databases. Last updated 2026-03-28.
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