Anodyne

Prenylamine
Generated by the Chemistry Development Kit (http://github.com/cdk)
Molecular structure via molpic based on CDK
Physical properties
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329.5 g/mol [1]
[1]
Structural Identifiers
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C24H27[1]
3,3-diphenyl-N-(1-phenylpropan-2-yl)propan-1-amine [1]
CC(CC1=CC=CC=C1)NCCC(C2=CC=CC=C2)C3=CC=CC=C3 [1]
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 [1]
InChIKeyIFFPICMESYHZPQ-UHFFFAOYSA-N [1]

Prenylamine

Prenylamine (also known as Prenylamine, Prenilamina, Prenylaminum, N-(3,3-Diphenylpropyl)-α-methylphenethylamine, B-436, 1-Phenyl-2-(1',1'-diphenylpropyl-3'-amino)propane, N-(1-Methyl-2-phenylethyl)-γ-phenylbenzenepropanamine, Benzenepropanamine, N-(1-methyl-2-phenylethyl)-γ-phenyl-, (3,3-diphenylpropyl)(1-phenylpropan-2-yl)amine or C01DX02) is a calcium channel blocker substance of the amphetamine class.

Chemistry

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Prenylamine is a racemic mixture of the

Stereoisomers
(R)-PrenylamineGenerated by the Chemistry Development Kit (http://github.com/cdk)
(S)-PrenylamineGenerated by the Chemistry Development Kit (http://github.com/cdk)

See also []

External links []

References []

  1. National Center for Biotechnology Information. PubChem Compound Summary for CID 9801, Prenylamine. Accessed July 20, 2025. https://pubchem.ncbi.nlm.nih.gov/compound/9801

  2. U.S. Food and Drug Administration; National Center for Advancing Translational Sciences. Prenylamine. UNII: K2OH82Z000. Global Substance Registration System. Accessed July 20, 2025. https://gsrs.ncats.nih.gov/ginas/app/beta/substances/K2OH82Z000