Anodyne

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Phenatine
Generated by the Chemistry Development Kit (http://github.com/cdk)
Molecular structure via molpic
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Physical properties
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Molecular mass240.30 g/mol [1]
Predicted LogP2.2 [1]
Structural Identifiers
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Molecular formulaC15H16N2O [1]
IUPAC nameN-(1-phenylpropan-2-yl)pyridine-3-carboxamide [1]
SMILESCC(CC1=CC=CC=C1)NC(=O)C2=CN=CC=C2 [1]
InChIInChI=1S/C15H16N2O/c1-12(10-13-6-3-2-4-7-13)17-15(18)14-8-5-9-16-11-14/h2-9,11-12H,10H2,1H3,(H,17,18) [1]
InChIKeyKJRJJAZBUWXZFN-UHFFFAOYSA-N [1]
Dosing

Phenatine

Phenatine (also known as Perviton, Fenatin, N-(α-Methylphenethyl)nicotinamide, Nicotinoyl-β-phenylisopropylamine, 3-Pyridinecarboxamide, N-(1-methyl-2-phenylethyl)-, Phenatin, N-(1-Methyl-2-phenylethyl)nicotinamide, Nicotinic acid β-phenylisopropylamide, Nicotinamide, N-(α-methylphenethyl)- or Oprea1_859298) is a stimulant substance of the amphetamine class.

Chemistry

Stereochemistry []

Phenatine is a racemic mixture of the :

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

Subjective effects
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See also []

  • Substituted amphetamines
  • Anodyne

    • External links []

    References []

    1. National Center for Biotechnology Information. PubChem Compound Summary for CID 120640, Phenatine. Accessed July 19, 2025. https://pubchem.ncbi.nlm.nih.gov/compound/120640

    2. U.S. Food and Drug Administration; National Center for Advancing Translational Sciences. Phenatine. UNII: 90O34W851E. Global Substance Registration System. Accessed July 19, 2025. https://gsrs.ncats.nih.gov/ginas/app/beta/substances/90O34W851E