Phenatine

Molecular structure via molpic based on CDK

Conformer []

Conformer structure via JSmol

Physical properties []
Molecular mass	240.30 g/mol ^[1]
Predicted LogP	2.2 ^[1]

Structural Identifiers []
Molecular formula	C₁₅H₁₆N₂O ^[1]
IUPAC name	N-(1-phenylpropan-2-yl)pyridine-3-carboxamide ^[1]
SMILES	CC(CC1=CC=CC=C1)NC(=O)C2=CN=CC=C2 ^[1]
InChI	InChI=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]
InChIKey	KJRJJAZBUWXZFN-UHFFFAOYSA-N ^[1]

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 enantiomers

Stereoisomers
(R)-Phenatine (S)-Phenatine

Subjective effects []

Physical effects
Abnormal heartbeat Appetite suppression Dehydration Dry mouth Increased blood pressure Increased heart rate Increased libido Restless legs Shakiness Stamina enhancement Stimulation Teeth grinding Vasoconstriction

Cognitive effects
Analysis enhancement Cognitive euphoria Compulsive redosing Disinhibition Ego inflation Focus enhancement Increased music appreciation Mania Motivation enhancement Suggestibility suppression Thought acceleration Wakefulness

External links []

References []

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

Anodyne