Anodyne| Fenethylline | |
|---|---|
| Salts [] | |
|---|---|
| Hydrochloride | |
| Molecular structure via molpic based on CDK |
| Physical properties [] | |
|---|---|
| Molecular mass | 341.4 g/mol [1] |
| Melting point | 227-229 [1] |
| Predicted LogP | 1.4 [1] |
| Structural Identifiers [] | |
|---|---|
| Molecular formula | C18H23N5O2 [1] |
| IUPAC name | 1,3-dimethyl-7-[2-(1-phenylpropan-2-ylamino)ethyl]purine-2,6-dione [1] |
| SMILES | CC(CC1=CC=CC=C1)NCCN2C=NC3=C2C(=O)N(C(=O)N3C)C [1] |
| InChI | InChI=1S/C18H23N5O2/c1-13(11-14-7-5-4-6-8-14)19-9-10-23-12-20-16-15(23)17(24)22(3)18(25)21(16)2/h4-8,12-13,19H,9-11H2,1-3H3 [1] |
| InChIKey | NMCHYWGKBADVMK-UHFFFAOYSA-N [1] |
Fenethylline
Fenethylline (also known as Fenetylline, Phenethylline, Amfetyline, Captagon, Fenetyllin, Amphetaminoethyltheophylline, Theophyllineethylamphetamine, Fenetylinum, Fenetilina or Fitton) is a codrug, prodrug and stimulant substance of the amphetamine class.
Chemistry
Salts []
Fenethylline is typically found in the form of its hydrochloride salt.
Stereochemistry []
Fenethylline is a racemic mixture of the enantiomers
| Stereoisomers |
|---|
Pharmacology
Fenethylline acts as a codrug for:
| Active metabolites [] |
|---|
Subjective effects
See also []
External links []
References []
National Center for Biotechnology Information. PubChem Compound Summary for CID 19527, Fenethylline. Accessed July 19, 2025. https://pubchem.ncbi.nlm.nih.gov/compound/19527
U.S. Food and Drug Administration; National Center for Advancing Translational Sciences. Fenethylline. UNII: YZ0N7VL5R3. Global Substance Registration System. Accessed July 19, 2025. https://gsrs.ncats.nih.gov/ginas/app/beta/substances/YZ0N7VL5R3