Anodyne| Pargyline | |
|---|---|
| Salts [] | |
|---|---|
| Hydrochloride | |
| Molecular structure via molpic based on CDK |
| Conformer [] | |
|---|---|
| Conformer structure via JSmol | |
| Physical properties [] | |
|---|---|
| Molecular mass | 159.23 g/mol [1] |
| Solubility | 9.98e-02 g/L [1] |
| Predicted LogP | 2.1 [1] |
| Structural Identifiers [] | |
|---|---|
| Molecular formula | C11H13N [1] |
| IUPAC name | N-benzyl-N-methylprop-2-yn-1-amine [1] |
| SMILES | CN(CC#C)CC1=CC=CC=C1 [1] |
| InChI | InChI=1S/C11H13N/c1-3-9-12(2)10-11-7-5-4-6-8-11/h1,4-8H,9-10H2,2H3 [1] |
| InChIKey | DPWPWRLQFGFJFI-UHFFFAOYSA-N [1] |
Pargyline
Pargyline (also known as N-Methyl-N-propargylbenzylamine, Pargylamine, Paragyline, Supirdyl, Eudatin, N-Methyl-N-2-propynylbenzylamine, Pargilina, Pargylinum, Benzenemethanamine, N-methyl-N-2-propynyl- or benzyl(methyl)(prop-2-yn-1-yl)amine) is a monoamine oxidase inhibitor substance of the benzylamine class.
Chemistry
Salts []
Pargyline is typically found in the form of its hydrochloride salt.
Stereochemistry []
Pargyline is a achiral mixture
See also []
External links []
References []
National Center for Biotechnology Information. PubChem Compound Summary for CID 4688, Pargyline. Accessed July 20, 2025. https://pubchem.ncbi.nlm.nih.gov/compound/4688
U.S. Food and Drug Administration; National Center for Advancing Translational Sciences. Pargyline. UNII: 9MV14S8G3E. Global Substance Registration System. Accessed July 20, 2025. https://gsrs.ncats.nih.gov/ginas/app/beta/substances/9MV14S8G3E