Bluedark| Pargyline | |
|---|---|
 |
| Salts [] | |
|---|---|
| Pargyline hydrochloride | |
|
| Molecular structure via molpic | |
|
| |
| Molecular formula | C11H13N |
|---|---|
| Molecular mass | 159.23 g/mol |
| Predicted LogP | 2.1 |
| Solubility | 9.98e-02 g/L |
| Chirality | achiral |
| Identifiers [] | |
|---|---|
| IUPAC name | N-benzyl-N-methylprop-2-yn-1-amine |
| SMILES | CN(CC#C)CC1=CC=CC=C1 |
| InChI | InChI=1S/C11H13N/c1-3-9-12(2)10-11-7-5-4-6-8-11/h1,4-8H,9-10H2,2H3 |
| InChIKey | DPWPWRLQFGFJFI-UHFFFAOYSA-N |
Pargyline
Pargyline (also known as N-Methyl-N-propargylbenzylamine, Pargylamine, Paragyline, Eudatin, Supirdyl, Pargylin, Eutonyl, N-Methyl-N-2-propynylbenzylamine, Pargilina or Benzyl-methyl-2-propinylamin)
Chemistry
Pargyline is typically found in the form of its hydrochloride salt.
Stereochemistry
Pargyline is a achiral mixturePharmacology
| Predicted binding sites (SwissTargetPredictions)[] | ||
|---|---|---|
| Target | Target Class | Probability |
| Sodium-dependent Norepinephrine | Transporter | 0.43 |
| Sodium-dependent Serotonin | Transporter | 0.43 |
| Sodium-dependent Dopamine | Transporter | 0.43 |
| Trace amine-associated | Receptor 1 | 0.43 |
| Trace amine-associated | Receptor 2 | 0.43 |
| Monoamine oxidase | Enzyme A | 0.34 |
| Monoamine oxidase | Enzyme B | 0.34 |
| Sigma non-opioid intracellular | Receptor 1 | 0.34 |
| Serotonin | Receptor 2A | 0.30 |
| Serotonin | Receptor 2C | 0.30 |