Pridinol
From Wikipedia, the free encyclopedia
| Systematic (IUPAC) name | |
|---|---|
| 1,1-diphenyl-3-(piperidin-1-yl)propan-1-ol | |
| Clinical data | |
| AHFS/Drugs.com | International Drug Names |
| Pregnancy cat. | ? |
| Legal status | ? |
| Identifiers | |
| CAS number | 511-45-5 |
| ATC code | M03BX03 |
| PubChem | CID 4904 |
| IUPHAR ligand | 4139 |
| DrugBank | DB00945 |
| ChemSpider | 4735 |
| UNII | 9E75Q6SUUB |
| ChEMBL | CHEMBL404215 |
| Chemical data | |
| Formula | C20H25NO |
| Mol. mass | 295.419 g/mol |
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Pridinol is a muscle relaxant.
There is some evidence in one of Paul Janssens first books that pridinol cannot simply be acylated to make a reverse ester of methadone. The reason for this is steric strain making the product unstable.
[edit] See also
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| This drug article relating to the musculoskeletal system is a stub. You can help Wikipedia by expanding it. |

