Pridinol
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Systematic (IUPAC) name | |
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1,1-diphenyl-3-(piperidin-1-yl)propan-1-ol | |
Clinical data | |
AHFS/Drugs.com | International Drug Names |
Legal status | ? |
Routes | oral, parenteral |
Identifiers | |
CAS number | 511-45-5 |
ATC code | M03BX03 |
PubChem | CID 4904 |
DrugBank | DB00945 |
ChemSpider | 4735 |
UNII | 9E75Q6SUUB |
ChEMBL | CHEMBL404215 |
Chemical data | |
Formula | C20H25NO |
Mol. mass | 295.419 g/mol |
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(what is this?) (verify) | |
Pridinol is a muscle relaxant.
There is some evidence in one of Paul Janssen's 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.
See also
- Trihexyphenidyl
- Gamfexidine
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