Phenampromide
From Wikipedia, the free encyclopedia
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Phenampromide
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| Systematic (IUPAC) name | |
| N-phenyl-N-(1-piperidin-1-ylpropan-2-yl)propanamide | |
| Identifiers | |
| CAS number | |
| ATC code | ? |
| PubChem | |
| Chemical data | |
| Formula | C17H26N2O |
| Mol. mass | 274.40 g/mol |
| SMILES | & |
| Synonyms | Phenampromide |
| Pharmacokinetic data | |
| Bioavailability | ? |
| Metabolism | ? |
| Half life | ? |
| Excretion | ? |
| Therapeutic considerations | |
| Pregnancy cat. |
? |
| Legal status | |
| Routes | ? |
Phenampromide is an opioid analgesic from the ampromide family of drugs, related to other drugs such as propiram and diampromide. It was invented in the 1960s.[1]
Phenampromide produces similar effects to other opioids, including analgesia, sedation, dizziness and nausea.
[edit] References
- ^ Portoghese PS. Stereochemical Studies on Medicinal Agents II. Absolute Configuration of (-)-Phenampromide. Journal of Medicinal Chemistry. 1965 Mar;8:147-50.

