 | |
| Clinical data | |
|---|---|
| Other names | 4-(diphenylmethoxy)-1-methyl-piperidine |
| AHFS/Drugs.com | International Drug Names |
| Routes of administration | Oral,Topical |
| ATC code | |
| Legal status | |
| Legal status |
|
| Pharmacokinetic data | |
| Eliminationhalf-life | 24–40 hours[1] |
| Identifiers | |
| |
| CAS Number |
|
| PubChemCID | |
| IUPHAR/BPS | |
| DrugBank |
|
| ChemSpider |
|
| UNII | |
| KEGG |
|
| ChEBI | |
| ChEMBL | |
| CompTox Dashboard(EPA) | |
| ECHA InfoCard | 100.005.170 |
| Chemical and physical data | |
| Formula | C19H23NO |
| Molar mass | 281.399 g·mol−1 |
| 3D model (JSmol) | |
| |
| |
| (verify) | |
Diphenylpyraline (DPP; sold asAllergen,Arbid,Belfene,Diafen,Hispril,Histyn,Lergobine,Lyssipol,Mepiben,Neargal) is afirst-generation antihistamine withanticholinergic effects of thediphenylpiperidine class.[2][3][4] It is marketed inEurope for the treatment ofallergies.[2][3][5] DPP has also been found to act as adopamine reuptake inhibitor and produceshyperactivity in rodents.[6] It has been shown to be useful in the treatment ofParkinsonism.[7]
| Dopaminergics |
| ||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|
| Anticholinergics | |||||||||||
| Others | |||||||||||
| |||||||||||
| D1-like |
| ||||||
|---|---|---|---|---|---|---|---|
| D2-like |
| ||||||
| DATTooltip Dopamine transporter (DRIsTooltip Dopamine reuptake inhibitors) |
| ||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| NETTooltip Norepinephrine transporter (NRIsTooltip Norepinephrine reuptake inhibitors) |
| ||||||||||||||
| SERTTooltip Serotonin transporter (SRIsTooltip Serotonin reuptake inhibitors) |
| ||||||||||||||
| VMATsTooltip Vesicular monoamine transporters | |||||||||||||||
| Others |
| ||||||||||||||
 | Thisdrug article relating to therespiratory system is astub. You can help Wikipedia byexpanding it. |
