3',4'-Methylenedioxy-α-pyrrolidinopropiophenone
From Wikipedia, the free encyclopedia
(Redirected from MDPPP)
Stimulant drugTemplate:SHORTDESC:Stimulant drug
Pharmaceutical compoundTemplate:SHORTDESC:Pharmaceutical compound
| File:MDPPP.svg | |
| File:3',4'-Methylenedioxy-α-pyrrolidinopropiophenone.png | |
| Clinical data | |
|---|---|
| Routes of administration | By mouth, insufflation, vaporization, IV, rectal, sublingual |
| ATC code |
|
| Legal status | |
| Legal status | |
| Pharmacokinetic data | |
| Metabolism | Hepatic[1][2] |
| Excretion | Primarily urine (renal) |
| Identifiers | |
| |
| CAS Number | |
| PubChem CID | |
| ChemSpider | |
| UNII | |
| E number | {{#property:P628}} |
| CompTox Dashboard (EPA) |
|
| ECHA InfoCard | {{#property:P2566}}Lua error in Module:EditAtWikidata at line 29: attempt to index field 'wikibase' (a nil value). |
| Chemical and physical data | |
| Formula | C14H17NO3 |
| Molar mass | 247.294 g·mol−1 |
| 3D model (JSmol) | |
| Chirality | Racemic mixture |
| |
| |
3',4'-Methylenedioxy-α-pyrrolidinopropiophenone (MDPPP) is a stimulant designer drug. It was sold in Germany in the late 1990s and early 2000s as an ingredient in imitation ecstasy (MDMA) pills.[3] It shares a similar chemical structure with α-PPP and MDPV,[4][1][2] and has been shown to have reinforcing effects in rats.[5]
Contents
Metabolism
[edit | edit source]MDPPP appears to have a similar metabolic fate as MDPV.[2]
Legal status
[edit | edit source]As of October 2015[update] MDPPP is a controlled substance in China.[6]
See also
[edit | edit source]- Substituted methylenedioxyphenethylamine
- α-Pyrrolidinopropiophenone (α-PPP)
- 4'-Methyl-α-pyrrolidinopropiophenone (MPPP)
- 4'-Methoxy-α-pyrrolidinopropiophenone (MOPPP)
- 3',4'-Methylenedioxy-α-pyrrolidinobutiophenone (MDPBP)
- Dimethylone
References
[edit | edit source]- ^ a b Lua error in Module:Citation/CS1/Configuration at line 2172: attempt to index field '?' (a nil value).
- ^ a b c Lua error in Module:Citation/CS1/Configuration at line 2172: attempt to index field '?' (a nil value).
- ^ Lua error in Module:Citation/CS1/Configuration at line 2172: attempt to index field '?' (a nil value).
- ^ Lua error in Module:Citation/CS1/Configuration at line 2172: attempt to index field '?' (a nil value).
- ^ Lua error in Module:Citation/CS1/Configuration at line 2172: attempt to index field '?' (a nil value).
- ^ Lua error in Module:Citation/CS1/Configuration at line 2172: attempt to index field '?' (a nil value).
| Phenethylamines |
| ||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Amphetamines |
| ||||||||||||||||
| Phentermines |
| ||||||||||||||||
| Cathinones |
| ||||||||||||||||
| Phenylisobutylamines (and further-extended) | |||||||||||||||||
| Catecholamines (and close relatives) |
| ||||||||||||||||
| Cyclized phenethylamines |
| ||||||||||||||||
| Related compounds |
| ||||||||||||||||
| Stub icon | This drug article relating to the nervous system is a stub. You can help Wikipedia by expanding it. |
Hidden categories:
- Pages with script errors
- Articles with short description
- Articles with missing files
- E number from Wikidata
- ECHA InfoCard ID from Wikidata
- Infobox drug articles with non-default infobox title
- Articles without EBI source
- Chemical pages without DrugBank identifier
- Articles without KEGG source
- Articles containing unverified chemical infoboxes
- Articles containing potentially dated statements from October 2015
- All articles containing potentially dated statements
- All stub articles