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ATC code |
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Identifiers | |
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CompTox Dashboard ( EPA) | |
ECHA InfoCard | 100.118.791 |
Chemical and physical data | |
Formula | C17H19NO |
Molar mass | 253.345 g·mol−1 |
3D model ( JSmol) | |
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(what is this?) (verify) |
Diphenylprolinol (D2PM), or (R/S)-(±)-diphenyl-2-pyrrolidinyl-methanol, is a norepinephrine-dopamine reuptake inhibitor which is used as a designer drug. [1]
The dextrorotary (R)-(+)- enantiomer is the more pharmacologically active, although a variety of related derivatives have been studied. [2]
Side effects including chest pain (suggestive of possible cardiovascular toxicity) have been seen following recreational use of diphenylprolinol, although it was combined with glaucine in a party pill product, thus making it impossible to say for certain which drug was responsible. [3]
Diphenylprolinol can be used to prepare the chiral CBS catalyst, which is used for enantioselective organic synthesis. [4]
Clinical data | |
---|---|
ATC code |
|
Legal status | |
Legal status | |
Identifiers | |
| |
CAS Number | |
PubChem CID | |
ChemSpider | |
UNII | |
CompTox Dashboard ( EPA) | |
ECHA InfoCard | 100.118.791 |
Chemical and physical data | |
Formula | C17H19NO |
Molar mass | 253.345 g·mol−1 |
3D model ( JSmol) | |
| |
| |
(what is this?) (verify) |
Diphenylprolinol (D2PM), or (R/S)-(±)-diphenyl-2-pyrrolidinyl-methanol, is a norepinephrine-dopamine reuptake inhibitor which is used as a designer drug. [1]
The dextrorotary (R)-(+)- enantiomer is the more pharmacologically active, although a variety of related derivatives have been studied. [2]
Side effects including chest pain (suggestive of possible cardiovascular toxicity) have been seen following recreational use of diphenylprolinol, although it was combined with glaucine in a party pill product, thus making it impossible to say for certain which drug was responsible. [3]
Diphenylprolinol can be used to prepare the chiral CBS catalyst, which is used for enantioselective organic synthesis. [4]