3,4-Isopropylidenedioxyamphetamine
Pharmaceutical compound
From Wikipedia, the free encyclopedia
3,4-Isopropylidenedioxyamphetamine (IDA) is a monoamine releasing agent (MRA) of the amphetamine family related to 3,4-methylenedioxyamphetamine (MDA) developed by David E. Nichols and colleagues.[1][2][3] It is considerably less potent than MDA as an MRA in vitro.[3][1] IDA fully substituted for MDMA and LSD in animal drug discrimination tests, albeit with 5- to 7-fold lower potency than MDA.[3][1]
Other namesIDA; Isopropylidenedioxyamphetamine
ATC code
- None
| Clinical data | |
|---|---|
| Other names | IDA; Isopropylidenedioxyamphetamine |
| Drug class | Monoamine releasing agent; Entactogen; Serotonergic psychedelic; Hallucinogen |
| ATC code |
|
| Identifiers | |
| |
| PubChem CID | |
| ChemSpider | |
| ChEMBL | |
| Chemical and physical data | |
| Formula | C12H17NO2 |
| Molar mass | 207.273 g·mol−1 |
| 3D model (JSmol) | |
| |
| |