3,4-Isopropylidenedioxyamphetamine
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Pharmaceutical compound
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Other names | IDA; Isopropylidenedioxyamphetamine |
Drug class | Monoamine releasing agent; Entactogen; Serotonergic psychedelic; Hallucinogen |
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Formula | C12H17NO2 |
Molar mass | 207.273 g·mol−1 |
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3,4-Isopropylidenedioxyamphetamine (IDA) is a monoamine releasing agent (MRA) of the amphetamine family related to 3,4-methylenedioxyamphetamine (MDA).[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]
See also
[edit]- 3,4-Ethylidenedioxyamphetamine (EIDA)
- 3,4-Ethylenedioxyamphetamine (EDA)
- 3,4-Ethylenedioxymethamphetamine (EDMA)
- 3,4-Ethylenedioxymethcathinone (EDMC)
References
[edit]- ^ a b c Nichols DE, Oberlender R, Burris K, Hoffman AJ, Johnson MP (November 1989). "Studies of dioxole ring substituted 3,4-methylenedioxyamphetamine (MDA) analogues". Pharmacol Biochem Behav. 34 (3): 571–576. doi:10.1016/0091-3057(89)90560-1. PMID 2623014.
- ^ Heal DJ, Gosden J, Smith SL (November 2018). "Evaluating the abuse potential of psychedelic drugs as part of the safety pharmacology assessment for medical use in humans". Neuropharmacology. 142: 89–115. doi:10.1016/j.neuropharm.2018.01.049. PMID 29427652.
- ^ a b c Sáez-Briones P, Hernández A (September 2013). "MDMA (3,4-Methylenedioxymethamphetamine) Analogues as Tools to Characterize MDMA-Like Effects: An Approach to Understand Entactogen Pharmacology". Curr Neuropharmacol. 11 (5): 521–534. doi:10.2174/1570159X11311050007. PMC 3763760. PMID 24403876.
Additionally, EDA (ethyl[idene]dioxyamphetamine) has been demonstrated to be nearly equipotent to MDA in its ability to induce [3H]5-HT and [3H]dopamine release from rat hippocampal slices, whereas IDA (isopropylidenedioxyamphetamine) was considerably less potent [114]. In drug discrimination experiments, complete substitution for LSD and MDMA was found for EDA and IDA, which also correlates in the latter case with [125I]DOI displacement.
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