4-APBT
Clinical data | |
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Other names | 4-(2-Aminopropyl)-1-benzothiophene |
Drug class | Serotonin–norepinephrine–dopamine releasing agent |
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Chemical and physical data | |
Formula | C11H13NS |
Molar mass | 191.29 g·mol−1 |
3D model (JSmol) | |
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4-APBT, also known as 4-(2-aminopropyl)-1-benzothiophene, is a monoamine releasing agent (MRA) of the amphetamine and benzothiophene families.[1][2] It acts specifically as a fairly well-balanced serotonin–norepinephrine–dopamine releasing agent (SNDRA), with EC50Tooltip half-maximal effective concentration values of 21.2 nM for serotonin, 46.2 nM for norepinephrine, and 66.6 nM for dopamine in rat brain synaptosomes.[2] 4-APBT was first described in the scientific literature by 2020.[1][2]
See also
References
- ^ a b Brandt SD, Carlino L, Kavanagh PV, Westphal F, Dreiseitel W, Dowling G, Baumann MH, Sitte HH, Halberstadt AL (August 2020). "Syntheses and analytical characterizations of novel (2-aminopropyl)benzo[b]thiophene (APBT) based stimulants". Drug Test Anal. 12 (8): 1109–1125. doi:10.1002/dta.2813. PMC 8281332. PMID 32372465.
- ^ a b c Rudin D, McCorvy JD, Glatfelter GC, Luethi D, Szöllősi D, Ljubišić T, Kavanagh PV, Dowling G, Holy M, Jaentsch K, Walther D, Brandt SD, Stockner T, Baumann MH, Halberstadt AL, Sitte HH (March 2022). "(2-Aminopropyl)benzo[β]thiophenes (APBTs) are novel monoamine transporter ligands that lack stimulant effects but display psychedelic-like activity in mice". Neuropsychopharmacology. 47 (4): 914–923. doi:10.1038/s41386-021-01221-0. PMC 8882185. PMID 34750565.
External links
DRAsTooltip Dopamine releasing agents |
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NRAsTooltip Norepinephrine releasing agents |
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SRAsTooltip Serotonin releasing agents |
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See also: Receptor/signaling modulators • Monoamine reuptake inhibitors • Adrenergics • Dopaminergics • Serotonergics • Monoamine metabolism modulators • Monoamine neurotoxins |
Phenethylamines |
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Amphetamines |
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