Drug intelligence / Profile preview

R-(+)-8-hydroxy-2-(di-n-propylamino)tetralin

Development stage
Preclinical
Modality
Small Molecules
Administration
Experimental (commonly Administered Subcutaneous, Intraperitoneal, Or Intracerebroventricular In Animals)[1]
01

Overview

R-(+)-8-hydroxy-2-(di-n-propylamino)tetralin is the R-enantiomer of 8-OH-DPAT, a synthetic small molecule and research tool compound primarily recognized as a **full agonist at the serotonin 1A (5-HT1A) receptor**, and also acts as an agonist at 5-HT7 receptors and as a serotonin reuptake inhibitor and releasing agent. It is structurally an aminotetralin derivative and has been used extensively to probe serotonergic pharmacology in animal models. The compound induces a variety of serotonergic effects, including antidepressant, anxiolytic, hypothermic, hypotensive, and other CNS-related activities. It has not been developed or marketed as a therapeutic drug, but is widely used in preclinical pharmacological research to understand the function of serotonergic systems.[1][3][5][8][10]

Other names
8-OH-DPAT(R)-(+)-8-hydroxy-DPAT(R)-(+)-8-OH-DPAT hydrobromide(R)-8-hydroxy-2-(di-n-propylamino)tetralin(R)-8-Hydroxy-2-dipropylaminotetralinR-(+)-8-Hydroxy-2-(di-n-propylamino)tetralin hydrobromideR-8-OH-DPATR8-OH-DPATR 8-OH-DPAT8-Hydroxy-2-(di-n-propylamino)tetralin8-hydroxy-dipropylaminotetralin8-hydroxy-N,N-dipropyl-2-aminotetralin
02

Targets

HTR7 (5-hydroxytryptamine receptor 7)SERT (Sodium-dependent serotonin transporter)HTR1A (Serotonin receptor 1A (5-hydroxytryptamine receptor 1A))

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