8-OH-DPAT
8-OH-DPAT is a potent and selective 5-HT agonist, with a pIC50 of 8.19 for 5-HT1A and a Ki of 466 nM for 5-HT7; 8-OH-DPAT weakly binds to 5-HT1B (pIC50, 5.42), 5-HT (pIC50 <5) .
Product Specifications
CAS Number
[78950-78-4]
Product Name Alternative
8-Hydroxy-DPAT
UNSPSC
12352005
Target
5-HT Receptor
Type
Reference compound
Related Pathways
GPCR/G Protein; Neuronal Signaling
Applications
Neuroscience-Neuromodulation
Field of Research
Neurological Disease
Assay Protocol
https://www.medchemexpress.com/8-OH-DPAT.html
Purity
99.87
Solubility
DMSO : 100 mg/mL (ultrasonic)
Smiles
OC1=C2CC(N(CCC)CCC)CCC2=CC=C1
Molecular Formula
C16H25NO
Molecular Weight
247.38
References & Citations
[1]DEREK N. MIDDLEMISS, et al. 8-HYDROXY-2- (DI-n-PROPYLAMINO) -TETRALIN DISCRIMINATES BETWEEN SUBTYPES OF|[2]Bard JA, et al. Cloning of a novel human serotonin receptor (5-HT7) positively linked to adenylate cyclase. J Biol Chem. 1993 Nov 5;268 (31) :23422-6.|[3]Mori T, et al. Narcolepsy-like sleep disturbance in orexin knockout mice are normalized by the 5-HT1A receptor agonist 8-OH-DPAT. Psychopharmacology (Berl) . 2016 Jun;233 (12) :2343-53.
Shipping Conditions
Room Temperature
Storage Conditions
-20°C, 3 years; 4°C, 2 years (Powder)
Scientific Category
Reference compound1
Clinical Information
No Development Reported
Isoform
5-HT1 Receptor;5-HT7 Receptor; mLAG-3; MUC3
Citation 01
Acta Pharmacol Sin. 2025 Oct 9.|J Ethnopharmacol. 2026 Feb 28:357:120876.|Mol Neurobiol. 2025 Nov 24;63 (1) :163.|Nature. 2024 Jun;630 (8015) :237-246.|Neurochem Int. 2025 Jan 28:105937.|SSRN. 2025 Jun 19.|Eur J Pharmacol. 2023 Dec 5:960:176147.
Available Sizes
Curated Selection
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