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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.

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