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L-745870

L-745870 is a potent, selective, brain-penetrant and orally active dopamine D4 receptor antagonist with a Ki of 0.43 nM. L-745870 shows weaker affinity for D2 (Ki of 960 nM) and D3 (Ki of 2300 nM) receptors, and exhibits moderate affinity for 5-HT2 receptors, sigma sites and α-adrenoceptors[1][2][3].

Product Specifications

CAS Number

[158985-00-3]

UNSPSC

12352005

Hazard Statement

H302, H315, H319, H335

Target

Dopamine 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/l-745870.html

Purity

99.92

Solubility

DMSO : 25 mg/mL (ultrasonic)

Smiles

ClC(C=C1)=CC=C1N(CC2)CCN2CC3=CNC4=NC=CC=C43

Molecular Formula

C18H19ClN4

Molecular Weight

326.82

Precautions

H302, H315, H319, H335

References & Citations

[1]Bristow LJ, et al. Schizophrenia and L-745,870, a novel dopamine D4 receptor antagonist. Trends Pharmacol Sci. 1997 Jun;18 (6) :186-8.|[2]Patel S, et al. Biological profile of L-745,870, a selective antagonist with high affinity for the dopamine D4 receptor. J Pharmacol Exp Ther. 1997 Nov;283 (2) :636-47.|[3]Kulagowski JJ, et al. 3- ((4- (4-Chlorophenyl) piperazin-1-yl) -methyl) -1H-pyrrolo-2,3-b-pyridine: an antagonist with high affinity and selectivity for the human dopamine D4 receptor. J Med Chem. 1996 May 10;39 (10) :1941-2.

Shipping Conditions

Room Temperature

Storage Conditions

4°C (Powder, protect from light)

Scientific Category

Reference compound1

Clinical Information

Phase 2

Isoform

D2 Receptor; D3 Receptor; D4 Receptor

Citation 01

Br J Cancer. 2024 Oct;131 (7) :1212-1223.|Research Square Preprint. 2023 Oct 3.|Psychopharmacology (Berl) . 2022 Nov;239 (11) :3551-3565.

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