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Luzindole Inhibitor

For Research Use Only. Not for use in diagnostic procedures. Catalog #: MBS5755126

Luzindole is a selective melatonin receptor antagonist. Luzindole inhibits experimental autoimmune encephalomyelitis and exerts antidepressant-like activity. Luzindole preferentially targets MT2 (Mel1b) over MT1 (Mel1a) with Ki values of 10.2 and 158nM for… More details

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Technical Datasheet View PDF
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Product Overview

Online Datasheet in PDF
Product Name
Luzindole, Inhibitor
Full Product Name
Luzindole
Product Synonym Names
N-0774
Form/Format
Solid. Powder
Purity/Purification
98.00%
Preparation and Storage
Store at -20 degree C for 3 years powder
-80 degree C for 2 years in solvent
Molecular Weight
292.37
Solubility
<1mg/ml refers to the product slightly soluble or insoluble
Formula
C19H20N2O
SMILES
CC(NCCC1=C(CC2=CC=CC=C2)NC3=C1C=CC=C3)=O
CAS Number
117946-91-5
Target & IC50
human MT2: ic50 10.2nM (ki)
human MT1: ic50 158nM (ki)
In Vitro
Luzindole (30mg/kg i.p.) decreases the time of immobility in a dose-dependent manner, the effect being more pronounced at midnight (60% reduction) than at noon (39% reduction). Luzindole (30mg/kg; i.p.; days 0-5) inhibits experimental autoimmune encephalomyelitis[2]. Luzindole (30mg/kg i.p.) did not modify the time of immobility either at noon or midnight in the albino ND/4 mouse, or in the C57BL/6J mouse, which does not produce melatonin[3]. The effect of luzindole is time-dependent, showing a maximal effect at 60 minutes. The anti-immobility effect of luzindole (10mg/kg i.p.) is prevented by the administration of melatonin (30mg/kg i.p.).

Structure of Luzindole, inhibitor

Luzindole Inhibitor – Cat# MBS5755126

Product References and Citations for Luzindole, inhibitor

Dubocovich ML, et al. Melatonin receptor antagonists that differentiate between the human Mel1a and Mel1b recombinant subtypes are used to assess the pharmacological profile of the rabbit retina ML1 presynaptic heteroreceptor. Naunyn Schmiedebergs Arch Pharmacol. 1997 Mar;355(3):365-75.
Dubocovich ML, et al. Melatonin receptor antagonists that differentiate between the human Mel1a and Mel1b recombinant subtypes are used to assess the pharmacological profile of the rabbit retina ML1 presynaptic heteroreceptor. Naunyn Schmiedebergs Arch Pharmacol. 1997 Mar;355(3):365-75.
Constantinescu CS, et al. Luzindole, a melatonin receptor antagonist, suppresses experimental autoimmune encephalomyelitis. Pathobiology. 1997;65(4):190-4.
Constantinescu CS, et al. Luzindole, a melatonin receptor antagonist, suppresses experimental autoimmune encephalomyelitis. Pathobiology. 1997;65(4):190-4.
DubocovichmL Antidepressant-like activity of the melatonin receptor antagonist, luzindole (N-0774), in the mouse behavioral despair test. Eur J Pharmacol. 1990 Jul 3;182(2):313-25.
DubocovichmL Antidepressant-like activity of the melatonin receptor antagonist, luzindole (N-0774), in the mouse behavioral despair test. Eur J Pharmacol. 1990 Jul 3;182(2):313-25.

Other Notes

Small volumes of Luzindole, inhibitor vial(s) may occasionally become entrapped in the seal of the product vial during shipment and storage. If necessary, briefly centrifuge the vial on a tabletop centrifuge to dislodge any liquid in the container`s cap. Certain products may require to ship with dry ice and additional dry ice fee may apply.

Searchable Terms for Luzindole purchase

MBS5755126 is an inhibitor targeting Luzindole.
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