Drug intelligence / Profile preview

lauflumide

Development stage
Preclinical
Lead developer
NLS Pharmaceutics
Modality
Small Molecules
Administration
Oral, Intraperitoneal
01

Overview

Lauflumide (also known as NLS-4, CRL-40,940, or flmodafinil) is a small molecule wake-promoting agent being developed by NLS Pharmaceutics. It is an optically pure R-enantiomer of a bis(p-fluoro)phenyl derivative of modafinil. The drug acts as a selective atypical dopamine reuptake inhibitor (DAT) and also binds to alpha-1A and alpha-1B adrenergic receptors, neuropeptide Y1 (NPY1) receptors (as an inverse agonist), and exhibits histamine H2 receptor activity. Lauflumide is intended for the treatment of various conditions characterized by excessive daytime sleepiness or cognitive impairment, including narcolepsy, idiopathic hypersomnia, attention deficit hyperactivity disorder (ADHD), and chronic fatigue syndrome (including Long-COVID-associated fatigue). Preclinical studies indicate that lauflumide is more potent than modafinil, providing a longer duration of wakefulness without a hypersomnia rebound effect.

Brand names
Quilience
Other names
flmodafinilbisfluoromodafinil2-((bis(4-fluorophenyl)methane)sulfinyl)acetamide
02

Targets

DAT (Dopamine plasma membrane transport protein)RXFP3 (Relaxin family peptide receptor 3)NPY1R (Neuropeptide Y receptor Y1)ADRA1A (α1A)ADRA1B (α1B)HRH2 (Histamine H2 Receptor)

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