Drug intelligence / Profile preview

magnesium acetyltaurate

Development stage
Preclinical
Lead developer
Synapharm
Modality
Small Molecules
Administration
Intravitreal, Oral
01

Overview

Magnesium acetyltaurate (MgAT) is a synthetic chelate of magnesium and N-acetyltaurine. It is designed to enhance the bioavailability of both magnesium and taurine, particularly for delivery to the central nervous system and the retina, as it crosses the blood-brain barrier more effectively than other magnesium salts. MgAT exhibits neuroprotective properties by acting as an antagonist at N-methyl-D-aspartate (NMDA) receptors, thereby mitigating glutamate-induced excitotoxicity. Additionally, it reduces oxidative and nitrosative stress by modulating the expression of nitric oxide synthase (NOS) isoforms—specifically restoring endothelial NOS (eNOS) while downregulating inducible (iNOS) and neuronal (nNOS) isoforms. Preclinical research in rat models of glaucoma suggests that MgAT can prevent retinal ganglion cell apoptosis and optic nerve degeneration, potentially through the activation of brain-derived neurotrophic factor (BDNF) pathways and the reduction of caspase-3 activity. It is also commercially available as a dietary supplement.

Brand names
ATA Mg
Other names
MgATMagnesium N-acetyltaurateMagnesium acetyl taurate
02

Targets

NOS1 (nNOS)NMDAR (Glutamate receptor ionotropic, NMDA)BDNF (Brain-derived neurotrophic factor)

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