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T3MG

Catalog No. T2455 Name Sigma Aldrich
CAS Number 63088-04-0 Website http://www.sigmaaldrich.com
M. F. C6H11NO4 Telephone 1-800-521-8956
M. W. 161.15584 Fax
Purity (single spot, TLC) Email
Storage Chembase ID: 1666

SYNONYMS

IUPAC name
(2R,3S)-2-amino-3-methylpentanedioic acid
IUPAC Traditional name
(3r)-3-methyl-L-glutamic acid
Synonyms
3MG
(±)-threo-3-Methylglutamic acid
threo-3-Methylglutamate

DATABASE IDS

CAS Number 63088-04-0
MDL Number MFCD09836097

PROPERTIES

Empirical Formula (Hill Notation) C6H11NO4
Purity (single spot, TLC)
Apperance white to off-white powder
Solubility H2O: >1.5 mg/dL
GHS Pictograms GHS07
GHS Signal Word Warning
GHS Hazard statements H315-H319-H335
European Hazard Symbols Irritant Irritant (Xi)
MSDS Link Download
GHS Precautionary statements P261-P305 + P351 + P338
Risk Statements 36/37/38
Safety Statements 26
Storage Temperature room temp
German water hazard class 3

DETAILS

Description (English)
Biochem/physiol Actions
T3MG is a selective inhibitor of excitatory amino acid transporters GLT-1, EAAT2, and EAAT4. T3MG has long been utilized as a gold standard in the study of general EAAT function. It has more recently been shown to be selective for EAAT2 and EAAT4 as compared to EAAT1 and EAAT3 in electrophysiology and glutamate/aspartate uptake assays. Although there are other EAAT2-selective compounds, this is the first tool with selectivity for EAAT4. T3MG is not a substrate for the transporters themselves, nor does it have activity at glutamate ion channels.
Description (简体中文)
Biochem/physiol Actions
T3MG is a selective inhibitor of excitatory amino acid transporters GLT-1, EAAT2, and EAAT4. T3MG has long been utilized as a gold standard in the study of general EAAT function. It has more recently been shown to be selective for EAAT2 and EAAT4 as compared to EAAT1 and EAAT3 in electrophysiology and glutamate/aspartate uptake assays. Although there are other EAAT2-selective compounds, this is the first tool with selectivity for EAAT4. T3MG is not a substrate for the transporters themselves, nor does it have activity at glutamate ion channels.

REFERENCES