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Merck

T2455

Sigma-Aldrich

T3MG

Sinónimos:

(±)-threo-3-Methylglutamic acid, 3MG, threo-3-Methylglutamate

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About This Item

Fórmula empírica (notación de Hill):
C6H11NO4
Número de CAS:
Peso molecular:
161.16
MDL number:
UNSPSC Code:
12352200
PubChem Substance ID:
NACRES:
NA.77

form

powder

color

white to off-white

solubility

H2O: >1.5 mg/dL

suitability

suitable for TLC (single spot)

storage temp.

room temp

SMILES string

C[C@@H](CC(O)=O)[C@@H](N)C(O)=O

InChI

1S/C6H11NO4/c1-3(2-4(8)9)5(7)6(10)11/h3,5H,2,7H2,1H3,(H,8,9)(H,10,11)/t3-,5+/m0/s1

InChI key

FHJNAFIJPFGZRI-WVZVXSGGSA-N

Categorías relacionadas

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.

Features and Benefits

This compound is featured on the Excitatory Amino Acid Transporters page of the Handbook of Receptor Classification and Signal Transduction. To browse other handbook pages, click here.

Preparation Note

T3MG dissolves in water at a concentration that is greater than 1.5 mg/ml.

pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable


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Lois Slator et al.
Journal of aerosol medicine and pulmonary drug delivery, 27 Suppl 1, S37-S43 (2014-01-31)
Valved holding chambers (VHCs) are accessory devices for pressurized metered dose inhalers (pMDIs). Use of a VHC may help overcome coordination issues associated with drug delivery via the pMDI alone. Previous work has established that aspects of VHC use, including
Guide to Receptors and Channels (GRAC), 4th Edition.
British journal of pharmacology, 158 Suppl 1, S1-254 (2009-11-04)

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