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Tocris/3-MATIDA/2196/50/50 mg

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货号: 2196/50

品牌: Tocris

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Description: Potent, selective mGlu₁ antagonist

Chemical Name: α-Amino-5-carboxy-3-methyl-2-thiopheneacetic acid

Purity: ≥99% (HPLC)

Biological Activity Technical Data Solubility Calculators Datasheets References

Biological Activity

Potent metabotropic glutamate mGlu₁ receptor antagonist (IC₅₀ = 6.3 μM at rat mGlu_1a). Displays ≥ 40-fold selectivity over other receptors: mGlu₅, mGlu₂, mGlu_4a (IC₅₀ > 300 μM), NMDA and AMPA (IC₅₀ = 250 μM). Neuroprotective in cultured murine cortical cells and rat hippocampal slice cultures in vitro. Reduces the volume of ischemia-induced brain infarcts in rats following systemic administration in vivo.

Technical Data

M. Wt	215.23
Formula	C₈H₉NO₄S
Storage	Store at +4°C
Purity	≥99% (HPLC)
CAS Number	518357-51-2
PubChem ID	10398360
InChI Key	KOMWRBFEDDEWEP-UHFFFAOYSA-N
Smiles	CC1=C(SC(=C1)C(O)=O)C(N)C(O)=O

The technical data provided above is for guidance only. For batch specific data refer to the Certificate of Analysis.

All Tocris products are intended for laboratory research use only.

Solubility Data

	Solvent	Max Conc. mg/mL	Max Conc. mM
Solubility
	1eq. NaOH	21.52	100
	DMSO	10.76	50

Preparing Stock Solutions

The following data is based on the product molecular weight 215.23. Batch specific molecular weights may vary from batch to batch due to solvent of hydration, which will affect the solvent volumes required to prepare stock solutions.

Concentration / Solvent Volume / Mass	1 mg	5 mg	10 mg
1 mM	4.65 mL	23.23 mL	46.46 mL
5 mM	0.93 mL	4.65 mL	9.29 mL
10 mM	0.46 mL	2.32 mL	4.65 mL
50 mM	0.09 mL	0.46 mL	0.93 mL

Product Datasheets

Certificate of Analysis / Product Datasheet

Safety Datasheet

References

References are publications that support the products' biological activity.

Moroni et al (2002) The novel and systemically active metabotropic glutamate 1 (mGlu1) receptor antagonist 3-MATIDA reduces post-ischemic neuronal death. Neuropharmacology 42 741 PMID: 12015200

Cozzi et al (2002) Metabotropic glutamate 1 (mGlu1) receptor antagonists enhance GABAergic neurotransmission: a mechanism for the attenuation of post-ischemic injury and epileptiform activity? Neuropharmacology 43 119 PMID: 12213266

Constantino et al (2004) Stereoselective synthesis and preliminary evaluation of (+)- and (-)-3-methyl-5-carboxy-thien-2-yl-glycine (3-MATIDA): identification of (+)-3-MATIDA as a novel mGluR1 competitive antagonist. Il Farmaco 59 93 PMID: 14871500

Keywords: 3-MATIDA, supplier, Potent, selective, mGlu1, mGluR1, antagonists, mGlur, Group, I, Receptors, mGlu5, mGluR5, Glutamate, Metabotropic, Glutamate, (Metabotropic), Group, I, Receptors, Glutamate, (Metabotropic), Group, I, Receptors, Tocris Bioscience

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