Description: Inactive isomer of (RS)-AMPA (Cat. No. 0169)
Chemical Name: (R)-α-Amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
Purity: ≥99% (HPLC)
Biological Activity
Technical Data
Solubility
Calculators
Datasheets
References
Biological Activity
Inactive enantiomer of AMPA. Active enantiomer (S)-AMPA (Cat. No 0254) and racemate (RS)-AMPA (Cat. No. 0169) also available.
Technical Data
M. Wt
186.17
Formula
C7H10N2O4
Storage
Store at RT
Purity
≥99% (HPLC)
CAS Number
83654-13-1
PubChem ID
6604707
InChI Key
UUDAMDVQRQNNHZ-RXMQYKEDSA-N
Smiles
N[C@@]([H])([C@@](O)=O)CC1=C(C)ON=C1O
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
phosphate buffered saline
1.86
10
water
1.86
10
Preparing Stock Solutions
The following data is based on the product molecular weight 186.17. 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
5.37 mL
26.86 mL
53.71 mL
5 mM
1.07 mL
5.37 mL
10.74 mL
10 mM
0.54 mL
2.69 mL
5.37 mL
50 mM
0.11 mL
0.54 mL
1.07 mL
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Product Datasheets
Certificate of Analysis / Product Datasheet
Safety Datasheet
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References
References are publications that support the products' biological activity.
Hansenet al (1983) Enzymic resolution and binding to rat brain membranes of the glutamic acid agonist α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid. J.Med.Chem. 26 901 PMID: 6133955
Lauridsenet al (1985) Ibotenic acid analogues. Synthesis, molecular flexibility, and in vitro activity of agonists and antagonists at central glutamic acid receptors. J.Med.Chem. 28 668 PMID: 2859375