Chemical Name: (S)-(-)-3-Amino-1-hydroxypyrrolidin-2-one
Purity: ≥98% (HPLC)
Biological Activity
Technical Data
Solubility
Calculators
Datasheets
References
Biological Activity
Possesses potent sedative and ataxic action, probably through disruption of striatal dopaminergic mechanisms. R-enantiomer (Cat. No. 0281) also available.
Technical Data
M. Wt
116.12
Formula
C4H8N2O2
Storage
Store at RT
Purity
≥98% (HPLC)
CAS Number
111821-58-0
PubChem ID
183351
InChI Key
HCKUBNLZMKAEIN-VKHMYHEASA-N
Smiles
N[C@H]1CCN(O)C1=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
Solubility
Soluble to 100 mM in water
Preparing Stock Solutions
The following data is based on the product molecular weight 116.12. 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
8.61 mL
43.06 mL
86.12 mL
5 mM
1.72 mL
8.61 mL
17.22 mL
10 mM
0.86 mL
4.31 mL
8.61 mL
50 mM
0.17 mL
0.86 mL
1.72 mL
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Product Datasheets
Certificate of Analysis is currently unavailable on-line. Please contact Customer Service
Safety Datasheet
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References
References are publications that support the products' biological activity.
Grobaskiet al (1997) Responses of rat substantia nigra dopamine-containing neurones to (-)-HA-966 in vitro. Br.J.Pharmacol. 120 575 PMID: 9051293
Shepard and Lehmann
(1992) (±)-1-Hydroxy-3-aminopyrrolidone-2 (HA-966) inhibits the activity of substantia nigra dopamine neurons through a non-N-methyl-D-aspartate receptor mediated mechanism. J.Pharmacol.Exp.Ther. 261 387 PMID: 1578355
Singhet al (1990) Enantiomers of HA-966 (3-amino-1-hydroxypyrrolidin-2-one) exhibit distinct central nervous system effects: (+)-HA-966 is a selective glycine/N-methyl-D-aspartate receptor antagonist, but (-)-HA966 is a potent γ-butyrolactone-like sedative. Proc.Natl.Acad.Sci.U.S.A. 87 347 PMID: 2153294