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123931-04-4

123931-04-4 Structure

123931-04-4 Structure
IdentificationBack Directory
[Name]

(R)-(+)-HA-966
[CAS]

123931-04-4
[Synonyms]

Zinc03791818
(R)-(+)-HA-966
R(+)-HA-966 R(+)-3-AMINO-1-HYDROX
R(+)-3-AMINO-1-HYDROXY-2-PYRROLIDINONE
(3R)-3-Amino-1-hydroxy-2-pyrrolidinone
(R)-(+)-3-AMINO-1-HYDROXYPYRROLIDIN-2-ONE
2-Pyrrolidinone, 3-amino-1-hydroxy-, (3R)-
(R)-3-amino-1-hydroxypyrrolidin-2-one 2,2,2-trifluoroacetate
[Molecular Formula]

C4H8N2O2
[MDL Number]

MFCD00078583
[MOL File]

123931-04-4.mol
[Molecular Weight]

116.12
Chemical PropertiesBack Directory
[Melting point ]

166℃
[Boiling point ]

258.6±50.0 °C(Predicted)
[density ]

1.436±0.06 g/cm3(Predicted)
[storage temp. ]

Desiccate at RT
[solubility ]

H2O: soluble
[form ]

solid
[pka]

7.19±0.20(Predicted)
[color ]

white
[optical activity]

[α]22/D +103°, c = 1 in H2O(lit.)
[Water Solubility ]

Soluble to 100 mM in water
Safety DataBack Directory
[WGK Germany ]

3
Hazard InformationBack Directory
[Uses]

(R)-(+)-HA-966 is an antagonist/partial agonist at the glycine site of the NMDA receptor.
[Biological Activity]

Antagonist/partial agonist at the glycine site of the NMDA receptor; able to cross the blood-brain barrier. Also available as part of the NMDA Receptor - Glycine Site Tocriset™ .
[in vivo]

(R)-(+)-HA-966 ((+)-HA-966; 10 mg/kg; IV) significantly attenuates the dose-dependent pressor response and the associated tachycardic response elicited by systemic NMDA (125, 250, 500, and 1000 mg/kg; i.v.)[3].
(+)-HA-966 (30, 100 mg/kg; IP) dose-dependently blocks the enhancement of dopamine synthesis induced in the nucleus accumbens by amphetamine, but is without effect on the increase in dopamine synthesis in the striatum in male BKTO mice (20-30g)[1].

Animal Model:Sprague-Dawley rats (11 to 12 weeks old)[3]
Dosage:10 mg/kg
Administration:IV
Result:Significantly attenuated the dose-dependent pressor response and the associated tachycardic response elicited by systemic NMDA.
[IC 50]

NMDA Receptor
[storage]

Desiccate at RT
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