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144912-63-0

144912-63-0 Structure

144912-63-0 Structure
IdentificationBack Directory
[Name]

2-(8,9-dioxo-2,6-diazabicyclo[5.2.0]non-1(7)-en-2-yl)ethylphosphonic acid
[CAS]

144912-63-0
[Synonyms]

WAY-126090
Perzinfotel
EAA-090 >=98% (HPLC)
2-(8,9-dioxo-2,6-diazabicyclo[5.2.0]non-1(7)-en-2-yl)ethylphosphonic acid
P-[2-(8,9-dioxo-2,6-diazabicyclo[5.2.0]non-1(7)-en-2-yl)ethyl]-phosphonic acid
Phosphonic acid, P-[2-(8,9-dioxo-2,6-diazabicyclo[5.2.0]non-1(7)-en-2-yl)ethyl]-
[Molecular Formula]

C9H13N2O5P
[MDL Number]

MFCD00912427
[MOL File]

144912-63-0.mol
[Molecular Weight]

260.18
Chemical PropertiesBack Directory
[Melting point ]

260-278 °C (decomp)
[Boiling point ]

518.3±60.0 °C(Predicted)
[density ]

1.60±0.1 g/cm3(Predicted)
[storage temp. ]

2-8°C
[solubility ]

H2O: ≥2mg/mL
[form ]

powder
[pka]

2.45±0.10(Predicted)
[color ]

light yellow to yellow
[Water Solubility ]

H2O: ≥2mg/mL
Safety DataBack Directory
[Hazard Codes ]

T
[Risk Statements ]

25
[Safety Statements ]

45
[RIDADR ]

UN 2811 6.1 / PGIII
[WGK Germany ]

3
Hazard InformationBack Directory
[Uses]

Treatment of neuropathic pain (NMDA receptor antagonist).
[Definition]

ChEBI: Perzinfotel is a dialkylarylamine and a tertiary amino compound.
[Biological Activity]

EAA-090 inhibits the binding of ligands to glutamate receptors and blocks NMDA-induced currents. It is neuroprotective against glutamate and ischemia-induced toxicity.''EAA-090 is a potent NMDA receptor antagonist with neuroprotective properties. In isoflurane-anesthetized dogsEAA-090 reduces the minimum alveolar concentration (MAC) of isoflurane and increases systolicmeanand diastolic arterial blood pressure.
[IC 50]

NMDA Receptor
[storage]

Store at -20°C
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