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NBQX (FG9202) GluR antagonist

Cat.No.S9686

NBQX (FG9202, NNC 079202) is a highly selective and competitive antagonist of AMPA receptor (AMPAR) with anti-epileptic effect.
NBQX (FG9202) GluR antagonist Chemical Structure

Chemical Structure

Molecular Weight: 336.28

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Quality Control

Batch: S968601 DMSO]67 mg/mL]false]Water]Insoluble]false]Ethanol]Insoluble]false Purity: 98.86%
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98.86

Solubility

In vitro
Batch:

DMSO : 67 mg/mL (199.23 mM)
(Moisture-contaminated DMSO may reduce solubility. Use fresh, anhydrous DMSO.)

Water : Insoluble

Ethanol : Insoluble

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In vivo
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Chemical Information, Storage & Stability

Molecular Weight 336.28 Formula

C12H8N4O6S

Storage (From the date of receipt) 3 years -20°C powder
CAS No. 118876-58-7 -- Storage of Stock Solutions

Synonyms NNC 079202 Smiles N[S](=O)(=O)C1=C2C(=CC=C1)C3=C(NC(=O)C(=O)N3)C=C2[N+]([O-])=O

Mechanism of Action

Targets/IC50/Ki
AMPAR
In vitro

NBQX (FG9202) is highly selective in vitro. The IC50 value for inhibition of AMPA-evoked inward currents is 0.4 μM for this compound, while it inhibits NMDA-induced currents with an IC50 value of 60 μM.

In vivo

Rats are intraperitoneally (i.p.) injected with pentylenetetrazole (PTZ, 50 mg/kg) for 28 consecutive days to establish chronic epilepsy models. Subsequently, NBQX (FG9202, 20 mg/kg, i.p.) is injected for 3 days for the observation of behavioral measurements of epilepsy. This compound normalizes perineuronal nets (PNNs), tenascin-R, aggrecan and neurocan levels. It is sufficient to decrease seizures through increasing the latency to seizures, decrease the duration of seizure onset, and reduce the scores for the severity of seizures.

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