DQP-997-74 (compound 2i) is a selective negative allosteric modulator of N-methyl-d-aspartate receptor (NMDAR), specifically targeting GluN2C/D (IC50: 0.069 µM and 0.035 µM), with blood-brain barrier penetrability. Where DQP refers to dihydroquinoline-pyrazoline. DQP-997-74 acts synergistically with the agonist glutamate to exhibit time-dependent enhanced potency in inhibiting hypersynchronous activity driven by high-frequency excitatory synaptic transmission. DQP-997-74 reduces the number of epileptogenesis in a murine model of tuberous sclerosis complex (TSC)-induced epilepsy. DQP-997-74 can be used for research on NMDAR-related neurological diseases[1].
Molekulargewicht:
570.37
Reinheit:
99.85
CAS Nummer:
[2377187-09-0]
Formel:
C28H19Cl2F2N3O4
Target-Kategorie:
iGluR
Anwendungsbeschreibung:
MCE Product type: Reference compound
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