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QNZ 46

Cat. No. M7175
QNZ 46 Structure
Size Price Availability Quantity
10mg USD 135  USD135 In stock
50mg USD 430  USD430 In stock
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Quality Control & Documentation
Biological Activity

QNZ 46 is a nR2C/NR2D-selective NMDA receptor non-competitive antagonist (IC50 values are 3, 6, 229, and >300, >300 μM for NR2D, NR2C, NR2A, NR2B, and GluR1, respectively). Requires binding of glutamate to the GluN2 subunit.

Chemical Information
Molecular Weight 443.41
Formula C24H17N3O6
CAS Number 1237744-13-6
Form Solid
Solubility (25°C) DMSO 4.43 mg/mL (with gentle warming)
Storage Powder          -20°C   3 years ;  4°C   2 years
In solvent       -80°C   6 months ;  -20°C   1 month
Conversion of different model animals based on BSA (PMID: 27057123)
Species Mouse Rat Rabbit Guinea pig Hamster Dog
Weight (kg) 0.02 0.15 1.8 0.4 0.08 10
Body Surface Area (m2) 0.007 0.025 0.15 0.05 0.02 0.5
Km factor 3 6 12 8 5 20
Animal A (mg/kg) = Animal B (mg/kg) multiplied by  Animal B Km
Animal A Km

For example, to modify the dose of Compound A used for a mouse (20 mg/kg) to a dose based on the BSA for a rat, multiply 20 mg/kg by the Km factor for a mouse and then divide by the Km factor for a rat. This calculation results in a rat equivalent dose for Compound A of 10 mg/kg.

References

[1] Markovič, et al. Drug Discov Today. Structural features of subtype-selective EP receptor modulators.

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