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JNJ 16259685

Cat. No. M6846

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JNJ 16259685 Structure
Synonym:

JNJ16259685

Size Price Availability Quantity
5mg USD 130 In stock
10mg USD 220 In stock
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Quality Control & Documentation
Biological Activity

JNJ 16259685 is a sub-nanomolar potent, non-competitive mGlu1 antagonist (Ki = 0.34 nM). JNJ16259685 inhibits glutamate-induced Ca2+ response at the human mGlu1 receptor with an IC50 value of 0.55 nM. JNJ16259685 is selective over mGlu5 (> 400-fold) and displays no activity at mGlu2, mGlu3, mGlu4, mGlu6, AMPA or NMDA receptors (IC50 > 10 μM).

Chemical Information
Molecular Weight 325.41
Formula C20H23NO3
CAS Number 409345-29-5
Solubility (25°C) DMSO ≥ 60 mg/mL
Storage Powder          -20°C   3 years ;  4°C   2 years
In solvent       -80°C   6 months ;  -20°C   1 month
References

[1] Dugovic, et al. J Pharmacol Exp Ther. Blockade of orexin-1 receptors attenuates orexin-2 receptor antagonism-induced sleep promotion in the rat.

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Keywords: JNJ 16259685, JNJ16259685 supplier, GluR, inhibitors, activators

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