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JNJ16259685

CAT: 0804-HY-100407-01Size: 5 mgDry Ice: NoHazardous: No
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CAT#:0804-HY-100407-01Size:5 mg
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24/48H Stock Items & 2 to 6 Weeks non Stock Items.
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Description
JNJ16259685 is a selective antagonist of mGlu1 receptor, and inhibits the synaptic activation of mGlu1 in a concentration-dependent manner with IC50 of 19 nM.
CAS Number
409345-29-5
UNSPSC
12352005
Hazard Statement
H302, H315, H319
Target
MGluR
Type
Reference compound
Related Pathways
GPCR/G Protein; Neuronal Signaling
Applications
Neuroscience-Neuromodulation
Field of Research
Neurological Disease
Assay Protocol
https://www.medchemexpress.com/JNJ16259685.html
Purity
99.94
Solubility
DMSO : ≥ 100 mg/mL
Smiles
O=C(C1=CC=C2N=C3C(CCCO3)=CC2=C1)[C@H]4CC[C@@H](OC)CC4
Molecular Formula
C20H23NO3
Molecular Weight
325.40
Precautions
H302, H315, H319
References & Citations
[1]Navarro JF, et al. JNJ16259685, a selective mGlu1 antagonist, suppresses isolation-induced aggression in male mice. Eur J Pharmacol. 2008 May 31;586 (1-3) :217-20.|[2]Hodgson RA, et al. Characterization of the selective mGluR1 antagonist, JNJ16259685, in rodent models of movement and coordination. Pharmacol Biochem Behav. 2011 Apr;98 (2) :181-7.|[3]Lavreysen H, et al. JNJ16259685, a highly potent, selective and systemically active mGlu1 receptor antagonist. Neuropharmacology. 2004 Dec;47 (7) :961-72.|[4]I Fukunaga , et al. Potent and Specific Action of the mGlu1 Antagonists YM-298198 and JNJ16259685 on Synaptic Transmission in Rat Cerebellar Slices. Br J Pharmacol. 2007 Jul;151 (6) :870-6.
Shipping Conditions
Room Temperature
Storage Conditions
-20°C, 3 years; 4°C, 2 years (Powder)
Scientific Category
Reference compound1
Clinical Information
No Development Reported
Isoform
MGluR1

Alternative Products

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JRA34529-01JNJ16259685
A20545-50JNJ16259685 50mg
A20545-25JNJ16259685 25mg
A20545-10JNJ16259685 10mg
A20545-100JNJ16259685 100mg
A20545-5JNJ16259685 5mg
A20545-2JNJ16259685 2mg
A20545-1JNJ16259685 1mg
A20545-10mM-DJNJ16259685 10mM * 1mL in DMSO

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