product summary
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company name :
Alomone Labs
product type :
chemical
product name :
JNJ 16259685
catalog :
J-110
more info or order :
image
image 1 :
Alomone Labs J-110 image 1
Western blot analysis of rat lung (lanes 1 and 3) rat tongue (lanes 2 and 4) human U-87 astrocytoma cells (lanes 5 and 7) and mouse MS1 endothelial cells (lanes 6 and 8) lysates: - 1256. Anti-GPR120/FFAR4 (extracellular) Antibody (#AFR-014) (1:200).3478. Anti-GPR120/FFAR4 (extracellular) Antibody preincubated with the negative control antigen.
product information
CAT :
J-110
SKU :
J-110_10 mg
Product Name :
JNJ 16259685
Group Type :
Non Antibodies
Product Type :
S. Molecules
Storage After Reconstitution :
The reconstituted solution can be stored at 4°C for up to 1 week. For longer periods (up to 6 months), small aliquots should be stored at -20°C. We do not recommend storing the product in working solutions for longer than a few days. Avoid multiple freeze-thaw cycles.
Shipping and storage :
Shipped at room temperature. Product as supplied can be stored intact at room temperature for several weeks. For longer periods, it should be stored at -20°C
Product Page - Scientific background :
JNJ 16259685 is a potent, specific, and non-competitive antagonist of mGluR1 displaying an IC50 of 19 nM1. The compound shows a much lower potency towards mGluR5 receptor1,2.Glutamate is the most abundant excitatory neurotransmitter in the central nervous system and it modulates activity of many types of synapses by activating in part metabotropic glutamate receptors (mGluRs). mGluRs consist of three groups: I, II, and III with a total of eight subtypes, mGluR1 to mGluR8.mGluR1 plays an important role in the central sensitization of pain and in various physiological functions including regulating ion channels, synaptic transmission, and synaptic plasticity2.
Supplier :
Alomone Labs
Target :
mGluR1
Long Description :
JNJ 16259685 (#J-110) is a highly pure, synthetic, and biologically active compound.
Short Description :
A Potent and Selective Antagonist of mGluR1
MW :
325.41
Source :
Synthetic
Molecular formula :
C20H23NO3.
Effective Concentration :
1 nM - 1 µM.
Activity :
JNJ 16259685 is a potent and selective non-competitive antagonist of mGluR1 receptors, inhibiting human mGluR1 and mGluR5 mediated glutamate-induced Ca2+ mobilization with IC50 values of 1.21 nM and 28.3 µM, respectively, whilst having no effect on a range of other receptor subtypes at over 10 µM1.It is systemically active, occupying central mGluR1 receptors in the rat cerebellum and thalamus (ED50 = 40 and 14 µg/kg, respectively) when administered subcutaneously1. JNJ 16259685 inhibits synaptic activation of mGluR1 in Purkinje cells in cerebellar slices with IC50 of 19 nM2.
Reconstitution and Solubility :
Soluble in DMSO. Centrifuge all product preparations before use (10000 x g 5 min).
Solubility :
Soluble in DMSO. Centrifuge all product preparations before use (10000 x g 5 min).
Storage of solutions :
-20°C.
Lead Time :
1-2 Business Days
Country of origin :
Israel/IL
Applications key :
Application key: FC- Flow cytometry, IFC- Indirect flow cytometry, IHC- Immunohistochemistry,LCI- Live cell imaging, Calcium imaging assay,Cell survival assay, Electrophysiology, Neurite outgrowth assay.
Purity :
>97%
CAS No :
409345-29-5
Form :
Lyophilized powder.
Comment :
Contact Alomone Labs for technical support and product customization
UNSPSC :
41116134
Bioassay Tested :
Yes
Chemical Name :
3,4-dihydro-2H-pyrano[2,3-b]quinolin-7-yl-(4-methoxycyclohexyl)methanone.
more info or order :
company information
Alomone Labs
Jerusalem BioPark (JBP), Hadassah Ein Kerem
P.O. Box 4287
Jerusalem 9104201
info@alomone.com
http://www.alomone.com
972 2 531 8002
headquarters: Israel