product summary
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company name :
Alomone Labs
product type :
chemical
product name :
JNJ-47965567
catalog :
J-115
more info or order :
product information
CAT :
J-115
SKU :
J-115_10 mg
Product Name :
JNJ-47965567
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-47965567 is a synthetic compound that acts as a potent, selective, and high affinity antagonist of P2X7 receptors. It inhibits BzATP-induced Ca2+ responses in human, rat and mouse P2X7 receptors with pIC50 values of 8.3, 7.2 and 7.5, respectively. JNJ-47965567 is centrally permeable and is active in vivo. The compound can be used as a tool to explore the role of P2X7 in models of CNS pathophysiology.Studies show that JNJ-47965567 may attenuate amphetamine induced hyperactivity and exhibits significant efficacy in rat models of neuropathic pain1.P2X receptors are detected in neuronal, muscular, epithelial and immune cells and have been shown to play a pivotal role in models of various pain conditions. P2X7 receptors are responsible for mediating the release of proinflammatory cytokines in inflammatory/immune conditions and pain1,2.
Supplier :
Alomone Labs
Target :
P2X7 receptors
Long Description :
JNJ-47965567 (#J-115) is a highly pure, synthetic, and biologically active compound.
Short Description :
A Potent and Selective Antagonist of P2X7 Receptors
MW :
488.65
Synonyms :
JNJ-479655, 2-(Phenylthio)-N-[[tetrahydro-4-(4-phenyl-1-piperazinyl)-2H-pyran-4-yl]methyl-3-pyridinecarboxamide
Source :
Synthetic
Molecular formula :
C28H32N4O2S.
Effective Concentration :
20 nM - 1 µM.
Activity :
JNJ-47965567 is a potent and highly selective antagonist of purinergic P2X7 receptors, shown to inhibit BzATP-induced Ca2+ responses at human, rat and mouse P2X7 receptors with pIC50 values of 8.3, 7.2 and 7.5, respectively. JNJ-47965567 is centrally permeable and active in vivo1.
Reconstitution and Solubility :
Soluble in DMSO. Centrifuge all products before handling (10000 x g 5 min).
Solubility :
Soluble in DMSO. Centrifuge all products before handling (10000 x g 5 min).
Storage of solutions :
-20°C. It is recommended to aliquot stock solutions to prevent repeated thawing and freezing.
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 :
>99% (HPLC)
CAS No :
1428327-31-4
Form :
Lyophilized Powder
Comment :
Contact Alomone Labs for technical support and product customization
UNSPSC :
41116134
Bioassay Tested :
Yes
Chemical Name :
N-[[4-(4-phenylpiperazin-1-yl)oxan-4-yl]methyl]-2-phenylsulfanylpyridine-3-carboxamide.
more info or order :
company information

Alomone Labs
Jerusalem BioPark (JBP), Hadassah Ein Kerem
P.O. Box 4287
Jerusalem 9104201
P.O. Box 4287
Jerusalem 9104201
info@alomone.com
http://www.alomone.com972 2 531 8002
headquarters: Israel
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