product summary
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company name :
Alomone Labs
product type :
chemical
product name :
ZINC58368839
catalog :
Z-135
more info or order :
citations: 1
Reference
Bin Dayel A, Evans R, Schmid R. Mapping the Site of Action of Human P2X7 Receptor Antagonists AZ11645373, Brilliant Blue G, KN-62, Calmidazolium, and ZINC58368839 to the Intersubunit Allosteric Pocket. Mol Pharmacol. 2019;96:355-363 pubmed publisher
image
image 1 :
Alomone Labs Z-135 image 1
Expression of Kir6.2 in mouse hippocampus - Immunohistochemical staining of perfusion-fixed frozen mouse brain sectionsusing Guinea pigAnti-Kir6.2 Antibody (#AGP-067) (1:300) followed by goat-anti-guinea pig-Cy3 antibody (red staining).Kir6.2staining appears in the hilus region in neuronal outlines (arrows). Nuclei are stained with DAPI (blue).
product information
CAT :
Z-135
SKU :
Z-135_10 mg
Product Name :
ZINC58368839
Group Type :
Non Antibodies
Product Type :
S. Molecules
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 :
ZINC58368839 inhibits P2X7 receptors by binding to the ATP-binding pocket of the receptor and demonstrates strong specificity towards human P2X7R over human P2X4R and rat P2X3R1. It inhibits BzATP-induced Ca2+ responses in HEK-hP2X7 cells with IC50 value of 4.8 µM1.P2X receptors are cationic trimeric channel complexes that function as ATP-gated Ca2+-permeable channels. They are considered to be an attractive therapeutic target. This family includes seven receptor subtypes: P2X1-P2X7. P2X7 receptors participate in a variety of cellular responses such as membrane permeabilization, activation of caspases, cytokine release, cell proliferation, and apoptosis. P2X7 receptors are ubiquitously expressed, and particularly in cells of haematopoietic origin1,2.
Supplier :
Alomone Labs
Target :
P2X7 channels
Long Description :
ZINC58368839 (#Z-135) is a highly pure, synthetic, and biologically active compound.
Short Description :
An Antagonist of P2X7 Receptors
MW :
329.39
Synonyms :
N-cycloheptyl-N-methyl-2-(5-nitro-1H-indol-1-yl)acetamide, T6869826, Z905437510
Source :
Synthetic
Molecular formula :
C18H23N3O3.
Effective Concentration :
5-50 µM.
Activity :
ZINC58368839 is a novel antagonist of purinergic P2X7 receptors, shown to inhibit BzATP-induced Ca2+ responses in HEK-hP2X7 cells with IC50 of 4.8 µM1.
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 :
>97%
CID :
51127177
Form :
Lyophilized Powder
Comment :
Contact Alomone Labs for technical support and product customization
UNSPSC :
41116134
Bioassay Tested :
Yes
Chemical Name :
N-cycloheptyl-N-methyl-2-(5-nitroindol-1-yl)acetamide.
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