Comparison

AZ11645373 European Partner

Item no. ALO-A-395-1g
Manufacturer Alomone
CASRN 227088-94-0
Amount 1 g
Quantity options 10 mg 1 g 25 mg 50 mg 5 mg
Category
Type Small Molecules
Format Lyophilized
Specific against other
Purity >95%
ECLASS 10.1 32160490
ECLASS 11.0 32160490
UNSPSC 12000000
Shipping Condition Room temperature
Available
Manufacturer - Type
Non Antibodies
Manufacturer - Category
S. Molecules
Manufacturer - Targets
P2X7 receptors
Country of Origin
Israel
Shipping Temperature
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
Storage Conditions
Storage as Solution: -20°C. It is recommended to aliquot stock solutions to prevent repeated thawing and freezing. - 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.
Molecular Weight
463, 51
Manufacturer - Format
Lyophilized Powder
Short description
A Potent and Selective Antagonist of Human P2X7 Receptors
Description
3-[1-[[(3'-Nitro[1, 1'-biphenyl]-4-yl)oxy]methyl]-3-(4-pyridinyl)propyl]-2, 4-thiazolidinedione - A Potent and Selective Antagonist of Human P2X7 Receptors
Reconstitution
Soluble in DMSO. Centrifuge all products before handling (10000 x g 5 min).
PH
7, 4
UNSPSC
41116134
Effective Concentration
0.1-5 µM.
Activity
AZ11645373 is a potent and selective antagonist of human P2X7 purinergic receptors (KB = 5-20 nM), significantly less active on rat receptors, and inactive on other P2X receptor subtypes1.
Solubility
Soluble in DMSO. Centrifuge all products before handling (10000 x g 5 min).
Bioassay tested
Yes
Chemical Name
3-[1-[4-(3-nitrophenyl)phenoxy]-4-pyridin-4-ylbutan-2-yl]-1, 3-thiazolidine-2, 4-dione.
Scientific Background
AZ11645373 is a potent and highly selective antagonist of the human P2X7 receptor. It demonstrates IC50 values ranging from 5 to 90 nm depending on the cellular assay1. AZ11645373 is inactive on other P2X receptor subtypes and significantly less active on rat receptors1.The P2X7 receptor is a member of ligand-gated ion channels activated by extracellular ATP. 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 highly expressed throughout autonomic, sensory and central neurons and in visceral smooth muscle, immune cells and epithelia1, 2.

Note: The presented information and documents (Manual, Product Datasheet, Safety Datasheet and Certificate of Analysis) correspond to our latest update and should serve for orientational purpose only. We do not guarantee the topicality. We would kindly ask you to make a request for specific requirements, if necessary.

All products are intended for research use only (RUO). Not for human, veterinary or therapeutic use.

Amount: 1 g
Available: In stock
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