product summary
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company name :
Alomone Labs
product type :
chemical
product name :
A-317491 sodium salt hydrate
catalog :
A-380
more info or order :
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Alomone Labs IRL-1620 activates Endothelin B receptor-mediated Ca2+ mobilization in CHO-K1-mt Aequorin cells. - Dose-response curve of normalized activation of Endothelin B receptor-mediated Ca2+mobilization evoked byIRL-1620(#SPE-220). Ca2+response was detected by measuring aequorin-derived fluorescence following application of IRL-1620 and Endothelin-1 at different concentrations. The EC50measured for IRL-1620 is 1.53 nM.
product information
CAT :
A-380
SKU :
A-380_10 mg
Product Name :
A-317491 sodium salt hydrate
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 :
A-317491 is a selective, competitive, non-nucleotide antagonist of P2X3 and P2X2/3 receptors. It is shown to inhibit human homomeric P2X3 and heteromeric P2X2/3 receptors with pIC50 values of ~7 and exhibits almost no antagonistic activity on other P2X family receptors1. The compound is active in chronic inflammatory and neuropathic pain models, but is ineffective in reducing nociception in animal models of acute, postoperative, and visceral pain.A-317491 is the chiral pure S-enantiomer, while the R-enantiomer, A-317344, shows lower activity at P2X3 and P2X2/3 receptors in vitro and lacks anti-nociceptive effects in animal models. A-317491 shows high systemic bioavailability following subcutaneous administration but lacks oral bioavailability. It is not susceptible to metabolic degradation1,2.P2X receptors are a family of ion channels gated by ATP. They are expressed in cell types of almost every origin, including neuronal, muscular, epithelial and immune and have been shown to play a pivotal role in models of various pain conditions3.
Supplier :
Alomone Labs
Target :
P2X3 receptors
Long Description :
A-317491 sodium salt hydrate (#A-380) is a highly pure, synthetic, and biologically active compound.
Short Description :
A Selective Antagonist of P2X3 and P2X2/3 Receptors
MW :
565.57 (free acid, anhydrous)
Source :
Synthetic
Molecular formula :
C33H27NO8 + xNa + xH2O.
Effective Concentration :
50 nM - 50 µM.
Activity :
A-317491 sodium salt hydrate is a selective antagonist of the P2X3 and P2X2/3 receptors. It was shown to inhibit human homomeric P2X3 and heteromeric P2X2/3 receptors with pIC50 values of ~7, whilst exhibiting little to no antagonistic activity on other P2X family receptors, and no effect on P2Y2 at over 10 µM1. This non-nucleotide antagonist reduces chronic inflammatory and neuropathic pain in the rat2.
Reconstitution and Solubility :
Up to 100 mM in DMSO. Centrifuge all product preparations before use (10000 x g 5 min).
Solubility :
Up to 100 mM 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 :
>98% (HPLC)
CAS No :
475205-49-3
Form :
Lyophilized Powder
Comment :
Contact Alomone Labs for technical support and product customization
UNSPSC :
41116134
Bioassay Tested :
Yes
Chemical Name :
5-[(3-phenoxyphenyl)methyl-[(1S)-1,2,3,4-tetrahydronaphthalen-1-yl]carbamoyl]benzene-1,2,4-tricarboxylic acid.
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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