AZ 10606120 dihydrochloride

Catalog #: 3323
15 Citations Datasheet / COA / SDS

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3323/10
3323/50

AZ 10606120 dihydrochloride | CAS No. 607378-18-7 | P2X Receptor Antagonists

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Description: Potent P2X7 antagonist

Chemical Name: N-[2-[[2-[(2-Hydroxyethyl)amino]ethyl]amino]-5-quinolinyl]-2-tricyclo[3.3.1.13,7]dec-1-ylacetamide dihydrochloride

Purity: ≥98%

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Product Details

Citations (15)

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Biological Activity

AZ 10606120 dihydrochloride is a potent P2X₇ receptor antagonist (K_D values are 1.4 and 19 nM at human and rat P2X₇ receptors respectively). Binds in a positive cooperative manner to sites distinct from, but coupled to, the ATP binding site and acts as a negative allosteric modulator. Inhibits tumor growth and displays antiangiogenic effects in mice.

Technical Data

M.Wt:

495.48

Formula:

C₂₅H₃₄N₄O₂.2HCl

Solubility:

Soluble to 25 mM in water and to 100 mM in DMSO

Purity:

≥98%

Storage:

Desiccate at RT

CAS No:

607378-18-7

The technical data provided above is for guidance only. For batch specific data refer to the Certificate of Analysis.
Tocris products are intended for laboratory research use only, unless stated otherwise.

Additional Information

Licensing Caveats:

Sold for research purposes under agreement from AstraZeneca

Background References

Expression of P2X7 receptor increases in vivo tumor growth.
Adinolfi et al.
Cancer Res., 2012;72:2957
Negative and positive allosteric modulators of the P2X₇ receptor.
Michel et al.
Br.J.Pharmacol., 2008;153:737
Direct labelling of the human P2X₇ receptor and identification of positive and negative cooperativity of binding.
Michel et al.
Br.J.Pharmacol., 2007;151:103
Agonist potency at P2X₇ receptors is modulated by structurally diverse lipids.
Michel and Fonfria
Br.J.Pharmacol., 2007;152:523

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*When preparing stock solutions always use the batch-specific molecular weight of the product found on the vial label and CoA (available online).

Citations for AZ 10606120 dihydrochloride

The citations listed below are publications that use Tocris products. Selected citations for AZ 10606120 dihydrochloride include:

15 Citations: Showing 1 - 10

Characterization of purinergic receptor expression in ARPKD cystic epithelia.
Authors: Palygin Et al.
Purinergic Signal 2018;14:485
Unique residues in the ATP gated human P2X7 receptor define a novel allosteric binding pocket for the selective antagonist AZ10606120
Authors: Allsopp
Sci Rep 2017;7(1)
Neutrophil P2X₇ receptors mediate NLRP3 inflammasome-dependent IL-1β secretion in response to ATP.
Authors: Karmakar Et al.
Nat.Commun. 2016;7:10555
Active Caspase-1 Induces Plasma Membrane Pores That Precede Pyroptotic Lysis and Are Blocked by Lanthanides
Authors: Russo Et al.
The Journal of Immunology 2016;197:1353
Selected ginsenosides of the protopanaxdiol series are novel positive allosteric modulators of P2X7 receptors.
Authors: Helliwell Et al.
Br J Pharmacol 2015;172:3326
The P2X7 receptor regulates cell survival, migration and invasion of pancreatic ductal adenocarcinoma cells.
Authors: Giannuzzo Et al.
Purinergic Signal 2015;14:203
Bile acid effects are mediated by ATP release and purinergic signalling in exocrine pancreatic cells.
Authors: Kowal Et al.
Mol Cancer 2015;13:28
Probenecid blocks human P2X7 receptor-induced dye uptake via a pannexin-1 independent mechanism.
Authors: Bhaskaracharya Et al.
PLoS One 2014;9:e93058
IKKα negatively regulates ASC-dependent inflammasome activation.
Authors: Martin Et al.
Nat Commun 2014;5:4977
Tanshinone II A sulfonate, but not tanshinone II A, acts as potent negative allosteric modulator of the human purinergic receptor P2X7.
Authors: Kaiser Et al.
J Pharmacol Exp Ther 2014;350:531

Natural compounds with P2X7 receptor-modulating properties.
Authors: Fischer Et al.
Purinergic Signal 2013;10:313

P2X7 receptor activation mediates organic cation uptake into human myeloid leukaemic KG-1 cells.
Authors: Gadeock Et al.
Mol Biol Cell 2012;8:669

Positive allosteric modulation by iverm. of human but not murine P2X7 receptors.
Authors: Nörenberg Et al.
Br J Pharmacol 2012;167:48

K+ depolarization evokes ATP, adenosine and glutamate release from glia in rat hippocampus: a microelectrode biosensor study.
Authors: Heinrich Et al.
Br J Pharmacol 2012;167:1003

Lack of neuroprotection in the absence of P2X7 receptors in toxin-induced animal models of Parkinson's disease.
Authors: Hracskó Et al.
Mol Neurodegener 2011;6:28

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