MedKoo Cat#: 524317 | Name: AZ-11645373
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Description:

WARNING: This product is for research use only, not for human or veterinary use.

AZ-11645373 is a potent and selective human P2X7 antagonist that is completely without effect at all other P2X subtypes. It also inhibits BzATP-mediated calcium influx and inhibits ATP-mediated IL-1β release.

Chemical Structure

AZ-11645373
AZ-11645373
CAS#227088-94-0

Theoretical Analysis

MedKoo Cat#: 524317

Name: AZ-11645373

CAS#: 227088-94-0

Chemical Formula: C24H21N3O5S

Exact Mass: 463.1201

Molecular Weight: 463.51

Elemental Analysis: C, 62.19; H, 4.57; N, 9.07; O, 17.26; S, 6.92

Price and Availability

Size Price Availability Quantity
10mg USD 550.00 2 Weeks
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Related CAS #
No Data
Synonym
AZ-11645373; AZ 11645373; AZ11645373; UNII-XY4SZP4C72; GTPL4142;
IUPAC/Chemical Name
2,4-Thiazolidinedione, 3-(1-(((3'-nitro(1,1'-biphenyl)-4-yl)oxy)methyl)-3-(4-pyridinyl)propyl)-
InChi Key
VQEHBLGYANQWEA-UHFFFAOYSA-N
InChi Code
InChI=1S/C24H21N3O5S/c28-23-16-33-24(29)26(23)21(7-4-17-10-12-25-13-11-17)15-32-22-8-5-18(6-9-22)19-2-1-3-20(14-19)27(30)31/h1-3,5-6,8-14,21H,4,7,15-16H2
SMILES Code
c1cc(cc(c1)[N+](=O)[O-])c2ccc(cc2)OCC(CCc3ccncc3)N4C(=O)CSC4=O
Appearance
Solid powder
Purity
>98% (or refer to the Certificate of Analysis)
Shipping Condition
Shipped under ambient temperature as non-hazardous chemical. This product is stable enough for a few weeks during ordinary shipping and time spent in Customs.
Storage Condition
Dry, dark and at 0 - 4 C for short term (days to weeks) or -20 C for long term (months to years).
Solubility
Soluble in DMSO, not in water
Shelf Life
>2 years if stored properly
Drug Formulation
This drug may be formulated in DMSO
Stock Solution Storage
0 - 4 C for short term (days to weeks), or -20 C for long term (months).
HS Tariff Code
2934.99.9001
More Info

Preparing Stock Solutions

The following data is based on the product molecular weight 463.51 Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which will affect the solvent volumes required to prepare stock solutions.

Recalculate based on batch purity %
Concentration / Solvent Volume / Mass 1 mg 5 mg 10 mg
1 mM 1.15 mL 5.76 mL 11.51 mL
5 mM 0.23 mL 1.15 mL 2.3 mL
10 mM 0.12 mL 0.58 mL 1.15 mL
50 mM 0.02 mL 0.12 mL 0.23 mL
1: Bartlett R, Yerbury JJ, Sluyter R. P2X7 receptor activation induces reactive oxygen species formation and cell death in murine EOC13 microglia. Mediators Inflamm. 2013;2013:271813. doi: 10.1155/2013/271813. Epub 2013 Jan 27. PubMed PMID: 23431238; PubMed Central PMCID: PMC3568910. 2: Sakowicz-Burkiewicz M, Kocbuch K, Grden M, Maciejewska I, Szutowicz A, Pawelczyk T. High glucose concentration impairs ATP outflow and immunoglobulin production by human peripheral B lymphocytes: involvement of P2X7 receptor. Immunobiology. 2013 Apr;218(4):591-601. doi: 10.1016/j.imbio.2012.07.010. Epub 2012 Jul 21. PubMed PMID: 22883563. 3: Hanamsagar R, Torres V, Kielian T. Inflammasome activation and IL-1β/IL-18 processing are influenced by distinct pathways in microglia. J Neurochem. 2011 Nov;119(4):736-48. doi: 10.1111/j.1471-4159.2011.07481.x. Epub 2011 Oct 11. PubMed PMID: 21913925; PubMed Central PMCID: PMC3202981. 4: Bradley HJ, Browne LE, Yang W, Jiang LH. Pharmacological properties of the rhesus macaque monkey P2X7 receptor. Br J Pharmacol. 2011 Sep;164(2b):743-54. doi: 10.1111/j.1476-5381.2011.01399.x. PubMed PMID: 21457228; PubMed Central PMCID: PMC3188921. 5: Lopez-Castejon G, Theaker J, Pelegrin P, Clifton AD, Braddock M, Surprenant A. P2X(7) receptor-mediated release of cathepsins from macrophages is a cytokine-independent mechanism potentially involved in joint diseases. J Immunol. 2010 Aug 15;185(4):2611-9. doi: 10.4049/jimmunol.1000436. Epub 2010 Jul 16. PubMed PMID: 20639492. 6: Michel AD, Ng SW, Roman S, Clay WC, Dean DK, Walter DS. Mechanism of action of species-selective P2X(7) receptor antagonists. Br J Pharmacol. 2009 Apr;156(8):1312-25. doi: 10.1111/j.1476-5381.2009.00135.x. Epub 2009 Mar 20. PubMed PMID: 19309360; PubMed Central PMCID: PMC2697735. 7: Stokes L, Jiang LH, Alcaraz L, Bent J, Bowers K, Fagura M, Furber M, Mortimore M, Lawson M, Theaker J, Laurent C, Braddock M, Surprenant A. Characterization of a selective and potent antagonist of human P2X(7) receptors, AZ11645373. Br J Pharmacol. 2006 Dec;149(7):880-7. Epub 2006 Oct 9. PubMed PMID: 17031385; PubMed Central PMCID: PMC2014691.