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Azeliragon

Chemical Structure : Azeliragon

CAS No.: 603148-36-3

Azeliragon (TTP488, PF-04494700)

Catalog No.: PC-45840Not For Human Use, Lab Use Only.

Azeliragon (TTP488, PF-04494700) is an orally bioavailable small molecule inhibitor of RAGE, inhibits sRAGE from binding to RAGE ligands, S100b, amphoterin and carboxymethyl-lysine.

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Purity & Documentation Purity: >98% (HPLC) Select Batch:

Biological Activity

Azeliragon (TTP488, PF-04494700) is an orally bioavailable small molecule inhibitor of RAGE, inhibits sRAGE from binding to RAGE ligands, S100b, amphoterin and carboxymethyl-lysine.
Azeliragon (TTP488, PF-04494700) has been shown to inhibit the binding of sRAGE to Aβ1-42 in a fluorescent polarization assay.
Azeliragon (TTP488, PF-04494700) reduces accumulation in the spleen of Aβ peptides and the expression of IL-6 and macrophage colony stimulating factor, reduces both inflammatory markers (TNF-α, TGF-β and IL-1) and CNS amyloid deposition.

Physicochemical Properties

M.Wt 532.116
Formula C32H38ClN3O2
Appearance Solid
CAS No.
Storage
Solide Powder
-20 °C 12 Months; 4°C 6 Months
In Solvent
-80 °C 6 Months; -20°C 6 Months
Shipping
Solubility

10 mM in DMSO

Chemical Name/SMILES

1-Propanamine, 3-[4-[2-butyl-1-[4-(4-chlorophenoxy)phenyl]-1H-imidazol-4-yl]phenoxy]-N,N-diethyl-

References

1. Sabbagh MN, et al. Alzheimer Dis Assoc Disord. 2011 Jul-Sep;25(3):206-12.

2. Chen Y, et al. J Immunol. 2008 Sep 15;181(6):4272-8.

3. Burstein AH, et al. BMC Neurol. 2014 Jan 15;14:12.

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