
Azeliragon
CAS No. 603148-36-3
Azeliragon( TTP-488 | PF-04494700 )
Catalog No. M15253 CAS No. 603148-36-3
An orally bioavailable small molecule inhibitor of RAGE.
Purity : >98% (HPLC)






Size | Price / USD | Stock | Quantity |
2MG | 30 | In Stock |
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5MG | 42 | In Stock |
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10MG | 72 | In Stock |
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25MG | 133 | In Stock |
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50MG | 237 | In Stock |
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100MG | 384 | In Stock |
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1G | Get Quote | In Stock |
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Biological Information
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Product NameAzeliragon
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NoteResearch use only, not for human use.
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Brief DescriptionAn orally bioavailable small molecule inhibitor of RAGE.
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DescriptionAn orally bioavailable small molecule inhibitor of RAGE; inhibits sRAGE from binding to RAGE ligands, S100b, amphoterin and carboxymethyl-lysine; has been shown to inhibit the binding of sRAGE to Aβ1-42 in a fluorescent polarization assay; 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.Alzheimer's Disease Phase 3 Clinical(In Vitro):Azeliragon (4 nM; 16 hours; T cells) treatment inhibits of wild type mice (WT) but not the deletion of the receptor (RAGE-/- mice) T cells and significant reduction in the production of IFN-γ.(In Vivo):Azeliragon (100 mcg/d; intraperitoneal injection; every day) treatment reduces syngeneic islet graft and islet allograft in NOD and B6 mice (Islets were isolated from young prediabetic NOD/LtJ mice and transplanted into NOD mice with spontaneous diabetes; islets were isolated from WT BALB/c mice and transplanted into B6 mice with diabetes).
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In VitroAzeliragon (4 nM; 16 hours; T cells) treatment inhibits of wild type mice (WT) but not the deletion of the receptor (RAGE-/- mice) T cells and significant reduction in the production of IFN-γ. Cell Viability Assay Cell Line:Purified T cells from RAGE-/- or WT B6 mice.Concentration:4 nM Incubation Time:16 hours Result:Inhibited of WT but not RAGE-/- T cells, and significantly reduced the level of IFN-γ.
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In VivoAzeliragon (100 mcg/d; intraperitoneal injection; every day) treatment reduces syngeneic islet graft and islet allograft in NOD and B6 mice (Islets were isolated from young prediabetic NOD/LtJ mice and transplanted into NOD mice with spontaneous diabetes; islets were isolated from WT BALB/c mice and transplanted into B6 mice with diabetes). Animal Model:Prediabetic NOD/LtJ (6-7 week old) mice, NOD mice with spontaneous diabetes, WT BALB/c mice (8-10 week old) and B6 mice with diabetes .Dosage:100 mcg/d Administration:Intraperitoneal injection; every day Result:Prolonged islet auto and allograft survival.
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SynonymsTTP-488 | PF-04494700
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PathwayOthers
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TargetOther Targets
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RecptorRAGE
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Research AreaNeurological Disease
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IndicationAlzheimer Disease
Chemical Information
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CAS Number603148-36-3
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Formula Weight532.116
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Molecular FormulaC32H38ClN3O2
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Purity>98% (HPLC)
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Solubility10 mM in DMSO
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SMILESCCCCC1=NC(=CN1C2=CC=C(C=C2)OC3=CC=C(C=C3)Cl)C4=CC=C(C=C4)OCCCN(CC)CC
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Chemical Name1-Propanamine, 3-[4-[2-butyl-1-[4-(4-chlorophenoxy)phenyl]-1H-imidazol-4-yl]phenoxy]-N,N-diethyl-
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
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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