
AZD5718
CAS No. 2041075-86-7
AZD5718( AZD-5718 | AZD 5718 )
Catalog No. M13174 CAS No. 2041075-86-7
AZD5718 (AZD-5718, AZD 5718) is a novel potent 5-lipoxygenase activating protein (FLAP) inhibitor with binding IC50 of 6.3 nM.
Purity : >98% (HPLC)






Size | Price / USD | Stock | Quantity |
2MG | 143 | Get Quote |
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5MG | 215 | Get Quote |
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10MG | 320 | Get Quote |
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25MG | 531 | Get Quote |
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50MG | 773 | Get Quote |
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100MG | 1062 | Get Quote |
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200MG | Get Quote | Get Quote |
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500MG | Get Quote | Get Quote |
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1G | Get Quote | Get Quote |
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Biological Information
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Product NameAZD5718
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NoteResearch use only, not for human use.
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Brief DescriptionAZD5718 (AZD-5718, AZD 5718) is a novel potent 5-lipoxygenase activating protein (FLAP) inhibitor with binding IC50 of 6.3 nM.
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DescriptionAZD5718 (AZD-5718, AZD 5718) is a novel potent 5-lipoxygenase activating protein (FLAP) inhibitor with binding IC50 of 6.3 nM; exhibits LTB4 inhibition in human whole blood assays with IC50 of 39 nM; reduce the production of pro-inflammatory and vasoactive leukotrienes both in vitro and in vivo.(In Vitro):Atuliflapon demonstrates a dose dependent and greater than 90% suppression of leukotriene production over 24 h.Atuliflapon exhibits an IC50 of 39 nM for LTB4.(In Vivo):Atuliflapon exhibits t1/2 of 0.45 h and 2.1 h in rat and dog by iv injection, respectively.Atuliflapon shows no inhibition of 5-LO pathway activity in rodent blood.
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In Vitro——
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In Vivo——
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SynonymsAZD-5718 | AZD 5718
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PathwayImmunology/Inflammation
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TargetFLAP
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RecptorFLAP
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Research Area——
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Indication——
Chemical Information
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CAS Number2041075-86-7
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Formula Weight446.511
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Molecular FormulaC24H26N6O3
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Purity>98% (HPLC)
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SolubilityIn Vitro:?DMSO : 125 mg/mL (279.96 mM)
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SMILES——
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Chemical Name(1R,2R)-2-[4-(3-Methyl-1H-pyrazol-5-yl)benzoyl]-N-(4-oxo-4,5,6,7-tetrahydropyrazolo[1,5-a]pyrazin-3-yl)cyclohexanecarboxamide
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. Ericsson H, et al. Clin Transl Sci. 2018 May;11(3):330-338.
2. Pettersen D, et al. J Med Chem. 2019 Mar 14. doi: 10.1021/acs.jmedchem.8b02004.
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