APX-115 freebase
CAS No. 1270084-92-8
APX-115 freebase( Ewha 18278 | APX 115 | APX115 )
Catalog No. M11132 CAS No. 1270084-92-8
APX-115 (Ewha 18278) is a first-in-class, orally active, pan-NADPH oxidase (Nox) inhibitor with Ki of 1.08, 0.57, 0.63 nM for Nox1, Nox2, and Nox4, respectively.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 1 mL x 10 mM in DMSO | 119 | In Stock |
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| 5MG | 93 | In Stock |
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| 10MG | 155 | In Stock |
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| 25MG | 330 | In Stock |
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| 50MG | 523 | In Stock |
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| 100MG | 805 | In Stock |
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| 200MG | 1107 | In Stock |
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| 500MG | Get Quote | In Stock |
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| 1G | Get Quote | In Stock |
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Biological Information
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Product NameAPX-115 freebase
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NoteResearch use only, not for human use.
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Brief DescriptionAPX-115 (Ewha 18278) is a first-in-class, orally active, pan-NADPH oxidase (Nox) inhibitor with Ki of 1.08, 0.57, 0.63 nM for Nox1, Nox2, and Nox4, respectively.
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DescriptionAPX-115 (Ewha 18278) is a first-in-class, orally active, pan-NADPH oxidase (Nox) inhibitor with Ki of 1.08, 0.57, 0.63 nM for Nox1, Nox2, and Nox4, respectively; shows no inhibitory activities on xanthine oxidase and glucose oxidase; inhibits the responses of BMMs to RANKL, including ROS generation, activation of MAPK and NF-κB, and osteoclast cells differentiation; protects db/db mice from renal injury.Diabetes Preclinical.
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In Vitro——
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In VivoAnimal Model:Six-week-old male diabetic db/db mice (C57BLKS/J-leprdb/leprdb)Dosage:60?mg/kg Administration:Oral gavage; per day; for 12 weeks Result:Significantly improved insulin resistance in diabetic mice.
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SynonymsEwha 18278 | APX 115 | APX115
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PathwayMembrane Transporter/Ion Channel
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TargetNADPH
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RecptorNADPH
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Research AreaMetabolic Disease
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IndicationDiabetes
Chemical Information
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CAS Number1270084-92-8
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Formula Weight279.343
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Molecular FormulaC17H17N3O
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Purity>98% (HPLC)
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SolubilityIn Vitro:?DMSO : 250 mg/mL (894.97 mM)
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SMILES——
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Chemical Name3-phenyl-1-(pyridin-2-yl)-4-propyl-1-5-hydroxypyrazol
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
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NoxA1ds
Potent and selective NADPH oxidase 1 (NOX1) inhibitor (IC50 = 20 nM). Exhibits selectivity for NOX1 over NOX2, NOX4, NOX5 and xanthine oxidase. Inhibits NOX1-derived O2- production in HT-29 human colon cancer cells. Attenuates VEGF-induced human pulmonary artery endothelial cell migration under hypoxic conditions in vitro. Cell permeable.
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GSK2795039
GSK2795039 inhibits reactive oxygen species (ROS) production and NADPH consumption. GSK2795039 decreases apoptosis. GSK2795039 is an inhibitor of NADPH oxidase 2 (NOX2) (pIC50: 6 in different cell-free assays). GSK2795039 (25 μM; 24 hours) decreases the combinatory effect of FeSO4 and LPS-increased levels of apoptosis.
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GKT137831
GKT137831 (Setanaxib, GKT-137831) is a potent, selective, dual NADPH oxidase Nox1/4 inhibitor with Ki of 110/140 nM.
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