GSK2593074A
CAS No. 1337531-06-2
GSK2593074A( GSK'074 | GSK-2593074A )
Catalog No. M11349 CAS No. 1337531-06-2
GSK2593074A (GSK'074, GSK-2593074A) is novel potent, selective RIP1/RIP3 kinase dual inhibitor.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 5MG | 260 | Get Quote |
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| 10MG | 410 | Get Quote |
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| 25MG | 687 | Get Quote |
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| 50MG | 963 | Get Quote |
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| 100MG | 1287 | 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 NameGSK2593074A
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NoteResearch use only, not for human use.
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Brief DescriptionGSK2593074A (GSK'074, GSK-2593074A) is novel potent, selective RIP1/RIP3 kinase dual inhibitor.
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DescriptionGSK2593074A (GSK'074, GSK-2593074A) is novel potent, selective RIP1/RIP3 kinase dual inhibitor, directly binds to RIP1 and RIP3 with Kd of 130 and 12 nM, respectively; potently inhibits necroptosis in various cell types (IC50=3 nM both in MOVAS and L929 cells), blocks necroptosis signaling pathway; inhibits RIP3-dependent RIP1-independent necroptosis and inflammation, but does not induce apoptosis; attenuates cell death and inflammation in calcium phosphate injured aortae.
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In VitroGSK2593074A (GSK’074; 0.01, 0.1, 1, 10, and 100 nM; 6?hours for MOVAS cells; 3 hours for L929 cells) completely rescues cells from necroptosis under different stimuli in both human and murine cells at IC50~3?nM. In multiple cell types including mouse SMCs, fibroblasts (L929), bone marrow derived macrophages (BMDM), and human colon epithelial cells (HT29), GSK2593074A inhibits necroptosis with an IC50 of ~3?nM. Cell Viability Assay Cell Line:Mouse smooth muscle cell line MOVAS; Mouse fibroblast cell line L929Concentration:0.01, 0.1, 1, 10, and 100 nM Incubation Time:6?hours for MOVAS cells; 3 hours for L929 cells Result:Inhibited MOVAS and L929 cells with the IC50 of 3 nM.
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In VivoGSK2593074A (GSK’074; 0.93?mg/kg/day; i.p. injection; 14 or 28 days) is administrated to Apoe-/- mice immediately following pump implantation. Compared to the DMSO group, GSK2593074A-treated mice show significantly alleviated aneurysm formation, reflected by a much smaller aortic dilatation (DMSO 85.39±15.76% vs GSK2593074A 36.28±5.76%; P<0.05) as well as a reduced abdominal aortic aneurysm (AAA) incidence (from 83.3 to 16.7%). GSK2593074A significantly decreases the extent of aortic expansion (DMSO 66.06±9.17% vs GSK2593074A 27.36±8.25%; P<0.05) . Animal Model:Apoe-/- female mice (9-10 months)Dosage:0.93?mg/kg/day; 200?μL Administration:Daily i.p. injection; 14 or 28 days Result:Inhibited aneurysm formation in mouse models of aneurysms.
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SynonymsGSK'074 | GSK-2593074A
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PathwayApoptosis
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TargetRIP kinase
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RecptorRIP kinase
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Research Area——
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Indication——
Chemical Information
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CAS Number1337531-06-2
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Formula Weight465.575
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Molecular FormulaC27H23N5OS
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Purity>98% (HPLC)
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SolubilityIn Vitro:?DMSO : 41.67 mg/mL (89.50 mM)
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SMILESCN1N=CC(C2=CN=C(N)C3=C2SC=C3C4=CC5=C(N(C(CC6=CC=CC=C6)=O)CC5)C=C4)=C1
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Chemical Name1-(5-(4-amino-7-(1-methyl-1H-pyrazol-4-yl)thieno[3,2-c]pyridin-3-yl)indolin-1-yl)-2-phenylethan-1-one
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. Zhou T, et al. Cell Death Dis. 2019 Mar 6;10(3):226.
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