- GSK583
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- $46.00 / 1mg
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2024-11-19
- CAS:1346547-00-9
- Min. Order:
- Purity: 99.06%
- Supply Ability: 10g
- GSK583
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- $1.00 / 1ASSAYS
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2019-09-06
- CAS:1346547-00-9
- Min. Order: 1ASSAYS
- Purity: 95%~99%
- Supply Ability: per week:100kg
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| Product Name: | GSK583 | | Synonyms: | GSK583;SK583;6-[(1,1-Dimethylethyl)sulfonyl]-N-(5-fluoro-1H-indazol-3-yl)-4-quinolinamine;RIP2 kinase inhibitor 583;CS-2216;GSK583, >98%;GSK-583;GSK 583;4-Quinolinamine, 6-[(1,1-dimethylethyl)sulfonyl]-N-(5-fluoro-1H-indazol-3-yl)- | | CAS: | 1346547-00-9 | | MF: | C20H19FN4O2S | | MW: | 398.45 | | EINECS: | | | Product Categories: | | | Mol File: | 1346547-00-9.mol |  |
| | GSK583 Chemical Properties |
| Boiling point | 652.9±55.0 °C(Predicted) | | density | 1.402±0.06 g/cm3(Predicted) | | storage temp. | under inert gas (nitrogen or Argon) at 2–8 °C | | solubility | Soluble in DMSO (up to at least 25 mg/ml). | | form | solid | | pka | 12.59±0.40(Predicted) | | color | Pale yellow | | Stability: | Stable for 1 year from date of purchase as supplied. Solutions in DMSO may be stored at -20° for up to 1 month. |
| | GSK583 Usage And Synthesis |
| Description | GSK583 (1346547-00-9) is a highly selective and potent inhibitor of RIP2 kinase, IC50?= 5 nM human and IC50?= 2 nM rat.1?It also potently inhibits isolated RIP3 kinase (IC50?= 5 nM) but is inactive against RIP3 in cellular assays due to a very low KM,ATP. GSK583 blocks NOD2 signaling by interfering with XIAP-RIP2 binding resulting in decreased cytokine and chemokine production.1,2 | | Uses | GSK 583, is a selective inhibitor of RIP-like interacting CLARP kinase RIP2 Kinase is a central component of the innate immune system and enables downstream signaling following activation of the pattern recognition receptors NOD1 and NOD2, leading to the production of inflammatory cytokines. | | in vivo | GSK583 (0.1, 1, and 10 mg/kg, p.o.) inhibits serum KC (the rodent orthologue of IL-8) levels in rats in a dose-dependent manner, with an IC50 derived from rat blood concentrations of 50 nM (or 20 ng/mL). Similarly, GSK583 inhibits serum KC levels and recruitment of neutrophils into the peritoneal cavity in mice in a dose-dependent manner, with an IC50 of 37 nM (15 ng/mL) derived from mouse blood concentration[1]. | | storage | Store at +4°C | | References | 1) Haile?et al.?(2016),?The Identification and Pharmacological Characterization of 6-(tert-Butylsulfonyl)-N-(5-fluoro-1H-indazol-3-yl)quinoline-4-amine; J. Med. Chem.,?59?4867
2) Goncharov?et al.?(2018),?Disruption of XIAP-RIP2 Association Blocks NOD2-Mediated Inflammatory Signaling; Mol. Cell,?69?551 |
| | GSK583 Preparation Products And Raw materials |
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