VRT-043198
VRT-043198 是 VX-765 (Belnacasan) 的活性代谢物，是有效的、选择性的、能透过血脑屏障的 caspase-1 的抑制剂。VRT-043198 对 caspase-1 和 caspase-4 的 Ki 值分别为 0.8 nM 和 0.6 nM。
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包装价格促销价数量
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5mg￥1625.001300.00- +
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10mg￥2725.002180.00- +
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25mg￥4850.003880.00- +
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50mg￥8100.006480.00- +
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100mg￥13350.0010680.00- +
- 货号: ajcx35324
- CAS: 244133-31-1
- 别名:
- 分子式: C22H29ClN4O6
- 分子量: 480.94
- 纯度: ＞98%
- 溶解度: DMSO : 180 mg/mL (374.27 mM; Need ultrasonic)|Methanol : 12.5 mg/mL (25.99 mM; Need ultrasonic)
- 储存: Store at -20°C
- 库存: 现货
Background
VRT-043198, the drug metabolite of VX-765 (Belnacasan), is a potent, selective and blood-brain barrier permeable inhibitor of interleukin-converting enzyme/caspase-1 subfamily caspases. VRT-043198 exhibits Ki values of 0.8 nM and 0.6 nM for ICE/caspase-1 and caspase-4, respectively[1].
VRT-043198 exhibits 100- to 10,000-fold selectivity against other caspase-3 and -6 to -9[1].VRT043198 inhibits the release of interleukin (IL)-1β and IL-18, but it has little effect on the release of several other cytokines, including IL-1α, tumor necrosis factor-, IL-6 and IL-8. VRT-043198 inhibited IL-1β release from both PBMCs (n = 8) and whole blood (n = 4) with IC50 values of 0.67±0.55 and 1.9±0.80 nM, respectively[1].VRT-043198 lacks potent antiapoptotic activity[1].
VX-765 is converted rapidly to VRT-043198 under the action of plasma and liver esterases and also much more slowly in aqueous solution[1].VX765 reduces disease severity and the expression of inflammatory mediators in models of rheumatoid arthritis and skin inflammation[1].VX765 (25, 50, 100, or 200 mg/kg) inhibits lipopolysaccharide-induced cytokine secretion[1].
[1]. Woods Wannamaker, et al. (S)-1-((S)-2-{[1-(4-amino-3-chloro-phenyl)-methanoyl]-amino}-3,3-dimethyl-butanoyl)-pyrrolidine-2-carboxylic acid ((2R,3S)-2-ethoxy-5-oxo-tetrahydro-furan-3-yl)-amide (VX-765), an orally available selective interleukin (IL)-converting enzyme/caspase-1 inhibitor, exhibits potent anti-inflammatory activities by inhibiting the release of IL-1beta and IL-18. J Pharmacol Exp Ther. 2007 May;321(2):509-16.
