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RN486

    
10mM in DMSO

RN486

源叶(MedMol)
T95422 一键复制产品信息
1242156-23-5
C35H35FN6O3
606.69
6-cyclopropyl-8-fluoro-2-(2-(hydroxymethyl)-3-(1-methyl-5-(5-(4-methylpiperazin-1-yl)pyridin-2-ylamino)-6-oxo-1,6-dihydropyridin-3-yl)phenyl)isoquinolin-1(2H)-one
货号 规格 价格 上海 北京 珠海 重庆 武汉 购买数量
T95422-1ml促销
10mM in DMSO

¥720.00 ¥648.00

货期:3-5天 - - - -
产品介绍 参考文献 质检证书(COA) 摩尔浓度计算器 相关产品
产品描述: BTK抑制剂;BTK Inhibitors;;InformationRN486 RN486 is a potent and selective BTK inhibitor with IC50 of 4 nM.TargetsBTK 4 nMIn vitroRN486 not only potently and selectively inhibits the Btk enzyme, but also displays functional activities in human cell-based assays in multiple cell types, blocking Fcε receptor cross-linking-induced degranulation in mast cells (IC50 = 2.9 nM), Fcγ receptor engagement-mediated tumor necrosis factor α production in monocytes (IC50 = 7.0 nM), and B cell antigen receptor-induced expression of an activation marker, CD69, in B cells in whole blood (IC50 = 21.0 nM). RN486 is able to block the signaling of BCR as demonstrated by a marked inhibition of phosphorylation of both Btk and PLCγ2 in B cells. RN486 displays a selective B cell inhibitory profile in BioMAP Systems.In vivoRN486 displays similar functional activities in rodent models, effectively preventing type I and type III hypersensitivity responses. More importantly, RN486 produces robust anti-inflammatory and bone-protective effects in mouse CIA and rat adjuvant-induced arthritis (AIA) models. In the AIA model, RN486 inhibits both joint and systemic inflammation either alone or in combination with methotrexate, reducing both paw swelling and inflammatory markers in the blood.
靶点: IC50: 4.0 nM (Btk);Kd: 0.31 nM (Btk)
保存条件: -80℃(运输条件:冰袋低温运输)
配置溶液浓度参考:
1mg 5mg 10mg
1 mM 1.648 ml 8.241 ml 16.483 ml
5 mM 0.33 ml 1.648 ml 3.297 ml
10 mM 0.165 ml 0.824 ml 1.648 ml
50 mM 0.033 ml 0.165 ml 0.33 ml
注意: 部分产品我司仅能提供部分信息,我司不保证所提供信息的权威性,仅供客户参考交流研究之用。

参考文献

质检证书(COA)

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摩尔浓度计算器

质量 (mg) = 浓度 (mM) x 体积 (mL) x 分子摩尔量 (g/mol)

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