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其他生物化学试剂

环丙基[4-[3-(1H-咪唑-5-基)丙氧基]苯 T6156

英文名称:Ruxolitinib (S enantiomer)
品牌 厂商性质 产地 货期
TargetMol 生产商 美国 现货

性能特点

生化试剂,可用于动物细胞实验

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产品参数
规格 CAS号 价格 操作
50 mg 941685-37-6 ¥2,323.00 询底价
5 mg 941685-37-6 ¥625.00 询底价
100 mg 941685-37-6 ¥3,715.00 询底价
1 mL 941685-37-6 ¥644.00 询底价
10 mg 941685-37-6 ¥929.00 询底价
产品介绍

Product Introduction
Bioactivity


英文名: Ruxolitinib (S enantiomer)

描述: Ruxolitinib S enantiomer (INCB18424) 是 Ruxolitinib 的 S 型对映体,是一种JAK 抑制剂。

细胞实验: Cell lines: Ba/F3 and HEL cells. Concentrations: 3 μM. Method: Cells are seeded at 2×103/well of white bottom 96-well plates,treated with INCB018424 from DMSO stocks (0.2% final DMSO concentration),and incubated for 48 hours at 37 ℃ in an atmosphere containing 5% CO2.Viability is measured by cellular ATP determination using the Cell-Titer Glo luciferase reagent or viable cell counting.Values are transformed to percent inhibition relative to vehicle control,and IC50 curves are fitted according to nonlinear regression analysis of the data using PRISM GraphPad.

激酶实验: Recombinant proteins expressed with Sf21 cells and baculovirus vectors are purified with affinity chromatography. JAK kinase assay is done by a homogeneous time-resolved fluorescence assay with the peptide substrate (-EQEDEPEGDYFEWLE). Each enzyme reaction is carried out with Ruxolitinib or control, JAK enzyme, 500 nM peptide, adenosine triphosphate (ATP; 1 mM), and 2% dimethyl sulfoxide (DMSO) for 1 hour. IC50 is the INCB018424 concentration required for inhibition of 50% of the fluorescent signal.

动物实验: Animal Models: JAK2V617F-driven mouse modelFormulation & . Dosages: 5% dimethyl acetamide,0.5% methylcellulose.180 mg/kg. Administration: Oral gavage

体外活性: INCB018424(180 mg/kg,口服,每天两次)显著减少JAK2V617F驱动的小鼠模型中脾肿大和炎性细胞因子的循环水平,并优先消灭肿瘤细胞,显著延长生存期,且未产生骨髓抑制或免疫抑制.上述小鼠在第22天存活率超过90%.15 mg Ruxolitinib处理骨髓纤维化患者,每天两次,在48周时,28%患者的脾脏体积减少至少35%.Ruxolitinib组的患者整体生活质量改善,与骨髓纤维化有关的症状减轻.

体内活性: INCB018424在Ba/F3细胞中以剂量依赖性方式显著增加细胞凋亡。INCB018424作用于Ba/F3细胞和HEL细胞,有效且选择性抑制JAK2V617F介导的信号和增殖。INCB018424(64 nM) 导致Ba/F3细胞线粒体去极化增加一倍。INCB018424抑制正常供体和真性红细胞增多症患者提供的红系祖细胞增殖,IC50分别为407 nM 和 223 nM。INCB018424表现出对红系细胞集落形成的有效作用,IC50为67 nM。

存储条件: Powder: -20°C for 3 years | In solvent: -80°C for 1 year

溶解度: DMSO : 57 mg/mL (186 mM)
Ethanol : 57 mg/mL (186 mM)
H2O : 5 mg/mL (16.32 mM)


关键字: S-INCB18424 | Ruxolitinib | INCB 018424 | INCB-18424 | Ruxolitinib (S enantiomer) | INCB-018424 | Janus kinase | JAK | inhibit | INCB 18424 | Inhibitor

相关产品: Tyrosine kinase inhibitor | ZAP-180013 | Beta-Hydroxyisovalerylshikonin | PP2 | SU 4981 | Vamotinib | Baricitinib phosphate | Brepocitinib | GSK 3 Inhibitor IX | NVP-BSK805 2HCl (1092499-93-8(free base))

相关库: Drug Repurposing Compound Library | FDA-Approved Kinase Inhibitor Library | Anti-Cancer Compound Library | Anti-Cancer Drug Library | Inhibitor Library | Kinase Inhibitor Library | Anti-Cancer Clinical Compound Library | Epigenetics Compound Library | Tyrosine Kinase Inhibitor Library | Anti-Cancer Approved Drug Library

环丙基[4-[3-(1H-咪唑-5-基)丙氧基]苯 T6156信息由TargetMol中国为您提供,如您想了解更多关于环丙基[4-[3-(1H-咪唑-5-基)丙氧基]苯 T6156报价、型号、参数等信息,欢迎来电或留言咨询。

注:该产品未在中华人民共和国食品药品监督管理部门申请医疗器械注册和备案,不可用于临床诊断或治疗等相关用途

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