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其他生物化学试剂

化合物CHZ868 TQ0061

英文名称:CHZ868
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
2 mg 1895895-38-1 ¥657.00 询底价
50 mg 1895895-38-1 面议 询底价
1 mL 1895895-38-1 ¥1,215.00 询底价
5 mg 1895895-38-1 面议 询底价
产品介绍

Product Introduction
Bioactivity


英文名: CHZ868

描述: CHZ868 是II型 JAK 抑制剂,具有潜在的抗肿瘤活性,可逆转 I 型 JAK 抑制剂的持续存在,可用于研究白血病。

细胞实验: CHZ868 is dissolved in DMSO to make 10 mM stock solution and diluted in culture media. Cells are treated with CHZ868 (0, 0.05, 0.1, 0.2 μM) or vehicle (DMSO). After 48 hr (Ba/F3 cells) or 72 hr (MHH-CALL4 and PDX cells), CellTiter-Glo Luminescent Cell Viability Assay is added (10 μL undiluted or 25 μL of a 1:2 dilution in each well) and plates are read [2].

动物实验: CHZ868 is reconstituted in 0.5% methylcellulose / 0.5% Tween-80 and administered at doses of 10 or 30 mg/kg/day by oral gavage. Pharmacokinetic/pharmacodynamic and efficacy studies in the mouse model of rhEpo-induced polycythemia are carried out essentially. Detection of STAT5 phosphorylation in spleen lysates by Meso Scale Discovery is performed [2].

体外活性: CHZ868 effectively inhibits constitutive phosphorylation of JAK2 and STAT5 in JAK2V617F SET2 cells. The compound demonstrates potent inhibition of SET2 cell proliferation (GI50=59nM) and exhibits 6-fold lower growth inhibitory activity against CMK cells (GI50=378nM)[1]. At a concentration of 100 nM, CHZ868 shows activity against 26 kinases, including JAK2 and TYK2. It is believed that CHZ868 interacts with the hinge region of JAK2 through two hydrogen bonds, formed between the amino-pyridine of CHZ868 and the backbone-NH/CO of L932, while the pyridine occupies the adenine pocket of the ATP binding site. CHZ868 effectively suppresses the growth of CRLF2-rearranged human B-ALL cells and disrupts JAK2 signaling[1].

体内活性: Characterized by high passive permeability, good metabolic stability, and low water solubility, CHZ868 also exhibits moderate blood clearance and good oral bioavailability, rendering it suitable for in vivo applications. In mice with human or murine B-ALL, CHZ868 enhances survival. When used in combination with dexamethasone, CHZ868 synergistically induces apoptosis in JAK2-dependent B-ALLs, leading to improved survival compared to CHZ868 alone[1].

存储条件: store at low temperaturePowder: -20°C for 3 years | In solvent: -80°C for 1 year

溶解度: DMSO : 50 mg/mL (118.08 mM)


关键字: CHZ-868 | CHZ868 | CHZ 868

相关产品: JAK 3 inhibitor IV | MM-589 | Brevilin A | Momelotinib sulfate | AZ960 | ABBV-712 | JAK-IN-27 | G5-7 | Ergosterol peroxide | AZ-3

相关库: Inhibitor Library

化合物CHZ868 TQ0061信息由TargetMol中国为您提供,如您想了解更多关于化合物CHZ868 TQ0061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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