化合物 CHIR-99021【252917-06-9】产品图
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化合物 CHIR-99021【252917-06-9】

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  • ¥257 - 5224
  • TargetMol
  • T2310
  • 2026年07月07日
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    • 技术资料
    • CAS号:

      252917-06-9

    • 规格:

      1mLx10mM(inDMSO)/1mg/2mg/5mg/10mg/25mg/50mg/100mg/200mg

    规格:1mLx10mM(inDMSO)产品价格:¥708.0
    规格:1mg产品价格:¥257.0
    规格:2mg产品价格:¥408.0
    规格:5mg产品价格:¥677.0
    规格:10mg产品价格:¥1128.0
    规格:25mg产品价格:¥1920.0
    规格:50mg产品价格:¥2728.0
    规格:100mg产品价格:¥3936.0
    规格:200mg产品价格:¥5224.0

    Product Introduction

    Bioactivity

    名称 CHIR-99021
    描述 CHIR-99021 (CT99021) is an activator of the Wnt/β-catenin signaling pathway and a GSK-3α/β inhibitor (IC50=10/6.7 nM) with selective and oral activity.CHIR-99021 induces cellular autophagy, which enhances self-renewal in mouse and human embryonic stem cells.
    细胞实验 The Wnt/beta-catenin reporter assay was performed with the M50 Super 8× TOPFlash and M51 Super 8× FOPFlash vector containing the firefly luciferase gene under the control of TCF/LEF binding sites or mutated bindings sites. 12,500 cells were seeded overnight on gelatine-coated 96-well plates in LIF-containing ES cell medium. On the next day, the cells were transfected using Lipofectamine with one of the aforementioned vectors plus pGL4.75 [hRluc/CMV] encoding the renilla luciferase reporter gene hRluc as a transfection control. Six hours after transfection the medium was changed to medium devoid of LIF, with reduced serum, and supplemented with 5 μM CHIR-99021. The Dual-Luciferase? reporter assay system was employed 48 and 72 h after the medium change to follow the luminescence reaction using a GloMax?-multi detection system [4].
    激酶实验 Kinases were purified from SF9 cells through the use of their His or Glu tag. Glu-tagged proteins were purified as described, and His-tagged proteins were purified according to the manufacturer's instructions. Kinase assays were performed in 96-well plates with appropriate peptide substrates in a 300-μl reaction buffer (variations on 50 mM Tris-HCl, pH 7.5, 10 mM MgCl2, 1 mM EGTA, 1 mM dithiothreitol, 25 mMβ-glycerophosphate, 1 mM NaF, and 0.01% bovine serum albumin). Peptides had Km values from 1 to 100 μM. CHIR 99021 or CHIR GSKIA was added in 3.5 μl of Me2SO, followed by ATP to a final concentration of 1 μM. After incubation, triplicate 100-μl aliquots were transferred to Combiplate 8 plates containing 100 μl/well of 50 μM ATP and 20 mM EDTA. After 1 hour, the wells were rinsed five times with phosphate-buffered saline, filled with 200 μl of scintillation fluid, sealed, and counted in a scintillation counter 30 min later. All of the steps were at room temperature. The percentage of inhibition was calculated as 100 × (inhibitor ? no enzyme control)/(Me2SO control ? no enzyme control) [4].
    动物实验 Blood was obtained by shallow tail snipping at lidocaine-anesthetized tips. Blood glucose was measured directly or heparinized plasma was collected for measurement of glucose or insulin. Animals were pre-bled and randomized to vehicle control or GSK-3 inhibitor treatment groups. For glucose tolerance tests (GTTs), animals fasted throughout the procedure with food removal early in the morning, 3 h before the first prebleed (db/db mice), or the previous night, 16 h before the bleed (ZDF rats). When the time course of plasma glucose and insulin changes in fasting ZDF rats was measured, food was removed ~16 h before test agent administration. The glucose challenges in the GTT were 1.35 g/kg i.p. (ipGTT) or 2 g/kg via oral gavage (oGTT). CHIR-99021 were formulated as solutions in 20 mmol/l citrate-buffered 15% Captisol or as fine suspensions in 0.5% carboxymethylcellulose [1].
    体外活性 方法:小鼠干细胞 ES-D3 用 CHIR-99021 (1-10 µM) 处理 72 h,使用 MTT 方法检测细胞生长抑制情况。 结果:CHIR-99021 剂量依赖性地抑制 ES-D3 细胞生长,IC50 为 4.9 µM。[1] 方法:小鼠胚胎干细胞 J1 mESCs 和小鼠胚胎瘤细胞 F9 mEC 用 CHIR-99021 (3 μM) 处理 24 h,使用 immunofluorescence 方法检测靶点蛋白表达水平。 结果:CHIR-99021 处理后,J1-mESCs 和 F9-mEC 细胞的细胞质和细胞核中的β-连环蛋白增加。[2] 方法:人 Tenon 成纤维细胞 HTFs 用 CHIR-99021 (5 μM) 处理 48 h,使用 Western Blot 方法检测靶点蛋白表达水平。 结果:CHIR-99021 处理使活性形式的 GSK-3β (p-GSK-3β (Y216)) 的产生显著减少。[3]
    体内活性 方法:为检测体内抗肿瘤活性,将 CHIR-99021 (37.5 mg/kg/第 0-3、6-10、13-17 和 20 天每天两次) 口服给药和 paclitaxel (10 mg/kg/第 0 天单次给药) 腹腔注射给携带人非小细胞肺癌肿瘤 H1975 的 Balb/c nude 小鼠。 结果:CHIR-99021 和 paclitaxel 在体内协同作用,抑制 NSCLC 肿瘤的生长。[4] 方法:为研究 GSK-3 的直接药理学抑制是否会改变酒精在小鼠体内的积极增强作用,将 CHIR-99021 (1-10 mg/kg) 单次腹腔注射给有酒精或蔗糖自给药史的 C57BL/6J 小鼠。 结果:CHIR-99021 剂量依赖性地增加了酒精强化反应,而对蔗糖自我给药或运动活性没有影响。CHIR-99021 显著降低了 pGSK-3β 在所有测试脑区的表达,仅在 NAcb 中降低了 PICK1 并增加了 GluA2 的总表达。[5]
    存储条件 Store at low temperature Powder: -20°C for 3 years | In solvent: -80°C for 1 year Shipping with blue ice/Shipping at ambient temperature.
    溶解度 10% DMSO+40% PEG300+5% Tween 80+45% Saline : 0.93 mg/mL (2 mM), Solution.
    DMSO : 105 mg/mL (225.64 mM), Sonication is recommended.
    关键字 β-catenin | βcatenin | Wnt/β-catenin | Wnt/betacatenin | Wnt/b-catenin | Wnt | Inhibitor | inhibit | GSK-3β | GSK-3α | GSK-3 | GSK3 | Glycogen synthase kinase-3 | Glycogen synthase kinase 3 | CT-99021 | CT 99021 | CHIR99021 | CHIR 99021 | beta-catenin | betacatenin | Beta catenin | bcatenin | Autophagy
    相关产品 Urea | Guanidine hydrochloride | Naringin | Aceglutamide | Alginic acid | Hemin | Hydroxychloroquine | Sildenafil citrate | Stavudine | Tamoxifen | Paeonol | Ethyl linoleate
    相关库 Inhibitor Library | Neuroprotective Compound Library | Bioactive Compound Library | Bioactive Compounds Library Max | Kinase Inhibitor Library | Highly Selective Inhibitor Library | Anti-Aging Compound Library | Antioxidant Compound Library | Membrane Protein-targeted Compound Library | Anti-Neurodegenerative Disease Compound Library | Immunology/Inflammation Compound Library | PI3K-AKT-mTOR Compound Library

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