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Lumacaftor

Lumacaftor

产品编号 T2595   CAS 936727-05-8
别名: 鲁玛卡托, VX-809, VRT 826809

Lumacaftor (VRT 826809) 是一种 CFTR 调节剂,可纠正 CFTR 蛋白的折叠和运输。它增强了 FRT 细胞中 F508del-CFTR 蛋白的成熟,EC50为100 nM。

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Lumacaftor Chemical Structure
Lumacaftor, CAS 936727-05-8
规格 价格/CNY 货期 数量
1 mg ¥ 290 现货
5 mg ¥ 663 现货
10 mg ¥ 913 现货
25 mg ¥ 1,250 现货
50 mg ¥ 1,490 现货
100 mg ¥ 1,960 现货
500 mg ¥ 4,760 现货
1 mL * 10 mM (in DMSO) ¥ 728 现货
千万补贴 助力科研
BCA蛋白浓度测定试剂盒限时半价
Venetoclax限时半价
MG-132限时半价
产品目录号及名称: Lumacaftor (T2595)
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纯度: 99.72%
纯度: 99.68%
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生物活性
化学信息
存储 & 溶解度
参考文献
产品描述 Lumacaftor (VRT 826809) is a CFTR modulator that corrects the folding and trafficking of CFTR protein. It enhances F508del-CFTR protein maturation in FRT cells (EC50: 100 nM).
靶点活性 F508del CFTR:0.1 μM (EC50, Fischer rat thyroid cells)
体外活性 In cultured human bronchial epithelial cells isolated from patients with CF homozygous for F508del, Lumacaftor (VX-809) improved F508del-CFTR processing in the endoplasmic reticulum and enhanced chloride secretion to approximately 14% of non-CF human bronchial epithelial cells (EC50: 81 nM), a level associated with mild CF in patients with less disruptive CFTR mutations [1]. VX-809 produced a concentration-dependent increase in the HRP luminescence signal after incubation with cells at 37°C or 27°C in both cell lines, with a similar EC50 value of approximately 0.3 μM [2].
激酶实验 In one set of assays, R1070W-?F508-CFTR-HRP (R1070W-HRP)–expressing CFBE41o? cells were incubated with 100 μl medium containing 25 μM test compounds and 0.5 μg/ml doxycycline for 24 hours at 37°C. In a second set of assays, ?F508-CFTR-HRP (?F508-HRP)–expressing CFBE41o? cells were incubated with 100 μl medium containing 25 μM test compounds, 2 μM VX-809, and 0.5 μg/ml doxycycline for 24 hours at 37°C. All compound plates contained negative controls (DMSO vehicle) and positive controls [2 μM VX-809]. In both assays, the cells were washed four times with PBS, and HRP activity was assayed by the addition of 50 μl/well of HRP substrate. After shaking for 5 minutes, chemiluminescence was measured using a Tecan Infinite M1000 plate reader (Tecan Groups Ltd, Mannedorf, Switzerland) equipped with an automated stacker (integration time, 100 milliseconds). Z′ is defined as = 1 ? [(3 × standard deviation of maximum signal control + 3 × standard deviation of minimum signal control)/absolute (mean of maximum signal control ? mean of minimum signal control)] [2].
细胞实验 FRT, HEK-293, or HBE cells expressing CFTR or F508del-CFTR were incubated for 24 h at 37 °C with or without VX-809 in the assay media. After incubation, cells were harvested in ice-cold D-PBS solution (without calcium and magnesium) and pelleted at 1,000 × g at 4 °C. Cell pellets were lysed in 1% Nonidet P-40, 0.5% sodium deoxycholate, 200 mM NaCl, 10 mM Tris, pH 7.8, and 1 mM EDTA plus protease inhibitor mixture (1:250) for 30 min on ice. Lysates were spun for 10 min at 10,000 × g at 4 °C to pellet nuclei and insoluble material. Approximately 12 μg total protein was heated in Laemmli buffer with 5% β-mercaptoethanol at 37 °C for 5 min and loaded onto a 3% to 8% Tris-acetate gel. The gel was transferred to nitrocellulose and processed for Western blotting by using monoclonal CFTR antibody 769 or polyclonal to GAPDH. Blots were developed by enhanced chemiluminescence. Quantification of the relative amounts of bands C and GAPDH was performed by using NIH ImageJ analysis of scanned films [1].
别名 鲁玛卡托, VX-809, VRT 826809
分子量 452.41
分子式 C24H18F2N2O5
CAS No. 936727-05-8

存储

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

溶解度

H2O: < 1 mg/mL (insoluble or slightly soluble)

Ethanol: 6 mg/mL (13.26 mM)

DMSO: 83 mg/mL (183.5 mM)

溶液配制表

可选溶剂 浓度 体积 质量 1 mg 5 mg 10 mg 25 mg
Ethanol / DMSO 1 mM 2.2104 mL 11.0519 mL 22.1038 mL 55.2596 mL
5 mM 0.4421 mL 2.2104 mL 4.4208 mL 11.0519 mL
10 mM 0.221 mL 1.1052 mL 2.2104 mL 5.526 mL
DMSO 20 mM 0.1105 mL 0.5526 mL 1.1052 mL 2.763 mL
50 mM 0.0442 mL 0.221 mL 0.4421 mL 1.1052 mL
100 mM 0.0221 mL 0.1105 mL 0.221 mL 0.5526 mL

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TargetMol Library Books参考文献

1. Van Goor F, et al. Correction of the F508del-CFTR protein processing defect in vitro by the investigational drug VX-809. Proc Natl Acad Sci U S A. 2011 Nov 15;108(46):18843-8. 2. Phuan PW, et al. Synergy-based small-molecule screen using a human lung epithelial cell line yields ΔF508-CFTR correctors that augment VX-809 maximal efficacy. Mol Pharmacol. 2014 Jul;86(1):42-51.

TargetMol Library Books文献引用

1. Sondo E, Cresta F, Pastorino C, et al. The L467F-F508del Complex Allele Hampers Pharmacological Rescue of Mutant CFTR by Elexacaftor/Tezacaftor/Ivacaftor in Cystic Fibrosis Patients: The Value of the Ex Vivo Nasal Epithelial Model to Address Non-Responders to CFTR-Modulating Drugs. International Journal of Molecular Sciences. 2022, 23(6): 3175. 2. Baldassarri M, Zguro K, Tomati V, et al.Gain-and Loss-of-Function CFTR Alleles Are Associated with COVID-19 Clinical Outcomes.Cells.2022, 11(24): 4096. 3. Tomati V, Costa S, Capurro V, et al.Rescue by elexacaftor-tezacaftor-ivacaftor of the G1244E cystic fibrosis mutation's stability and gating defects are dependent on cell background.Journal of Cystic Fibrosis.2022
(R)-Elexacaftor GlyH-101 CFTR corrector 9 (R)-BPO-27 Cavosonstat DNDS KM11060 IOWH-032

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该产品包含在如下化合物库中:
抗癌临床化合物库 抗癌上市药物库 EMA 上市药物库 药物功能重定位化合物库 抗癌药物库 FDA 上市药物库 抗纤维化化合物库 抗癌化合物库 临床期小分子药物库 经典已知活性库

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Keywords

Lumacaftor 936727-05-8 Autophagy Membrane transporter/Ion channel CFTR 鲁玛卡托 VX 809 VX809 VX-809 Cystic fibrosis transmembrane conductance regulator VRT826809 Inhibitor VRT-826809 inhibit VRT 826809 inhibitor

 

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