Tezacaftor (VX-661)

目录号:S7059 批次号:S705903

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化学数据

化学结构式 别名 N/A 储存条件
(自收到货起)
3年 / -20°C / 粉状
1年 / -80°C / 溶于溶剂
化学式

C26H27F3N2O6

分子量 520.5 CAS号 1152311-62-0
Solubility (25°C)* 体外 DMSO 100 mg/mL (192.12 mM)
Ethanol 100 mg/mL (192.12 mM)
Water Insoluble
体内
(现配现用)
均匀悬浊液
CMC-NA
≥5mg/ml 均匀悬浊液可用于口服和腹腔注射。以 1 mL 工作液为例,取 5 mg该产品加到 1 ml CMC-NA 溶液中,混合均匀,即可得工作液浓度为 5 mg/ml的均匀悬浊液。
澄清溶液
5%DMSO 40%PEG300 5%Tween80 50%ddH2O

该配方已经过Selleck实验室实测。如果上述溶解方案不能满足您的需求,可联系Selleck销售提供定制化测试。

5.000mg/ml (9.61mM) 以 1 mL 工作液为例,取50μL100mg/ml的澄清DMSO储备液加到400μL PEG300中,混合均匀使其澄清;向上述体系中加入50μLTween80,混合均匀使其澄清;然后继续加入500μL ddH2O定容至 1 mL。工作液请现配现用!
* <1 mg/ml means slightly soluble or insoluble.
* Please note that Selleck tests the solubility of all compounds in-house, and the actual solubility may differ slightly from published values. This is normal and is due to slight batch-to-batch variations.

制备储备液

生物活性

产品描述 Tezacaftor (VX-661)是第二个F508del CFTR校正药物,协助CFTR蛋白到达细胞表面。Phase 2。
靶点
F508del-CFTR [1]
(Cell-free assay)
体外研究

VX-661是CFTR校正药物,使F508del突变通道避免降解且转运到细胞膜上。

推荐的实验操作(此推荐来自于公开的文献所以Selleck并不保证其有效性)

客户使用selleck产品的实验数据

数据来源于[Data independently produced by Sci Transl Med, 2014, 6(246), 246ra96]

数据来源于[Data independently produced by , , J Cyst Fibros, 2018, doi:10.1016/j.jcf.2018.07.001]

数据来源于[Data independently produced by , , NPJ Genom Med. 2017, 2:12]

Tezacaftor (VX-661)在文献中得到引用

Endometrium-derived organoids from cystic fibrosis patients and mice as new models to study disease-associated endometrial pathobiology [ Cell Mol Life Sci, 2025, 82(1):109] PubMed: 40074868
Inflammation-induced loss of CFTR-expressing airway ionocytes in non-eosinophilic asthma [ Respirology, 2025, 30(1):25-40] PubMed: 39358991
Global functional genomics reveals GRK5 as a cystic fibrosis therapeutic target synergistic with current modulators [ iScience, 2025, 28(3):111942] PubMed: 40040803
Human Induced Lung Organoids: A Promising Tool for Cystic Fibrosis Drug Screening [ Int J Mol Sci, 2025, 26(2)437] PubMed: 39859153
Inhibitors of the ubiquitin‑proteasome system rescue cellular levels and ion transport function of pathogenic pendrin (SLC26A4) protein variants [ Int J Mol Med, 2025, 55(5)69] PubMed: 40052591
Evaluation of the response to elexacaftor-tezacaftor-ivacaftor of the rare CFTR variants L383S, I507del, L1065P and R1066H in intestinal organoid-derived epithelial monolayers [ J Cyst Fibros, 2025, S1569-1993(25)00059-1] PubMed: 39979195
Septin-dependent defense mechanisms against Pseudomonas aeruginosa are stalled in cystic fibrosis bronchial epithelial cells [ Eur J Cell Biol, 2024, 103(2):151416] PubMed: 38636185
Ligand-based virtual-screening identified a novel CFTR ligand which improves the defective cell surface expression of misfolded ABC transporters [ Front Pharmacol, 2024, 15:1370676] PubMed: 38666024
Comprehensive Assessment of CFTR Modulators' Therapeutic Efficiency for N1303K Variant [ Int J Mol Sci, 2024, 25(5)2770] PubMed: 38474016
Estimation of Chloride Channel Residual Function and Assessment of Targeted Drugs Efficiency in the Presence of a Complex Allele [L467F;F508del] in the CFTR Gene [ Int J Mol Sci, 2024, 25(19)10424] PubMed: 39408749

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如果需要长期保存,请于零下二十度低温保存。禁止用于人体及治疗!

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