艾力替尼,Allitinib tosylate

艾力替尼|T6331|TargetMol

1篇文献
价格 463 1160 1860
包装 1mg 5mg 10mg
最小起订量 1mg
发货地 上海
更新日期 2025-11-17
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产品详情

中文名称:艾力替尼英文名称:Allitinib tosylate
CAS:1050500-29-2品牌: TargetMol
产地: 美国保存条件: Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.
纯度规格: 98.68%产品类别: 抑制剂
货号: T6331
2025-11-17 艾力替尼 Allitinib tosylate 1mg/463RMB;5mg/1160RMB;10mg/1860RMB 463 TargetMol 美国 Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature. 98.68% 抑制剂

Product Introduction

Bioactivity

名称Allitinib tosylate
描述Allitinib tosylate (AST-1306) is a novel irreversible inhibitor of EGFR and ErbB2 with IC50 of 0.5 nM and 3 nM, respectively.
细胞实验Cell (including Calu-3, A-549 cell line et al.) proliferation is evaluated using the SRB (Sulforhodamine B) assay. Briefly, cells are seeded into 96-well plates and grown for 24 hours. The cells are then treated with increasing concentrations of AST-1306 and grown for a further 72 hours. The medium remains unchanged until the completion of the experiment. The cells are then fixed with 10% precooled trichloroacetic acid (TCA) for 1 hour at 4 °C and stained for 15 min at room temperature with 100 μL of 4 mg/mL SRB solution in 1% acetic acid. The SRB is then removed, and the cells are quickly rinsed five times with 1% acetic acid. After cells are air-dried, protein-bound dye is dissolved in 150 μL of 10 mM Tris base for 5 min and measured at 515 nm using a multiwell spectrophotometer. The inhibition rate on cell proliferation is calculated as (1 - A515 treated/A515 control) × 100%. The IC50 value is obtained by the Logit method and is determined from the results of at least 3 independent tests.(Only for Reference)
激酶实验Tyrosine kinase assays: The tyrosine kinase activities are determined in 96-well ELISA plates precoated with 20 μg/mL Poly (Glu,Tyr)4:1. First, 80 μL of 5 μM ATP solution diluted in kinase reaction buffer (50 mM HEPES pH 7.4, 20 mM MgCl2, 0.1 mM MnCl2, 0.2 mM Na3VO4, 1 mM DTT) is added to each well. Various concentrations of AST-1306 diluted in 10 μL of 1% DMSO (v/v) are then added to each reaction well, with 1% DMSO (v/v) used as the negative control. Subsequently, the kinase reaction is initiated by the addition of purified tyrosine kinase proteins diluted in 10 μL of kinase reaction buffer solution. Experiments at each concentration are performed in duplicate. After incubation for 60 min at 37 °C, the plate is washed three times with phosphate buffered saline (PBS) containing 0.1% Tween 20 (T-PBS). Next, 100 μL anti-phosphotyrosine antibody (PY99, 1:500 dilution) diluted in T-PBS containing 5 mg/mL BSA is added. After 30 min incubation at 37 °C, the plate is washed three times as before. Horseradish peroxidase-conjugated goat anti-mouse IgG (100 μL) diluted 1:2000 in T-PBS containing 5 mg/mL BSA is added. The plate is reincubated at 37 °C for 30 min, and then washed with PBS. Finally, 100 μL of a solution containing 0.03 % Water2 and 2 mg/mL o-phenylenediamine in 0.1 M citrate buffer, pH 5.5, is added and samples are incubated at room temperature until color emerged. The reaction is terminated by the addition of 50 μL of 2 M H2SO4, and the plate is read using a multi-well spectrophotometer at 490 nm. The inhibition rate (%) is calculated using the following equation: [1-(A490 treated /A490 control)] ×100%. IC50 values are determined from the results of at least three independent tests and calculated by Logit method.
体外活性Allitinib同时针对 ErB2 和 EGFR T790M/L858R 双突变体。 Allitinib的活性大约是 lapatinib 的 500 倍,并且针对 ErbB 家族激酶相较于其他激酶家族(包括 PDGFR、KDR 和 c-Met)的选择性超过 3000 倍。 Allitinib可能与 EGFR 和 ErbB2 的特定氨基酸残基形成共价结合。 Allitinib以浓度依赖的方式显著抑制 HIH3T3-EGFR T790M/L858R 细胞的生长,并有效抑制这些细胞中 EGFR 的磷酸化。此外, Allitinib在浓度依赖的方式中阻断带有 EGFR T790M/L858R 突变的 NCI-H1975 细胞的生长,并阻断 EGFR 及其下游途径的磷酸化。同时, Allitinib以剂量依赖的方式明显抑制 A549 细胞中 EGF 诱导的 EGFR 磷酸化。 Allitinib抑制 EGFR 和 ErbB2 的磷酸化及包括 A549 细胞、Calu-3 细胞和 SK-OV-3 细胞在内的人类癌症细胞的下游信号传导。[1]
体内活性每日两次口服AST-1306能显著防止SK-OV-3和Calu-3异种移植模型中的肿瘤生长。在SK-OV-3模型中,经过7天的AST-1306治疗,肿瘤几乎消失。相反,在HO-8910和A549异种移植模型中,AST-1306仅轻微抑制肿瘤生长。因此,AST-1306在过表达ErbB2的肿瘤模型中的抗肿瘤效能大于在低表达ErbB2的模型中。AST-1306具有良好的耐受性。虽然Lapatinib在这些过表达ErbB2的肿瘤模型中显示出抗肿瘤活性,但与Lapatinib相比,AST-1306在相同剂量和计划下治疗SK-OV-3异种移植肿瘤模型时更加有效。此外,每日两次口服AST-1306连续3周显著抑制了FVB-2/Nneu模型中的肿瘤生长。治疗11天后,肿瘤几乎完全消失。治疗期间,小鼠体重减少不到20%。[1]
存储条件Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.
溶解度H2O : < 1 mg/mL (insoluble or slightly soluble)
Ethanol : < 1 mg/mL (insoluble or slightly soluble)
10% DMSO+40% PEG300+5% Tween 80+45% Saline : 4 mg/mL (6.44 mM), Sonication is recommended.
DMSO : 114 mg/mL (183.55 mM), Sonication is recommended.
关键字TsOH | HER2/ErbB2 | FLT1 | EGFR (T790M/L858R) | EGFR | AST6 | AST1306 | AST 6 | AST 1306 | anilino-quinazoline
相关产品Neratinib | Lapatinib | Chalcone | Gefitinib | Erlotinib | Osimertinib | Erlotinib hydrochloride | Gilteritinib | Afatinib | Lidocaine Hydrochloride hydrate | Genistein | Sorafenib
相关库抑制剂库 | 抗癌活性化合物库 | 经典已知活性库 | 已知活性化合物库 | 激酶抑制剂库 | 高选择性抑制剂库 | 免疫/炎症分子化合物库 | 膜蛋白靶向化合物库 | 药物功能重定位化合物库 | 酪氨酸激酶分子库 | 抗癌临床化合物库 | 抗癌药物库
关键字: 艾力替尼|||AST-1306 TsOH|||AST-1306 (TsOH)|TargetMol

公司简介

TargetMol Chemicals Inc. 总部位于马萨诸塞州波士顿,致力于为全球生化领域科学家的研究提供专业的产品和服务。TargetMol?品牌的客户群分布于40多个国家和地区,已发展成为全球知名的化合物库和小分子化合物研究供应商。 TargetMol?可提供160多种满足不同需求的化合物库,以及多种类型的生化试剂产品,包括12000多种抑制剂、16000多种天然产物和各类多肽、抗体、生命科学试剂盒等,此外,我们还建设有CADD(计算机辅助药物设计)研究中心、药理实验室、药化合成平台三大技术中心,全方位满足客户的定制需求。 凭借我们优质的产品和服务、快速高效的全球供应链和专业的技术支持,我们将有效帮助您缩短研发周期,取得更成功的结果。
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