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Zosuquidar trihydrochloride

Synonyms: 唑喹达三盐酸盐, Zosuquidar 3HCl, Zosuquidar (LY335979) 3HCl, RS 33295-198 trihydrochloride, RS 33295-198 (D06387) 3HCl, LY-335979 trihydrochloride
货号 T6018Cas号 167465-36-3 一键复制产品信息纯度: 99.97%
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Zosuquidar trihydrochloride (LY-335979 trihydrochloride) 是一种高选择性、强效的 P - 糖蛋白(P-gp, ABCB1)竞争性抑制剂,Ki 值为 59 nM。Zosuquidar trihydrochloride 具有抗肿瘤活性,可用于白血病等肿瘤研究。

Zosuquidar trihydrochloride

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纯度: 99.97%

货号 T6018Cas号 167465-36-3

别名 唑喹达三盐酸盐, Zosuquidar 3HCl, Zosuquidar (LY335979) 3HCl, RS 33295-198 trihydrochloride, RS 33295-198 (D06387) 3HCl, LY-335979 trihydrochloride

Zosuquidar trihydrochloride (LY-335979 trihydrochloride) 是一种高选择性、强效的 P - 糖蛋白(P-gp, ABCB1)竞争性抑制剂,Ki 值为 59 nM。Zosuquidar trihydrochloride 具有抗肿瘤活性,可用于白血病等肿瘤研究。

Zosuquidar trihydrochloride
其他形式的 “Zosuquidar trihydrochloride”:
规格价格库存数量
1 mg
¥ 315
现货
2 mg
¥ 449
现货
5 mg
¥ 745
现货
10 mg
¥ 1,070
现货
25 mg
¥ 1,790
现货
50 mg
¥ 2,650
现货
100 mg
¥ 3,980
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实验操作小课堂
常见问题解答
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选择批次:
纯度: 99.97%
资源下载: COA LCMS HNMR产品操作手册

产品介绍


生物活性
产品描述
Zosuquidar trihydrochloride (LY-335979 trihydrochloride) is a highly selective, potent competitive inhibitor of P-glycoprotein (P-gp, ABCB1) with a Ki value of 59 nM. Zosuquidar trihydrochloride exhibits antitumor activity and can be used in research on tumors such as leukemia.
靶点活性
MDR:6 μM-16 μM, SW620 cells:0.059 μM, P-gp:60 nM (Ki)
体外活性

方法:在 P-gp 高表达的细胞系中加入 P-gp 抑制剂 Zosuquidar trihydrochloride (0.3 μM),同时加入 AVE9633 或 DM4 (3.125, 6.25, 12.5, 25, 50, 100 and 200 nM),AVE9633 处理 4 天,DM4 处理 3 天。单层细胞外排实验检测 P-gp 抑制。
结果:Zosuquidar trihydrochloride 完全恢复了 P-gp 表达细胞对 AVE9633 和 DM4 的敏感性。[1]
方法:从 High-Five 昆虫细胞制备的表达野生型或突变型 P-gp 的粗膜。将膜蛋白与不同浓度抑制剂(zosuquidar, elacridar, tariquidar,浓度范围 0-100 μM)在 37°C 孵育,加入 5 mM ATP 启动反应,20 分钟后 用 SDS 终止,通过比色法检测无机磷释放量。
结果:在野生型 P-gp 中,Zosuquidar trihydrochloride 等抑制剂浓度依赖性抑制基础 ATP 酶活性,IC₅₀在 10-30 nM 范围。[2]

体内活性

方法:野生型小鼠通过颈动脉插管,以恒定流速(2.5 mL/min)向大脑灌注含有药物(imatinib, 0.05 - 50 μM; Zosuquidar trihydrochloride, 0.5 μM)的生理缓冲液。灌注结束后,立即处死小鼠,取脑组织测定药物浓度,计算脑摄取率。
结果:Zosuquidar trihydrochloride 使 imatinib 脑摄取增加 2.5 倍。[3]

激酶实验
ATPase Assay : P-Glycoprotein ATPase activity is measured by the liberation of inorganic phosphate from ATP. The assay is measured in a 96-well plate for 90 min at 37 °C. Membranes (8 μg-10 μg protein) are incubated in a total volume of 100 μL of buffer A containing 5 mM sodium azide, 1 mM ouabain, 1 mM EGTA, 3 mM ATP, an ATP regenerating system composed of 5 mM phosphoenolpyruvate, and 3.6 units/mL pyruvate kinase in the presence and absence of 1 mM sodium vanadate. Pgp-ATPase activity is defined as the vanadate-sensitive portion of the total ATPase activity. Plates are read 3 minutes after the addition of the detection solution. The absorbance is measured at 690 nm by a microtiter dish reader. A phosphate standard curve is used to calculate the μMol of phosphate formed. Samples are measured in triplicate.
细胞实验
Cell viability is determined using a modified 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide dye reduction method. Cells are harvested during logarithmic growth phase, and seeded in 96-well plates. The cells are then cultured for 72 hours in the presence of oncolytics with or without modulators. MCF-7 and MCF-7/ADR cells are incubated 24 hours before the addition of the drug with and without the LY335979. LY335979 is prepared as 2 mM DMSO stocks and added to wells to give final concentrations ranging from 0.05 to 5 μM. After 72 hours, 20 μL of freshly prepared 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (5 mg/mL in Dulbecco's PBS) is added to each well and incubated for 4 hours in a 37 °C incubator containing 5% CO2. Cells are pelleted in a Sorvall RT6000B centrifuge, 70 μL of medium is carefully removed from each well, and 100 μL of 2-propanol/0.04 N HC1 is added. Cells are resuspended 5-10 times with a Multipipettor or until no particulate matter is visible. Plates are immediately read on a Titertek Multiskan MCC/340 microplate reader Flow Laboratories with a test wavelength of 570 nm and a reference wavelength of 630 nm. Controls are measured in quadruplicate and modulators are measured in duplicate. Cytotoxicity analyses are also performed using the CeliTiter 96 AQueous assay kit.(Only for Reference)
别名
唑喹达三盐酸盐, Zosuquidar 3HCl, Zosuquidar (LY335979) 3HCl, RS 33295-198 trihydrochloride, RS 33295-198 (D06387) 3HCl, LY-335979 trihydrochloride
化学信息
分子量636.99
分子式C32H31F2N3O2·3HCl
CAS No.167465-36-3
SmilesFC1([C@@]2([H])[C@]1([H])C3=CC=CC=C3[C@H](N4CCN(CC4)C[C@@H](O)COC5=CC=CC6=C5C=CC=N6)C7=CC=CC=C72)F.Cl.Cl.Cl
密度no data available
储存&溶解度
存储

Store under nitrogen Powder: -20°C for 3 years Shipping with blue ice/Shipping at ambient temperature.

实际储存温度请以COA为准

溶解度信息
DMSO: 80.83 mg/mL (126.89 mM), Sonication is recommended.
溶液配制表
DMSO
1mg5mg10mg50mg
1 mM1.5699 mL7.8494 mL15.6988 mL78.4942 mL
5 mM0.3140 mL1.5699 mL3.1398 mL15.6988 mL
10 mM0.1570 mL0.7849 mL1.5699 mL7.8494 mL
20 mM0.0785 mL0.3925 mL0.7849 mL3.9247 mL
50 mM0.0314 mL0.1570 mL0.3140 mL1.5699 mL
100 mM0.0157 mL0.0785 mL0.1570 mL0.7849 mL
该溶液配制表仅适用于固体产品。对于液体产品,请根据标明的浓度或密度计算稀释方案。

Handling Instruction | TargetMol 化合物与蛋白结合的复合物

T6018_2

Zosuquidar and UIC2 Fab complex of human-mouse chimeric ABCB1 (ABCB1HM)

计算器

  • 摩尔浓度 计算器
  • 稀释 计算器
  • 配液 计算器
  • 分子量 计算器

体内实验配液计算器

请在以下方框中输入您的动物实验信息后点击计算,可以得到母液配置方法和体内配方的制备方法:
比如您的给药剂量是10 mg/kg,每只动物体重20 g,给药体积100 μL, 一共给药动物10只,您使用的配方为 10% DMSO + 40% PEG300 + 5% Tween 80 + 45% Saline / PBS / ddH2O, 那么您的工作液浓度为2 mg/mL
母液配置方法:2 mg 药物溶于 100 μL DMSO ( 母液浓度为 20 mg/mL ), 如您需要配置的浓度超过该产品的溶解度,请先与我们联系。
体内配方的制备方法:100 μL DMSO 母液, 添加 400 μL PEG300 混匀澄清, 再加 50 μL Tween 80, 混匀澄清, 再加 450 μL Saline / PBS / ddH2O 混匀澄清
以上为“体内实验配液计算器”的使用方法举例,并不是具体某个化合物的推荐配制方式,请根据您的实验动物和给药方式选择适当的溶解方案。
方案所需的各类助溶剂如: DMSOPEG300PEG400Tween 80SBE-β-CD玉米油等, 均可在TargetMol网站点击购买。
1 请输入动物实验的基本信息
mg/kg
g
μL
2 请输入动物体内配方组成,不同的产品配方组成不同,如有配方需求,可先联系我们提供正确的体内配方。
% DMSO
%
% Tween 80
% Saline/PBS/ddH2O

剂量转换

对于不同动物的给药剂量换算,您也可以参考 更多

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