Home>>Signaling Pathways>> Membrane Transporter/Ion Channel>> Potassium Channel>>TASK-1-IN-1

TASK-1-IN-1

目录号 : GC69992

TASK-1-IN-1 是一种有效的选择性的 TASK-1 (Potassium Channel) 抑制剂,IC50 为 148 nM。TASK-1-IN-1 对 TASK-3 通道 (IC50 为 1750 nM) 的抑制作用降低,并且对其他 K+ 通道没有显着影响。TASK-1-IN-1 具有抗癌作用。

TASK-1-IN-1 Chemical Structure

Cas No.:600125-11-9

规格 价格 库存 购买数量
10mg
¥1,440.00
现货
25mg
¥3,150.00
现货
50mg
¥4,950.00
现货
100mg
¥7,650.00
现货

电话:400-920-5774 Email: sales@glpbio.cn

Customer Reviews

Based on customer reviews.

Sample solution is provided at 25 µL, 10mM.

产品描述 化学性质 产品文档

产品文档

Quality Control & SDS

View current batch:

IC50: 148 nM (TASK-1) and 1750 nM (TASK-3)[1]

TASK-1-IN-1 is a potent and selective TASK-1 (Potassium Channel) inhibitor with an IC50 of 148 nM. TASK-1-IN-1 shows a reduced inhibition of TASK-3 channels (IC50 of 1750 nM) and not a significant effect on other K+ channels. TASK-1-IN-1 has anticancer effects.

TASK-1-IN-1 (compound F3) blocks cell proliferation and viability in the MCF-7 cancer cell line but not in TASK-1 knockdown MCF-7 cells, indicating that it is acting in TASK-1 channels[1].

Cell Proliferation Assay[1]

Cell Line: MCF-7 cells
Concentration: 10 μM
Incubation Time: 96 hours
Result: Showed an antiproliferative activity of ∼45% on the cell line MCF-7.

[1]. BÁrbara ArÉvalo, et al. Selective TASK-1 Inhibitor with a Defined Structure-Activity Relationship Reduces Cancer Cell Proliferation and Viability. J Med Chem. 2022 Nov 24;65(22):15014-15027.

溶解性数据

制备储备液
1 mg 5 mg 10 mg
1 mM 2.9035 mL 14.5176 mL 29.0352 mL
5 mM 0.5807 mL 2.9035 mL 5.807 mL
10 mM 0.2904 mL 1.4518 mL 2.9035 mL
  • 摩尔浓度计算器

  • 稀释计算器

  • 分子量计算器

质量
=
浓度
x
体积
x
分子量
 
 
 
*在配置溶液时,请务必参考产品标签上、MSDS / COA(可在Glpbio的产品页面获得)批次特异的分子量使用本工具。

计算

动物体内配方计算器 (澄清溶液)

第一步:请输入基本实验信息(考虑到实验过程中的损耗,建议多配一只动物的药量)
给药剂量 mg/kg 动物平均体重 g 每只动物给药体积 ul 动物数量
第二步:请输入动物体内配方组成(配方适用于不溶于水的药物;不同批次药物配方比例不同,请联系GLPBIO为您提供正确的澄清溶液配方)
% DMSO % % Tween 80 % saline
计算重置