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HSP27 inhibitor J2

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产品编号 T7265Cas号 2133499-85-9
别名 J2

HSP27 inhibitor J2 (J2) 是一种HSP27抑制剂,可显著增强 17-AAG 的抗增殖活性,并对顺铂诱导的肺癌细胞生长抑制具有敏感性。它显著诱导异常 HSP27 二聚体形成并抑制HSP27巨聚合物的产生,从而具有抑制HSP27的伴侣功能和降低细胞保护功能的作用。

HSP27 inhibitor J2
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HSP27 inhibitor J2

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纯度: 99.51%
产品编号 T7265 别名 J2Cas号 2133499-85-9

HSP27 inhibitor J2 (J2) 是一种HSP27抑制剂,可显著增强 17-AAG 的抗增殖活性,并对顺铂诱导的肺癌细胞生长抑制具有敏感性。它显著诱导异常 HSP27 二聚体形成并抑制HSP27巨聚合物的产生,从而具有抑制HSP27的伴侣功能和降低细胞保护功能的作用。

规格价格库存数量
1 mg¥ 1,230现货
2 mg¥ 1,720现货
5 mg¥ 2,660现货
10 mg¥ 3,990现货
25 mg¥ 6,320现货
50 mg¥ 8,520现货
100 mg¥ 11,500现货
1 mL x 10 mM (in DMSO)¥ 3,630现货
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TargetMol 的所有产品仅用作科学研究或药证申报,不能被用于人体,我们不向个人提供产品和服务。请您遵守承诺用途,不得违反法律法规规定用于任何其他用途。

产品介绍

生物活性
产品描述
HSP27 inhibitor J2 (J2) (J2) is a HSP27 inhibitor, inhibits a production of HSP27 giant polymers, thereby having an effect of inhibiting a chaperone function of the HSP27 and reducing a cell protection function.
体内活性
HSP27 inhibitor J2与氨甲蝶呤在辐射诱导的肺炎症反应中的比较研究中显示,J2处理显著抑制了肺组织中的免疫细胞浸润,显示了J2的抗炎潜力。通过微型CT分析评估的J2处理小鼠的正常肺体积。J2处理的小鼠逆转了辐射诱导的呼吸困难。然而,氨甲蝶呤与J2相比未显示显著的辐射防护效果。在HSP27转基因小鼠中,我们观察到与野生型小鼠相比,免疫细胞招募增加且正常肺体积减少。辐射后增加的ROS产生和氧化应激经J2处理后得到下调,证明了J2的抗氧化特性。J2可能是治疗辐射诱导肺损伤的有效疗法[1]。
动物实验
Male C57BL/6 mice (age, 6 weeks; weight, 20–25 g), and were acclimatized (n = 5 per cage) for a week before irradiation. A single dose of 75 Gy was delivered to the left lung in a single fraction using image-guided small-animal irradiator (X-RAD 320) that was equipped with a collimator system composed of 3.5-cm-thick copper to produce focal radiation beams, as well as an imaging subsystem consisting of a fluorescent screen coupled to a charge-coupled-device camera. We selected 3-mm collimators to mimic clinical SBRT conditions by irradiating only a small volume of tissue. The mice were divided into six groups (n = 6–8 per group) as follows: (1) control (C);(2) irradiation (IR) - mice were exposed to a single dose of 75 Gy delivered to the left lung in a single fraction; (3) irradiation + J2 (IR + J2) ?15 mg/kg of J2 was intraperitoneal administered on every other day after irradiation;(4) irradiation + amifostine (IR + Ami) ?100 mg/kg of amifostine were intraperitoneal administered on every other day after irradiation; (5) J2 only (J2) ?15 mg/kg of J2 were intraperitoneal administered on every other day without irradiation; (6) Amifostine only (Ami) ?100 mg/kg of amifostine were intraperitoneal administered on every other day without irradiation. On day 14, mice were sacrificed by CO2 asphyxiation, and their lung tissues were collected for analysis[1].
别名J2
化学信息
分子量264.3
分子式C13H12O4S
CAS No.2133499-85-9
SmilesCc1cc(=O)c2c(O)cc(OCC3CS3)cc2o1
密度1.419 g/cm3 (Predicted)
储存&溶解度
存储Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
溶解度信息
DMSO: 22.5 mg/mL (85.13 mM)
溶液配制表
1mg5mg10mg50mg
1 mM3.7836 mL18.9179 mL37.8358 mL189.1790 mL
5 mM0.7567 mL3.7836 mL7.5672 mL37.8358 mL
10 mM0.3784 mL1.8918 mL3.7836 mL18.9179 mL
20 mM0.1892 mL0.9459 mL1.8918 mL9.4589 mL
50 mM0.0757 mL0.3784 mL0.7567 mL3.7836 mL

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:
TargetMol | Animal experiments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 μLTargetMol | Animal experiments 一共给药动物 10 只 ,您使用的配方为 5% TargetMol | reagent DMSO+ 30%PEG300+ 5%Tween 80 + 60% 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 50 μLDMSOTargetMol | reagent ( 母液浓度为 40 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:50μLDMSOTargetMol | reagent 母液,添加 300 μLPEG300TargetMol | reagent 混匀澄清,再加 50μLTween 80, 混匀澄清,再加 600μLddH2OTargetMol | reagent 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。

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
%ddH2O

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