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GW3965 hydrochloride

Synonyms: GW3965 HCl
货号 T6310Cas号 405911-17-3 一键复制产品信息纯度: 99.51%
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GW3965 hydrochloride (GW3965 HCl) 属于合成小分子,是一种肝X受体(LXR)激动剂(hLXRα EC50=190 nM;hLXRβ EC50=30 nM),具有亚型选择性、细胞渗透性和口服活性。用于代谢、炎症及神经病理性疼痛相关研究。

GW3965 hydrochloride

一键复制产品信息
Rating icon 很棒

纯度: 99.51%

货号 T6310Cas号 405911-17-3

别名 GW3965 HCl

GW3965 hydrochloride (GW3965 HCl) 属于合成小分子,是一种肝X受体(LXR)激动剂(hLXRα EC50=190 nM;hLXRβ EC50=30 nM),具有亚型选择性、细胞渗透性和口服活性。用于代谢、炎症及神经病理性疼痛相关研究。

GW3965 hydrochloride
其他形式的 “GW3965 hydrochloride”:
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规格价格库存数量
1 mg
¥ 228
现货
2 mg
¥ 329
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5 mg
¥ 578
现货
10 mg
¥ 828
现货
25 mg
¥ 1,680
现货
50 mg
¥ 3,230
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100 mg
¥ 4,780
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500 mg
¥ 9,870
现货
1 mL x 10 mM (in DMSO)
¥ 789
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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: 99.03%
颜色: 白色
性状: Solid
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
GW3965 hydrochloride (GW3965 HCl) belongs to synthetic small molecules and is a liver X receptor (LXR) agonist (hLXRα EC50 = 190 nM; hLXRβ EC50 = 30 nM) with subtype selectivity, cell permeability, and oral activity. This compound is used in research related to metabolism, inflammation, and neuropathic pain.
靶点活性
LXRα (human):190 nM (EC50), LXRβ (human):30 nM (EC50)
体外活性

方法:将脓毒症小鼠分离的脾脏髓源性抑制细胞(MDSCs)与1 μM GW3965 hydrochloride共孵育1小时,采用流式细胞术检测细胞凋亡。
结果:GW3965 hydrochloride可诱导脾脏MDSCs凋亡。[1]
方法:采用吉非替尼耐药的非小细胞肺癌PC9细胞,以5 μM GW3965 hydrochloride单独或联合吉非替尼处理48小时,通过MTT法检测细胞活力,Western blot检测自噬相关蛋白LC3 II/I及Beclin 1表达,AO染色观察自噬体形成,流式细胞术评估细胞凋亡。
结果:GW3965 hydrochloride联合吉非替尼较单药组协同抑制细胞活力,上调LC3 II/I比值及Beclin 1表达,增加自噬体积累及凋亡率。[2]

体内活性

方法:采用胶原酶诱导脑出血小鼠模型,GW3965 hydrochloride以10 mg/kg剂量腹腔注射,溶于50% DMSO,术后1小时开始给药,每日一次,连续7天。
结果:GW3965 hydrochloride治疗组病灶体积减小、血肿清除加快、白质损伤减轻,并促进神经功能恢复。[3]
方法:采用盲肠结扎穿孔(CLP)诱导的脓毒症小鼠模型,GW3965 hydrochloride以3 mg/kg剂量皮下注射,溶于5% DMSO/30% PEG300/5% Tween 80/60% ddH₂O,于术后1、6、12、24、48、72小时共给药6次。
结果:GW3965 hydrochloride提高小鼠存活率,减轻多器官损伤,降低血清炎症因子水平。[4]

激酶实验
Steady-state drug accumulation assay: AuxB1 and CHrB30 cells are grown to confluency in 12-well (24 mm) tissue culture dishes and the steady-state accumulation of [3H]-vinblastine is measured. Accumulation is initiated by the addition of 0.1 μ Ci [3H]-vinblastine and unlabelled vinblastine to a final concentration of 100 nM . The accumulation of [3H]-paclitaxel is measured using 0.1 μ Ci [3H]-paclitaxel and unlabelled drug to a final concentration of 1 μM . Cells are incubated in a reaction volume of 1 mL for 60 min at 37 ℃ under 5% CO2 in order to reach steady-state. The effect of the modulators XR9576 on [3H]-ligand accumulation is investigated in the concentration range 10-9 - 10-6 M. Modulators are added from a DMSO stock giving a final solvent concentration of 0.2 % (v/v). Following cell harvesting, accumulated drug is measured by liquid scintillation counting and normalized for cell protein content. Plots of amount accumulated as a function of modulator concentration are fitted with the general dose-response equation: Y={(a-b)/(1+(X/c)d)}+b Where: Y=response; a=initial response; b=final response; c=EC50 concentration; d=slope value; X=drug concentration.
细胞实验
Cells are seeded in 96 wells and are treated after 24 hours with different drugs indicated in each experiment in medium containing 1% FBS or lipoprotein deficient serum. Relative proliferation is determined using Cell Proliferation Assay Kit. Cells are incubated 1.5 hrs after adding tetrazolium salt WST-1 [2-(4-iodophenyl)-3- (4-nitrophenyl)-5-(2, 4-disulfo-phenyl)-2H-tetrazolium, monosodium salt] at 5% CO2, 37oC and the absorbance of the treated and untreated cells are measured using a microplate reader at 420 to 480 nm. Cells seeded in 12 well plates are counted using a hemocytometer, and dead cells are assessed using trypan blue exclusion assays.
别名
GW3965 HCl
化学信息
分子量618.51
分子式C33H31ClF3NO3·HCl
CAS No.405911-17-3
Smilesc1ccc(cc1)C(CN(CCCOc1cccc(c1)CC(=O)O)Cc1c(c(ccc1)C(F)(F)F)Cl)c1ccccc1.Cl
密度no data available
储存&溶解度
存储

Store at low temperature,Keep away from moisture Powder: -20°C for 3 years | In solvent: -80°C for 1 year 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: 71.2 mg/mL (115.12 mM), Sonication is recommended.
Ethanol: 12.4 mg/mL (20.05 mM), Sonication is recommended.
体内实验配方
10% DMSO+40% PEG300+5% Tween 80+45% Saline: 2 mg/mL (3.23 mM), Sonication is recommended.
请按顺序添加溶剂,在添加下一种溶剂之前,尽可能使溶液澄清。如有必要,可通过加热、超声、涡旋处理进行溶解。工作液建议现配现用。以上配方仅供参考,体内配方并不是绝对的,请根据不同情况进行调整。
溶液配制表
Ethanol/DMSO
1mg5mg10mg50mg
1 mM1.6168 mL8.0839 mL16.1679 mL80.8394 mL
5 mM0.3234 mL1.6168 mL3.2336 mL16.1679 mL
10 mM0.1617 mL0.8084 mL1.6168 mL8.0839 mL
20 mM0.0808 mL0.4042 mL0.8084 mL4.0420 mL
DMSO
1mg5mg10mg50mg
50 mM0.0323 mL0.1617 mL0.3234 mL1.6168 mL
100 mM0.0162 mL0.0808 mL0.1617 mL0.8084 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。

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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