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Resatorvid
本产品不向个人销售,仅用作科学研究,不用于任何人体实验及非科研性质的动物实验。
Resatorvid图片
CAS NO:243984-11-4
包装与价格:
包装价格(元)
10 mM * 1 mL in DMSO电议
5mg电议
10mg电议
50mg电议
100mg电议
200mg电议
500mg电议

产品名称
瑞沙托维
TAK-242
CLI-095
产品介绍
Resatorvid (TAK-242) 是一种选择性的TLR4信号传导抑制剂。Resatorvid 抑制NOTNF-αIL-6的产生,其IC50值分别为 1.8 nM,1.9 nM,1.3 nM。Resatorvid 下调TLR4下游信号分子 MyD88 和 TRIF 的表达。Resatorvid 抑制自噬 (autophagy),并在各种炎症性疾病中起关键作用。
生物活性

Resatorvid (TAK-242) is a selectiveToll-like receptor 4 (TLR4)inhibitor. Resatorvid inhibitsNO, TNF-αandIL-6production withIC50sof 1.8 nM, 1.9 nM and 1.3 nM, respectively. Resatorvid downregulates expression ofTLR4downstream signaling moleculesMyD88and TRIF. Resatorvid inhibitsautophagyand plays pivotal role in various inflammatory diseases[1][2].

IC50& Target[1][2]

TLR4

 

IL-6

1.3 nM (IC50)

TNF-R

1.9 nM (IC50)

体外研究
(In Vitro)

Resatorvid suppresses the production of NO, TNF-α, and IL-6 from LPS-stimulated human peripheral blood mononuclear cells (PBMCs) atIC50values from 11 to 33 nM[1].
Resatorvid (1-100 nM; 4 hours) inhibits mRNA expression of IL-6 and TNF-α induced by LPS and IFN-γ in RAW264.7 cells[1].
Resatorvid (1-100 nM; 15 minutes; PBMCs cells) markedly inhibits the LPS-induced phosphorylation of extracellular signal-regulated kinase 1/2 (Erk1/2), p38, and JNK/SAPK as well as degradation of IκBβ at a concentration of 100 nM[1].

RT-PCR[1]

Cell Line:RAW264.7 cells
Concentration:1 nM, 10 nM, 100 nM
Incubation Time:4 hours
Result:TNF-α and IL-6 mRNA expression levels were clearly suppressed at concentrations of 10 to 100 nM.

Western Blot Analysis[1]

Cell Line:PBMCs cells
Concentration:1 nM, 10 nM, 100 nM
Incubation Time:15 minutes
Result:The phosphorylation of mitogen-activated protein kinases induced by LPS was also inhibited in a concentration-dependent manner.
体内研究
(In Vivo)

Resatorvid (TAK-242; 3 mg/kg; intraperitoneal injection; for 2 days; male C57BL/6 mice) pretreatment markedly and significantly reverses the LPS-induced body weight loss, TA muscle loss, and muscle strength loss. TAK-242 reverses the LPS-induced shrinkage of muscle fibres and increases the interstitial space. TAK-242 blocks systemic catabolic cytokine release and skeletal muscle proteolysis in LPS-administered mice[3].

Animal Model:Male C57BL/6 mice (8-12 weeks of age) treated with lipopolysaccharide (LPS)[3]
Dosage:3 mg/kg
Administration:Intraperitoneal injection; for 2 days
Result:Pretreatment of mice reduced or reversed all the detrimental effects of LPS.
Clinical Trial
分子量

361.82

性状

Solid

Formula

C15H17ClFNO4S

CAS 号

243984-11-4

中文名称

瑞沙托维

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式
Powder-20°C3 years
4°C2 years
In solvent-80°C6 months
-20°C1 month
溶解性数据
In Vitro: 

DMSO : 100 mg/mL(276.38 mM;Need ultrasonic)

配制储备液
浓度溶剂体积质量1 mg5 mg10 mg
1 mM2.7638 mL13.8190 mL27.6381 mL
5 mM0.5528 mL2.7638 mL5.5276 mL
10 mM0.2764 mL1.3819 mL2.7638 mL
*

请根据产品在不同溶剂中的溶解度选择合适的溶剂配制储备液;一旦配成溶液,请分装保存,避免反复冻融造成的产品失效
储备液的保存方式和期限:-80℃, 6 months; -20℃, 1 month。-80℃ 储存时,请在 6 个月内使用,-20℃ 储存时,请在 1 个月内使用。

In Vivo:

请根据您的实验动物和给药方式选择适当的溶解方案。以下溶解方案都请先按照In Vitro方式配制澄清的储备液,再依次添加助溶剂:

——为保证实验结果的可靠性,澄清的储备液可以根据储存条件,适当保存;体内实验的工作液,建议您现用现配,当天使用; 以下溶剂前显示的百
分比是指该溶剂在您配制终溶液中的体积占比;如在配制过程中出现沉淀、析出现象,可以通过加热和/或超声的方式助溶

  • 1.

    请依序添加每种溶剂: 5% DMSO    40%PEG300   5%Tween-80   50% saline

    Solubility: 5.5 mg/mL (15.20 mM); Suspended solution; Need ultrasonic

  • 2.

    请依序添加每种溶剂: 5% DMSO    95% (20%SBE-β-CDin saline)

    Solubility: 5.5 mg/mL (15.20 mM); Suspended solution; Need ultrasonic

  • 3.

    请依序添加每种溶剂: 10% DMSO    90% saline

    Solubility: 5 mg/mL (13.82 mM); Suspended solution; Need ultrasonic

  • 4.

    请依序添加每种溶剂: 10% DMSO    40%PEG300   5%Tween-80   45% saline

    Solubility: ≥ 2.75 mg/mL (7.60 mM); Clear solution

    此方案可获得 ≥ 2.75 mg/mL (7.60 mM,饱和度未知) 的澄清溶液。

    以 1 mL 工作液为例,取 100 μL 27.5 mg/mL 的澄清 DMSO 储备液加到 400 μL PEG300 中,混合均匀;向上述体系中加入50 μL Tween-80,混合均匀;然后继续加入 450 μL生理盐水定容至 1 mL。

    将 0.9 g 氯化钠,完全溶解于 100 mL ddH2O 中,得到澄清透明的生理盐水溶液
  • 5.

    请依序添加每种溶剂: 10% DMSO    90% (20%SBE-β-CDin saline)

    Solubility: 2.75 mg/mL (7.60 mM); Suspended solution; Need ultrasonic

    此方案可获得 2.75 mg/mL (7.60 mM) 的均匀悬浊液,悬浊液可用于口服和腹腔注射。

    以 1 mL 工作液为例,取 100 μL 27.5 mg/mL 的澄清 DMSO 储备液加到 900 μL20% 的 SBE-β-CD 生理盐水水溶液中,混合均匀。

    将 2 g 磺丁基醚 β-环糊精加入 5 mL 生理盐水中,再用生理盐水定容至 10 mL,完全溶解,澄清透明
  • 6.

    请依序添加每种溶剂: 10% DMSO    90%corn oil

    Solubility: ≥ 2.75 mg/mL (7.60 mM); Clear solution

    此方案可获得 ≥ 2.75 mg/mL (7.60 mM,饱和度未知) 的澄清溶液,此方案不适用于实验周期在半个月以上的实验。

    以 1 mL 工作液为例,取 100 μL 27.5 mg/mL 的澄清 DMSO 储备液加到 900 μL玉米油中,混合均匀。

  • 7.

    请依序添加每种溶剂: 5% DMSO   95% saline

    Solubility: 2.5 mg/mL (6.91 mM); Suspended solution; Need ultrasonic

  • 8.

    请依序添加每种溶剂: 1% DMSO    99% saline

    Solubility: 0.5 mg/mL (1.38 mM); Suspended solution; Need ultrasonic

*以上所有助溶剂都可在本网站选购。