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TCS JNK 5a

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纯度: 99.51%

货号 T2234Cas号 312917-14-9

别名 SC-202671, SC202671, SC 202671, N-(3-氰基-4,5,6,7-四氢苯并[b]噻吩-2-基)-1-萘甲酰胺, N-(3-Cyano-4,5,6,7-tetrahydrobenzo[b]thienyl-2-yl)-1-naphthalenecarboxamide, JNK Inhibitor IX

TCS JNK 5a (SC202671) 是一种 JNK2和 JNK3的有效抑制剂,pIC50分别为 6.5和 6.7。

TCS JNK 5a
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TCS JNK 5a

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Rating icon 很棒

纯度: 99.51%

货号 T2234 别名 SC-202671, SC202671, SC 202671, N-(3-氰基-4,5,6,7-四氢苯并[b]噻吩-2-基)-1-萘甲酰胺, N-(3-Cyano-4,5,6,7-tetrahydrobenzo[b]thienyl-2-yl)-1-naphthalenecarboxamide, JNK Inhibitor IXCas号 312917-14-9

TCS JNK 5a (SC202671) 是一种 JNK2和 JNK3的有效抑制剂,pIC50分别为 6.5和 6.7。

规格价格库存数量
1 mg
¥ 145
现货
5 mg
¥ 372
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10 mg
¥ 578
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25 mg
¥ 1,050
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50 mg
¥ 1,790
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100 mg
¥ 2,770
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500 mg
¥ 6,350
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1 mL x 10 mM (in DMSO)
¥ 397
现货
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产品介绍


TCS JNK 5a AI Summary
TCS JNK 5a inhibits human truncated JNK3 with an IC50 value of 199.53 nM and human JNK2alpha2 with an IC50 value of 316.23 nM. It shows negligible inhibitory activity against a range of kinases including CDK2, p38alpha, Alk5, cFms, EGFR, ErbB2, GSK3-beta, PLK1, Src, Tie2, and VegFr2, with IC50 values exceeding 10,000 nM for these targets. In addition to its kinase inhibition profile, TCS JNK 5a demonstrates inhibitory activity against various viruses including Lassa Virus and Marburg Virus, and inhibits the proliferation of Plasmodium falciparum strains (3D7, DD2, HB3) with potency values ranging from 10.6 nM to 11875.4 nM. Further, this compound shows complex bioactivity, with minor inhibition percentages at 1 µM concentration on targets such as IKK-alpha (-1.0% to 2.0%), IKK-beta (-2.0% to 0.0%), and IKK-epsilon (-2.0% to -3.0%). It significantly inhibits Mer Kinase (78.0% at 10 µM), and presents varying inhibition on TBK1 (-3.0% to -4.0% at 1 µM). TCS JNK 5a inhibits Firefly Luciferase with an AC50 value of 18337.4 nM as indicated by GSK_PKIS assays and shows moderate inhibition of the SARS-CoV-2 3CL-Pro protease (15.68% at 20 µM) using FRET methodology. Additionally, it provides slight antiviral activity by inhibiting SARS-CoV-2 induced cytotoxicity in VERO-6 cells (1.37% inhibition at 10 µM over 48 hours exposure to 0.01 MOI). Finally, in a primary screen using the NF54 nanoGlo assay, TCS JNK 5a had a Z score of 3.59 and an inhibition of -21.0% at a 2 µM concentration over 72 hours..
Note: Summary generated by AI. Data source: ChEMBL
生物活性
产品描述
TCS JNK 5a (SC202671) is an effective, specific inhibitor of JNK3(pIC50= 6.7), JNK2(pIC50=6.5).
靶点活性
JNK3:6.7(pIC50), JNK2:6.5(pIC50)
体内活性

在人皮肤成纤维细胞中,JNK inhibitor IX能够介导c-Jun氨基末端激酶抑制丝氨酸残基上c-ABL的完全去磷酸化,从而显著降低caspase-3活性。

别名SC-202671, SC202671, SC 202671, N-(3-氰基-4,5,6,7-四氢苯并[b]噻吩-2-基)-1-萘甲酰胺, N-(3-Cyano-4,5,6,7-tetrahydrobenzo[b]thienyl-2-yl)-1-naphthalenecarboxamide, JNK Inhibitor IX
化学信息
分子量332.42
分子式C20H16N2OS
CAS No.312917-14-9
SmilesO=C(NC1=C(C#N)C2=C(CCCC2)S1)C1=C2C=CC=CC2=CC=C1
密度1.32 g/cm3 at 20℃
储存&溶解度
存储Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.
溶解度信息
DMSO: 3.33 mg/mL (10.02 mM), Sonication is recommended.
溶液配制表
DMSO
1mg5mg10mg50mg
1 mM3.0082 mL15.0412 mL30.0824 mL150.4121 mL
5 mM0.6016 mL3.0082 mL6.0165 mL30.0824 mL
10 mM0.3008 mL1.5041 mL3.0082 mL15.0412 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:
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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