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Tinoridine

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纯度: 99.08%

货号 T50001Cas号 24237-54-5

别名 替诺立定, ethyl 2-amino-6-benzyl-4H,5H,6H,7H-thieno[2,3-c]pyridine-3-carboxylate

Tinoridine 通过抑制环氧合酶-2(COX-2)的产生来发挥作用,具有抗炎、抗过敏和抗凝血等活性。

Tinoridine
其他形式的 “Tinoridine”:

Tinoridine

一键复制产品信息
Rating icon 很棒

纯度: 99.08%

货号 T50001 别名 替诺立定, ethyl 2-amino-6-benzyl-4H,5H,6H,7H-thieno[2,3-c]pyridine-3-carboxylateCas号 24237-54-5

Tinoridine 通过抑制环氧合酶-2(COX-2)的产生来发挥作用,具有抗炎、抗过敏和抗凝血等活性。

规格价格库存数量
100 mg
¥ 137
现货
200 mg
¥ 193
现货
1 mL x 10 mM (in DMSO)
¥ 99
现货
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产品介绍


Tinoridine AI Summary
Tinoridine exhibits allosteric modulatory activity at the human adenosine A1 receptor with an EC50 of 10300.0 nM, causing a half-maximal allosteric effect on [125I]-ABA dissociation from the receptor-G protein ternary complex. It retains 44.9% activity at a concentration of 50 µM after 10 minutes of radioligand dissociation. Additionally, Tinoridine displays a diverse range of bioactivities, including inhibition of Menin-MLL interaction, modulation of Lamin A splicing, inhibition of Cruzain and Tau fibril formation, and activity against several other targets such as Sfp phosphopantetheinyl transferase, Fructose-1,6-bisphosphate aldolase, VHR1, Histone lysine methyltransferase G9a, 15-hLO-2, vitamin D receptor, and malarial parasite plastid. It also blocks entry of pathogens like Ebola and Lassa viruses, induces DNA re-replication in normal breast cells, and inhibits DNA repair enzyme TDP1. The compound demonstrates a high clearance rate of 71.2 mL.min-1.g-1 in human liver microsomes at 1 µM, suggesting efficient liver metabolism. It exhibits moderate liver toxicity, with some instances of severe hepatitis, chronic liver disease, and cirrhosis, but no evidence of cytolytic or cholestatic liver toxicity, granulomatous hepatitis, or vascular disease association. Despite its broad bioactivity, Tinoridine shows weak antiviral activity against SARS-CoV-2, with an IC50 value greater than 20000.0 nM..
Note: Summary generated by AI. Data source: ChEMBL
生物活性
产品描述
Tinoridine is a quinoline derivative analog that acts by inhibiting the production of cyclooxygenase-2 (COX-2). It has anti-inflammatory, anti-allergic and anticoagulant activities.
靶点活性
CYP2D6 (human):0.0098µM
别名替诺立定, ethyl 2-amino-6-benzyl-4H,5H,6H,7H-thieno[2,3-c]pyridine-3-carboxylate
化学信息
分子量316.42
分子式C17H20N2O2S
CAS No.24237-54-5
SmilesCCOC(=O)c1c(N)sc2CN(Cc3ccccc3)CCc12
密度1.256 g/cm3
颜色Yellow
物理性状Solid
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: 50 mg/mL (158.02 mM), Sonication is recommended.
溶液配制表
DMSO
1mg5mg10mg50mg
1 mM3.1604 mL15.8018 mL31.6036 mL158.0178 mL
5 mM0.6321 mL3.1604 mL6.3207 mL31.6036 mL
10 mM0.3160 mL1.5802 mL3.1604 mL15.8018 mL
20 mM0.1580 mL0.7901 mL1.5802 mL7.9009 mL
50 mM0.0632 mL0.3160 mL0.6321 mL3.1604 mL
100 mM0.0316 mL0.1580 mL0.3160 mL1.5802 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20g,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%Saline/PBS/ddH2O, 那么您的工作液浓度为2mg/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 50μLTween80, 混匀澄清,再加 600μLSaline/PBS/ddH2OTargetMol | 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。

方案所需的各类助溶剂如: DMSOPEG300 / PEG400Tween 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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