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Felbinac

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Rating icon 很棒

纯度: 99.47%

货号 T0888Cas号 5728-52-9

别名 Dapson, 4-联苯乙酸, 4-Biphenylacetic acid

Felbinac (Dapson) 是非甾体抗炎药,可用于肌肉炎症和关节炎的研究。

Felbinac
其他形式的 “Felbinac”:

Felbinac

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Rating icon 很棒

纯度: 99.47%

货号 T0888 别名 Dapson, 4-联苯乙酸, 4-Biphenylacetic acidCas号 5728-52-9

Felbinac (Dapson) 是非甾体抗炎药,可用于肌肉炎症和关节炎的研究。

规格价格库存数量
500 mg
¥ 331
现货
1 g
¥ 415
现货
1 mL x 10 mM (in DMSO)
¥ 415
现货
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纯度: 99.47%
颜色: 白色
性状: Solid
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产品介绍


Felbinac AI Summary
Felbinac exhibits a rapid absorption profile in rats, achieving maximum plasma concentration (Cmax) of 32508.83 nM within 0.5 hours (Tmax = 0.5 hr) and a mean residence time (MRT) of 6.6 hours. It demonstrates oral bioavailability in rats at 18.1% (F = 18.1%). The compound also shows notable bioactivities such as antioxidant and anti-inflammatory effects, as well as analgesic activity in animal models. For instance, it reduces myeloperoxidase, superoxide dismutase, catalase activities, and lipid peroxidation in rats' stomachs and alleviates carrageenan-induced paw edema in Sprague-Dawley rats. Moreover, Felbinac exhibits broad-spectrum bioactivities: - It acts as a modulator of Lamin A Splicing (potency: 2511.9 nM) and an agonist of the Thyroid Stimulating Hormone Receptor (potency: 5011.9 nM). - It activates intracellular cAMP concentrations in Parental HEK 293 cells by targeting the Thyroid Stimulating Hormone Receptor (potency: 5011.9 nM). - It demonstrates dual cytoprotective action in a Cell Model of Huntington (potency: 0.0501 nM) and inhibitory activity against Human alpha-Glucosidase (potency: 12589.3 nM). - It shows activity against Ebola Virus entry in screening assays with AC50 values ranging from 25.12 uM to 44668.4 nM. - It inhibits firefly luciferase and TDP-43 with potencies of 30131.3 nM and 35481.3 nM, respectively. - It acts as a cyclooxygenase COX-1 enzyme inhibitor (IC50: 894.0 nM) and inhibits human MRP4 activity in uptake assays (IC50: 8200.0 nM). Regarding antiviral activity, Felbinac shows limited effect against SARS-CoV-2 in multiple assays, including a low inhibition index (0.2263) in Vero E6 cells and an inhibition rate of 4.64% in Caco-2 cells. The compound exhibits an IC50 value greater than 20000.0 nM against SARS-CoV-2 in VERO-6 cells but shows inhibitory effects against the 3CL-Pro protease with an inhibition rate of 8.275% at 20 µM. Finally, Felbinac exhibits minor inhibitory effects on human HDAC6 enzyme activity, with 10.58% inhibition using a commercial peptide substrate, but lesser inhibition in custom peptide assays. Its binding affinity and receptor interactions suggest broad, albeit generally weak, bioactivities that require further exploration to fully characterize its therapeutic potential..
Note: Summary generated by AI. Data source: ChEMBL
生物活性
产品描述
Felbinac (Dapson), a topical medicine, is an active metabolite of fenbufen. It is belonging to the family of medicines known as non-steroidal anti-inflammatory drugs (NSAIDs) of the arylpropionic acid class, which is used to treat muscle arthritis and inflammation.
靶点活性
COX-2:976 nM, COX-1:865.68 nM
别名Dapson, 4-联苯乙酸, 4-Biphenylacetic acid
化学信息
分子量212.24
分子式C14H12O2
CAS No.5728-52-9
SmilesOC(=O)CC1=CC=C(C=C1)C1=CC=CC=C1
密度1.165 g/cm3
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: 30 mg/mL (141.35 mM), Sonication is recommended.
体内实验配方
10% DMSO+40% PEG300+5% Tween 80+45% Saline: 2 mg/mL (9.42 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
DMSO
1mg5mg10mg50mg
1 mM4.7116 mL23.5582 mL47.1165 mL235.5824 mL
5 mM0.9423 mL4.7116 mL9.4233 mL47.1165 mL
10 mM0.4712 mL2.3558 mL4.7116 mL23.5582 mL
20 mM0.2356 mL1.1779 mL2.3558 mL11.7791 mL
50 mM0.0942 mL0.4712 mL0.9423 mL4.7116 mL
100 mM0.0471 mL0.2356 mL0.4712 mL2.3558 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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