购物车
  • TargetMol
    您的购物车当前为空

N-Phenylacrylamide

Synonyms: N-苯基丙烯酰胺
货号 T9322Cas号 2210-24-4 一键复制产品信息 纯度: 99.99%
Rating icon 很棒

N-Phenylacrylamide 通过荧光转酰胺法抑制人重组 TGM2。

N-Phenylacrylamide

一键复制产品信息
Rating icon 很棒

纯度: 99.99%

货号 T9322Cas号 2210-24-4

别名 N-苯基丙烯酰胺

N-Phenylacrylamide 通过荧光转酰胺法抑制人重组 TGM2。

N-Phenylacrylamide
规格价格库存数量
1 g
¥ 99
现货
1 mL x 10 mM (in DMSO)
¥ 108
现货
库存状态实时更新,以官网显示为准,现货产品可直接加购物车下单
大包装 & 定制
加入购物车
TargetMol的所有产品仅用作科学研究或药证申报,不能被用于人体,我们不向个人提供产品和服务。请您遵守承诺用途,不得违反法律法规规定用于任何其他用途。
实验操作小课堂
常见问题解答
查看更多

选择批次:
纯度: 99.99%
颜色: 白色
性状: solid

产品介绍


N-Phenylacrylamide AI Summary
N-Phenylacrylamide is a bioactive inhibitor of human recombinant Transglutaminase 2 (TG2), with an IC50 value of 43000.0 nM based on fluorescent transamidation assay results. It exhibits various pharmacokinetic properties, including a half-life of 4.983 hours in phosphate buffer at pH 7.4 at a concentration of 50 uM in the presence of glutathione. It shows intrinsic clearance rates in human and rat hepatocytes of approximately 30.9 and 32.36 uL/min/(10^6 cells), respectively, indicating moderate metabolism and elimination in liver cells. Additionally, N-Phenylacrylamide inhibits several enzymes—such as West Nile virus NS2B-NS3 protease, Dengue virus serotype 2 NS2B-NS3 protease, Bovine thrombin, human and Escherichia coli MetAP, and wild-type Escherichia coli Mur enzymes—with inhibition rates of less than 15.0%. It also inhibits human FBPase by 17.0% at 500 uM. Furthermore, the compound demonstrates GSH reactivity and forms adducts, evident from RP-HPLC analysis, and shows a pseudo-first-order reaction with GSH at 37°C (K = 13.0 x 10^-3/min) with a half-life of 0.88 hours for GSH reactivity. In terms of thiol reactivity, N-Phenylacrylamide has a pseudo-first-order rate constant of 1.6 x 10^-4/s in a PBS/DMSO buffer environment. When tested against cysteine in PBS buffer using NMR assay, it has a half-life of 2.3 hours and a rate constant of 8.38 x 10^-5/s. Additionally, it shows a half-life of 4.75 hours in GSH reactivity assessment using DNTB and exhibits a Gibbs free energy change of 24.1 kcal/mol at 1 uM concentration within 120 minutes, with a pseudo-first-order rate constant of 3.87 x 10^-3/min and a half-life of 2.983 hours under pH 7.4 phosphate buffer conditions. N-Phenylacrylamide also manifests cytotoxicity against HeLa cells, with an EC50 greater than 100,000.0 nM, further highlighting its potential bioactivity and reactivity in various biological contexts..
Note: Summary generated by AI. Data source: ChEMBL
生物活性
产品描述
N-Phenylacrylamide inhibit human recombinant TGM2 by fluorescent transamidation assay.
靶点活性
TGase 2:43 µM
别名N-苯基丙烯酰胺
化学信息
分子量147.17
分子式C9H9NO
CAS No.2210-24-4
SmilesC=CC(=O)Nc1ccccc1
密度1.31g/cm3
储存&溶解度
存储
溶解度信息
DMSO: 55 mg/mL (373.72 mM), Sonication is recommended.
溶液配制表
DMSO
1mg5mg10mg50mg
1 mM6.7949 mL33.9743 mL67.9486 mL339.7432 mL
5 mM1.3590 mL6.7949 mL13.5897 mL67.9486 mL
10 mM0.6795 mL3.3974 mL6.7949 mL33.9743 mL
20 mM0.3397 mL1.6987 mL3.3974 mL16.9872 mL
50 mM0.1359 mL0.6795 mL1.3590 mL6.7949 mL
100 mM0.0679 mL0.3397 mL0.6795 mL3.3974 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

Related Tags: buy N-Phenylacrylamide | purchase N-Phenylacrylamide | N-Phenylacrylamide cost | order N-Phenylacrylamide | N-Phenylacrylamide chemical structure | N-Phenylacrylamide formula | N-Phenylacrylamide molecular weight