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Mafenide hydrochloride

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纯度: 98.34%

货号 T1026Cas号 138-37-4

别名 盐酸磺胺米隆, 4-Aminomethylbenzenesulfonamide hydrochloride

Mafenide hydrochloride (4-Aminomethylbenzenesulfonamide hydrochloride) 是一种有效的磺酰胺类抗菌剂,可用于烧伤创面。它通过抑制核苷酸合成,对革兰氏阳性和革兰氏阴性生物均具有活性。

Mafenide hydrochloride
其他形式的 “Mafenide hydrochloride”:

Mafenide hydrochloride

一键复制产品信息
Rating icon 很棒

纯度: 98.34%

货号 T1026 别名 盐酸磺胺米隆, 4-Aminomethylbenzenesulfonamide hydrochlorideCas号 138-37-4

Mafenide hydrochloride (4-Aminomethylbenzenesulfonamide hydrochloride) 是一种有效的磺酰胺类抗菌剂,可用于烧伤创面。它通过抑制核苷酸合成,对革兰氏阳性和革兰氏阴性生物均具有活性。

规格价格库存数量
25 mg
¥ 289
现货
50 mg
¥ 413
现货
100 mg
¥ 578
现货
200 mg
¥ 849
现货
500 mg
¥ 1,420
现货
1 mL x 10 mM (in DMSO)
¥ 166
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产品介绍


Mafenide hydrochloride AI Summary
Mafenide hydrochloride exhibits a broad spectrum of bioactivities, including the inhibition of tau fibril formation, inducing DNA re-replication in SW480 colon adenocarcinoma cells, and inhibiting human tyrosyl-DNA phosphodiesterase 1 (TDP1). It also shows efficacy in blocking Ebola virus entry and modulating insulin secretion in INS-1E cells. This compound demonstrates significant potency in both nanomolar and micromolar ranges across various assays. In addition to its antiviral properties, Mafenide hydrochloride inhibits sodium fluorescein uptake in OATP1B1 and OATP1B3-transfected CHO cells, achieving inhibition rates of 81.65% and 85.4% at a 10 µM concentration, respectively. It also acts as an inhibitor of human carbonic anhydrase enzymes, displaying greater potency against carbonic anhydrase 1 (Ki = 170.0 nM) relative to carbonic anhydrase 2 (Ki = 25000.0 nM). Specifically related to SARS-CoV-2, Mafenide hydrochloride exhibits weak activity in preventing cell death in Vero E6 cells, with a very low inhibition index of 0.01527. It inhibits SARS-CoV-2 induced cytotoxicity in Caco-2 and Vero-6 cells, with inhibition rates of -2.65% and 0.12%, respectively, at 10 µM after 48 hours exposure. Additionally, the compound inhibits the SARS-CoV-2 3CL-Pro protease by 17.39% at a concentration of 20 µM, as measured by a FRET assay..
Note: Summary generated by AI. Data source: ChEMBL
生物活性
产品描述
Mafenide hydrochloride (4-Aminomethylbenzenesulfonamide hydrochloride) is a sulfonamide that inhibits the enzyme carbonic anhydrase and is used as topical anti-infective, especially in burn therapy.
别名盐酸磺胺米隆, 4-Aminomethylbenzenesulfonamide hydrochloride
化学信息
分子量222.69
分子式C7H11ClN2O2S
CAS No.138-37-4
SmilesCl.NCc1ccc(cc1)S(=O)(=O)N
密度no data available
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
H2O: 197.6 mM, Sonication is recommended.
DMSO: 55 mg/mL (246.98 mM), Sonication is recommended.
溶液配制表
H2O/DMSO
1mg5mg10mg50mg
1 mM4.4905 mL22.4527 mL44.9055 mL224.5274 mL
5 mM0.8981 mL4.4905 mL8.9811 mL44.9055 mL
10 mM0.4491 mL2.2453 mL4.4905 mL22.4527 mL
20 mM0.2245 mL1.1226 mL2.2453 mL11.2264 mL
50 mM0.0898 mL0.4491 mL0.8981 mL4.4905 mL
100 mM0.0449 mL0.2245 mL0.4491 mL2.2453 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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