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Bromhexine hydrochloride

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纯度: 99.98%

货号 T0828Cas号 611-75-6

别名 盐酸溴己新, Bromhexine HCl, Bisolvon, Auxit

Bromhexine hydrochloride (Bisolvon) 是TMPRSS2蛋白酶的一种特异性有效抑制剂,IC50为 0.75 μM。它可预防和控制SARS-CoV-2感染。它是一种粘液溶解剂,用于治疗与粘稠或过多粘液相关的呼吸系统疾病。

Bromhexine hydrochloride
其他形式的 “Bromhexine hydrochloride”:

Bromhexine hydrochloride

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Rating icon 很棒

纯度: 99.98%

货号 T0828 别名 盐酸溴己新, Bromhexine HCl, Bisolvon, AuxitCas号 611-75-6

Bromhexine hydrochloride (Bisolvon) 是TMPRSS2蛋白酶的一种特异性有效抑制剂,IC50为 0.75 μM。它可预防和控制SARS-CoV-2感染。它是一种粘液溶解剂,用于治疗与粘稠或过多粘液相关的呼吸系统疾病。

规格价格库存数量
1 g
¥ 198
现货
5 g
¥ 237
待询
1 mL x 10 mM (in DMSO)
¥ 237
现货
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产品介绍


Bromhexine hydrochloride AI Summary
Bromhexine hydrochloride exhibits a wide range of bioactivities across various assays related to cellular functions, enzyme inhibition, and antiviral properties. It shows potency in assays such as modulators of Lamin A splicing, inhibitors of ROR gamma transcriptional activity, activators and inhibitors of Cytochrome P450 3A4, compounds blocking the interaction between CBF-beta and RUNX1 for the treatment of acute myeloid leukemia, and inhibitors of the malarial parasite plastid. Additionally, it inhibits human tyrosyl-DNA phosphodiesterase 1 (TDP1) in both absence and presence of CPT. It also demonstrates the ability to inhibit the binding or entry into cells for Lassa Virus, Marburg Virus, and Ebola Virus. Specifically, it inhibits sodium fluorescein uptake in OATP1B3-transfected CHO cells by 95.98% and in OATP1B1-transfected CHO cells by 103.11% at a concentration of 10 µM. Despite its broad bioactivity, Bromhexine hydrochloride shows minimal activity in inhibiting cell viability of SARS-CoV-2 (strain BavPat1) infected Vero E6 cells, with a very low inhibition index of 0.00411. However, it exhibits modest antiviral activity against SARS-CoV-2, with an inhibition rate of -38.2% in Caco-2 cells at 10 µM after 48 hours. Furthermore, it inhibits the SARS-CoV-2 3CL-Pro protease by 13.35% at a concentration of 20 µM, as determined by a FRET assay using a peptide substrate. Lastly, Bromhexine hydrochloride inhibits SARS-CoV-2 induced cytotoxicity of VERO-6 cells at a 10 µM concentration after 48 hours exposure, with an inhibition rate of 0.29%, as determined by high content imaging..
Note: Summary generated by AI. Data source: ChEMBL
生物活性
产品描述
Bromhexine hydrochloride (Bisolvon) is a mucolytic agent used in the treatment of respiratory disorders associated with viscid or excessive mucus.
别名盐酸溴己新, Bromhexine HCl, Bisolvon, Auxit
化学信息
分子量412.59
分子式C14H21Br2ClN2
CAS No.611-75-6
SmilesCl.CN(Cc1cc(Br)cc(Br)c1N)C1CCCCC1
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
DMSO: 5.63 mg/mL (13.65 mM), Sonication is recommended.
Ethanol: 5 mg/mL (12.12 mM), Sonication is recommended.
H2O: < 1 mg/mL (insoluble or slightly soluble)
溶液配制表
Ethanol/DMSO
1mg5mg10mg50mg
1 mM2.4237 mL12.1186 mL24.2371 mL121.1857 mL
5 mM0.4847 mL2.4237 mL4.8474 mL24.2371 mL
10 mM0.2424 mL1.2119 mL2.4237 mL12.1186 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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