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HBED

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纯度: 98.58%

货号 T32046Cas号 35998-29-9

别名 CHEL-II, CHELII, CHEL II

HBED (CHELII) 是一种铁螯合剂,可用于治疗慢性铁过载和急性铁中毒的研究。

HBED
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HBED

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纯度: 98.58%

货号 T32046 别名 CHEL-II, CHELII, CHEL IICas号 35998-29-9

HBED (CHELII) 是一种铁螯合剂,可用于治疗慢性铁过载和急性铁中毒的研究。

规格价格库存数量
2 mg
¥ 143
现货
5 mg
¥ 198
现货
10 mg
¥ 289
现货
25 mg
¥ 458
现货
50 mg
¥ 662
现货
100 mg
¥ 968
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500 mg
¥ 2,380
现货
1 mL x 10 mM (in DMSO)
¥ 195
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产品介绍


HBED AI Summary
HBED demonstrates multiple bioactivities related to iron metabolism and toxicity in animal models. When administered intraperitoneally at different dosages, it affects iron levels in various organs such as the spleen, liver, feces, and urine, with both increases and decreases observed. The LD50 value for intraperitoneal administration in an iron overload rat model is greater than or equal to 800.0 mg/kg. The compound has varying ionization constants (pKa values) and differences in partition coefficients (logP) in different solvents, indicating its interactions in various pH environments and biological systems. It is suitable for use in organic solvents such as MeOH, chloroform, and cyclohexane, which highlights its applicability in different experimental setups or biological assays. Despite its low absorption rate of 5.0% in the human GI-tract and low effective permeability across a hexadecane membrane (Log Pe value of -5.1 cm s-1), the compound has near-neutral partitioning (LogD value of -0.2). HBED exhibits strong iron chelating activity, evidenced by a high stability constant of the Fe3+-compound complex (log K value of 40.0). It serves as a transporter substrate and shows interactions with various transporters in human Caco2 cells. The compound's efflux ratios vary with and without specific inhibitors, and its permeability is influenced by P-gp and MRP2 inhibitors, showing a high transporter substrate index ratio when treated with the MRP2 inhibitor MK571..
Note: Summary generated by AI. Data source: ChEMBL
生物活性
产品描述
HBED (CHELII) is an iron chelator and can be used in research on the treatment of chronic iron overload and acute iron poisoning.
别名CHEL-II, CHELII, CHEL II
化学信息
分子量388.41
分子式C20H24N2O6
CAS No.35998-29-9
SmilesC(N(CCN(CC1=C(O)C=CC=C1)CC(O)=O)CC(O)=O)C2=C(O)C=CC=C2
密度1.374g/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: 5 mg/mL (12.87 mM), Sonication is recommended.
溶液配制表
DMSO
1mg5mg10mg50mg
1 mM2.5746 mL12.8730 mL25.7460 mL128.7300 mL
5 mM0.5149 mL2.5746 mL5.1492 mL25.7460 mL
10 mM0.2575 mL1.2873 mL2.5746 mL12.8730 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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