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HBED

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Catalog No. T32046Cas No. 35998-29-9
Alias CHEL-II, CHELII, CHEL II

HBED (CHELII) is an iron chelator and can be used in research on the treatment of chronic iron overload and acute iron poisoning.

HBED

HBED

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Purity: 98.58%
Catalog No. T32046Alias CHEL-II, CHELII, CHEL IICas No. 35998-29-9
HBED (CHELII) is an iron chelator and can be used in research on the treatment of chronic iron overload and acute iron poisoning.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
10 mg$40In StockIn Stock
25 mg$64In StockIn Stock
50 mg$91In StockIn Stock
100 mg$132In StockIn Stock
500 mg$322-In Stock
1 mL x 10 mM (in DMSO)$39In StockIn Stock
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In Stock Estimated shipping dateUSA Warehouse[1-2 days] Global Warehouse[5-7 days]
This molecule is a custom-made product. TargetMol has an excellent synthesis team with the experience and capability to provide you with cost-effective products.If you have any questions, please feel free to contact us. We are committed to serving you wholeheartedly.
All TargetMol products are for research purposes only and cannot be used for human consumption. We do not provide products or services to individuals. Please comply with the intended use and do not use TargetMol products for any other purpose.
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Purity:98.58%
Appearance:Solid
Color:White
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Product Introduction

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
Bioactivity
Description
HBED (CHELII) is an iron chelator and can be used in research on the treatment of chronic iron overload and acute iron poisoning.
SynonymsCHEL-II, CHELII, CHEL II
Chemical Properties
Molecular Weight388.41
FormulaC20H24N2O6
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
Relative Density.1.374g/cm3
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.
Solubility Information
DMSO: 5 mg/mL (12.87 mM), Sonication is recommended.
Solution Preparation Table
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

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In Vivo Formulation Calculator (Clear solution)

Please enter your animal experiment information in the following box and click Calculate to obtain the stock solution preparation method and in vivo formula preparation method:
TargetMol | Animal experiments For example, if the intended dosage is 10 mg/kg for animals weighing 20 g , with a dosing volume of 100 μL per animal, TargetMol | Animal experiments and a total of 10 animals are to be administered, using a formulation of TargetMol | reagent 10% DMSO+ 40% PEG300+ 5% Tween 80+ 45% Saline/PBS/ddH2O , the resulting working solution concentration would be 2 mg/mL.
Stock Solution Preparation:

Dissolve 2 mg of the compound in 100 μL DMSOTargetMol | reagent to obtain a stock solution at a concentration of 20 mg/mL . If the required concentration exceeds the compound's known solubility, please contact us for technical support before proceeding.

Preparation of the In Vivo Formulation:

1) Add 100 μL of the DMSOTargetMol | reagent stock solution to 400 μL PEG300TargetMol | reagent and mix thoroughly until the solution becomes clear.

2) Add 50 μL Tween 80 and mix well until fully clarified.

3) Add 450 μL Saline,PBS or ddH2OTargetMol | reagent and mix thoroughly until a homogeneous solution is obtained.

This example is provided solely to demonstrate the use of the In Vivo Formulation Calculator and does not constitute a recommended formulation for any specific compound. Please select an appropriate dissolution and formulation strategy based on your experimental model and route of administration.
All co-solvents required for this protocol, includingDMSO, PEG300/PEG400, Tween 80, SBE-β-CD, and Corn oil, are available for purchase on the TargetMol website.
1 Enter information below:
mg/kg
g
μL
2 Enter the in vivo formulation:
% DMSO
%
% Tween 80
% Saline/PBS/ddH2O

Dose Conversion

You can also refer to dose conversion for different animals. More Dose Conversion

Tech Support

Please see Inhibitor Handling Instructions for more frequently ask questions. Topics include: how to prepare stock solutions, how to store products, and cautions on cell-based assays & animal experiments, etc

Keywords

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