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Iminostilbene

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Catalog No. T0598Cas No. 256-96-2
Alias Dibenzazepine

Iminostilbene (Dibenzazepine) (Dibenzazepine) is a chemical precursor of carbamazepine which is used primarily in the treatment of epilepsy and neuropathic pain.

Iminostilbene

Iminostilbene

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Purity: 98.50%
Catalog No. T0598Alias DibenzazepineCas No. 256-96-2
Iminostilbene (Dibenzazepine) (Dibenzazepine) is a chemical precursor of carbamazepine which is used primarily in the treatment of epilepsy and neuropathic pain.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
1 g$29In StockIn Stock
1 mL x 10 mM (in DMSO)$29In StockIn Stock
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In Stock Estimated shipping dateUSA Warehouse[1-2 days] Global Warehouse[5-7 days]
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:98.50%
Appearance:Solid
Color:Yellow
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Product Introduction

Iminostilbene AI Summary
Iminostilbene shows a broad spectrum of bioactivities and potential therapeutic applications. It inhibits AAPH-induced hemolysis in human erythrocytes in a dose-dependent manner, highlighting its protective effects against oxidative damage. The compound exhibits inhibitory effects in multiple assays, such as ATPase activity of TAg, Tau fibril formation, ROR gamma transcriptional activity, lipid storage in Drosophila cells, human alpha-Glucosidase activity, JMJD2A-Tudor Domain, Histone Lysine Methyltransferase G9a, BAZ2B, Polymerase Iota, MgcRacGAP, integrin-mediated alleviation for muscular dystrophy, human tyrosyl-DNA phosphodiesterase 1, and PTHR. Moreover, Iminostilbene demonstrates limited cytotoxic activity against UV-irradiated human U937 cells with an IC50 of 2580.0 nM and against human HepG2 cells with an IC50 value greater than 158489.32 nM in a 48-hour CCK8 assay. The compound also possesses antibacterial activity, inhibiting Escherichia coli and Pseudomonas aeruginosa to some extent, while showing minimal effects against Klebsiella pneumoniae, Staphylococcus aureus, and Acinetobacter baumannii. Additionally, Iminostilbene exhibits antifungal activity against Candida albicans but not against Cryptococcus neoformans. These diverse bioactivities suggest that Iminostilbene has potential uses in treating various diseases and biological pathways..
Note: Summary generated by AI. Data source: ChEMBL
Bioactivity
Description
Iminostilbene (Dibenzazepine) (Dibenzazepine) is a chemical precursor of carbamazepine which is used primarily in the treatment of epilepsy and neuropathic pain.
SynonymsDibenzazepine
Chemical Properties
Molecular Weight193.24
FormulaC14H11N
Cas No.256-96-2
SmilesN1C2=CC=CC=C2C=CC2=C1C=CC=C2
Relative Density.1.116 g/cm3
Storage & Solubility Information
StorageIn solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.
Solubility Information
H2O: Limited solubility
DMSO: 50 mg/mL (258.75 mM), Sonication is recommended.
In Vivo Formulation
10% DMSO+40% PEG300+5% Tween 80+45% Saline: 2 mg/mL (10.35 mM), Sonication is recommended.
Please add the solvents sequentially, clarifying the solution as much as possible before adding the next one. Dissolve by heating and/or sonication if necessary. Working solution is recommended to be prepared and used immediately. The formulation provided above is for reference purposes only. In vivo formulations may vary and should be modified based on specific experimental conditions.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM5.1749 mL25.8746 mL51.7491 mL258.7456 mL
5 mM1.0350 mL5.1749 mL10.3498 mL51.7491 mL
10 mM0.5175 mL2.5875 mL5.1749 mL25.8746 mL
20 mM0.2587 mL1.2937 mL2.5875 mL12.9373 mL
50 mM0.1035 mL0.5175 mL1.0350 mL5.1749 mL
100 mM0.0517 mL0.2587 mL0.5175 mL2.5875 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

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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

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