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Mitonafide

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Catalog No. T25817Cas No. 54824-17-8
Alias NSC-300288, NSC300288, NSC 300288

Mitonafide (NSC-300288) suppresses the activity of M. tuberculosis NAD+ dependent DNA ligase A. Mitonafide is a DNA intercalating agent.

Mitonafide

Mitonafide

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Purity: 99.89%
Catalog No. T25817Alias NSC-300288, NSC300288, NSC 300288Cas No. 54824-17-8
Mitonafide (NSC-300288) suppresses the activity of M. tuberculosis NAD+ dependent DNA ligase A. Mitonafide is a DNA intercalating agent.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
1 mg$30In StockIn Stock
2 mg$40In StockIn Stock
5 mg$64In StockIn Stock
10 mg$97In StockIn Stock
25 mg$198In StockIn Stock
50 mg$328In StockIn Stock
100 mg$537In StockIn Stock
200 mg$767In StockIn Stock
500 mg$1,150In Stock-
1 mL x 10 mM (in DMSO)$71In StockIn Stock
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In Stock Estimated shipping dateUSA Warehouse[1-2 days] Global Warehouse[5-7 days]
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Purity:99.89%
Appearance:Solid
Color:White
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Product Introduction

Mitonafide AI Summary
Mitonafide exhibits a variety of potent bioactivities, particularly related to DNA binding and antiproliferative effects against cancer cell lines. It has demonstrated DNA binding affinity comparable to ethidium bromide, with a C50 value of 11.0 µM and a dissociation constant (KD) of log 5.16. Furthermore, it shows significant cytotoxicity against multiple human cancer cell lines, including HT-29 with an IC50 of 600.0 nM, A549, SK-MEL-2, HL-60, and MCF-7, along with notable inhibition of cell growth in these lines. The compound's binding affinity, as measured by melting temperature changes, ranges with the highest Delta Tm of 17.2°C for specific DNA sequences, suggesting a role in stabilizing these structures. This compound also exhibits antiproliferative activity under hypoxic conditions in A375 and V79 cells. Additionally, it shows effective anticancer activity in xenografted mice models, with substantial inhibition of tumor growth at various doses. Mitonafide also disrupts specific molecular pathways and targets, including Nrf2 and Importin beta complex formation, indicating broad bioactivity and potential as an antitumor agent..
Note: Summary generated by AI. Data source: ChEMBL
Bioactivity
Description
Mitonafide (NSC-300288) suppresses the activity of M. tuberculosis NAD+ dependent DNA ligase A. Mitonafide is a DNA intercalating agent.
SynonymsNSC-300288, NSC300288, NSC 300288
Chemical Properties
Molecular Weight313.31
FormulaC16H15N3O4
Cas No.54824-17-8
SmilesCN(C)CCN1C(=O)c2cccc3cc(cc(C1=O)c23)[N+]([O-])=O
Relative Density.1.384g/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: 13 mg/mL (41.49 mM), Sonication is recommended.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM3.1917 mL15.9586 mL31.9173 mL159.5864 mL
5 mM0.6383 mL3.1917 mL6.3835 mL31.9173 mL
10 mM0.3192 mL1.5959 mL3.1917 mL15.9586 mL
20 mM0.1596 mL0.7979 mL1.5959 mL7.9793 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:
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μL
2 Enter the in vivo formulation:
% DMSO
%
% Tween 80
% Saline/PBS/ddH2O

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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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