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DMNB

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Catalog No. T8637Cas No. 20357-25-9
Alias 6-Nitroveratraldehyde

DMNB (6-Nitroveratraldehyde) is DNA-dependent protein kinase (DNA-PK) inhibitor with IC50 of 15 μM, an enzyme involved in the non-homologous end-joining (NHEJ) pathway of double-stranded DNA break (DSB) repair in human cells.

DMNB

DMNB

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Purity: 97.87%
Catalog No. T8637Alias 6-NitroveratraldehydeCas No. 20357-25-9
DMNB (6-Nitroveratraldehyde) is DNA-dependent protein kinase (DNA-PK) inhibitor with IC50 of 15 μM, an enzyme involved in the non-homologous end-joining (NHEJ) pathway of double-stranded DNA break (DSB) repair in human cells.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
200 mg$29-In 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]
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Purity:97.87%
Appearance:Solid
Color:White
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Product Introduction

DMNB AI Summary
DMNB demonstrates bioactivity as both an inhibitor and activator across various biological processes and enzyme assays. It inhibits human Jumonji Domain Containing 2E (JMJD2E), Tau Fibril Formation, Aldehyde Dehydrogenase 1 (ALDH1A1), 15-human lipoxygenase, Fructose-1,6-bisphosphate Aldolase, Hydroxyacyl-Coenzyme A Dehydrogenase, Type II, DNA-dependent protein kinase (DNA-PK), and Cytochrome P450 3A4, with potency values ranging from 177.8 nM to 39810.7 nM. Notably, it also serves as an activator of Cytochrome P450 3A4. In the context of antiviral activity, DMNB inhibits 5.75% of SARS-CoV-2 induced cytotoxicity in Caco-2 cells and shows slight inhibition of SARS-CoV-2 3CL-Pro protease by 0.8005% at 20 µM. However, it exhibited very minimal antiviral activity (-0.08%) against SARS-CoV-2 in VERO-6 cells under the same conditions. Furthermore, DMNB acts as a substrate for recombinant Haemophilus influenzae Chloramphenicol nitroreductase expressed in Escherichia coli, with an activity level of 132.0% under specific assay conditions involving NADPH. It also demonstrates varying inhibitory effects on human HDAC6, showing an 11.84% inhibition with a commercial peptide substrate but a decrease in activity (-2.7% inhibition) with a custom peptide substrate, highlighting the dependency on the assay's specific conditions..
Note: Summary generated by AI. Data source: ChEMBL
Bioactivity
Description
DMNB (6-Nitroveratraldehyde) is DNA-dependent protein kinase (DNA-PK) inhibitor with IC50 of 15 μM, an enzyme involved in the non-homologous end-joining (NHEJ) pathway of double-stranded DNA break (DSB) repair in human cells.
Synonyms6-Nitroveratraldehyde
Chemical Properties
Molecular Weight211.17
FormulaC9H9NO5
Cas No.20357-25-9
SmilesCOC1=C(OC)C=C(C(C=O)=C1)[N+]([O-])=O
Relative Density.1.4194 g/cm3 (Estimated)
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: 22.5 mg/mL (106.55 mM), Sonication is recommended.
In Vivo Formulation
10% DMSO+40% PEG300+5% Tween 80+45% Saline: 2 mg/mL (9.47 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 mM4.7355 mL23.6776 mL47.3552 mL236.7761 mL
5 mM0.9471 mL4.7355 mL9.4710 mL47.3552 mL
10 mM0.4736 mL2.3678 mL4.7355 mL23.6776 mL
20 mM0.2368 mL1.1839 mL2.3678 mL11.8388 mL
50 mM0.0947 mL0.4736 mL0.9471 mL4.7355 mL
100 mM0.0474 mL0.2368 mL0.4736 mL2.3678 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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