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Cyanoacetohydrazide

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Catalog No. T0704Cas No. 140-87-4
Alias Cyanoacetic hydrazide, 2-Cyanoacetohydrazide

Cyanoacetohydrazide (Cyanoacetic hydrazide) is an anti-TB drug. It has also been used to derive compounds that may have antitumor properties.

Cyanoacetohydrazide

Cyanoacetohydrazide

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Purity: 99.78%
Catalog No. T0704Alias Cyanoacetic hydrazide, 2-CyanoacetohydrazideCas No. 140-87-4
Cyanoacetohydrazide (Cyanoacetic hydrazide) is an anti-TB drug. It has also been used to derive compounds that may have antitumor properties.
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1 g$29-In 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:99.78%
Appearance:Solid
Color:Yellow
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Product Introduction

Cyanoacetohydrazide AI Summary
Cyanoacetohydrazide demonstrates multi-faceted bioactivities, including antiviral, enzymatic inhibitory, and anti-cytotoxic effects. It exhibits significant inhibition of Glutaminase (GLS) with a potency of 15848.9 nM. In assays targeting the Ebola virus, Cyanoacetohydrazide shows AC50 values ranging from 2511.9 nM to 3.981 µM. Its antiviral properties extend to SARS-CoV-2, where it inhibits induced cytotoxicity in both Caco-2 and VERO-6 cells at a 10 µM concentration, achieving inhibition rates of -1.94% and 0.21%, respectively. Moreover, the compound shows limited inhibition of the SARS-CoV-2 3CL-Pro protease, with a 12.61% inhibition observed at 20 µM. Additionally, Cyanoacetohydrazide inhibits human HDAC6 enzymatic activity with a substantial inhibition of -66.26% using a commercial peptide substrate, though a lesser inhibition of -1.29% is noted with a custom peptide substrate. The IC50 values for inhibiting SARS-CoV-2 induced cytotoxicity in VERO-6 cells are greater than 20000.0 nM and 19952.62 nM, underscoring potential antiviral effects at higher concentrations..
Note: Summary generated by AI. Data source: ChEMBL
Bioactivity
Description
Cyanoacetohydrazide (Cyanoacetic hydrazide) is an anti-TB drug. It has also been used to derive compounds that may have antitumor properties.
SynonymsCyanoacetic hydrazide, 2-Cyanoacetohydrazide
Chemical Properties
Molecular Weight99.09
FormulaC3H5N3O
Cas No.140-87-4
SmilesNNC(=O)CC#N
Relative Density.1.222 g/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: 45 mg/mL (454.13 mM), Sonication is recommended.
In Vivo Formulation
10% DMSO+40% PEG300+5% Tween 80+45% Saline: 2 mg/mL (20.18 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 mM10.0918 mL50.4592 mL100.9184 mL504.5918 mL
5 mM2.0184 mL10.0918 mL20.1837 mL100.9184 mL
10 mM1.0092 mL5.0459 mL10.0918 mL50.4592 mL
20 mM0.5046 mL2.5230 mL5.0459 mL25.2296 mL
50 mM0.2018 mL1.0092 mL2.0184 mL10.0918 mL
100 mM0.1009 mL0.5046 mL1.0092 mL5.0459 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

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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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