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Malonic acid

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Catalog No. T5291Cas No. 141-82-2
Alias Propanedioic Acid, Carboxyacetic Acid, 1,3-Propanedioic Acid

Malonic acid (propanedioic acid) is the archetypal example of a competitive inhibitor: it acts against succinate dehydrogenase (complex II) in the respiratory electron transport chain. Malonic acid is found to be associated with malonyl-CoA decarboxylase deficiency, which is an inborn error of metabolism.

Malonic acid

Malonic acid

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Purity: 99.53%
Catalog No. T5291Alias Propanedioic Acid, Carboxyacetic Acid, 1,3-Propanedioic AcidCas No. 141-82-2
Malonic acid (propanedioic acid) is the archetypal example of a competitive inhibitor: it acts against succinate dehydrogenase (complex II) in the respiratory electron transport chain. Malonic acid is found to be associated with malonyl-CoA decarboxylase deficiency, which is an inborn error of metabolism.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
25 mg$46In StockIn Stock
50 mg$66In StockIn Stock
100 mg$96In StockIn Stock
500 mg$138In StockIn Stock
1 g$209In StockIn Stock
1 mL x 10 mM (in DMSO)$45In 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:99.53%
Appearance:Solid
Color:White
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Product Introduction

Malonic acid AI Summary
Malonic acid exhibits a range of bioactivities. It has shown antileukemic activity in in vivo studies against P-388 lymphocytic leukemia in male mice, with an average survival increase to 11.0 days at a dose of 0.6 mg/kg/day and a T/C value of 114.0%. The compound also demonstrates inhibitory activity against the SH2 domain of human p60 c-Src tyrosine kinase with an IC50 greater than 40,000,000 nM. It acts as an inhibitor of mouse recombinant serine racemase with a Ki of 71,000 nM and an IC50 of 24,900 nM for inhibiting serine racemase using L-serine as substrate. Additionally, Malonic acid inhibits DDO and DAO with various IC50 values, including 1,355,000 nM for DDO and greater than 10,000,000 nM for DAO. It binds to 6-His-tagged human LDHA in the presence of NADH with a Kd of 5,000,000 nM and shows inhibitory activity against human recombinant serine racemase with Ki values ranging from 59,000 nM to 66,000 nM. Malonic acid demonstrates cytotoxicity against HEK293 cells with an IC50 of 9,700,000 nM and inhibits SARS-CoV-2 with an IC50 greater than 20,000 nM. Its inhibitory effects extend to the human serine racemase C2D2 mutant (IC50 of 770,000 nM) and recombinant human serine racemase (inhibition ranging from 51.0% to 62.0% at concentrations of 0.1 to 1 mM). Potentiometric titration using the Noyes method determined its pKa2 to be 5.78. These diverse activities suggest its potential as a multi-target bioactive compound..
Note: Summary generated by AI. Data source: ChEMBL
Bioactivity
Description
Malonic acid (propanedioic acid) is the archetypal example of a competitive inhibitor: it acts against succinate dehydrogenase (complex II) in the respiratory electron transport chain. Malonic acid is found to be associated with malonyl-CoA decarboxylase deficiency, which is an inborn error of metabolism.
SynonymsPropanedioic Acid, Carboxyacetic Acid, 1,3-Propanedioic Acid
Chemical Properties
Molecular Weight104.06
FormulaC3H4O4
Cas No.141-82-2
SmilesOC(=O)CC(O)=O
Relative Density.no data available
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: 250 mg/mL (2402.46 mM), Sonication is recommended.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM9.6098 mL48.0492 mL96.0984 mL480.4920 mL
5 mM1.9220 mL9.6098 mL19.2197 mL96.0984 mL
10 mM0.9610 mL4.8049 mL9.6098 mL48.0492 mL
20 mM0.4805 mL2.4025 mL4.8049 mL24.0246 mL
50 mM0.1922 mL0.9610 mL1.9220 mL9.6098 mL
100 mM0.0961 mL0.4805 mL0.9610 mL4.8049 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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2 Enter the in vivo formulation:
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%
% Tween 80
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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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