1. Membrane Transporter/Ion Channel Metabolic Enzyme/Protease NF-κB Immunology/Inflammation
  2. Na+/K+ ATPase Mitochondrial Metabolism Reactive Oxygen Species (ROS)
  3. 3-Methylglutaric acid

3-Methylglutaric acid is a non-selective inhibitor of mitochondrial function and Na+, K+-ATPase, with an inhibition rate of 30% on rat cortical synaptosomal Na+, K+-ATPase. 3-Methylglutaric acid can induce reactive oxygen species (ROS) generation, thereby causing oxidative damage and inhibiting mitochondrial redox potential and ion pump function of cell membranes. 3-Methylglutaric acid can be used to study the neuropathological mechanisms of metabolic diseases and the role of oxidative stress-mediated neuronal damage in neurodegeneration.

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3-Methylglutaric acid Chemical Structure

3-Methylglutaric acid Chemical Structure

CAS No. : 626-51-7

Size Price Stock Quantity
Solid + Solvent (Highly Recommended)
10 mM * 1 mL in DMSO
ready for reconstitution
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Solution
10 mM * 1 mL in DMSO In-stock
Solid
500 mg In-stock
1 g In-stock
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Customer Review

Based on 1 publication(s) in Google Scholar

Other Forms of 3-Methylglutaric acid:

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Description

3-Methylglutaric acid is a non-selective inhibitor of mitochondrial function and Na+, K+-ATPase, with an inhibition rate of 30% on rat cortical synaptosomal Na+, K+-ATPase. 3-Methylglutaric acid can induce reactive oxygen species (ROS) generation, thereby causing oxidative damage and inhibiting mitochondrial redox potential and ion pump function of cell membranes. 3-Methylglutaric acid can be used to study the neuropathological mechanisms of metabolic diseases and the role of oxidative stress-mediated neuronal damage in neurodegeneration[1][2][3][4].

IC50 & Target

Human Endogenous Metabolite

 

In Vitro

3-Methylglutaric acid (0.1-5.0 mM; 1 h) inhibits the mitochondrial redox potential of rat cortical synaptosomes, and the reduction rate of Resazurin (HY-118540) is reduced by 25%[1].
3-Methylglutaric acid (0.1-5.0 mM; 1 h) significantly inhibits the synaptosomal Na+,K+-ATPase activity by 30%, and this inhibitory effect can be completely reversed by the antioxidants creatine and melatonin[1].
3-Methylglutaric acid (0.1-5.0 mM; 1 h) induces synaptosomal ROS generation and increases the DCFH oxidation level by 30%[1].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Cell Viability Assay[1]

Cell Line: Rat cerebral cortex synaptosomes (viability assessed by LDH release)
Concentration: 0.1 mM, 1.0 mM, 5.0 mM
Incubation Time: 1 h, 2 h
Result: Unchanged LDH leakage compared to control (≤10% of total release), indicating no significant membrane damage or cell death at tested concentrations.
In Vivo

3-Methylglutaric acid (10 μmol/g for the first time, followed by two doses of 5 μmol/g each; ip; 90 min between each dose, single cycle) induces oxidative stress, mitochondrial dysfunction, and neuronal damage in the liver and cerebral cortex in male Wistar rats, while Bezafibrate (HY-B0637) (30-100 mg/kg/day, pretreatment by oral gavage for 7 days) significantly reverses the above effects[2][3].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Animal Model: Male Wistar rats (80-100 g, 23 days old), hepatic and cerebral cortex injury model induced by MGA[2][3]
Dosage: 10 μmol/g (first injection), 5 μmol/g (subsequent two injections); with or without Bezafibrate (30 or 100 mg/kg/day, dissolved in corn oil)
Administration: Intraperitoneal injection, three doses with 90-min intervals on the same day;
while Bezafibrate administratied via Oral gavage, once daily for 7 consecutive days before 3-Methylglutaric acid administration.
Result: Significantly increased malondialdehyde (MDA) levels (lipid peroxidation) in liver and cerebral cortex, decreased reduced glutathione (GSH) content, and altered activities of antioxidant enzymes (catalase ↑, glutathione peroxidase ↓, glucose-6-phosphate dehydrogenase ↓).
Bezafibrate (100 mg/kg/day) completely prevented MDA increase and GSH depletion, and partially normalized enzyme activities.
Molecular Weight

146.14

Formula

C6H10O4

CAS No.
Appearance

Solid

Color

White to off-white

SMILES

O=C(O)CC(C)CC(O)=O

Structure Classification
Initial Source
Shipping

Room temperature in continental US; may vary elsewhere.

Storage
Powder -20°C 3 years
4°C 2 years
In solvent -80°C 6 months
-20°C 1 month
Solvent & Solubility
In Vitro: 

H2O : ≥ 100 mg/mL (684.28 mM)

DMSO : 100 mg/mL (684.28 mM; Need ultrasonic; Hygroscopic DMSO has a significant impact on the solubility of product, please use newly opened DMSO)

*"≥" means soluble, but saturation unknown.

Preparing
Stock Solutions
Concentration Solvent Mass 1 mg 5 mg 10 mg
1 mM 6.8428 mL 34.2138 mL 68.4275 mL
5 mM 1.3686 mL 6.8428 mL 13.6855 mL
View the Complete Stock Solution Preparation Table

* Please refer to the solubility information to select the appropriate solvent. Once prepared, please aliquot and store the solution to prevent product inactivation from repeated freeze-thaw cycles.
Storage method and period of stock solution: -80°C, 6 months; -20°C, 1 month. When stored at -80°C, please use it within 6 months. When stored at -20°C, please use it within 1 month.

* Note: If you choose water as the stock solution, please dilute it to the working solution, then filter and sterilize it with a 0.22 μm filter before use.

  • Molarity Calculator

  • Dilution Calculator

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

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Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

This equation is commonly abbreviated as: C1V1 = C2V2

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In Vivo:

Select the appropriate dissolution method based on your experimental animal and administration route.

For the following dissolution methods, please ensure to first prepare a clear stock solution using an In Vitro approach and then sequentially add co-solvents:
To ensure reliable experimental results, the clarified stock solution can be appropriately stored based on storage conditions. As for the working solution for in vivo experiments, it is recommended to prepare freshly and use it on the same day.
The percentages shown for the solvents indicate their volumetric ratio in the final prepared solution. If precipitation or phase separation occurs during preparation, heat and/or sonication can be used to aid dissolution.

  • Protocol 1

    Add each solvent one by one:  10% DMSO    40% PEG300    5% Tween-80    45% Saline

    Solubility: ≥ 2.5 mg/mL (17.11 mM); Clear solution

    This protocol yields a clear solution of ≥ 2.5 mg/mL (saturation unknown).

    Taking 1 mL working solution as an example, add 100 μL DMSO stock solution (25.0 mg/mL) to 400 μL PEG300, and mix evenly; then add 50 μL Tween-80 and mix evenly; then add 450 μL Saline to adjust the volume to 1 mL.

    Preparation of Saline: Dissolve 0.9 g sodium chloride in ddH₂O and dilute to 100 mL to obtain a clear Saline solution.
  • Protocol 2

    Add each solvent one by one:  10% DMSO    90% (20% SBE-β-CD in Saline)

    Solubility: ≥ 2.5 mg/mL (17.11 mM); Clear solution

    This protocol yields a clear solution of ≥ 2.5 mg/mL (saturation unknown).

    Taking 1 mL working solution as an example, add 100 μL DMSO stock solution (25.0 mg/mL) to 900 μL 20% SBE-β-CD in Saline, and mix evenly.

    Preparation of 20% SBE-β-CD in Saline (4°C, storage for one week): 2 g SBE-β-CD powder is dissolved in 10 mL Saline, completely dissolve until clear.
In Vivo Dissolution Calculator
Please enter the basic information of animal experiments:

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g

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(per animal)

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Number of animals

Recommended: Prepare an additional quantity of animals to account for potential losses during experiments.
Calculation results:
Working solution concentration: mg/mL
This product has good water solubility, please refer to the measured solubility data in water/PBS/Saline for details.
The concentration of the stock solution you require exceeds the measured solubility. The following solution is for reference only.If necessary, please contact MedChemExpress (MCE).
Purity & Documentation

Purity: ≥98.0%

References

Complete Stock Solution Preparation Table

* Please refer to the solubility information to select the appropriate solvent. Once prepared, please aliquot and store the solution to prevent product inactivation from repeated freeze-thaw cycles.
Storage method and period of stock solution: -80°C, 6 months; -20°C, 1 month. When stored at -80°C, please use it within 6 months. When stored at -20°C, please use it within 1 month.

Optional Solvent Concentration Solvent Mass 1 mg 5 mg 10 mg 25 mg
H2O / DMSO 1 mM 6.8428 mL 34.2138 mL 68.4275 mL 171.0688 mL
5 mM 1.3686 mL 6.8428 mL 13.6855 mL 34.2138 mL
10 mM 0.6843 mL 3.4214 mL 6.8428 mL 17.1069 mL
15 mM 0.4562 mL 2.2809 mL 4.5618 mL 11.4046 mL
20 mM 0.3421 mL 1.7107 mL 3.4214 mL 8.5534 mL
25 mM 0.2737 mL 1.3686 mL 2.7371 mL 6.8428 mL
30 mM 0.2281 mL 1.1405 mL 2.2809 mL 5.7023 mL
40 mM 0.1711 mL 0.8553 mL 1.7107 mL 4.2767 mL
50 mM 0.1369 mL 0.6843 mL 1.3686 mL 3.4214 mL
60 mM 0.1140 mL 0.5702 mL 1.1405 mL 2.8511 mL
80 mM 0.0855 mL 0.4277 mL 0.8553 mL 2.1384 mL
100 mM 0.0684 mL 0.3421 mL 0.6843 mL 1.7107 mL

* Note: If you choose water as the stock solution, please dilute it to the working solution, then filter and sterilize it with a 0.22 μm filter before use.

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Product Name:
3-Methylglutaric acid
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HY-113410
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