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  3. Acetyl-L-carnitine

Acetyl-L-carnitine  (Synonyms: O-Acetyl-L-carnitine; ALCAR)

Cat. No.: HY-113218 Purity: ≥98.0%
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Acetyl-L-carnitine (O-Acetyl-L-carnitine; ALCAR) is an orally active mitochondrial energy metabolism regulator and neuroprotectant that can penetrate the blood-brain barrier. Acetyl-L-carnitine selectively enters cells and the brain through the organic cation transporter OCTN2. Acetyl-L-carnitine can participate in fatty acid β-oxidation, promote acetylcholine synthesis, regulate mitochondrial function and inhibit oxidative stress as an acetyl donor. Acetyl-L-carnitine exerts its activity by enhancing energy metabolism, protecting neurons and improving synaptic plasticity. Acetyl-L-carnitine is mainly used in the study of neurodegenerative diseases and metabolic disorder-related diseases such as neonatal hypoxic-ischemic brain damage, Alzheimer's disease, and depression.

For research use only. We do not sell to patients.

Acetyl-L-carnitine Chemical Structure

Acetyl-L-carnitine Chemical Structure

CAS No. : 3040-38-8

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Based on 2 publication(s) in Google Scholar

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Description

Acetyl-L-carnitine (O-Acetyl-L-carnitine; ALCAR) is an orally active mitochondrial energy metabolism regulator and neuroprotectant that can penetrate the blood-brain barrier. Acetyl-L-carnitine selectively enters cells and the brain through the organic cation transporter OCTN2. Acetyl-L-carnitine can participate in fatty acid β-oxidation, promote acetylcholine synthesis, regulate mitochondrial function and inhibit oxidative stress as an acetyl donor. Acetyl-L-carnitine exerts its activity by enhancing energy metabolism, protecting neurons and improving synaptic plasticity. Acetyl-L-carnitine is mainly used in the study of neurodegenerative diseases and metabolic disorder-related diseases such as neonatal hypoxic-ischemic brain damage, Alzheimer's disease, and depression[1][2][3].

IC50 & Target

Human Endogenous Metabolite

 

In Vitro

Cell Viability and Apoptosis:
Acetyl-L-carnitine (1 mM; 30 min) significantly inhibits 1 μg/mL Doxycycline (HY-N0565)-induced caspase-3/9 activation, reduces reactive oxygen species (ROS) generation and apoptosis, and maintains glutathione levels in thioredoxin TRX2-deficient DT40 cells[1].

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

Cell Viability Assay[1]

Cell Line: TRX2-/- DT40 cells (chicken B-cell line)
Concentration: 1 mM
Incubation Time: 30 min pretreatment before 1 μg/mL Doxycycline induction
Result: Reduced activation of caspase-3 and caspase-9, key markers of mitochondrial apoptosis pathway, compared to untreated cells.
Decrease 40% in intracellular ROS levels, indicating attenuation of oxidative stress.
Maintained glutathione levels in both cytosol and mitochondria, preventing redox imbalance caused by TRX2 deficiency.
Resulted 35% reduction in apoptotic cell population, confirming protective effects against mitochondrial-dependent apoptosis.
In Vivo

Acetyl-L-carnitine (100 mg/kg; intraperitoneal injection; once daily; 14 days) significantly alleviates brain damage in the hypoxic-ischemic brain damage (HIBD) model of neonatal rats, improves neurological function, reduced oxidative stress levels, and decreases cell apoptosis[2].
Acetyl-L-carnitine (300 mg/kg; oral gavage; once daily; 28 days) improves cognitive function in the cognitive impairment model of aged rats, enhances synaptic plasticity in the hippocampus, and increases the expression of brain-derived neurotrophic factor (BDNF)[3].

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

Animal Model: Neonatal Sprague-Dawley rats (male, 18-22g, postnatal day 7), hypoxic-ischemic brain damage (HIBD) model[2]
Dosage: 100 mg/kg
Administration: Intraperitoneal injection, once daily, for 14 consecutive days starting 24 hours after HIBD induction
Result: Brain injury: Reduced infarct volume by 40% compared to the HIBD control group as measured by triphenyltetrazolium chloride (TTC) staining.
Neurological function: Improved neurological scores, including motor function, sensory function, and balance, as evaluated by a modified neurological severity score (mNSS).
Molecular Weight

203.24

Formula

C9H17NO4

CAS No.
Appearance

Solid

Color

White to off-white

SMILES

C[N+](C)(C)C[C@H](OC(C)=O)CC([O-])=O

Structure Classification
Initial Source

Homo sapiens

Shipping

Room temperature in continental US; may vary elsewhere.

Storage

Store at room temperature 3 years

In solvent -80°C 2 years
-20°C 1 year
Solvent & Solubility
In Vitro: 

H2O : 350 mg/mL (1722.10 mM; Need ultrasonic)

Preparing
Stock Solutions
Concentration Solvent Mass 1 mg 5 mg 10 mg
1 mM 4.9203 mL 24.6015 mL 49.2029 mL
5 mM 0.9841 mL 4.9203 mL 9.8406 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, 2 years; -20°C, 1 year. When stored at -80°C, please use it within 2 years. When stored at -20°C, please use it within 1 year.

* 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 Dissolution Calculator
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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
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, 2 years; -20°C, 1 year. When stored at -80°C, please use it within 2 years. When stored at -20°C, please use it within 1 year.

Optional Solvent Concentration Solvent Mass 1 mg 5 mg 10 mg 25 mg
H2O 1 mM 4.9203 mL 24.6015 mL 49.2029 mL 123.0073 mL
5 mM 0.9841 mL 4.9203 mL 9.8406 mL 24.6015 mL
10 mM 0.4920 mL 2.4601 mL 4.9203 mL 12.3007 mL
15 mM 0.3280 mL 1.6401 mL 3.2802 mL 8.2005 mL
20 mM 0.2460 mL 1.2301 mL 2.4601 mL 6.1504 mL
25 mM 0.1968 mL 0.9841 mL 1.9681 mL 4.9203 mL
30 mM 0.1640 mL 0.8200 mL 1.6401 mL 4.1002 mL
40 mM 0.1230 mL 0.6150 mL 1.2301 mL 3.0752 mL
50 mM 0.0984 mL 0.4920 mL 0.9841 mL 2.4601 mL
60 mM 0.0820 mL 0.4100 mL 0.8200 mL 2.0501 mL
80 mM 0.0615 mL 0.3075 mL 0.6150 mL 1.5376 mL
100 mM 0.0492 mL 0.2460 mL 0.4920 mL 1.2301 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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  • Do most proteins show cross-species activity?

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