1. Metabolic Enzyme/Protease Apoptosis NF-κB Protein Tyrosine Kinase/RTK PI3K/Akt/mTOR Epigenetics Immunology/Inflammation
  2. Endogenous Metabolite Apoptosis Bcl-2 Family NF-κB Survivin Src Akt AMPK NO Synthase
  3. Propionyl-L-carnitine

Propionyl-L-carnitine is an orally active L-carnitine derivative. Propionyl-L-carnitine has a high affinity for muscle L-carnitine transferase. Propionyl-L-carnitine increases Apoptosis, Bax, and reduces NF-κB, VCAM-1, MCP-1, and survivin. Propionyl-L-carnitine activates Src kinase, Akt, induces p-AMPK and nitric oxide synthesis. Propionyl-L-carnitine alleviates cardiovascular disease, obesity, and colitis.

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

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Propionyl-L-carnitine Chemical Structure

Propionyl-L-carnitine Chemical Structure

CAS No. : 20064-19-1

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Based on 1 publication(s) in Google Scholar

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  • Biological Activity

  • Purity & Documentation

  • References

  • Customer Review

Description

Propionyl-L-carnitine is an orally active L-carnitine derivative. Propionyl-L-carnitine has a high affinity for muscle L-carnitine transferase. Propionyl-L-carnitine increases Apoptosis, Bax, and reduces NF-κB, VCAM-1, MCP-1, and survivin. Propionyl-L-carnitine activates Src kinase, Akt, induces p-AMPK and nitric oxide synthesis. Propionyl-L-carnitine alleviates cardiovascular disease, obesity, and colitis[1][2][3][4][5][6][7][8][9][10].

IC50 & Target

IC50: muscular carnitine transferase[1]

In Vitro

Propionyl-L-carnitine (0-100 μM; 0-8 h) induces eNOS activation and nitric oxide synthesis in endothelial cells HAEC via PI3 and Akt kinases[2].
Propionyl-L-carnitine (100 μM; 6-24 h) induces IκB-α mRNA, and inhibits p65 and p50 in intimal cells[3].

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

Western Blot Analysis[2]

Cell Line: HAEC
Concentration: 25, 50, 75, 100 μM
Incubation Time: 2, 4, 6, 8 h
Result: Increased eNOS phosphorylation and activity in a concentration- and time-dependent manner.
Increased eNOS activity by 350% at 50 μM.
Induced Akt activation.
Activated Src kinase.
Induced phosphorylation of AMPK.
In Vivo

Propionyl-L-carnitine (120 mg/kg; p.o.; daily; starting immediately after aortic injury and lasting for 15 days) reduces the relative aortic intimal volume, increases apoptosis, up-regulates Bax without changing the Bcl-2 level, and reduces NF-κB, VCAM-1, MCP-1, and survivin in rats[3].
Propionyl-L-carnitine (30-120 mg/kg/day, p.o., drinking water) enhances wound healing and counteracts microvascular endothelial cell dysfunction in rats[4].
Propionyl-L-carnitine (3.6 mg/mL, infused into the renal artery at the rate of 0.4 mL/min) prevents renal function deterioration due to ischemia/reperfusion in male Sprague-Dawley rats[5].
Propionyl-L-carnitine (200 mg/kg/day, p.o., 4 weeks) corrects metabolic and cardiovascular alterations in diet-induced obese mice and improves liver respiratory chain activity[6].
Propionyl-L-carnitine (25  mg/kg, intrarectal, twice daily, for 1 week; 120 mg/kg, p.o., once daily, for 1 week) reduces intestinal damage and microvascular dysfunction in rat TNBS-induced acute and reactivated colitis[7].
Propionyl-L-carnitine (200 mg/kg, p.o., drinking water) increases NO synthesis by enhancing eNOS expression in spontaneously hypertensive rats[8].
Propionyl-L-carnitine (500 mg/kg, i.p., 10 successive days) prevents the progression of Cisplatin (HY-17394)-induced cardiomyopathy in a carnitine-depleted rat model[9].
Propionyl-L-carnitine (200 mg/kg per d, p.o., 20 weeks) reduces body weight and hyperinsulinaemia in obese Zucker rats[10].

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

Animal Model: Male Wistar rats (200-225 g, 13-14 weeks old), skin flap model and full-thickness skin wound model[4]
Dosage: For the skin flap model, 100 mg/kg (dissolved in drinking water); for the full-thickness skin wound model, 30 mg/kg, 60 mg/kg, 120 mg/kg (dissolved in water).
Administration: Oral gavage (p.o.), drinking water
Result: Showed a faster blood flow recovery of the flap, an improved viability, reduced ROS production, increased NO level and iNOS expression (In the skin flap model).
Reduced the necrotic skin area after 8 days (in the skin flap model).
Had faster re-epithelialization, increased CD31+ capillaries, iNOS, VEGF and PlGF expression, and reduced Nox4+ microvessels (in the full-thickness skin wound model).
Molecular Weight

217.26

Formula

C10H19NO4

CAS No.
Appearance

Solid

Color

White to off-white

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 : ≥ 250 mg/mL (1150.70 mM)

*"≥" means soluble, but saturation unknown.

Preparing
Stock Solutions
Concentration Solvent Mass 1 mg 5 mg 10 mg
1 mM 4.6028 mL 23.0139 mL 46.0278 mL
5 mM 0.9206 mL 4.6028 mL 9.2056 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.

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  • 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
Please enter the basic information of animal experiments:

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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
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 1 mM 4.6028 mL 23.0139 mL 46.0278 mL 115.0695 mL
5 mM 0.9206 mL 4.6028 mL 9.2056 mL 23.0139 mL
10 mM 0.4603 mL 2.3014 mL 4.6028 mL 11.5070 mL
15 mM 0.3069 mL 1.5343 mL 3.0685 mL 7.6713 mL
20 mM 0.2301 mL 1.1507 mL 2.3014 mL 5.7535 mL
25 mM 0.1841 mL 0.9206 mL 1.8411 mL 4.6028 mL
30 mM 0.1534 mL 0.7671 mL 1.5343 mL 3.8357 mL
40 mM 0.1151 mL 0.5753 mL 1.1507 mL 2.8767 mL
50 mM 0.0921 mL 0.4603 mL 0.9206 mL 2.3014 mL
60 mM 0.0767 mL 0.3836 mL 0.7671 mL 1.9178 mL
80 mM 0.0575 mL 0.2877 mL 0.5753 mL 1.4384 mL
100 mM 0.0460 mL 0.2301 mL 0.4603 mL 1.1507 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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Propionyl-L-carnitine
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