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Trimetazidine

Name: Trimetazidine
Brand: TargetMol
SKU: T22444
Price: 30 USD
Availability: InStock
Rating: 5 (10 reviews)

🥰Excellent

Catalog No. T22444Cas No. 5011-34-7

Trimetazidine is a non-haemodynamic antianginal agent that selectively inhibits the mitochondrial enzyme 3-ketoacyl coenzyme A thiolase (LC 3-KAT), thereby preventing β-oxidation of free fatty acids, with an IC50 value of 75 nM. Trimetazidine prevents ischaemia-reperfusion injury by altering cardiac metabolism, exhibiting antioxidant and anti-ischaemic effects.

Trimetazidine

🥰Excellent

Purity: 99.9%

Catalog No. T22444Cas No. 5011-34-7

Pack Size	Price	USA Warehouse	Global Warehouse
5 mg	$32	-	In Stock
10 mg	$44	In Stock	In Stock
25 mg	$57	In Stock	In Stock
50 mg	$70	In Stock	In Stock
1 mL x 10 mM (in DMSO)	$30	-	In Stock

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In Stock Estimated shipping dateUSA Warehouse[1-2 days] Global Warehouse[5-7 days]

This molecule is a custom-made product. TargetMol has an excellent synthesis team with the experience and capability to provide you with cost-effective products. However, due to objective factors, there is a small probability that the synthesis may not be successful during the R&D process. We appreciate your understanding. If you have any questions, please feel free to contact us. We are committed to serving you wholeheartedly.

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Purity:99.9%

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COA HNMR LCMS

Product Introduction

Bioactivity

Description	Trimetazidine is a non-haemodynamic antianginal agent that selectively inhibits the mitochondrial enzyme 3-ketoacyl coenzyme A thiolase (LC 3-KAT), thereby preventing β-oxidation of free fatty acids, with an IC50 value of 75 nM. Trimetazidine prevents ischaemia-reperfusion injury by altering cardiac metabolism, exhibiting antioxidant and anti-ischaemic effects.
Targets&IC50	Long chain 3-ketoyl coenzyme A thiolase:75 nM
In vitro	Methods: Mouse C2C12 myoblasts were treated with Trimetazidine (50–200 μM, 6 hours), and cell viability was measured using CCK-8 reagent. Result: Trimetazidine at concentrations of 150 μM and 200 μM significantly reversed dexamethasone-induced cell death.[1]
In vivo	Methods: Trimetazidine (5 mg/kg, administered intraperitoneally for 12 consecutive days) was injected into C26 colon carcinoma mice to study the "exercise-mimicking" effects of trimetazidine in a cancer cachexia mouse model. Results: Trimetazidine enhanced metabolic adaptive mechanisms in cancer cachexia mice by mimicking the effects of exercise, including increased grip strength, elevated proportion of slow muscle fibers, upregulated PGC1α expression, and enhanced mitochondrial biogenesis and oxidative metabolism. [2]

Chemical Properties

Molecular Weight	266.34
Formula	C₁₄H₂₂N₂O₃
Cas No.	5011-34-7
Smiles	COc1ccc(CN2CCNCC2)c(OC)c1OC
Relative Density.	1.092 g/cm3
Color	White
Appearance	Viscous

Storage & Solubility Information

Storage

keep away from direct sunlight | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.

Solubility Information

DMSO: 85.00 mg/mL (319.14 mM), Sonication is recommended.

In Vivo Formulation

10% DMSO+40% PEG300+5% Tween 80+45% Saline: 3.3 mg/mL (12.39 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

	1mg	5mg	10mg	50mg
1 mM	3.7546 mL	18.7730 mL	37.5460 mL	187.7300 mL
5 mM	0.7509 mL	3.7546 mL	7.5092 mL	37.5460 mL
10 mM	0.3755 mL	1.8773 mL	3.7546 mL	18.7730 mL
20 mM	0.1877 mL	0.9386 mL	1.8773 mL	9.3865 mL
50 mM	0.0751 mL	0.3755 mL	0.7509 mL	3.7546 mL
100 mM	0.0375 mL	0.1877 mL	0.3755 mL	1.8773 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 mother liquor preparation method and in vivo formula preparation method:

For example, your dosage is 10 mg/kg Each animal weighs 20 g, and the dosage volume is 100 μL . TargetMol | Animal experiments

A total of 10 animals were administered, and the formula you used is 5% TargetMol | reagent

DMSO+30% PEG300+5% Tween 80+60% Saline/PBS/ddH₂O. So your working solution concentration is 2 mg/mL。

Mother liquor preparation method: 2 mg of drug dissolved in 50 μL DMSO TargetMol | reagent

(mother liquor concentration of 40 mg/mL), if you need to configure a concentration that exceeds the solubility of the product, please contact us first.

Preparation method for in vivo formula: Take 50 μL DMSO TargetMol | reagent

main solution, add 300 μLPEG300 TargetMol | reagent

mix well and clarify, then add 50 more μL Tween 80, mix well and clarify, then add 600 more μLSaline/PBS/ddH₂O TargetMol | reagent

mix well and clarify

For Reference Only. Please develop an appropriate dissolution method based on your laboratory animals and route of administration.

All types of co-solvents required for the protocol, such asDMSO, PEG300/ PEG400, Tween 80, SBE-β-CD, corn oil are available for purchase on the TargetMol website with a simple click.

Dose Conversion

You can also refer to dose conversion for different animals. More Dose Conversion

Tech Support

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