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Trimetazidine dihydrochloride

🥰Excellent
Catalog No. T0988Cas No. 13171-25-0
Alias Yoshimilon, Vastarel F, Kyurinett

Trimetazidine dihydrochloride (Vastarel F) can improve myocardial glucose utilization by inhibiting fatty acid metabolism. Trimetazidine is the first cytoprotective anti-ischemic agent, also used as a vasodilator in ischemic heart disease or angina.

Trimetazidine dihydrochloride

Trimetazidine dihydrochloride

🥰Excellent
Purity: 99.31%
Catalog No. T0988Alias Yoshimilon, Vastarel F, KyurinettCas No. 13171-25-0
Trimetazidine dihydrochloride (Vastarel F) can improve myocardial glucose utilization by inhibiting fatty acid metabolism. Trimetazidine is the first cytoprotective anti-ischemic agent, also used as a vasodilator in ischemic heart disease or angina.
Pack SizePriceAvailabilityQuantity
25 mg$34In Stock
50 mg$47In Stock
100 mg$68In Stock
500 mg$165In Stock
1 mL x 10 mM (in DMSO)$30In Stock
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Purity:99.31%
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Product Introduction

Bioactivity
Description
Trimetazidine dihydrochloride (Vastarel F) can improve myocardial glucose utilization by inhibiting fatty acid metabolism. Trimetazidine is the first cytoprotective anti-ischemic agent, also used as a vasodilator in ischemic heart disease or angina.
Targets&IC50
Long-chain 3-ketoacyl thiolase (mitochondrial):75 nM
In vitro
Trimetazidine up-regulates miR-21 expression, then miR-21 targets PTEN increasing the PI3K pathway and finally the activation of this pathway counteracts the apoptotic effect of hypoxia/reperfusion[3].
In vivo
The administration of TMZ reduces myocardial infarction size in WT C57BL/6J hearts. Both AMPK and ERK signaling pathways mediate the cardioprotection of TMZ against ischemic injury. Trimetazidine Shifts Metabolism from Fatty Acid Oxidation to Glucose Oxidation and improves Contractile Functions of Cardiomyocytes during Hypoxia[2].
Cell Research
The H9C2 cells are randomly assigned into three groups: Sham group, in which the cells are treated with 0μM TMZ for 48 h and then cultured under normal oxygenation conditions (5% CO2, and 95% air); H/R group, in which cells are treated with 0 μM TMZ for 48 h and then cultured under H/R conditions; and H/R+TMZ group, in which cells are treated with 10 μM TMZ for 48 h and then subjected to H/R treatment. (Only for Reference)
AliasYoshimilon, Vastarel F, Kyurinett
Chemical Properties
Molecular Weight339.258
FormulaC14H24Cl2N2O3
Cas No.13171-25-0
SmilesCl.Cl.COC1=C(OC)C(OC)=C(CN2CCNCC2)C=C1
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.
Solubility Information
DMSO: 65 mg/mL (191.59 mM), Sonication is recommended.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM2.9476 mL14.7380 mL29.4761 mL147.3805 mL
5 mM0.5895 mL2.9476 mL5.8952 mL29.4761 mL
10 mM0.2948 mL1.4738 mL2.9476 mL14.7380 mL
20 mM0.1474 mL0.7369 mL1.4738 mL7.3690 mL
50 mM0.0590 mL0.2948 mL0.5895 mL2.9476 mL
100 mM0.0295 mL0.1474 mL0.2948 mL1.4738 mL

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