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Methyl 3,4,5-trimethoxycinnamate

CAS# 7560-49-8

Methyl 3,4,5-trimethoxycinnamate

2D Structure

Catalog No. BCN4589----Order now to get a substantial discount!

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Quality Control of Methyl 3,4,5-trimethoxycinnamate

3D structure

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Methyl 3,4,5-trimethoxycinnamate

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Chemical Properties of Methyl 3,4,5-trimethoxycinnamate

Cas No. 7560-49-8 SDF Download SDF
PubChem ID 735846 Appearance Powder
Formula C13H16O5 M.Wt 252.26
Type of Compound Phenylpropanoids Storage Desiccate at -20°C
Synonyms 20329-96-8;Methyl trans-3-(3,4,5-trimethoxyphenyl)acrylate
Solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
Chemical Name methyl (E)-3-(3,4,5-trimethoxyphenyl)prop-2-enoate
SMILES COC1=CC(=CC(=C1OC)OC)C=CC(=O)OC
Standard InChIKey KLXHCGFNNUQTEY-AATRIKPKSA-N
Standard InChI InChI=1S/C13H16O5/c1-15-10-7-9(5-6-12(14)17-3)8-11(16-2)13(10)18-4/h5-8H,1-4H3/b6-5+
General tips For obtaining a higher solubility , please warm the tube at 37 ℃ and shake it in the ultrasonic bath for a while.Stock solution can be stored below -20℃ for several months.
We recommend that you prepare and use the solution on the same day. However, if the test schedule requires, the stock solutions can be prepared in advance, and the stock solution must be sealed and stored below -20℃. In general, the stock solution can be kept for several months.
Before use, we recommend that you leave the vial at room temperature for at least an hour before opening it.
About Packaging 1. The packaging of the product may be reversed during transportation, cause the high purity compounds to adhere to the neck or cap of the vial.Take the vail out of its packaging and shake gently until the compounds fall to the bottom of the vial.
2. For liquid products, please centrifuge at 500xg to gather the liquid to the bottom of the vial.
3. Try to avoid loss or contamination during the experiment.
Shipping Condition Packaging according to customer requirements(5mg, 10mg, 20mg and more). Ship via FedEx, DHL, UPS, EMS or other couriers with RT, or blue ice upon request.

Source of Methyl 3,4,5-trimethoxycinnamate

The herbs of Alstonia yunnanensis

Biological Activity of Methyl 3,4,5-trimethoxycinnamate

DescriptionMethyl 3,4,5-trimethoxycinnamate may protect the heart from arrhythmias via its inhibitory effect on calcium channel.
TargetsCalcium Channel | Potassium Channel
In vitro

Potential antiarrhythmic effect of methyl 3,4,5-trimethoxycinnamate, a bioactive substance from roots of polygalae radix: suppression of triggered activities in rabbit myocytes.[Pubmed: 23196428 ]

Biol Pharm Bull. 2013;36(2):238-44.

3,4,5-Trimethoxycinnamic acid (TMCA), Methyl 3,4,5-trimethoxycinnamate (M-TMCA) and p-methoxycinnamic acid (PMCA) have been identified as the major bioactive components in the serum collected from rats treated with oral administration of Polygalae Radix ("YuanZhi," the roots of Polygala tenuifolia WILLD.), a traditional Chinese medicine used to relieve insomnia, anxiety and heart palpitation.
METHODS AND RESULTS:
Among three bioactive substances of Polygala metabolites, only Methyl 3,4,5-trimethoxycinnamate (15-30 µM) significantly shortened action potential duration at 50% and 90% repolarization (APD(50) and APD(90)) in cardiomyocytes in a concentration-dependent and a reversible manner. Methyl 3,4,5-trimethoxycinnamate also inhibited L-type calcium current (I(Ca,L)), but showed effect on neither transient outward potassium current (I(to)) nor steady-state potassium current (I(K,SS)). Furthermore, Methyl 3,4,5-trimethoxycinnamate abolished isoprenaline plus BayK8644-induced early afterdepolarizations (EADs) and suppressed delayed afterdepolarizations (DADs) and triggered activities (TAs).
CONCLUSIONS:
These findings suggest that Methyl 3,4,5-trimethoxycinnamate may protect the heart from arrhythmias via its inhibitory effect on calcium channel.

Methyl 3,4,5-trimethoxycinnamate Dilution Calculator

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Methyl 3,4,5-trimethoxycinnamate Molarity Calculator

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Preparing Stock Solutions of Methyl 3,4,5-trimethoxycinnamate

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 3.9642 mL 19.8208 mL 39.6416 mL 79.2833 mL 99.1041 mL
5 mM 0.7928 mL 3.9642 mL 7.9283 mL 15.8567 mL 19.8208 mL
10 mM 0.3964 mL 1.9821 mL 3.9642 mL 7.9283 mL 9.9104 mL
50 mM 0.0793 mL 0.3964 mL 0.7928 mL 1.5857 mL 1.9821 mL
100 mM 0.0396 mL 0.1982 mL 0.3964 mL 0.7928 mL 0.991 mL
* Note: If you are in the process of experiment, it's necessary to make the dilution ratios of the samples. The dilution data above is only for reference. Normally, it's can get a better solubility within lower of Concentrations.

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References on Methyl 3,4,5-trimethoxycinnamate

Potential antiarrhythmic effect of methyl 3,4,5-trimethoxycinnamate, a bioactive substance from roots of polygalae radix: suppression of triggered activities in rabbit myocytes.[Pubmed:23196428]

Biol Pharm Bull. 2013;36(2):238-44. Epub 2012 Nov 29.

3,4,5-Trimethoxycinnamic acid (TMCA), Methyl 3,4,5-trimethoxycinnamate (M-TMCA) and p-methoxycinnamic acid (PMCA) have been identified as the major bioactive components in the serum collected from rats treated with oral administration of Polygalae Radix ("YuanZhi," the roots of Polygala tenuifolia WILLD.), a traditional Chinese medicine used to relieve insomnia, anxiety and heart palpitation. The present study was designed to investigate its direct electrophysiological effects on isolated ventricular myocytes from rabbits. Whole-cell configuration of the patch-clamp technique was used to measure action potential (AP) and membrane currents in single ventricular myocytes enzymatically isolated from adult rabbit hearts. Ca(2+) transients were recorded in myocytes loaded with the Ca(2+) indicator Fluo-4AM. Among three bioactive substances of Polygala metabolites, only M-TMCA (15-30 microM) significantly shortened action potential duration at 50% and 90% repolarization (APD(50) and APD(90)) in cardiomyocytes in a concentration-dependent and a reversible manner. M-TMCA also inhibited L-type calcium current (I(Ca,L)), but showed effect on neither transient outward potassium current (I(to)) nor steady-state potassium current (I(K,SS)). Furthermore, M-TMCA abolished isoprenaline plus BayK8644-induced early afterdepolarizations (EADs) and suppressed delayed afterdepolarizations (DADs) and triggered activities (TAs). This potential anti-arrhythmic effects were likely attributed by the inhibition of I(Ca,L) and the suppression of intracellular Ca(2+) transients, which consequently suppress the generation of transient inward current (I(ti)). These findings suggest that M-TMCA may protect the heart from arrhythmias via its inhibitory effect on calcium channel.

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