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3,4,5-Trihydroxycinnamic acid decyl ester

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Catalog No. T39189Cas No. 1770778-45-4

3,4,5-Trihydroxycinnamic acid decyl ester, an effective inhibitor of lipid absorption and accumulation, exhibits anti-obesity properties and acts as a pancreatic lipase inhibitor, with an EC50 of approximately 0.9 μM.

3,4,5-Trihydroxycinnamic acid decyl ester

3,4,5-Trihydroxycinnamic acid decyl ester

🥰Excellent
Purity: 98.28%
Catalog No. T39189Cas No. 1770778-45-4
3,4,5-Trihydroxycinnamic acid decyl ester, an effective inhibitor of lipid absorption and accumulation, exhibits anti-obesity properties and acts as a pancreatic lipase inhibitor, with an EC50 of approximately 0.9 μM.
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1 mg$69In Stock
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Purity:98.28%
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Product Introduction

Bioactivity
Description
3,4,5-Trihydroxycinnamic acid decyl ester, an effective inhibitor of lipid absorption and accumulation, exhibits anti-obesity properties and acts as a pancreatic lipase inhibitor, with an EC50 of approximately 0.9 μM.
Targets&IC50
Pancreatic lipase:0.9 μM (EC50)
In vitro
3,4,5-Trihydroxycinnamic acid decyl ester (30 μM) inhibits pancreatic lipase activity by approximately 92% in vitro[1]. This compound exhibits dose-dependent inhibition of pancreatic lipase between 0.1-40 μM, with an EC50 around 0.9 μM[1]. Additionally, it prevents lipid accumulation during 3T3-L1 cell differentiation, indicating potential in influencing lipid metabolism[1].
In vivo
3,4,5-Trihydroxycinnamic acid decyl ester (30-150 mg/kg; p.o.) effectively suppresses the elevation of blood triglyceride (TG) levels in 6-week-old male ddY mice administered corn oil orally, with the compound showing a dose-dependent reduction in plasma TG levels at dosages of 30 mg/kg and 150 mg/kg[1].
Chemical Properties
Molecular Weight336.42
FormulaC19H28O5
Cas No.1770778-45-4
SmilesCCCCCCCCCCOC(=O)\C=C\c1cc(O)c(O)c(O)c1
Relative Density.1.143 g/cm3 (Predicted)
Storage & Solubility Information
Storagestore at low temperature | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
Solubility Information
DMSO: 80 mg/mL (237.80 mM), Sonication is recommended.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM2.9725 mL14.8624 mL29.7247 mL148.6237 mL
5 mM0.5945 mL2.9725 mL5.9449 mL29.7247 mL
10 mM0.2972 mL1.4862 mL2.9725 mL14.8624 mL
20 mM0.1486 mL0.7431 mL1.4862 mL7.4312 mL
50 mM0.0594 mL0.2972 mL0.5945 mL2.9725 mL
100 mM0.0297 mL0.1486 mL0.2972 mL1.4862 mL

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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:
TargetMol | Animal experimentsFor 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% ddH2O. So your working solution concentration is 2 mg/mL。
Mother liquor preparation method: 2 mg of drug dissolved in 50 μL DMSOTargetMol | 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 DMSOTargetMol | reagent main solution, add 300 μLPEG300TargetMol | reagent mix well and clarify, then add 50 more μL Tween 80, mix well and clarify, then add 600 more μLddH2OTargetMol | reagent mix well and clarify
For Reference Only. Please develop an appropriate dissolution method based on your laboratory animals and route of administration.
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