(E/Z)-Polydatin
Based on 1 Customer Validation
(E/Z)-Polydatin ((E/Z)-Piceid) is a mixture of the E/Z configurations of Polydatin (HY-N0120A). Polydatin can be isolated from Polygonum cuspidatum, grapes, peanuts, red wine, hop pellets, cocoa-containing products and chocolate products. Polydatin exhibits multiple biological properties, such as anti-platelet aggregation, anti-low-density lipoprotein oxidation, cardioprotective activity, anti-inflammatory and immunomodulatory functions. Polydatin shows favorable cytotoxic effects against various tumor cell lines, including cervical cancer cells, liver cancer cells, and nasopharyngeal carcinoma cells.
For research use only. We do not sell to patients.
- Purity: 98.06%
- CAS No.: 65914-17-2
- Formula: C20H22O8
- Molecular Weight:390.38
-
Storage:Powder -20°C, 3 years , 4°C, 2 years ; In solvent -80°C, 2 years , -20°C, 1 year
To place orders, for customer services and technical support, please contact: MedChemExpress USA
Tel: 609-228-6898 E-mail: [email protected] [email protected]
-
Biological Activity
-
Chemical Information
-
Solvent & Solubility
- Purity & Documentation
- References
-
Help & FAQs
Biological Activity
|
Cell Line
|
Type | Value | Description | References |
|---|---|---|---|---|
| C8166 | CC50 |
>200 μg/mL
Compound: Piceid
|
Cytotoxicity against human C8166 cells assessed as inhibition of cell growth by MTT assay
Cytotoxicity against human C8166 cells assessed as inhibition of cell growth by MTT assay
|
[PMID: 32652408] |
| HEK293 | IC50 |
>100 μM
Compound: Piceid
|
Anticancer activity against human HEK293 cells assessed as cell growth inhibition incubated for 3 days by MTT assay
Anticancer activity against human HEK293 cells assessed as cell growth inhibition incubated for 3 days by MTT assay
|
[PMID: 32485531] |
| HT-29 | IC50 |
18 μM
Compound: Piceid
|
Anticancer activity against human HT-29 cells assessed as cell growth inhibition incubated for 3 days by MTT assay
Anticancer activity against human HT-29 cells assessed as cell growth inhibition incubated for 3 days by MTT assay
|
[PMID: 32485531] |
| MCF7 | IC50 |
38 μM
Compound: Piceid
|
Anticancer activity against human MCF7 cells assessed as cell growth inhibition incubated for 3 days by MTT assay
Anticancer activity against human MCF7 cells assessed as cell growth inhibition incubated for 3 days by MTT assay
|
[PMID: 32485531] |
| Platelet | IC50 |
32.55 μg
Compound: 1, piceid
|
Inhibition of collagen-induced platelet aggregation in human platelet-rich plasma
Inhibition of collagen-induced platelet aggregation in human platelet-rich plasma
|
[PMID: 9392877] |
| Platelet | IC50 |
49.27 μg
Compound: 1, piceid
|
Inhibition of adrenaline-induced platelet aggregation in human platelet-rich plasma
Inhibition of adrenaline-induced platelet aggregation in human platelet-rich plasma
|
[PMID: 9392877] |
| Platelet | IC50 |
57.21 μg
Compound: 1, piceid
|
Inhibition of arachidonic acid-induced platelet aggregation in human platelet-rich plasma
Inhibition of arachidonic acid-induced platelet aggregation in human platelet-rich plasma
|
[PMID: 9392877] |
| Platelet | IC50 |
84.9 μg
Compound: 1, piceid
|
Inhibition of adenosine diphosphate-induced platelet aggregation in human platelet-rich plasma
Inhibition of adenosine diphosphate-induced platelet aggregation in human platelet-rich plasma
|
[PMID: 9392877] |
| RAW264.7 | IC50 |
13.5 μM
Compound: trans-Piceid
|
inhibitory concentration against PGE-2 production in LPS-stimulated RAW264.7 cells
inhibitory concentration against PGE-2 production in LPS-stimulated RAW264.7 cells
|
[PMID: 15501064] |
Polydatin exhibits multiple biological properties, such as anti-platelet aggregation, anti-low-density lipoprotein oxidation, cardioprotective activity, anti-inflammatory and immunomodulatory functions. Polydatin shows favorable cytotoxic effects against various tumor cell lines, including cervical cancer cells, liver cancer cells, and nasopharyngeal carcinoma cells[1].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
Chemical Information
-
CAS No. 65914-17-2
-
Appearance Solid
-
Molecular Weight 390.38
-
Formula C20H22O8
-
Color White to off-white
-
SMILES
O[C@H]([C@H]([C@@H]([C@@H](CO)O1)O)O)[C@@H]1OC2=CC(/C=C/C3=CC=C(O)C=C3)=CC(O)=C2
-
Synonyms
(E/Z)-Piceid
-
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 2 years -20°C 1 year
Solvent & Solubility
DMSO : 150 mg/mL (384.24 mM; Need ultrasonic; Hygroscopic DMSO has a significant impact on the solubility of product, please use newly opened DMSO)
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, 2 years; -20°C, 1 year. When stored at -80°C, please use it within 2 years. When stored at -20°C, please use it within 1 year.
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, 2 years; -20°C, 1 year. When stored at -80°C, please use it within 2 years. When stored at -20°C, please use it within 1 year.
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)
Select the appropriate dissolution method based on your experimental animal and administration route.
- For the following dissolution methods, please ensure to first prepare a clear stock solution using an In Vitro approach and then sequentially add co-solvents:
- To ensure reliable experimental results, the clarified stock solution can be appropriately stored based on storage conditions. As for the working solution for In Vivo experiments, it is recommended to prepare freshly and use it on the same day.
- The percentages shown for the solvents indicate their volumetric ratio in the final prepared solution. If precipitation or phase separation occurs during preparation, heat and/or sonication can be used to aid dissolution.
Add each solvent one by one: 10% DMSO 40% PEG300 5% Tween-80 45% Saline
Solubility: ≥ 2.5 mg/mL (6.40 mM); Clear solution
This protocol yields a clear solution of ≥ 2.5 mg/mL (saturation unknown).
Taking 1 mL working solution as an example, add 100 μL DMSO stock solution (25.0 mg/mL) to 400 μL PEG300, and mix evenly; then add 50 μL Tween-80 and mix evenly; then add 450 μL Saline to adjust the volume to 1 mL.
Preparation of Saline: Dissolve 0.9 g sodium chloride in ddH₂O and dilute to 100 mL to obtain a clear Saline solution.
Add each solvent one by one: 10% DMSO 90% (20% SBE-β-CD in Saline)
Solubility: ≥ 2.5 mg/mL (6.40 mM); Clear solution
This protocol yields a clear solution of ≥ 2.5 mg/mL (saturation unknown).
Taking 1 mL working solution as an example, add 100 μL DMSO stock solution (25.0 mg/mL) to 900 μL 20% SBE-β-CD in Saline, and mix evenly.
Preparation of 20% SBE-β-CD in Saline (4°C, storage for one week): 2 g SBE-β-CD powder is dissolved in 10 mL Saline, completely dissolve until clear.
Please enter the basic information of animal experiments:
-
-
-
-
Recommended: Prepare an additional quantity of animals to account for potential losses during experiments.
Please enter your animal formula composition:
-
%DMSO +
Recommended: Keep the proportion of DMSO in working solution below 2% if your animal is weak.
-
%+
-
+%Tween-80 + +
-
%Saline +
The co-solvents required include: DMSO, . All of co-solvents are available by MedChemExpress (MCE). , Tween 80. All of co-solvents are available by MedChemExpress (MCE).
Working solution concentration: 0.22 mg/mL
Method for preparing stock solution: mg drug dissolved in μL DMSO. Stock solution concentration: mg/mL.
1. Take μL DMSO stock solution;
2. Add μL .
μL , mix evenly;
3. Then add μL Tween 80, mix evenly;
4. Then add μL
Please ensure that the stock solution in the first step is dissolved to a clear state, and add co-solvents in sequence. You can use ultrasonic heating (ultrasonic cleaner, recommended frequency 20-40 kHz), vortexing, etc. to assist dissolution.
Purity & Documentation
-
Data Sheet (270 KB)
-
SDS (394 KB)
- English - EN (394 KB)
- Français - FR (394 KB)
- Deutsch - DE (394 KB)
- Norwegian - NO (394 KB)
- Español - ES (394 KB)
- Swedish - SV (394 KB)
- Italian - IT (394 KB)
- Korean - KR (394 KB)
- Portuguese - PT (394 KB)
-
Handling Instructions (2659 KB)
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, 2 years; -20°C, 1 year. When stored at -80°C, please use it within 2 years. When stored at -20°C, please use it within 1 year.
| Optional Solvent | Concentration Solvent Mass | 1 mg | 5 mg | 10 mg | 25 mg |
|---|---|---|---|---|---|
| DMSO | 1 mM | 2.5616 mL | 12.8080 mL | 25.6161 mL | 64.0402 mL |
| 5 mM | 0.5123 mL | 2.5616 mL | 5.1232 mL | 12.8080 mL | |
| 10 mM | 0.2562 mL | 1.2808 mL | 2.5616 mL | 6.4040 mL | |
| 15 mM | 0.1708 mL | 0.8539 mL | 1.7077 mL | 4.2693 mL | |
| 20 mM | 0.1281 mL | 0.6404 mL | 1.2808 mL | 3.2020 mL | |
| 25 mM | 0.1025 mL | 0.5123 mL | 1.0246 mL | 2.5616 mL | |
| 30 mM | 0.0854 mL | 0.4269 mL | 0.8539 mL | 2.1347 mL | |
| 40 mM | 0.0640 mL | 0.3202 mL | 0.6404 mL | 1.6010 mL | |
| 50 mM | 0.0512 mL | 0.2562 mL | 0.5123 mL | 1.2808 mL | |
| 60 mM | 0.0427 mL | 0.2135 mL | 0.4269 mL | 1.0673 mL | |
| 80 mM | 0.0320 mL | 0.1601 mL | 0.3202 mL | 0.8005 mL | |
| 100 mM | 0.0256 mL | 0.1281 mL | 0.2562 mL | 0.6404 mL |
(E/Z)-Polydatin Related Classifications
HY-N0120 Related Classifications
Powered by Bioz