1. Apoptosis Metabolic Enzyme/Protease Immunology/Inflammation NF-κB Anti-infection
  2. Apoptosis Reactive Oxygen Species (ROS) Bacterial SARS-CoV
  3. Hydroxytyrosol

Hydroxytyrosol  (Synonyms: DOPET; 3,4-Dihydroxyphenethyl alcohol; 3-Hydroxytyrosol)

Cat. No.: HY-N0570 Purity: 98.24%
Handling Instructions Technical Support

Hydroxytyrosol (DOPET) is a phenol found in the olive oil. Hydroxytyrosol can alleviate oxidative stress and improve mitochondrial function, thereby exerting neuroprotective effects. Hydroxytyrosol can induce cancer cells apoptosis via inducing ROS production. Hydroxytyrosol shows antibacterial and antiviral effect. Hydroxytyrosol can be used for the researches of cancer, infection, inflammation, immunology, metabolic, neurological and cardiovascular disease, such as colon cancer, diabetes, Alzheimer's Disease and atherosclerosis.

For research use only. We do not sell to patients.

Hydroxytyrosol

Hydroxytyrosol Chemical Structure

CAS No. : 10597-60-1

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10 mM * 1 mL in DMSO
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Customer Review

Based on 6 publication(s) in Google Scholar

Other Forms of Hydroxytyrosol:

Top Publications Citing Use of Products
  • Biological Activity

  • Purity & Documentation

  • References

  • Customer Review

Description

Hydroxytyrosol (DOPET) is a phenol found in the olive oil. Hydroxytyrosol can alleviate oxidative stress and improve mitochondrial function, thereby exerting neuroprotective effects. Hydroxytyrosol can induce cancer cells apoptosis via inducing ROS production. Hydroxytyrosol shows antibacterial and antiviral effect. Hydroxytyrosol can be used for the researches of cancer, infection, inflammation, immunology, metabolic, neurological and cardiovascular disease, such as colon cancer, diabetes, Alzheimer's Disease and atherosclerosis[1][2][3][4][5][6][7][8].

IC50 & Target

Microbial Metabolite

 

Cellular Effect
Cell Line Type Value Description References
DG-75 IC50
58 μg/mL
Compound: 2, HT
Cytotoxicity against human DG75 cells after 48 hrs by MTT assay
Cytotoxicity against human DG75 cells after 48 hrs by MTT assay
[PMID: 18823782]
HeLa IC50
70 μg/mL
Compound: 2, HT
Cytotoxicity against human HeLa cells after 48 hrs by MTT assay
Cytotoxicity against human HeLa cells after 48 hrs by MTT assay
[PMID: 18823782]
MDCK CC50
> 172.11 μM
Compound: 4b
Cytotoxicity against MDCK cells after 72 hrs by MTT assay
Cytotoxicity against MDCK cells after 72 hrs by MTT assay
[PMID: 24803363]
MDCK IC50
17.53 μM
Compound: 4b
Antiviral activity against Influenza A virus (A/Vietnam/1194/2004(H5N1)) infected in MDCK cells assessed as inhibition of viral replication after 2 to 3 days by crystal violet staining-based plaque reduction assay
Antiviral activity against Influenza A virus (A/Vietnam/1194/2004(H5N1)) infected in MDCK cells assessed as inhibition of viral replication after 2 to 3 days by crystal violet staining-based plaque reduction assay
[PMID: 24803363]
MRC5 IC50
> 50 μM
Compound: 2; HT
Cytotoxicity against human MRC5 cells assessed as inhibition of cell proliferation measured after 72 hrs by MTT assay
Cytotoxicity against human MRC5 cells assessed as inhibition of cell proliferation measured after 72 hrs by MTT assay
[PMID: 27155468]
Platelet IC50
27 μM
Compound: Htyr; Hydroxytyrosol
Inhibition of ADP-induced platelet aggregation in human platelet rich plasma preincubated for 10 mins
Inhibition of ADP-induced platelet aggregation in human platelet rich plasma preincubated for 10 mins
[PMID: 26225717]
Platelet IC50
67 μM
Compound: Htyr; Hydroxytyrosol
Inhibition of collagen-induced platelet aggregation in human platelet rich plasma preincubated for 10 mins
Inhibition of collagen-induced platelet aggregation in human platelet rich plasma preincubated for 10 mins
[PMID: 26225717]
SK-BR-3 IC50
201.1 μM
Compound: Hydroxytyrosol
Antiproliferative activity against human SKBR3 cells after 72 hrs by MTT reduction assay
Antiproliferative activity against human SKBR3 cells after 72 hrs by MTT reduction assay
[PMID: 28551177]
In Vitro

Hydroxytyrosol inhibits cells proliferation and inhibits LPS (HY-D1056)-induced TNF-a, IL-1b, IL-6 and IL-17 secretion in splenocytes and peritoneal macrophages from SLE mice[4].
Hydroxytyrosol (100 μg/mL) inhibits Staphylococcus aureus with the highest Zone of inhibition of 30 mm, and Staphylococcus epidermidis of 25 mm[5].
Hydroxytyrosol shows MIC of 3.125 μg/mL against Staphylococcus aureus[5].
Hydroxytyrosol (50-200 μg/mL, 24-48 h) inhibits proliferation, decreases mitochondrial membrane potential and induces apoptosis and ROS production in DLD1 cells[7].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Cell Proliferation Assay[7]

Cell Line: DLD1 cells
Concentration: 50, 100 and 200 μg/mL
Incubation Time:
Result: Inhibited the growth of DLD1 cells in a concentration and time-dependent manner.
In Vivo

Hydroxytyrosol (20-40 mg/kg, i.g., daily for 10 days) inhibits inflammation and increases survival rate in LPS (HY-D1056)-mediated septic mice[1].
Hydroxytyrosol (10 mg/kg, p.o., daily for 10 weeks) increases atherosclerotic lesion in Apo E deficient mice with low cholesterol-diet[2].
Hydroxytyrosol (5 mg/kg, i.g., daily for 6 months) improves cognitive function in APP/PS1 mice[3].
Hydroxytyrosol (0.4 mg, p.o., daily for 6 months) prevents Pristine (HY-N7819)-induced systemic lupus erythematous (SLE) in mice[4].
Hydroxytyrosol (1-10 mg/kg, p.o., daily for 2 months) shows neuroprotective effect in diabetic rats[6].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Animal Model: LPS (HY-D1056) )-mediated septic mice models[1]
Dosage: 20 and 40 mg/kg
Administration: Orally gavage, daily for 10 days
Result: Increased survival rate.
Inhibited the incidence of oxidative damage in splenic tissue.
Decreased total leukocytes count, C-reactive protein, monocyte chemoattractant protein-1, and myeloperoxidase levels.
Suppressed the production levels of tumor necrosis factor-a, interleukin-1b, and interleukin-6.
Increased mRNA expression of inducible nitric oxide synthase and nitric oxide production.
Animal Model: APP/PS1 mice[3]
Dosage: 5 mg/kg
Administration: Orally gavage, daily for 6 months
Result: Decreased levels of brain inflammatory markers.
Ameliorated mitochondrial dysfunction.
Reduced mitochondrial carbonyl protein.
Enhanced SOD-2 expression.
Reversed the phase 2 enzyme system.
Had no effects on brain Aβ accumulation.
Animal Model: Pristane-induced systemic lupus erythematous mice[4]
Dosage: 0.4 mg
Administration: Orally administration, daily for 6 months
Result: Reduced paw swelling.
Showed a slightly reduction of spleen and thymus.
Animal Model: Diabetic rats[6]
Dosage: 1, 5 and 10 mg/kg
Administration: Orally administration, daily for 2 months
Result: Reduced lipid peroxidation and nitrosative stress.
Reduced prostaglandin E2 and interleukin 1ß.
Reduced cell death.
Clinical Trial
Molecular Weight

154.16

Formula

C8H10O3

CAS No.
Appearance

Solid-Liquid Mixture

Color

Light yellow to yellow

SMILES

OC1=CC=C(CCO)C=C1O

Structure Classification
Initial Source
Shipping

Room temperature in continental US; may vary elsewhere.

Storage
Pure form -20°C 3 years
4°C 2 years
In solvent -80°C 6 months
-20°C 1 month
Solvent & Solubility
In Vitro: 

DMSO : 125 mg/mL (810.85 mM; Need ultrasonic; Hygroscopic DMSO has a significant impact on the solubility of product, please use newly opened DMSO)

H2O : 100 mg/mL (648.68 mM; Need ultrasonic)

Ethanol : 50 mg/mL (324.34 mM; Need ultrasonic)

Preparing
Stock Solutions
Concentration Solvent Mass 1 mg 5 mg 10 mg
1 mM 6.4868 mL 32.4338 mL 64.8677 mL
5 mM 1.2974 mL 6.4868 mL 12.9735 mL
View the 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, 6 months; -20°C, 1 month. When stored at -80°C, please use it within 6 months. When stored at -20°C, please use it within 1 month.

* Note: If you choose water as the stock solution, please dilute it to the working solution, then filter and sterilize it with a 0.22 μm filter before use.

  • Molarity Calculator

  • Dilution Calculator

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

Mass
=
Concentration
×
Volume
×
Molecular Weight *

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

This equation is commonly abbreviated as: C1V1 = C2V2

Concentration (start)

C1

×
Volume (start)

V1

=
Concentration (final)

C2

×
Volume (final)

V2

In Vivo:

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.

  • Protocol 1

    Add each solvent one by one:  10% DMSO    40% PEG300    5% Tween-80    45% Saline

    Solubility: ≥ 2.08 mg/mL (13.49 mM); Clear solution

    This protocol yields a clear solution of ≥ 2.08 mg/mL (saturation unknown).

    Taking 1 mL working solution as an example, add 100 μL DMSO stock solution (20.8 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.
  • Protocol 2

    Add each solvent one by one:  10% DMSO    90% (20% SBE-β-CD in Saline)

    Solubility: ≥ 2.08 mg/mL (13.49 mM); Clear solution

    This protocol yields a clear solution of ≥ 2.08 mg/mL (saturation unknown).

    Taking 1 mL working solution as an example, add 100 μL DMSO stock solution (20.8 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.
In Vivo Dissolution Calculator
Please enter the basic information of animal experiments:

Dosage

mg/kg

Animal weight
(per animal)

g

Dosing volume
(per animal)

μL

Number of animals

Recommended: Prepare an additional quantity of animals to account for potential losses during experiments.
Calculation results:
Working solution concentration: mg/mL
This product has good water solubility, please refer to the measured solubility data in water/PBS/Saline for details.
The concentration of the stock solution you require exceeds the measured solubility. The following solution is for reference only.If necessary, please contact MedChemExpress (MCE).
Purity & Documentation

Purity: 99.60%

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, 6 months; -20°C, 1 month. When stored at -80°C, please use it within 6 months. When stored at -20°C, please use it within 1 month.

Optional Solvent Concentration Solvent Mass 1 mg 5 mg 10 mg 25 mg
Ethanol / H2O / DMSO 1 mM 6.4868 mL 32.4338 mL 64.8677 mL 162.1692 mL
5 mM 1.2974 mL 6.4868 mL 12.9735 mL 32.4338 mL
10 mM 0.6487 mL 3.2434 mL 6.4868 mL 16.2169 mL
15 mM 0.4325 mL 2.1623 mL 4.3245 mL 10.8113 mL
20 mM 0.3243 mL 1.6217 mL 3.2434 mL 8.1085 mL
25 mM 0.2595 mL 1.2974 mL 2.5947 mL 6.4868 mL
30 mM 0.2162 mL 1.0811 mL 2.1623 mL 5.4056 mL
40 mM 0.1622 mL 0.8108 mL 1.6217 mL 4.0542 mL
50 mM 0.1297 mL 0.6487 mL 1.2974 mL 3.2434 mL
60 mM 0.1081 mL 0.5406 mL 1.0811 mL 2.7028 mL
80 mM 0.0811 mL 0.4054 mL 0.8108 mL 2.0271 mL
100 mM 0.0649 mL 0.3243 mL 0.6487 mL 1.6217 mL

* Note: If you choose water as the stock solution, please dilute it to the working solution, then filter and sterilize it with a 0.22 μm filter before use.

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    Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

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Hydroxytyrosol
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