1. Epigenetics PI3K/Akt/mTOR Protein Tyrosine Kinase/RTK NF-κB Metabolic Enzyme/Protease
  2. AMPK VEGFR PI3K Akt NF-κB Cytochrome P450
  3. Alizarin

Alizarin is a natural dye. Alizarin can be extracted from the roots of madder plant. Alizarin activates AMPK and VEGFR2/eNOS pathway. Alizarin regulates PI3K/Akt and inhibits NF-κB pathway. Alizarin enhances CYP1A1 enzyme activity. Alizarin has protective effects on hypertension and vascular endothelial dysfunction. Alizarin has anti-tumor activity against multiple cancers including pancreatic cancer, breast cancer, osteosarcoma and liver cancer. Alizarin has been widely used as a pigment in textile fabrics and paintings.

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

Alizarin

Alizarin Chemical Structure

CAS No. : 72-48-0

Size Price Stock Quantity
Solid + Solvent (Highly Recommended)
10 mM * 1 mL in DMSO
ready for reconstitution
In-stock
Solution
10 mM * 1 mL in DMSO In-stock
Solid
500 mg In-stock
1 g In-stock
5 g In-stock
10 g   Get quote  
50 g   Get quote  

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This product is a controlled substance and not for sale in your territory.

Customer Review

Based on 1 publication(s) in Google Scholar

Other Forms of Alizarin:

Top Publications Citing Use of Products

1 Publications Citing Use of MCE Alizarin

  • Biological Activity

  • Purity & Documentation

  • References

  • Customer Review

Description

Alizarin is a natural dye. Alizarin can be extracted from the roots of madder plant. Alizarin activates AMPK and VEGFR2/eNOS pathway. Alizarin regulates PI3K/Akt and inhibits NF-κB pathway. Alizarin enhances CYP1A1 enzyme activity. Alizarin has protective effects on hypertension and vascular endothelial dysfunction. Alizarin has anti-tumor activity against multiple cancers including pancreatic cancer, breast cancer, osteosarcoma and liver cancer. Alizarin has been widely used as a pigment in textile fabrics and paintings[1][2][3][4][5][6][7].

Cellular Effect
Cell Line Type Value Description References
A549 IC50
> 50 μM
Compound: Alizarin
Cytotoxicity against human A549 cells after 48 hrs by MTT assay
Cytotoxicity against human A549 cells after 48 hrs by MTT assay
[PMID: 24953029]
CNE IC50
> 100 μM
Compound: Alizarin
Cytotoxicity against human CNE cells after 48 hrs by MTT assay
Cytotoxicity against human CNE cells after 48 hrs by MTT assay
[PMID: 24953029]
HCT-116 IC50
> 50 μM
Compound: Alizarin
Cytotoxicity against human HCT116 cells after 48 hrs by MTT assay
Cytotoxicity against human HCT116 cells after 48 hrs by MTT assay
[PMID: 24953029]
HUVEC IC50
> 50 μM
Compound: Alizarin
Cytotoxicity against HUVEC after 48 hrs by MTT assay
Cytotoxicity against HUVEC after 48 hrs by MTT assay
[PMID: 24953029]
HeLa IC50
> 100 μM
Compound: Alizarin
Cytotoxicity against human HeLa cells after 48 hrs by MTT assay
Cytotoxicity against human HeLa cells after 48 hrs by MTT assay
[PMID: 24953029]
HepG2 IC50
> 50 μM
Compound: Alizarin
Cytotoxicity against human HepG2 cells after 48 hrs by MTT assay
Cytotoxicity against human HepG2 cells after 48 hrs by MTT assay
[PMID: 24953029]
KB IC50
15.65 μM
Compound: Alizarin
Cytotoxicity against human KB cells after 48 hrs by MTT assay
Cytotoxicity against human KB cells after 48 hrs by MTT assay
[PMID: 24953029]
KG-1a EC50
60.2 μM
Compound: 2
Antiproliferative activity against human KG-1a cells assessed as decrease in cell viability incubated for 72 hrs by trypan blue exclusion assay
Antiproliferative activity against human KG-1a cells assessed as decrease in cell viability incubated for 72 hrs by trypan blue exclusion assay
[PMID: 36215859]
MGC-803 IC50
39.35 μM
Compound: Alizarin
Cytotoxicity against human MGC803 cells after 48 hrs by MTT assay
Cytotoxicity against human MGC803 cells after 48 hrs by MTT assay
[PMID: 24953029]
NCI-H460 IC50
> 50 μM
Compound: Alizarin
Cytotoxicity against human NCI-H460 cells after 48 hrs by MTT assay
Cytotoxicity against human NCI-H460 cells after 48 hrs by MTT assay
[PMID: 24953029]
In Vitro

Alizarin (5-80 μM, 24-72 h) inhibits the growth of pancreatic cancer cells by abrogating NF-κB activation[1].
Alizarin (0.01-200 μM, 48 h) enhances CYP1A1 enzyme activity and induces transcriptional changes in hepatoma cells HepG2[2].
Alizarin (5-50  µg/mL, 24-144 h) strongly inhibits the osteosarcoma (IC50 for Saos-2, MG-63, and U-2OS cells, 27.5, 29.0, and 69.9 µg/ml, respectively) and breast carcinoma (IC50 for MDA-MB-231 cells, 62.1 µg/mL) cell proliferation[3].

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

Cell Viability Assay[3]

Cell Line: Saos-2, MG-63, and U-2 OS
Concentration: 5, 10, 25, 50 µg/mL
Incubation Time: 24, 48, 72, and 144 h
Result: Induced a dose-dependent inhibition of cell growth over time in osteosarcoma and breast cancer cell lines.
Showed lower effect in respect with the two osteosarcoma cell lines MG-63 and Saos-2 at the higher concentration.
In Vivo

Alizarin (24-96 mg/kg, 10 days) increase glucose uptake through PI3K/Akt signaling and improve Alloxan (HY-W017227)-induced diabetic mice[4].
Alizarin (100 mg/kg/d, p.o., 6 weeks) shows antihypertensive effect in SHR by activating VEGFR2/eNOS pathway, attenuating oxidative stress-induced mitochondrial damage and premature senescence[5].
Alizarin (10 mg/kg, p.o., 4 weeks) shows protective effect on vascular endothelial dysfunction in rats via inhibiting the type 2 diabetes-induced synthesis of THBS1 and activating the AMPK signaling pathway[6].

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

Animal Model: Male spontaneously hypertensive rat (SHR) (200-300 g)[5]
Dosage: 100 mg/kg
Administration: Oral gavage (p.o.), 6 weeks
Result: Reduced blood pressure in SHR, attenuated thoracic aortic injury, and increased endothelial dependent relaxation (EDR) in aortic rings.
Elevated activity and phosphorylation level of VEGFR2 and eNOS.
Attenuated endothelial dysfunction caused by hypertension through suppressing oxidative stress.
Ameliorated oxidative stress-induced mitochondrial damage.
Clinical Trial
Molecular Weight

240.21

Formula

C14H8O4

CAS No.
Appearance

Solid

Color

Orange to reddish brown

SMILES

O=C1C2=C(C=CC=C2)C(C3=CC=C(O)C(O)=C13)=O

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 6 months
-20°C 1 month
Solvent & Solubility
In Vitro: 

DMSO : 25 mg/mL (104.08 mM; Need ultrasonic; Hygroscopic DMSO has a significant impact on the solubility of product, please use newly opened DMSO)

H2O : < 0.1 mg/mL (insoluble)

Preparing
Stock Solutions
Concentration Solvent Mass 1 mg 5 mg 10 mg
1 mM 4.1630 mL 20.8151 mL 41.6302 mL
5 mM 0.8326 mL 4.1630 mL 8.3260 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.

  • Molarity Calculator

  • Dilution Calculator

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

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Molecular Weight *

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

This equation is commonly abbreviated as: C1V1 = C2V2

Concentration (start)

C1

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Volume (start)

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C2

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V2

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
Purity & Documentation

Purity: 99.48%

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
DMSO 1 mM 4.1630 mL 20.8151 mL 41.6302 mL 104.0756 mL
5 mM 0.8326 mL 4.1630 mL 8.3260 mL 20.8151 mL
10 mM 0.4163 mL 2.0815 mL 4.1630 mL 10.4076 mL
15 mM 0.2775 mL 1.3877 mL 2.7753 mL 6.9384 mL
20 mM 0.2082 mL 1.0408 mL 2.0815 mL 5.2038 mL
25 mM 0.1665 mL 0.8326 mL 1.6652 mL 4.1630 mL
30 mM 0.1388 mL 0.6938 mL 1.3877 mL 3.4692 mL
40 mM 0.1041 mL 0.5204 mL 1.0408 mL 2.6019 mL
50 mM 0.0833 mL 0.4163 mL 0.8326 mL 2.0815 mL
60 mM 0.0694 mL 0.3469 mL 0.6938 mL 1.7346 mL
80 mM 0.0520 mL 0.2602 mL 0.5204 mL 1.3009 mL
100 mM 0.0416 mL 0.2082 mL 0.4163 mL 1.0408 mL
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Help & FAQs
  • Do most proteins show cross-species activity?

    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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Product Name:
Alizarin
Cat. No.:
HY-N0563
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