1. Apoptosis NF-κB Metabolic Enzyme/Protease Immunology/Inflammation Autophagy
  2. Apoptosis Reactive Oxygen Species Autophagy
  3. Daucosterol

Daucosterol  (Synonyms: Eleutheroside A; β-Sitosterol β-D-glucoside)

Cat. No.: HY-N0410 Purity: 93.98%
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Daucosterol is an orally active natural sterol compound, which has anti-inflammatory, anticancer and immunomodulatory activities. Daucosterol inhibits cancer cell proliferation by inducing autophagy through ROS-dependent manner. Daucosterol also inhibits colon cancer growth by inducing apoptosis, inhibiting cell migration and invasion and targeting caspase signalling pathway.

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

Daucosterol Chemical Structure

Daucosterol Chemical Structure

CAS No. : 474-58-8

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Customer Review

Based on 6 publication(s) in Google Scholar

Top Publications Citing Use of Products

    Daucosterol purchased from MedChemExpress. Usage Cited in: Eur J Pharmacol. 2019 Jul 15;855:112-123.  [Abstract]

    Western blot analysis of p53 expression and phosphorylation in DS treated A549 cells with the indicated concentrations after 72 h incubation. DS up-regulates p53 expression and phosphorylation which resulted in activation of downstream regulator p21.
    • Biological Activity

    • Purity & Documentation

    • References

    • Customer Review

    Description

    Daucosterol is an orally active natural sterol compound, which has anti-inflammatory, anticancer and immunomodulatory activities. Daucosterol inhibits cancer cell proliferation by inducing autophagy through ROS-dependent manner. Daucosterol also inhibits colon cancer growth by inducing apoptosis, inhibiting cell migration and invasion and targeting caspase signalling pathway[1][2][3].

    Cellular Effect
    Cell Line Type Value Description References
    A2780 IC50
    > 10 μg/mL
    Compound: page 1629, R26C1
    Cytotoxicity against human A2780 cells after 96 hrs by MTT assay
    Cytotoxicity against human A2780 cells after 96 hrs by MTT assay
    [PMID: 17125236]
    A549 IC50
    > 10 μg/mL
    Compound: page 1629, R26C1
    Cytotoxicity against human A549 cells after 96 hrs by MTT assay
    Cytotoxicity against human A549 cells after 96 hrs by MTT assay
    [PMID: 17125236]
    A549 IC50
    > 20 μg/mL
    Compound: 10
    Cytotoxicity against human A549 cells by MTT assay
    Cytotoxicity against human A549 cells by MTT assay
    [PMID: 22413887]
    A549 GI50
    35.5 μM
    Compound: 6
    Growth inhibition of human A549 cells by MTT assay
    Growth inhibition of human A549 cells by MTT assay
    [PMID: 20153184]
    A549 ED50
    4.73 μg/mL
    Compound: beta-sitosterol-beta-D-glucopyranoside
    Cytotoxicity against human A549 cells after 7 days
    Cytotoxicity against human A549 cells after 7 days
    [PMID: 1453182]
    Bel-7402 IC50
    > 10 μg/mL
    Compound: page 1629, R26C1
    Cytotoxicity against human Bel-7402 cells after 96 hrs by MTT assay
    Cytotoxicity against human Bel-7402 cells after 96 hrs by MTT assay
    [PMID: 17125236]
    BGC-823 IC50
    > 10 μg/mL
    Compound: page 1629, R26C1
    Cytotoxicity against human BGC-823 cells after 96 hrs by MTT assay
    Cytotoxicity against human BGC-823 cells after 96 hrs by MTT assay
    [PMID: 17125236]
    Ca9-22 IC50
    > 20 μg/mL
    Compound: 10
    Cytotoxicity against human Ca9-22 cells by MTT assay
    Cytotoxicity against human Ca9-22 cells by MTT assay
    [PMID: 22413887]
    HCT-8 IC50
    > 10 μg/mL
    Compound: page 1629, R26C1
    Cytotoxicity against human HCT8 cells after 96 hrs by MTT assay
    Cytotoxicity against human HCT8 cells after 96 hrs by MTT assay
    [PMID: 17125236]
    Hep 3B2 IC50
    > 20 μg/mL
    Compound: 10
    Cytotoxicity against human Hep3B cells by MTT assay
    Cytotoxicity against human Hep3B cells by MTT assay
    [PMID: 22413887]
    HepG2 IC50
    > 20 μg/mL
    Compound: 10
    Cytotoxicity against human HepG2 cells by MTT assay
    Cytotoxicity against human HepG2 cells by MTT assay
    [PMID: 22413887]
    HL-60 GI50
    50.8 μM
    Compound: 6
    Growth inhibition of human HL60 cells by MTT assay
    Growth inhibition of human HL60 cells by MTT assay
    [PMID: 20153184]
    HT-1080 ED50
    > 100 μM
    Compound: 15
    Antiproliferative activity against human HT1080 cells by MTT assay
    Antiproliferative activity against human HT1080 cells by MTT assay
    [PMID: 11277741]
    HT-29 ED50
    4.44 x 10-1 μg/mL
    Compound: beta-sitosterol-beta-D-glucopyranoside
    Cytotoxicity against human HT-29 cells after 7 days
    Cytotoxicity against human HT-29 cells after 7 days
    [PMID: 1453182]
    HT-29 GI50
    46.8 μM
    Compound: 6
    Growth inhibition of human HT-29 cells by MTT assay
    Growth inhibition of human HT-29 cells by MTT assay
    [PMID: 20153184]
    MCF7 IC50
    > 20 μg/mL
    Compound: 10
    Cytotoxicity against human MCF7 cells by MTT assay
    Cytotoxicity against human MCF7 cells by MTT assay
    [PMID: 22413887]
    MCF7 ED50
    44.39 μg/mL
    Compound: beta-sitosterol-beta-D-glucopyranoside
    Cytotoxicity against human MCF7 cells after 7 days
    Cytotoxicity against human MCF7 cells after 7 days
    [PMID: 1453182]
    MDA-MB-231 IC50
    > 20 μg/mL
    Compound: 10
    Cytotoxicity against human MDA-MB-231 cells by MTT assay
    Cytotoxicity against human MDA-MB-231 cells by MTT assay
    [PMID: 22413887]
    NCI-H460 IC50
    > 50 μM
    Compound: 3
    Cytotoxicity against human NCI-H460 cells incubated for 24 hrs by MTT assay
    Cytotoxicity against human NCI-H460 cells incubated for 24 hrs by MTT assay
    [PMID: 28606759]
    SK-OV-3 GI50
    29.8 μM
    Compound: 6
    Growth inhibition of human SKOV3 cells by MTT assay
    Growth inhibition of human SKOV3 cells by MTT assay
    [PMID: 20153184]
    In Vitro

    Daucosterol (0.01-100 μM, 48 h) inhibits the proliferation of MCF-7, AGS, MGC803 and BGC823 cells in a dose-dependent manner, with IC50s of 19.96 μM, 3.13 μM, 24.19 μM and 16.95 μM, respectively[1].
    Daucosterol (50 μM, 24 h) significantly increases ROS production in MCF-7 and BGC823 cells[1].
    Daucosterol (0-80 μM, 48 h) inhibits proliferation and promotes apoptosis in PC3 and LNCap cells[2].

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

    Western Blot Analysis[2]

    Cell Line: PC3 and LNCap cells
    Concentration: 0-80 μM
    Incubation Time: 48 h
    Result: Increased the expressions of cleaved caspase 3, cleaved caspase 9, Bax protein, LC3II/LC3I ration and Beclin 1.
    Decreased the the expressions of Bax protein and p62.
    In Vivo

    Daucosterol (0.5-2.5 mg/kg, p.o., once per day for 7 days) significantly inhibits the H22 tumor growth in ICR mice inoculated with H22 hepatoma cells[1].

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

    Molecular Weight

    576.85

    Formula

    C35H60O6

    CAS No.
    Appearance

    Solid

    Color

    White to off-white

    SMILES

    C[C@H](CC[C@@H](CC)C(C)C)[C@](CC1)([H])[C@]2(C)[C@]1([H])[C@]([C@]3([H])CC2)([H])CC=C([C@]3(C)CC4)C[C@H]4O[C@@]5([H])[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O5

    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
    In Vitro: 

    DMSO : 3.33 mg/mL (5.77 mM; Need ultrasonic; Hygroscopic DMSO has a significant impact on the solubility of product, please use newly opened DMSO)

    Preparing
    Stock Solutions
    Concentration Solvent Mass 1 mg 5 mg 10 mg
    1 mM 1.7336 mL 8.6678 mL 17.3355 mL
    5 mM 0.3467 mL 1.7336 mL 3.4671 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, 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.

    • Molarity Calculator

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

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    This equation is commonly abbreviated as: C1V1 = C2V2

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    In Vivo Dissolution Calculator
    Please enter the basic information of animal experiments:

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    Purity & Documentation
    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 1.7336 mL 8.6678 mL 17.3355 mL 43.3388 mL
    5 mM 0.3467 mL 1.7336 mL 3.4671 mL 8.6678 mL
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    • 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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