1. GPCR/G Protein Metabolic Enzyme/Protease
  2. EBI2/GPR183 Endogenous Metabolite
  3. 7α,25-Dihydroxycholesterol

7α,25-Dihydroxycholesterol  (Synonyms: 7α,25-OHC)

Cat. No.: HY-113962 Purity: 99.88%
Handling Instructions Technical Support

7α, 25-dihydroxycholesterol (7α,25-OHC) is a potent and selective agonist and endogenous ligand of the orphan GPCR receptor EBI2 (GPR183). 7α, 25-dihydroxycholesterol is highly potent at activating EBI2 (EC50=140 pM; Kd=450 pM). 7α, 25-dihydroxycholesterol can serve as a chemokine directing migration of B cells, T cells and dendritic cells.

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

CAS No. : 64907-22-8

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
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Customer Review

Based on 3 publication(s) in Google Scholar

Other Forms of 7α,25-Dihydroxycholesterol:

Top Publications Citing Use of Products
Cell Proliferation/Viability Assay
Flow Cytometry
Cell Migration/Invasion Assay
WB

    7α,25-Dihydroxycholesterol purchased from MedChemExpress. Usage Cited in: Clin Exp Metastasis. 2025 Aug 4;42(5):44.  [Abstract]

    A549 and PC-9 cells were treated with 5 µM 7α,25-Dihydroxycholesterol (7α,25-OHC) for 24 h and/or 10 µM GSK682753A for 24 h and then examined for cell phenotypes. Cell viability was assessed using CCK-8 assays at 24-, 48-, and 72-hour after treatment.

    7α,25-Dihydroxycholesterol purchased from MedChemExpress. Usage Cited in: Clin Exp Metastasis. 2025 Aug 4;42(5):44.  [Abstract]

    A549 and PC-9 cells were treated with 5 µM 7α,25-Dihydroxycholesterol (7α,25-OHC) for 24 h and/or 10 µM GSK682753A for 24 h and then examined for cell phenotypes. Cell apoptosis was quantified by flow cytometry using Annexin V-FITC/PI staining.

    7α,25-Dihydroxycholesterol purchased from MedChemExpress. Usage Cited in: Clin Exp Metastasis. 2025 Aug 4;42(5):44.  [Abstract]

    A549 and PC-9 cells were treated with 5 µM 7α,25-Dihydroxycholesterol (7α,25-OHC) for 24 h and/or 10 µM GSK682753A for 24 h and then examined for cell phenotypes. Transwell migration assays were used to quantify cell migration at 24 hours.

    7α,25-Dihydroxycholesterol purchased from MedChemExpress. Usage Cited in: Clin Exp Metastasis. 2025 Aug 4;42(5):44.  [Abstract]

    A549 cells were treated with 5 µM 7α,25-Dihydroxycholesterol (7α,25-OHC) for 24 h and/or 10 µM GSK682753A for 24 h and then examined for cell phenotypes. The protein levels of ERK and Akt pathways related proteins, including phosphorylated ERK1/2, total ERK1/2, phosphorylated Akt and total Akt, were analyzed by Immunoblotting.

    7α,25-Dihydroxycholesterol purchased from MedChemExpress. Usage Cited in: Cell Metab. 2023 Nov 7;35(11):1915-1930.e8.  [Abstract]

    Transwell migration of CD7+ and CD7− monocytes transfected with si-Scramble or si-Gpr183 to 7α,25-Dihydroxycholesterol (7α,25-OHC).

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    • Biological Activity

    • Purity & Documentation

    • References

    • Customer Review

    Description

    7α, 25-dihydroxycholesterol (7α,25-OHC) is a potent and selective agonist and endogenous ligand of the orphan GPCR receptor EBI2 (GPR183). 7α, 25-dihydroxycholesterol is highly potent at activating EBI2 (EC50=140 pM; Kd=450 pM). 7α, 25-dihydroxycholesterol can serve as a chemokine directing migration of B cells, T cells and dendritic cells[1][2].

    IC50 & Target[1]

    Human Endogenous Metabolite

     

    In Vitro

    In vitro, 7α, 25-dihydroxycholesterol (7α,25-OHC) stimulates the migration of EBI2-expressing mouse B and T cells with half-maximum effective concentration values around 500 pM, but had no effect on EBI2-deficient cells[1].

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

    In Vivo

    EBI2-deficient B cells or normal B cells desensitized by 7α,25-Dihydroxycholesterol (1 μM; 1.5 hours) pre-treatment shows reduced homing to follicular areas of the spleen[1].

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

    Molecular Weight

    418.65

    Formula

    C27H46O3

    CAS No.
    Appearance

    Solid

    Color

    White to off-white

    SMILES

    C[C@@]12[C@](CC[C@]2([H])[C@H](C)CCCC(C)(O)C)([H])[C@@]3([H])[C@]([C@@]4(C(C[C@@H](O)CC4)=C[C@H]3O)C)([H])CC1

    Structure Classification
    Initial Source
    Shipping

    Room temperature in continental US; may vary elsewhere.

    Storage
    Powder -20°C 3 years
    In solvent -80°C 6 months
    -20°C 1 month
    Solvent & Solubility
    In Vitro: 

    DMSO : 4.55 mg/mL (10.87 mM; Need ultrasonic; Hygroscopic DMSO has a significant impact on the solubility of product, please use newly opened DMSO)

    Ethanol : < 1 mg/mL (insoluble)

    Preparing
    Stock Solutions
    Concentration Solvent Mass 1 mg 5 mg 10 mg
    1 mM 2.3886 mL 11.9432 mL 23.8863 mL
    5 mM 0.4777 mL 2.3886 mL 4.7773 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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    Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

    This equation is commonly abbreviated as: C1V1 = C2V2

    Concentration (start)

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    In Vivo:

    For the following dissolution methods, please prepare the working solution directly. It is recommended to prepare fresh solutions and use them promptly within a short period of time.
    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:  15% Cremophor EL    85% Saline

      Solubility: 5 mg/mL (11.94 mM); Suspended solution; Need ultrasonic

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

    Dosage

    mg/kg

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    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: 99.88%

    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 2.3886 mL 11.9432 mL 23.8863 mL 59.7158 mL
    5 mM 0.4777 mL 2.3886 mL 4.7773 mL 11.9432 mL
    10 mM 0.2389 mL 1.1943 mL 2.3886 mL 5.9716 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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    Inquiry Information

    Product Name:
    7α,25-Dihydroxycholesterol
    Cat. No.:
    HY-113962
    Quantity:
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