2. GPCR/G Protein Metabolic Enzyme/Protease
  3. EBI2/GPR183 Endogenous Metabolite
  4. 7α,25-Dihydroxycholesterol

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

Cat. No.: HY-113962 Purity: 98.68%
SDS COA Handling Instructions

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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.

7α,25-Dihydroxycholesterol Chemical Structure

7α,25-Dihydroxycholesterol Chemical Structure

CAS No. : 64907-22-8

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1 mg USD 55 In-stock
5 mg USD 250 In-stock
10 mg USD 480 In-stock
25 mg USD 1060 In-stock
50 mg USD 1850 In-stock
100 mg USD 3250 In-stock
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Based on 1 publication(s) in Google Scholar

Other Forms of 7α,25-Dihydroxycholesterol:

7α,25-Dihydroxycholesterol Related Antibodies

Top Publications Citing Use of Products

1 Publications Citing Use of MCE 7α,25-Dihydroxycholesterol

  • 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.

7α,25-Dihydroxycholesterol Related Antibodies
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

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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:

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

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: ≥99.0%

SDS (252 KB)

COA (249 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, 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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7α,25-Dihydroxycholesterol Related Classifications

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.

Keywords:

7α,25-Dihydroxycholesterol64907-22-87α,25-OHCEBI2/GPR183Endogenous MetaboliteendogenousligandGPCRreceptorBcellsTimmuneresponsemigrationoxysterolsInhibitorinhibitorinhibit

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