Glabridin

Catalog No.S3786 Batch:S378601

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Technical Data

Formula

C20H20O4

Molecular Weight 324.37 CAS No. 59870-68-7
Solubility (25°C)* In vitro DMSO 64 mg/mL (197.3 mM)
* <1 mg/ml means slightly soluble or insoluble.
* Please note that Selleck tests the solubility of all compounds in-house, and the actual solubility may differ slightly from published values. This is normal and is due to slight batch-to-batch variations.
* Room temperature shipping (Stability testing shows this product can be shipped without any cooling measures.)

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Biological Activity

Description Glabridin (Q-100692, KB-289522, LS-176045), one of the active phytochemicals in licorice extract, binds to and activates the ligand binding domain of PPARγ, as well as the full length receptor. It is also a GABAA receptor positive modulator promoting fatty acid oxidation and improving learning and memory.
Targets
PPARγ [1]
(Cell-free assay)
α1β2γ2 (GABAA receptor) [3] α1β3γ2 (GABAA receptor) [3] α1β2 (GABAA receptor) [3] α1β1γ2 (GABAA receptor) [3]
6.3 μM(EC50) 6.83 μM(EC50) 9.63 μM(EC50) 17.23 μM(EC50)
In vitro Glabridin induces dose-dependent increase in estrogenic activity and cell proliferation in Ishikawa cells. Glabridin exerts estrogenic activity via the ER-α-SRC-1-co-activator complex[1]. Glabridin has substantial neuroprotective effects, as indicated by the reduced cell death, apoptosis, DNA fragmentation, probably through the regulation of bcl-2, Bax and caspase-3 which are all closely related to cell apoptotic process[2].
In vivo Glabridin at 25mg/kg by intraperitoneal injection, but not at 5mg/kg, significantly decreases the focal infarct volume, cerebral histological damage and apoptosis in MCAO rats compared to sham-operated rats. Glabridin significantly attenuates the level of brain malonyldialdehyde (MDA) in MCAO rats, while it elevates the level of two endogenous antioxidants in the brain, i.e. superoxide dismutase (SOD) and reduced glutathione (GSH). Co-treatment with glabridin significantly inhibits the staurosporine-induced cytotoxicity and apoptosis of cultured rat cortical neurons in a concentration-dependent manner. Consistently, glabridin significantly reduces the DNA laddering caused by staurosporine in a concentration-dependent manner. Glabridin has a neuroprotective effect via modulation of multiple pathways associated with apoptosis. Glabridin appears to achieve steady state concentrations slowly in humans. The limited penetration of glabridin into the brain due to the activity of P-glycoprotein in the blood-brain barrier may also lessen the activity of glabridin at low doses[2].

Protocol (from reference)

Cell Assay:[1]
  • Cell lines

    Ishikawa cells

  • Concentrations

    1nM to 10μM

  • Incubation Time

    72 h

  • Method

    The effect of the extracts on cell proliferation are estimated using MTT assay. Briefly, 10μL of 5 mg/ml MTT is added to each well after incubation with test compounds for 72 h. DMSO is then added to dissolve the formazan and the plate read at 595 nm. The cell proliferation of control cells is 100.00% and any increase or decrease in cell proliferation of treated cells is compared to the control cells. All experimental conditions are assayed in triplicate.

Animal Study:[2]
  • Animal Models

    Male healthy Sprague-Dawley rats

  • Dosages

    5 mg/kg and 25 mg/kg

  • Administration

    i.p.

Selleck's Glabridin has been cited by 1 publication

Glabridin inhibits osteoarthritis development by protecting chondrocytes against oxidative stress, apoptosis and promoting mTOR mediated autophagy [ Life Sci, 2021, S0024-3205(20)31752-5] PubMed: 33417956

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SHIPPING AND STORAGE
Selleck products are transported at room temperature. If you receive the product at room temperature, please rest assured, the Selleck Quality Inspection Department has conducted experiments to verify that the normal temperature placement of one month will not affect the biological activity of powder products. After collecting, please store the product according to the requirements described in the datasheet. Most Selleck products are stable under the recommended conditions.

NOT FOR HUMAN, VETERINARY DIAGNOSTIC OR THERAPEUTIC USE.