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Glycyrrhizin

Actions Biologically active constituent in the sweet root of Glycyrrhiza species (licorice) . Antiviral. Packaging 25,100 g in poly bottle (In Vitro) :Glycyrrhizic acid shows a series of anti-cancer-related pharmacological activities, such as broad-spectrum anti-cancer ability, resistance to the tissue toxicity caused by chemotherapy and radiation, drug absorption enhancing effects and anti-multidrug resistance (MDR) mechanisms, as a carrier material in drug delivery systems.In intestinal NCI-H716 cells that secretes GLP-1, Glycyrrhizic acid promotes GLP-1 secretion with a marked elevation of calcium levels. Glycyrrhizic acid can enhance GLP-1 secretion through TGR5 activation.Glycyrrhizic acid can form a stable transparent low-molecular-weight hydrogels (LMWHs) at 37°C in physiological phosphate buffered saline (PBS) with nanoclusters as the microstructures. (In Vivo) :In type 1-like diabetic rats induced by streptozotocin (STZ-treated rats), Glycyrrhizic acid increases the level of plasma GLP-1, which is blocked by triamterene at a dose sufficient to inhibit Takeda G-protein-coupled receptor 5 (TGR5) . Glycyrrhizic acid (Glycyrrhizic acid; 50 mg/kg, i.p.) significantly decreases the levels of TgAb, HMGB1, TNF-α, IL-6, IL-1β in mice.

Product Specifications

CAS Number

1405-86-3

Product Name Alternative

Glycyrrhizic Acid

Purity

>98% (HPLC)

Solubility

Ethanol: 165 mg/mL (200.5 mM) ; Water: 20 mg/mL (24.3 mM) ; DMSO: 117 mg/mL (142.17 mM)

Smiles

O[C@@H] ([C@@H] ([C@@H] (C (O) =O) O1) O) [C@@H] (O[C@H]2[C@@H] ([C@H] ([C@@H] ([C@@H] (C (O) =O) O2) O) O) O) [C@H]1O[C@@H] (C (C) ([C@] (CC[C@@] ([C@@]3 (CC[C@]4 (CC[C@] (C[C@]4 (C3=C5) [H]) (C (O) =O) C) C) C) 6C) 7[H]) C) CC[C@]7 (C) [C@@]6 ([H]) C5=O

Molecular Formula

C42H62O16

Molecular Weight

822.93

Storage Conditions

Storage temperature: -20°C. Stability: ≥ 2 years

Notes

For research use only.

Other Product Names

(2S,3S,4S,5R,6R) -6- (((2S,3R,4S,5S,6S) -6-carboxy-2- (((3R,4aR,6aR,6bS,8aS,11R,12aR,14aR,14bS) -11-carboxy-4,4,6a,6b,8a,11,14b-heptamethyl-14-oxo-1,2,3,4,4a,5,6,6a,6b,7,8,8a,9,10,11,12,12a,14,14a,14b-icosahydropicen-3-yl) oxy) -4,5-dihydroxytetrahydro-2H-pyran-3-yl) oxy) -3,4,5-trihydroxytetrahydro-2H-pyran-2-carboxylic acid

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