β-Glucogallin


CAS No. : 13405-60-2

(Synonyms: Glucogallin; 1-O-Galloyl-β-D-glucose)

13405-60-2
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Cat. No. : HY-133708
M.Wt: 332.26
Formula: C13H16O10
Purity: >98 %
Solubility: DMSO : 100 mg/mL (ultrasonic);H2O : 6.25 mg/mL (ultrasonic)
Introduction of 13405-60-2 :

β-Glucogallin is an orally active and selective aldose reductase (AKR1B1) inhibitor with an IC50 value of 58 μM when using Glyceraldehyde (HY-128748) as AKR1B1 substrate. β-Glucogallin reduces ROS, PDGF, RAGE, and NF-κB. β-Glucogallin increases SOD. β-Glucogallin has antioxidant and hepatoprotective effects. β-Glucogallin can be used in retinal research[1][2][3][4][5]. IC50 & Target:IC50: 58 μM (AKR1B1) when using Glyceraldehyde (HY-128748) as AKR1B1 substrate In Vitro: β-Glucogallin (100 μM; 2 h) can reduce Methylglyoxal-induced oxidative stress in human retinal epithelial cells ARPE-19, decreasing intracellular ROS levels[1].
β-Glucoside inhibits AKR1B1 with Glyceraldehyde (HY-128748) as substrate, with an IC50 value of 58 μM[2].
β-Glucogallin (30 μM; 72 h) can inhibit sorbitol accumulation under hyperglycemic conditions in a transgenic mouse lens organ culture model, with an inhibition rate of 73%[2].
β-Glucogallin can inhibit the activity of AKR1B1 and prevent Sorbitol (HY-B0400) accumulation in RAW264.7 murine macrophage cells, with an inhibition rate of approximately 50%[3].
In Vivo: β-Glucogallin (300-1200 mg/kg; p.o.; once daily; 10 days) improves Carbon tetrachloride (HY-Y0298)-induced hepatotoxicity in female Wistar rats[4].

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