Astilbin – 10 mg

Brand:
Cayman
CAS:
29838-67-3
Storage:
-20
UN-No:
Non-Hazardous - /

Astilbin is a flavonoid that has been found in S. glabra and has diverse biological activities.{48502,48503,48504} It inhibits cisplatin-induced increases in apoptosis and accumulation of reactive oxygen species (ROS) in HEK293 cells when used at a concentration of 200 μM.{48502} Astilbin (50 mg/kg) increases renal glutathione (GSH) levels and superoxide dismutase (SOD) and catalase activity and reduces serum creatinine and blood urea nitrogen (BUN) levels, renal IL-1β, IL-6, and TNF-α levels, apoptosis in kidney tissue, and kidney injury in a mouse model of cisplatin-induced nephrotoxicity. It reduces loss of dopaminergic neurons in the substantia nigra and increases striatal GSH levels and SOD activity in a mouse model of MPTP-induced Parkinson’s disease when administered at a dose of 50 mg/kg per day.{48503} Astilbin also reduces descent time in a pole test and increases traction test score in a mouse model of Parkinson’s disease, indicating reduced motor deficits. It reduces cell viability of MDA-MB-231 and MCF-7 cells (IC50s = 167.9 and 191.6 μM, respectively), as well as inhibits migration and increases apoptosis when used at concentrations of 50 and 200 μM.{48504} Astilbin (20 mg/kg every other day for 14 days) reduces tumor growth in an MCF-7 mouse xenograft model.  

 

Available on backorder

SKU: 28267 - 10 mg Category:

Description

A flavonoid with diverse biological activities; inhibits cisplatin-induced increases in apoptosis and ROS in HEK293 cells at 200 μM; increases renal GSH levels and SOD and catalase activity and reduces serum creatinine and BUN levels, renal IL-1β, IL-6, and TNF-α levels, apoptosis in kidney tissue, and kidney injury in a mouse model of cisplatin-induced nephrotoxicity at 50 mg/kg; reduces loss of dopaminergic neurons in the substantia nigra and increases striatal GSH levels and SOD activity in a mouse model of MPTP-induced Parkinson’s disease at 50 mg/kg per day; reduces motor deficits in a mouse model of Parkinson’s disease; reduces cell viability of MDA-MB-231 and MCF-7 cells (IC50s = 167.9 and 191.6 μM, respectively), as well as inhibits migration and increases apoptosis at 50 and 200 μM; reduces tumor growth in an MCF-7 mouse xenograft model at 20 mg/kg every other day for 14 days


Formal name: (2R,3R)-3-[(6-deoxy-α-L-mannopyranosyl)oxy]-2-(3,4-dihydroxyphenyl)-2,3-dihydro-5,7-dihydroxy-4H-1-benzopyran-4-one

Synonyms:  Taxifolin 3-O-rhamnoside

Molecular weight: 450.4

CAS: 29838-67-3

Purity: ≥98%

Formulation: A crystalline solid