Uses of Licochalcone
A medical and stereoisomer technology, applied in the field of licorice chalcone, can solve the problems of limited use, high price, serious side effects, etc., to increase the level of GSH, reduce the area of liver necrosis, and reduce the level of ALT and AST Effect
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Embodiment 1
[0057] Embodiment 1, the activating effect of licorice chalcone on Nrf2
[0058] In this example, the effect of licorice chalcone on the viability of HepG2 cells and the activity of Nrf2 / ARE reporter gene was investigated.
[0059] 1. Experimental materials and methods
[0060] (1) Glycyrrhizalcone was purchased from Chengdu Mansite Biotechnology Co., Ltd., and its H-NMR and C-NMR spectra were as follows: figure 1 and figure 2 shown. The human liver cancer cell line HepG2 was purchased from the American Type Culture Collection (ATCC), and the cells in the logarithmic growth phase were used in the experiments.
[0061] HepG2 cells were stably transfected with Nrf2 luciferase reporter gene using Lipofectamine 2000 (Life Technologies), and the resulting cells were called HepG2C8 cells. After HepG2C8 cells were seeded in 24-well plates for 12 hours, licochalcone of specified concentration was added respectively, the cells were lysed after 6 hours, the luciferase activity was ...
Embodiment 2
[0066] Example 2, the application of licorice chalcone in the preparation of products that activate Nrf2 and / or AMPK signaling pathways, antioxidant enzyme inducers and anti-aging products
[0067] 1. Experimental materials and methods
[0068] (1) MEFs cells were obtained from C57 mouse embryos at 13.5 days of pregnancy (Mingyu Chen, Experimental Animal Science). After MEFs cells in the logarithmic growth phase were inoculated in 6-well plates for 24 hours, licochalcone of specified concentration was added respectively, and culture was continued for 6 hours or specified time. The supernatant was discarded, and the cells were lysed with TRIZOL buffer (Beijing Quanshijin Biotechnology Co., Ltd.) to extract total RNA. Then qPCR method was used to detect the mRNA levels of HO-1 and NQO-1.
[0069] (2) 24 hours after the MEFs cells were seeded in a 60mm dish, licochalcone of specified concentration was added respectively, and the culture was continued for 6 hours or specified ti...
Embodiment 3
[0084] Example 3, Application of Glycyrrhizalcone in the Preparation of Antioxidant Enzyme Inducers and Anti-Skin Cancer Cell Transformation Products
[0085] 1. Experimental materials and methods
[0086] (1) JB6P+ cells in the logarithmic growth phase (ATCC) were inoculated on a 6-well plate for 24 hours, then licorice chalcones of specified concentrations were added, and the culture was continued for 72 hours. The supernatant was discarded, and the cells were lysed with TRIZOL buffer to extract total RNA. Then the mRNA levels of Nrf2, HO-1, Gclc and NQO-1 were detected by qPCR method.
[0087] (2) 24 hours after the JB6P+ cells were inoculated in the 6-well plate, licochalcone of the specified concentration was added respectively, and the culture was continued for 72 hours. The supernatant was discarded, the cells were lysed with RIPA buffer, and the protein concentration was determined by BCA method. 20 μg of protein from each sample was separated by SDS-polyacrylamide ...
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