Phloretin ic50 glut1
WebbPhloretin inhibits Yeast-made GLUT1 as well as Human erythrocyte GLUT1 with IC50values of 49 μM and 61 μM, ... Phloretin (NSC 407292; RJC 02792) is extracted from Prunus mandshurica, which has the potential for the treatment of rheumatoid arthritis ... EGT-0001442, THR-1442) is a potent and selective SGLT2 inhibitor with an IC50 of 2 nM. KGA ... Webb12 aug. 2006 · Immunostaining showed that GLUT1 was significantly increased in hypoxic regions of the human colon ... Inhibition of glucose uptake by phloretin sensitized cancer cells to DNR for its anticancer activity and apoptosis to overcome drug ... (IC50 = 50 nM, 44 nM in hypoxia vs. IC50 = 11 and 21 nM in normoxia in SW620 ...
Phloretin ic50 glut1
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Webb1 mars 2012 · Glut1, Glut2 and glycogen synthase mRNA were expressed in the control. However, these expressions were suppressed in mHAT-9a cells in the presence of … WebbPhloretin inhibits Yeast-made GLUT1 as well as Human erythrocyte GLUT1 with IC50values of 49 μM and 61 μM, respectively.Phloretin has the potential for the treatment of …
Webb8 aug. 2012 · Other Glut1 inhibitors and glucose transport inhibitors, such as fasentin and phloretin , were also shown to be effective in reducing cancer cell growth. A group of inhibitors of glucose transporters has been recently identified with IC 50 values lower than 20 μmol/L for inhibiting cancer cell growth ( 18 ).
Webb2 jan. 2024 · Phloretin inhibits the active transport of glucose into cells by SGLT1 and SGLT2.IC50 Value: 49 +/- 12 microM [4]Target: SGLT1/2in vitro: Phlorizin blocks glucose … WebbGlucose transporter 1 (GLUT1) serves as a ubiquitously expressed glucose transporter, which could activate inflammatory response by mediating glycolysis. Phloretin (PHL), an …
Webb17 okt. 2024 · After 30 min, they were intraperitoneally injected with 200 μl of 20 wt% glucose solution, followed by an intravenous injection of the GLUT1 inhibitor phloretin (10–50 mg/kg) 38 at 20 min after ...
Webb5 mars 2010 · Other hexoses transported by GLUT1 are galactose, mannose, and glucosamine . When expressed in S. cerevisae, rat GLUT1 showed a K m for D-glucose of … philippines new years dayWebb26 jan. 2024 · Examining their specificity for GLUT1-5 revealed that the most potent GLUT3 inhibitor (G3iA, IC50 ~ 7 µM) was most selective for GLUT3, inhibiting less strongly only … trunc redshiftWebbBackground: Chronic renal failure (CRF) is associated with increased cardiovascular mortality, and medial vascular smooth muscle cell (VSMC) hypertrophy, proliferation, and calcification play a pivotal role in uremic vasculopathy. Glucose transporter-1 (GLUT1) facilitates the transport of glucose into VSMCs, and GLUT1 overexpression associated … trunc powerappsWebbPhloretin also inhibits a variety of urea transporters. [6] [7] It induces urea loss and diuresis when coupled with high protein diets. Phloretin has been found to inhibit weight gain … philippines next topWebb16 dec. 2006 · IC 50 indicates flavonoid concentration at which sugar uptake was decreased by half compared with control without flavonoid. For experiments describing quercetin uptake by intestinal sugar transporters in injected oocytes, five or more oocytes were used for each experimental condition. philippines next holidayWebb22 sep. 2015 · In this study, inhibition of five glycolysis pathway molecules (GLUT1, HKII, PFKFB3, PDHK1 and LDH) using 9 inhibitors (Phloretin, Quercetin, STF31, WZB117, 3PO, … philippines nickel companiesWebbGLUT activity was partially inhibited by cytochalasin B (IC (50) = 0.44 +/- 0.1; K (i) = 0.3 +/- 0.1 microM) and phloretin (IC (50) = 8.7 microM) in AS-30D hepatocarcinoma. At physiological glucose, GLUT1 and GLUT3 were the predominant active isoforms in HeLa cells and AS-30D cells, respectively. truncreg tobit