MDL | - |
---|---|
Molecular Weight | 450.39 |
Molecular Formula | C21H22O11 |
SMILES | O=C(C1=CC=C(O[C@H]2[C@@H]([C@H]([C@@H]([C@@H](CO)O2)O)O)O)C(O)=C1O)/C=C/C3=CC=C(O)C(O)=C3 |
Marein has the neuroprotective effect due to a reduction of damage to mitochondria function and activation of the AMPK signal pathway . Marein improves insulin resistance induced by high glucose in HepG2 cells through CaMKK/AMPK/GLUT1 to promote glucose uptake, through IRS/Akt/GSK-3β to increase glycogen synthesis, and through Akt/FoxO1 to decrease gluconeogenesis. Marein is a HDAC inhibitor with an IC 50 of 100 µM. Marein has beneficial antioxidative, antihypertensive, antihyperlipidemic and antidiabetic effects [1] [2] [3] .
IC50: 100 µM (HDAC) [3]
Marein (0-1000 µM; 24 h) inhibits HDAC activity and TNFα-induced NF-κB activation with IC
50
values of 100 and >200 μM, respectively
[1]
.
Marein (1.25-40 μM; 24 h) promotes glucose uptake in HepG2 cells
[2]
.
Marein (5-10 μM; 24 h) promotes GLUT1 translocation from intercellular vesicles to the plasma membrane, increases hepatic glycogen content and down-regulates expression levels of G6Pase and PEPCK in HepG2 cells
[2]
.
Marein (5-10 μM; 24 h) stimulates 2-NBDG uptake, and it can be reduced by STO-609 and compound C which is a inhibitor of AMPK
[2]
.
Marein (0-40 μM; 24 h) affects the cytotoxicity of MG in PC12 cells
[3]
.
MCE has not independently confirmed the accuracy of these methods. They are for reference only.
Western Blot Analysis [2]
Cell Line: | HepG2 cell line |
Concentration: | 5 and 10 μM |
Incubation Time: | 24 hours |
Result: | Increased GLUT1 translocation to plasma membrane and decreased the phosphorylation level of AS160 and GSK-3β in HepG2 cells. |
Western Blot Analysis [2]
Cell Line: | HepG2 cell line |
Concentration: | 10 μM |
Incubation Time: | 0-10 hours |
Result: | Time- and dose-dependently induced phosphorylation of AMPK and Akt in HepG2 cells. |
Cell Viability Assay [3]
Cell Line: | PC12 cell line |
Concentration: | 0-40 μM |
Incubation Time: | 24 hours |
Result: | Prevened MG-induced loss of viability in PC12 cells. |
Apoptosis Analysis [3]
Cell Line: | PC12 cell line |
Concentration: | 5-10 μM |
Incubation Time: | 30 min |
Result: | Protected PC12 cells from MG-induced apoptosis. |
Western Blot Analysis [3]
Cell Line: | PC12 cell line |
Concentration: | 5-10 μM |
Incubation Time: | 30 min |
Result: | Increased phospho-AMPKα (Thr172) in PC12 cells. |
Solid
Room temperature in continental US; may vary elsewhere.
4°C, protect from light
* In solvent : -80°C, 6 months; -20°C, 1 month (protect from light)
DMSO : 25 mg/mL ( 55.51 mM ; Need ultrasonic)
Concentration Solvent Mass | 1 mg | 5 mg | 10 mg |
---|
1 mM | 2.2203 mL | 11.1015 mL | 22.2030 mL |
5 mM | 0.4441 mL | 2.2203 mL | 4.4406 mL |
10 mM | 0.2220 mL | 1.1101 mL | 2.2203 mL |