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Catalog: | HY-N6258 |
Brand: | MCE |
CAS: | 6894-43-5 |
MDL | - |
---|---|
Molecular Weight | 314.42 |
Molecular Formula | C20H26O3 |
SMILES | C[C@]12[C@@]3([H])[C@@]4(CC[C@]1([H])C5=C(OC=C5)C=C2)C[C@@]([C@](CO)(O)C4)([H])CC3 |
AMPK; adipogenesis; apoptosis [1]
Kahweol (20-40 μM; 24 hours) decreases TGF-β-induced CTGF protein expression in AML12 and LX2 cells
[1]
.
Kahweol (20-40 μM; 1 hour) decreases TGF-β-induced phospho-Smad2/3 expression in AML12 cells, but does not affect expression in LX2 cells
[1]
.
Kahweol (20-40 μM) significantly decreased TGF-β-stimulated phospho-ERK and JNK expression in primary hepatocytes only
[1]
.
kahweol (0-25 μg/ml; 6-24 hours) increased the phosphorylation of AMPK and its downstream target Acetyl-CoA carboxylase (ACC) in a time-dependent manner in 3T3-L1 cells
[2]
.
kahweol (0-25 μg/ml) significantly affects protein expression of PPARγ, C/EBPα, FABP4, and FASN, that regulate adipocyte differentiation and lipid metabolism
[2]
.
MCE has not independently confirmed the accuracy of these methods. They are for reference only.
Western Blot Analysis [2]
Cell Line: | 3T3-L1 cells |
Concentration: | 0, 5, 10, 25 μg/ml |
Incubation Time: | |
Result: | Reduced PPARγ, C/EBPα, FABP4, and FASN expression in a dose-dependent manner. |
Solid
Room temperature in continental US; may vary elsewhere.
Powder | -20°C | 3 years |
---|---|---|
In solvent | -80°C | 6 months |
-20°C | 1 month |
DMSO : ≥ 33.33 mg/mL ( 106.00 mM )
* "≥" means soluble, but saturation unknown.
Concentration Solvent Mass | 1 mg | 5 mg | 10 mg |
---|
1 mM | 3.1805 mL | 15.9023 mL | 31.8046 mL |
5 mM | 0.6361 mL | 3.1805 mL | 6.3609 mL |
10 mM | 0.3180 mL | 1.5902 mL | 3.1805 mL |
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