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Catalog: | HY-N10335 |
Brand: | MCE |
CAS: | 64761-48-4 |
MDL | - |
---|---|
Molecular Weight | 310.34 |
Molecular Formula | C19H18O4 |
SMILES | O=C1C=C(CC2)C3=C([C@H]4C(C5O6)C3[C@@]2([C@H](C)[C@H]5O4)C6=O)C(C)=C1 |
Harringtonolide is a potent RACK1 inhibitor ( IC 50 =39.66 μM in A375 cells). Harringtonolide inhibits the epithelial-mesenchymal transition (EMT) process and cell proliferation by affecting the interaction between FAK and RACK1 . Harringtonolide has plant growth inhibitory, antiviral, anti-inflammatory, and antiproliferation activities [1] .
IC 50 : 39.66 μM (RACK1) in A375 cells [1]
Harringtonolide (0-50 μM; 24 hours) exhibits good antiproliferation activity in A375 cells with IC
50
of 39.66 μM
[1]
.
Harringtonolide (0-20 μM; 1 hour) restrains the proteolysis of RACK1 by Pronase, and protects temperature-dependent degradation of RACK1
[1]
.
Harringtonolide (0-4 μM; 24 hours) suppresses the phosphorylation of FAK dose-dependently and inhibits Src and STAT3, the downstream proteins of FAK
[1]
.
Harringtonolide (0-4 μM; 24 hours) dose-dependently inhibits the RACK1–FAK interaction in A375 cells
[1]
.
MCE has not independently confirmed the accuracy of these methods. They are for reference only.
Cell Proliferation Assay
Cell Line: | A375 melanoma cells [1] |
Concentration: | 0-50 μM |
Incubation Time: | 24 hours |
Result: | Showed good antiproliferation activity with IC 50 of 39.66 μM. |
Western Blot Analysis
Cell Line: | A375 melanoma cells [1] |
Concentration: | 0, 0.5, 1, 2, 4 μM |
Incubation Time: | 24 hours |
Result: | Suppressed the phosphorylation of FAK dose-dependently and inhibited Src and STAT3, the downstream proteins of FAK. |
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)
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