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Oleandrin

Chemical Structure : Oleandrin

CAS No.: 465-16-7

Oleandrin (PBI-05204)

Catalog No.: PC-27802Not For Human Use, Lab Use Only.

Oleandrin (PBI-05204) is a cardenolide glycoside that induce fatal poisonings, inhibits Na,K-ATPase catalytic activity with IC50 of 0.62 uM, also blocks NF-kappaB activation induced by phorbol ester and lipopolysaccharide, blocks AP-1 activation induced by TNF, suppresses inflammation and tumorigenesis.

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Biological Activity

Oleandrin (PBI-05204) is a cardenolide glycoside that induce fatal poisonings, inhibits Na,K-ATPase catalytic activity with IC50 of 0.62 uM, also blocks NF-kappaB activation induced by phorbol ester and lipopolysaccharide, blocks AP-1 activation induced by TNF, suppresses inflammation and tumorigenesis.

Physicochemical Properties

M.Wt 576.73
Formula C32H48O9
Appearance Solid
CAS No.
Storage
Solide Powder
-20°C 12 Months; 4°C 6 Months
In Solvent
-80°C 6 Months; -20°C 6 Months
Shipping
Solubility

10 mM in DMSO

Chemical Name/SMILES

(3S,5R,8R,9S,10S,13R,14S,16S,17R)-14-Hydroxy-3-(((2R,4S,5S,6S)-5-hydroxy-4-methoxy-6-methyltetrahydro-2H-pyran-2-yl)oxy)-10,13-dimethyl-17-(5-oxo-2,5-dihydrofuran-3-yl)hexadecahydro-1H-cyclopenta[a]phenanthren-16-yl acetate

References

1. Yang P, et al. Mol Carcinog. 2014 Apr;53(4):253-63.

2. Garofalo S, et al. J Neurosci. 2017 Apr 5;37(14):3926-3939.

3. Jortani SA, et al. Clin Chem. 1996 Oct;42(10):1654-8.

4. Manna SK, et al. Cancer Res. 2000 Jul 15;60(14):3838-47.

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