Chemical Structure : Oleandrin
CAS No.: 465-16-7
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.
| Packing | Price | Stock | Quantity |
|---|---|---|---|
| 5 mg | $148 | In stock | |
| 10 mg | $218 | In stock | |
| 25 mg | $358 | In stock | |
| 50 mg | Get quote | ||
| 100 mg | Get quote |
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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.
| M.Wt | 576.73 | |
| Formula | C32H48O9 | |
| Appearance | Solid | |
| Storage |
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| 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 |
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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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