| Name | 3-{4-[(2S,4S,5S,3R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)(2H-3,4,5,6-tetrahydropyran-2-yloxy)]phenyl}-5-hydroxy-7-methoxychromen-4-one |
|---|---|
| Synonyms |
3-(4-β-D-glucopyranosyloxy-phenyl)-5-hydroxy-7-methoxy-chromen-4-one
5-Hydroxy-7-methoxy-3-[4-((2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-hydroxymethyl-tetrahydro-pyran-2-yloxy)-phenyl]-chromen-4-one prunetin-4'-O-β-D glucopyranoside prunetrin Prunetin 4'-O-β-D-glucopyranoside prunetin 4'-O-[β-D-glucopyranoside] 4',5-dihydroxy-7-methoxyisoflavone-4'-O-β-D-glucopyranoside |
| Description | Prunetin (Trifoside), an O-methylated isoflavone found in Prunus yedoensis, possesses anti-inflammatory activities[1][2]. |
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| Related Catalog | |
| In Vitro | Prunetin inhibits LPS-induced nitric oxide and prostaglandin E2 production through the suppression of iNOS and COX-2 at the transcriptional level[1]. Prunetin inhibits lipopolysaccharide-induced inflammatory cytokine production and MUC5AC expression by inactivating the TLR4/MyD88 pathway in human nasal epithelial cells[2]. |
| References |
| Molecular Formula | C22H22O10 |
|---|---|
| Molecular Weight | 446.40400 |
| Exact Mass | 446.12100 |
| PSA | 159.05000 |
| LogP | 0.35290 |