Prunetrin structure
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Common Name | Prunetrin | ||
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CAS Number | 154-36-9 | Molecular Weight | 446.40400 | |
Density | N/A | Boiling Point | N/A | |
Molecular Formula | C22H22O10 | Melting Point | N/A | |
MSDS | N/A | Flash Point | N/A |
Use of PrunetrinPrunetin (Trifoside), an O-methylated isoflavone found in Prunus yedoensis, possesses anti-inflammatory activities[1][2]. |
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 |
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Synonym | More Synonyms |
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 |
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Molecular Weight | 446.40400 |
Exact Mass | 446.12100 |
PSA | 159.05000 |
LogP | 0.35290 |
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 |