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154-36-9

154-36-9 structure
154-36-9 structure
  • Name: Prunetrin
  • Chemical 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
  • CAS Number: 154-36-9
  • Molecular Formula: C22H22O10
  • Molecular Weight: 446.40400
  • Catalog: Research Areas Inflammation/Immunology
  • Create Date: 2018-06-28 17:00:10
  • Modify Date: 2025-08-25 14:39:09
  • Prunetin (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
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].
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

[1]. Yang G, et al. Anti-inflammatory effect of prunetin via the suppression of NF-κB pathway. Food Chem Toxicol. 2013;58:124-132.

[2]. Hu H, et al. Prunetin inhibits lipopolysaccharide-induced inflammatory cytokine production and MUC5AC expression by inactivating the TLR4/MyD88 pathway in human nasal epithelial cells. Biomed Pharmacother. 2018;106:1469-1477.

Molecular Formula C22H22O10
Molecular Weight 446.40400
Exact Mass 446.12100
PSA 159.05000
LogP 0.35290
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