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tricetin

Structure via PubChem · Public domain (PubChem)

EntityQ15303946· pop 7· linked from 65 articles

Also known as 3',4',5,5',7-pentahydroxyflavone, 5,7-DIHYDROXY-2-(3,4,5-TRIHYDROXYPHENYL)-4H-CHROMEN-4-ONE

Tricetin is a flavone, a type of flavonoid. It is a rare aglycone found in the pollen of members of the Myrtaceae, subfamily Leptospermoideae, such as Eucalyptus globulus. This compound shows anticancer effects on human breast adenocarcinoma MCF-7 cells. Moreover. a potent anti-inflammatory effect of tricetin has also been demonstrated in a model of acute pancreatitis. This observation was explained by the compound's radical scavenging effects, its inhibitory effect on the DNA damage sensor enzyme poly (ADP-ribose) polymerase-1 (PARP1) and PARP1-mediated cell death and suppression of inflammat

In the Vinony graph

Vinony's link graph records 65 inbound references to tricetin, and connects out to Myrtaceae, digital object identifier and International Standard Serial Number.

Vinony files it under Chembox image size set, ECHA InfoCard ID from Wikidata and Flavones.

Vinony links it to 6 Wikipedia language editions.

Chemical data

Formula
C15H10O7
Molecular weight
302.23 g/mol
IUPAC name
5,7-dihydroxy-2-(3,4,5-trihydroxyphenyl)chromen-4-one
SMILES
C1=C(C=C(C(=C1O)O)O)C2=CC(=O)C3=C(C=C(C=C3O2)O)O
InChIKey
ARSRJFRKVXALTF-UHFFFAOYSA-N
XLogP
1
Polar surface area
127 Ų
H-bond donors
5
H-bond acceptors
7
Formal charge
0

via PubChem

Drug data · ChEMBL

Molecule type
Small molecule

via ChEMBL · EBI

Wikidata facts

Subclass of
flavone
Mass
302.043
Show 5 more facts
canonical SMILES
C1=C(C=C(C(=C1O)O)O)C2=CC(=O)C3=C(C=C(C=C3O2)O)O
chemical formula
C₁₅H₁₀O₇
found in taxon
Larix sibirica
has characteristic
bitterness
Commons category
Tricetin
Sources (2)

via Wikidata · CC0

~1 min read

Encyclopedic overview

2 sections
Contents
  • See also
  • References

Tricetin is a flavone, a type of flavonoid. It is a rare aglycone found in the pollen of members of the Myrtaceae, subfamily Leptospermoideae, such as Eucalyptus globulus. This compound shows anticancer effects on human breast adenocarcinoma MCF-7 cells. Moreover. a potent anti-inflammatory effect of tricetin has also been demonstrated in a model of acute pancreatitis. This observation was explained by the compound's radical scavenging effects, its inhibitory effect on the DNA damage sensor enzyme poly (ADP-ribose) polymerase-1 (PARP1) and PARP1-mediated cell death and suppression of inflammatory gene expression.

== See also == Tricin synthase produces tricin or tricetin 3′,5′-dimethyl ether Tricetin 3′,4′,5′-O-trimethyltransferase

Excerpted from Wikipedia’s “tricetin” article, available under the CC BY-SA 4.0 licence.

Available in 6 languages

via Wikidata sitelinks · CC0

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