Tricin Explained

Tricin is a chemical compound. It is an O-methylated flavone, a type of flavonoid. It can be found in rice bran[1] and sugarcane.[2]

Glycosides

Biosynthesis

The biosynthesis of flavones has not yet been elucidated in full; however, most of the mechanistic and enzymatic steps have been discovered and studied. In biosynthesizing tricin, there is first stepwise addition of malonyl-CoA via the polyketide pathway and p-coumaroyl-CoA via the phenylpropanoid pathway.[3] These additions are mediated by the sequential action of chalcone synthase and chalcone isomerase to yield naringenin chalcone and the flavanone, naringenin, respectively. CYP93G1 of the CYP450 superfamily in rice then desaturates naringenin into apigenin. After this step, it is proposed that flavonoid 3',5'-hydroxylase (F3',5'H) changes apigenin into tricetin.[4] Upon formation of tricetin, 3'-O-methyltransferase and 5'-O-methyltransferase add methoxy groups to tricetin to form tricin.

Other compounds formed from tricin

Three flavonolignans derived from tricin have been isolated from oats Avena sativa.[5]

Notes and References

  1. http://mct.aacrjournals.org/content/4/9/1287.abstract The rice bran constituent tricin potently inhibits cyclooxygenase enzymes and interferes with intestinal carcinogenesis in ApcMin mice
  2. 27598841 . 10.1590/0001-3765201620150349 . 88 . 3 . Phenolic compounds and anticancer activity of commercial sugarcane cultivated in Brazil . An. Acad. Bras. Ciênc. . 1201–9 . Alves . VG . Souza . AG . Chiavelli . LU . Ruiz . AL . Carvalho . JE . Pomini . AM . Silva . CC . 2016. free .
  3. 10.1007/s11101-009-9161-5 . 9 . 3 . Tricin—a potential multifunctional nutraceutical . 2009 . Phytochemistry Reviews . 413–424 . Zhou . Jian-Min . Ibrahim . Ragai K.. 27161417 .
  4. 24843076 . 10.1104/pp.114.239723 . 165 . 3 . Cytochrome P450 93G1 Is a Flavone Synthase II That Channels Flavanones to the Biosynthesis of Tricin O-Linked Conjugates in Rice . 4081339 . Plant Physiol . 1315–1327 . Lam . PY . Zhu . FY . Chan . WL . Liu . H . Lo . C . 2014.
  5. 10.1021/np049636k . 15730266 . 68 . 2 . Flavonolignans from Avena sativa . 2005 . Journal of Natural Products . 289–292 . Wenzig . Eva.