Misplaced Pages

Ayanin: Difference between revisions

Article snapshot taken from Wikipedia with creative commons attribution-sharealike license. Give it a read and then ask your questions in the chat. We can research this topic together.
Browse history interactively← Previous editContent deleted Content addedVisualWikitext
Revision as of 16:32, 29 April 2023 editLegionMammal978 (talk | contribs)Extended confirmed users7,894 edits move systematic name← Previous edit Latest revision as of 00:08, 9 November 2023 edit undoOAbot (talk | contribs)Bots440,440 editsm Open access bot: doi updated in citation with #oabot. 
Line 43: Line 43:
'''Ayanin''' is an ], a type of flavonoid. It is the 3,7,4'-tri-''O''-methylated ] of ]. '''Ayanin''' is an ], a type of flavonoid. It is the 3,7,4'-tri-''O''-methylated ] of ].


It can be found in '']''. It can also be synthesized.<ref>{{cite journal | doi = 10.1002/jhet.5570130629| title = Partial methylation of quercetin: Direct synthesis of tamarixetin, ombuin and ayanin| journal = Journal of Heterocyclic Chemistry| volume = 13| issue = 6| pages = 1293–1295| year = 1976| last1 = Rao| first1 = Koppaka V.| last2 = Owoyale| first2 = Jacob A.}}</ref> It can be found in '']''. It can also be synthesized.<ref>{{cite journal | doi = 10.1002/jhet.5570130629| title = Partial methylation of quercetin: Direct synthesis of tamarixetin, ombuin and ayanin| journal = Journal of Heterocyclic Chemistry| volume = 13| issue = 6| pages = 1293–1295| year = 1976| last1 = Rao| first1 = Koppaka V.| last2 = Owoyale| first2 = Jacob A.| doi-access = free}}</ref>


== Biosynthesis == == Biosynthesis ==

Latest revision as of 00:08, 9 November 2023

Ayanin
Chemical structure of ayanin
Names
IUPAC name 3′,5-Dihydroxy-3,4′,7-trimethoxyflavone
Systematic IUPAC name 5-Hydroxy-2-(3-hydroxy-4-methoxyphenyl)-3,7-dimethoxy-4H-1-benzopyran-4-one
Other names
  • 3,7,4'-Tri-O-methylquercetin
  • 3,7,4'-Trimethylquercetin
Identifiers
CAS Number
3D model (JSmol)
ChEBI
ChEMBL
ChemSpider
PubChem CID
UNII
CompTox Dashboard (EPA)
InChI
  • InChI=1S/C18H16O7/c1-22-10-7-12(20)15-14(8-10)25-17(18(24-3)16(15)21)9-4-5-13(23-2)11(19)6-9/h4-8,19-20H,1-3H3Key: KPCRYSMUMBNTCK-UHFFFAOYSA-N
  • InChI=1/C18H16O7/c1-22-10-7-12(20)15-14(8-10)25-17(18(24-3)16(15)21)9-4-5-13(23-2)11(19)6-9/h4-8,19-20H,1-3H3Key: KPCRYSMUMBNTCK-UHFFFAOYAE
SMILES
  • COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)OC)O)OC)O
  • O=C1c3c(O/C(=C1/OC)c2ccc(OC)c(O)c2)cc(OC)cc3O
Properties
Chemical formula C18H16O7
Molar mass 344.319 g·mol
Density 1.454 g/mL
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). checkverify (what is  ?) Infobox references
Chemical compound

Ayanin is an O-methylated flavonol, a type of flavonoid. It is the 3,7,4'-tri-O-methylated derivative of quercetin.

It can be found in Croton schiedeanus. It can also be synthesized.

Biosynthesis

The enzyme 3,7-dimethylquercetin 4'-O-methyltransferase uses S-adenosyl methionine and rhamnazin to produce S-adenosylhomocysteine and ayanin.

References

  1. Rao, Koppaka V.; Owoyale, Jacob A. (1976). "Partial methylation of quercetin: Direct synthesis of tamarixetin, ombuin and ayanin". Journal of Heterocyclic Chemistry. 13 (6): 1293–1295. doi:10.1002/jhet.5570130629.
Flavonols and their conjugates
Backbone
Aglycones
Flavonols
Aglycones
Conjugates
Glycosides of herbacetin
Glycosides of kaempferol
Glycosides of myricetin
Conjugates of quercetin
Sulfates
Glycosides
O-Methylated flavonols
Aglycones
Glycosides
of isorhamnetin
other
Derivative flavonols
Aglycones
Glycosides
Pyranoflavonols
Aglycones
Furanoflavonols
Aglycones
Glycosides
Semisynthetic
Glycosides


Stub icon

This article about an aromatic compound is a stub. You can help Misplaced Pages by expanding it.

Categories: