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Patuletin

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Patuletin
Chemical structure of patuletin
Names
IUPAC name 2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-6-methoxychromen-4-one
Other names 6-Methoxyquercetin
Quercetagetin 6-methyl ether
2-(3,4-Dihydroxyphenyl)-3,5,7-trihydroxy-6-methoxy-4-benzopyrone
Identifiers
CAS Number
3D model (JSmol)
ECHA InfoCard 100.007.529 Edit this at Wikidata
PubChem CID
CompTox Dashboard (EPA)
SMILES
  • COC1=C(C=C2C(=C1O)C(=O)C(=C(O2)C3=CC(=C(C=C3)O)O)O)O
Properties
Chemical formula C16H12O8
Molar mass 332.26 g/mol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). Infobox references
Chemical compound

Patuletin is an O-methylated flavonol. It can be found in the genus Eriocaulon.

Glycosides

Patuletin glycosides can be found in Ipomopsis aggregata.

Patuletin-3-O-rutinoside can be isolated from the aerial parts of Echinacea angustifolia.

Patuletin acetylrhamnosides can be isolated from Kalanchoe brasiliensis.

References

  1. Quercetagetin and patuletin in Eriocaulon. E. C. Bate-Smith and J. B. Harborne, Phytochemistry, Volume 8, Issue 6, June 1969, Pages 1035-1037
  2. Identification of eupalitin, eupatolitin and patuletin glycosides in Ipomopsis aggregata. D.M. Smith, C.W. Glennie and J.B. Harborne, Phytochemistry, Volume 10, Issue 12, December 1971, Pages 3115-3120
  3. Patuletin-3-O-Rutinoside from the Aerial Parts of Echinacea angustifolia. Lin L., Qiu S., Lindenmaier M., He X., Featherstone T. and Cordell G.A., Pharmaceutical Biology (Formerly International Journal of Pharmacognosy), Volume 40, Number 2, April 2002 , pp. 92-95
  4. Patuletin acetylrhamnosides from Kalanchoe brasiliensis as inhibitors of human lymphocyte proliferative activity. Costa, S S, Jossang, A, Bodo, B, Souza, M L and Moraes, V L, J-Nat-Prod. 1994 Nov; 57(11): 1503-10
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

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