tulipanin
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Tulipanin — IUPAC name (2S,3R,4S,5S,6R) 2 [5,7 dihydroxy 2 (3,4,5 trihydroxyphenyl)chromenylium 3 yl]oxy 6 [[(2R,3R,4R,5R,6S) 3,4,5 trihydroxy 6 methylox … Wikipedia
Delphinidin — IUPAC name 2 (3,4,5 trihydroxyphenyl)chromenylium 3,5,7 triol … Wikipedia
Cyanidin — IUPAC name 2 (3,4 Dihydroxyphenyl) chromenylium 3,5,7 triol … Wikipedia
Malvin — For other uses, see Malvin (disambiguation). Malvin IUPAC name (2S,3R,4S,5S,6R) 2 [ [7 hydroxy 2 (4 hydr … Wikipedia
Malvidin — IUPAC name 3,5,7 trihydroxy 2 (4 hydroxy 3,5 dimethoxyphenyl)chromenium … Wikipedia
Chrysanthemin — IUPAC name (2S,3R,4S,5S,6R) 2 [2 (3,4 dihydroxyphenyl) 5,7 dihydroxychromenylium 3 yl]oxy 6 (hydroxymethyl)oxan … Wikipedia
Copigmentation — is a phenomenon where pigmentation due to anthocyanidins is reinforced by the presence of other colorless flavonoids known as cofactors or “copigments”. There is a formation of a non covalently linked complex. An example is the bluish purple… … Wikipedia
Columnidin — Other names 5,7,8,3′,4′ pentahydroxyflavylium[1] … Wikipedia
Antirrhinin — IUPAC name (2S,3R,4S,5S,6R) 2 [2 (3,4 dihydroxyphenyl) 5,7 dihydroxychromenylium 3 yl]oxy 6 [[(2R,3R,4R,5R,6S) 3,4,5 trihydroxy 6 methylo … Wikipedia
Myrtillin — IUPAC name (2 S ,3 R ,4 S ,5 S ,6 R ) 2 [5,7 dihydroxy 2 (3,4,5 trihydroxyphenyl)chromenylium 3 yl]oxy 6 (hydroxymethyl)oxane 3,4,5 … Wikipedia
