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. Author manuscript; available in PMC: 2009 Nov 26.
Published in final edited form as: Curr Anal Chem. 2008 Apr 1;4(2):75–101. doi: 10.2174/157341108784587795

Table 1.

Naturally Occurring Anthocyanidins

Anthocyanidin Abbreviation Substitution Pattern
3 5 6 7 3′ 4′ 5′
Apigeninidin Ap H OH H OH H OH H
Aurantinidin Au OH OH OH OH H OH H
Capensinidin Cp OH OMe H OH OMe OH OMe
Cyanidin Cy OH OH H OH OH OH H
Delphinidin Dp OH OH H OH OH OH OH
Europinidin Eu OH OMe H OH OMe OH OH
Hirsutidin Hs OH OH H OMe OMe OH OMe
6-Hydroxycyanidin 6-OHCy OH OH OH OH OH OH H
6-Hydroxydelphinidin 6-OHDp OH OH OH OH OH OH OH
Luteolinidin Lt H OH H OH OH OH H
Malvidin Mv OH OH H OH OMe OH OMe
5-Methylcyanidin 5-MCy OH OMe H OH OH OH H
Pelargonidin Pg OH OH H OH H OH H
Peonidin Pn OH OH H OH OMe OH H
Petunidin Pt OH OH H OH OMe OH OH
Pulchellidin PI OH OMe H OH OH OH OH
Riccionidin A* H H OH OH H OH H
Rosinidin Rs OH OH H OMe OMe OH H
Tricetinidin Tr H OH H OH OH OH OH

Bold type indicates the most commonly found anthocyanidins.

*

2′OH and an ether connection between 3 & 6′.