anthocyanidin
Sign in to saveAlso known as anthocyanidins
thumb|right|200px|Molecule in 3D of the anthocyanidin cyanidin
Wikidata facts
- Subclass of
- aglycone
- Image
- Anthocyanidin num.png
Show 5 more facts
- canonical SMILES
- [*]c1c([*])c([*])c(c([*])c1[*])-c1[o+]c2c([*])c([*])c([*])c([*])c2c([*])c1[*]
- SMARTS notation
- [cX3]1([OX2H1,OX1-])[cX3;H0,H1][cH1][cX3]([cX3H1][cX3;H0,H1]1)[cX3]1[o&+&X2][cX3]2[cX3H1][cX3]([cX3;H0,H1][cX3]([cX3]2[cX3H1][cX3]([OX2H1,OX1-])1)O)O
- Commons category
- Anthocyanidins
- topic's main category
- Category:Anthocyanidins
- CXSMILES
- [*]c1c([*])c([*])c(c([*])c1[*])-c1[o+]c2c([*])c([*])c([*])c([*])c2c([*])c1[*] |$R;;;R;;R;;;R;;R;;;;;R;;R;;R;;R;;;R;;R$|
Sources (3)
via Wikidata · CC0
~4 min read
Encyclopedic overview
5 sectionsContents
- Classification
- Natural occurrence
- Effect of pH
- References
- External links
thumb|right|200px|Molecule in 3D of the anthocyanidin cyanidin
Anthocyanidins are common plant pigments, the aglycones of anthocyanins. They are based on the flavylium cation, an oxonium ion, with various groups substituted for its hydrogen atoms. They generally change color from red through purple, blue, and bluish green as a function of pH.
Excerpted from Wikipedia’s “anthocyanidin” article, available under the CC BY-SA 4.0 licence.