Delphinidin
| Delphinidin | |
|---|---|
 |
|
|
2-(3,4,5-trihydroxyphenyl)chromenylium-3,5,7-triol |
|
| Identifiers | |
| CAS number | 13270-61-6  , [528-53-0] (chloride) |
| PubChem | 68245 |
| ChemSpider | 114185 |
| ChEBI | CHEBI:28436 |
| ChEMBL | CHEMBL590878 , CHEMBL276780 |
| Jmol-3D images | Image 1 Image 2 |
|
|
|
|
| Properties | |
| Molecular formula | C15H11O7 |
| Molar mass | 303.24 g mol−1 |
 (verify) (what is:  / ?)Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa) |
|
| Infobox references | |
Delphinidin is an anthocyanidin, a primary plant pigment, and also an antioxidant.[1] Delphinidin gives blue hues to flowers like violas and delphiniums. It also gives the blue-red color of the grape that produces Cabernet Sauvignon, and can be found in cranberries and Concord grapes as well as pomegranates.[2]
Delphinidin, like nearly all other anthocyanidins, is pH-sensitive, and changes from blue in basic solution to red in acidic solution.
Glycosides [edit]
Myrtillin (Delphinidin-3-O-glucoside) and tulipanin (delphinidin-3-O-rutinoside) can be found in blackcurrant pomace.
Violdelphin (Delphinidin 3-rutinoside-7-O-(6-O-(4-(6-O-(4-hydroxybenzoyl)-beta-D-glucosyl)oxybenzoyl)-beta-D-glucoside) is responsible for purplish blue flower color of Aconitum chinense.[3]
See also [edit]
- Prodelphinidin, a type of condensed tannins
References [edit]
- ^ Afaq, F.; Syed, D. N.; Malik, A.; Hadi, N.; Sarfaraz, S.; Kweon, M.-H.; Khan, N.; Zaid, M. A.; Mukhtar, H. (2007). "Delphinidin, an Anthocyanidin in Pigmented Fruits and Vegetables, Protects Human HaCaT Keratinocytes and Mouse Skin Against UVB-Mediated Oxidative Stress and Apoptosis". Journal of Investigative Dermatology 127 (1): 222–232. doi:10.1038/sj.jid.5700510. PMID 16902416.
- ^ Ribéreau-Gayon, J.; Ribéreau-Gayon, P. (1958). "The Anthocyans and Leucoanthocyans of Grapes and Wines". American Journal of Enology and Viticulture 9: 1–9.
- ^ Violdelphin on PubChem
|
||||||||||||||||||||||||||||||||
