Misplaced Pages

Delphinidin-3-O-(6-p-coumaroyl)glucoside

Article snapshot taken from Wikipedia with creative commons attribution-sharealike license. Give it a read and then ask your questions in the chat. We can research this topic together.
(Redirected from Delphinidin 3-(6-p-coumaroyl)glucoside)
Delphinidin-3-O-(6-p-coumaroyl)glucoside
Names
IUPAC name 3′,4′,5,5′,7-Pentahydroxy-3-{6-O--β-D-galactopyranosyloxy}flavylium
Systematic IUPAC name (4S,4R,4S,4S,4R,8E)-1,1,1,2,2,4,4,4,10-Nonahydroxy-7-oxo-3,6-dioxa-2λ-2(2,3)-benzopyrana-4(2,6)-oxana-1,10(1)-dibenzenadecaphan-8-en-2-ylium
Other names Delphinidin-3-O-p-coumaroyl glucoside
Identifiers
CAS Number
3D model (JSmol)
ChEBI
ChemSpider
KEGG
PubChem CID
CompTox Dashboard (EPA)
InChI
  • InChI=1S/C30H26O14/c31-15-4-1-13(2-5-15)3-6-24(36)41-12-23-26(38)27(39)28(40)30(44-23)43-22-11-17-18(33)9-16(32)10-21(17)42-29(22)14-7-19(34)25(37)20(35)8-14/h1-11,23,26-28,30,38-40H,12H2,(H5-,31,32,33,34,35,36,37)/p+1/t23-,26-,27+,28-,30-/m1/s1Key: DHTPVCYNNWQRMN-LHRGPQAGSA-O
  • InChI=1/C30H26O14/c31-15-4-1-13(2-5-15)3-6-24(36)41-12-23-26(38)27(39)28(40)30(44-23)43-22-11-17-18(33)9-16(32)10-21(17)42-29(22)14-7-19(34)25(37)20(35)8-14/h1-11,23,26-28,30,38-40H,12H2,(H5-,31,32,33,34,35,36,37)/p+1/t23-,26-,27+,28-,30-/m1/s1Key: DHTPVCYNNWQRMN-LEURJHHLBH
SMILES
  • c1cc(ccc1/C=C/C(=O)OC2((((O2)Oc3cc4c(cc(cc4c3c5cc(c(c(c5)O)O)O)O)O)O)O)O)O
Properties
Chemical formula C
30H
27O
14
Molar mass 611.52 g/mol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). Infobox references
Chemical compound

Delphinidin 3-O-(6-p-coumaroyl)glucoside is a p-coumaroylated anthocyanin. It can be found in some red Vitis vinifera grape cultivars (like Graciano) and in red wine.

It is formed by the enzyme anthocyanin 3-O-glucoside 6″-O-hydroxycinnamoyltransferase from delphinidin 3-O-glucoside and p-coumaroyl-CoA in the anthocyanin biosynthesis pathway.

See also

References

  1. "Showing Compound Delphinidin 3-(6-p-coumaroylglucoside) (FDB017204) - FooDB". foodb.ca.
  2. Núñez, V.; Monagas, M.; Gomez Cordovés, M. C.; Bartolomé, B. (2004). "Vitis vinifera L. cv. Graciano grapes characterized by its anthocyanin profile". Postharvest Biology and Technology. 31: 69–79. doi:10.1016/S0925-5214(03)00140-6.
  3. "Delphinidin 3-(6-p-coumaroyl)glucoside on www.phenol-explorer.eu". Archived from the original on 2011-12-30. Retrieved 2012-02-21.
  4. Delphinidin 3-(6-p-coumaroyl)glucoside synthesis reaction on www.kegg.jp
Anthocyanidins and their anthocyanin glucosides
3-Hydroxyanthocyanidins
3-Deoxyanthocyanidins
O-Methylated anthocyanidins
Anthocyanins
(anthocyaninidin glycosides)
Glucosides:

Diglucosides:

Others glycosides:

Acylated anthocyanins
Acetylated anthocyanins
  • Cyanidin 3-O-(6-acetyl)glucoside
  • Delphinidin 3-O-(6-acetyl)glucoside
  • Malvidin 3-O-(6-acetyl)glucoside
  • Petunidin 3-O-(6-acetyl)galactoside
  • Petunidin 3-O-(6-acetyl)glucoside
  • Peonidin 3-O-(6-acetyl)glucoside
  • Coumaroylated anthocyanins
    (cis- and trans-)
    Caffeoylated anthocyanins
    Malonylated anthocyanins
    Acylated anthocyanin diglycosides
    Flavanol-anthocyanin adducts
    Miscellaneous
    Stub icon

    This article about an aromatic compound is a stub. You can help Misplaced Pages by expanding it.

    Categories: