Services
Research
Training
Industry
About us
ChEBI
Examples:
iron*
,
InChI=1S/CH4O/c1-2/h2H,1H3
,
caffeine
Advanced
Home
Advanced Search
Browse
Documentation
Download
Tools
About ChEBI
Submit
Contact us
DiNA
Statistics
Entity of the Month
Periodic Table
Ontology
Train online
User Manual
Annotation Manual
Developer Manual
FAQ's
BiNChE
libChEBI
Web Services
ChEBI
> Main
CHEBI:6674 - malvidin
Main
ChEBI Ontology
Automatic Xrefs
Reactions
Pathways
Models
ChEBI Name
malvidin
ChEBI ID
CHEBI:6674
Definition
An anthocyanidin cation that is delphinidin carrying methyl substituents at positions 3' and 5'.
Stars
This entity has been manually annotated by the ChEBI Team.
Supplier Information
Download
Molfile
XML
SDF
Find compounds which contain this structure
Find compounds which resemble this structure
Take structure to the Advanced Search
Wikipedia
License
Read full article at Wikipedia
Formula
C17H15O7
Net Charge
+1
Average Mass
331.29680
Monoisotopic Mass
331.08123
InChI
InChI=1S/C17H14O7/c1-
22-
14-
3-
8(4-
15(23-
2)
16(14)
21)
17-
12(20)
7-
10-
11(19)
5-
9(18)
6-
13(10)
24-
17/h3-
7H,1-
2H3,(H3-
,18,19,20,21)
/p+1
InChIKey
KZMACGJDUUWFCH-UHFFFAOYSA-O
SMILES
COc1cc(cc(OC)c1O)-c1[o+]c2cc(O)cc(O)c2cc1O
Roles Classification
Biological Role
(s):
metabolite
Any intermediate or product resulting from metabolism. The term 'metabolite' subsumes the classes commonly known as primary and secondary metabolites.
biological pigment
An endogenous molecular entity that results in a colour of an organism as the consequence of the selective absorption of light.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing
malvidin (
CHEBI:6674
)
has functional parent
delphinidin (
CHEBI:28436
)
malvidin (
CHEBI:6674
)
has role
biological pigment (
CHEBI:26130
)
malvidin (
CHEBI:6674
)
has role
metabolite (
CHEBI:25212
)
malvidin (
CHEBI:6674
)
is a
5-hydroxyanthocyanidin (
CHEBI:140277
)
malvidin (
CHEBI:6674
)
is conjugate acid of
malvidin(1−) (
CHEBI:144781
)
Incoming
malvidin 3-
O
-β-
D
-glucoside (
CHEBI:31799
)
has functional parent
malvidin (
CHEBI:6674
)
malvidin 3-
O
-(6-
O
-(
E
)-4-coumaroyl-β-
D
-glucoside) (
CHEBI:75693
)
has functional parent
malvidin (
CHEBI:6674
)
malvidin 3-
O
-(6-
O
-(
Z
)-4-coumaroyl-β-
D
-glucoside) (
CHEBI:75691
)
has functional parent
malvidin (
CHEBI:6674
)
malvidin 3-
O
-(6-
O
-acetyl-β-
D
-glucoside) (
CHEBI:75689
)
has functional parent
malvidin (
CHEBI:6674
)
malvidin 3-
O
-{6-
O
-[(
E
)-caffeoyl]-β-
D
-glucoside} (
CHEBI:131453
)
has functional parent
malvidin (
CHEBI:6674
)
malvidin 3-
O
-{6-
O
-[(
Z
)-caffeoyl]-β-
D
-glucoside} (
CHEBI:131452
)
has functional parent
malvidin (
CHEBI:6674
)
malvin (
CHEBI:75030
)
has functional parent
malvidin (
CHEBI:6674
)
malvidin(1−) (
CHEBI:144781
)
is conjugate base of
malvidin (
CHEBI:6674
)
IUPAC Name
3,5,7-trihydroxy-2-(4-hydroxy-3,5-dimethoxyphenyl)chromenium
Synonyms
Sources
3',5'-Dimethoxy-3,4',5,7-tetrahydroxyflavylium acid anion
ChemIDplus
Malvidin
KEGG COMPOUND
Manual Xrefs
Databases
C00020647
KNApSAcK
C08716
KEGG COMPOUND
CPD-15051
MetaCyc
LMPK12010004
LIPID MAPS
Malvidin
Wikipedia
View more database links
Registry Numbers
Types
Sources
10463-84-0
CAS Registry Number
ChemIDplus
1691742
Reaxys Registry Number
Reaxys
1691742
Beilstein Registry Number
ChemIDplus
Citation
Type
Source
23755222
PubMed citation
Europe PMC
Last Modified
29 March 2018