CHEBI:28436 - delphinidin

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ChEBI Name delphinidin
ChEBI ID CHEBI:28436
Definition An anthocyanidin cation consisting of benzopyrylium with hydroxy substituents at the 3-, 5- and 7-positions and a 3,4,5-trihydroxyphenyl group at the 2-position. It is a plant pigment responsible for the colours of the plants of the genera Viola and Delphinium.
Stars This entity has been manually annotated by the ChEBI Team.
Secondary ChEBI IDs CHEBI:4382, CHEBI:23600
Supplier Information
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Roles Classification
Biological Role(s): biological pigment
An endogenous molecular entity that results in a colour of an organism as the consequence of the selective absorption of light.
plant metabolite
Any eukaryotic metabolite produced during a metabolic reaction in plants, the kingdom that include flowering plants, conifers and other gymnosperms.
Application(s): antineoplastic agent
A substance that inhibits or prevents the proliferation of neoplasms.
Related Structures
delphinidin is a Functional Parent of
delphinidin 3-O-rutinoside-7-O-beta-D-glucoside
Mass : 773.669
Formula : C33H41O21
145693
delphinidin 3-O-beta-D-sambubioside
Mass : 597.49890
Formula : C26H29O16
74810
delphinidin 3-O-(6-O-(Z)-4-coumaroyl-beta-D-glucoside)
Mass : 611.52700
Formula : C30H27O14
75675
delphinidin 3-O-(6-O-(E)-4-coumaroyl-beta-D-glucoside)
Mass : 611.52700
Formula : C30H27O14
75677
delphinidin 3-O-(6-O-acetyl-beta-D-glucoside)
Mass : 507.42090
Formula : C23H23O13
75678
delphinidin 3-O-beta-D-glucoside-5-O-beta-D-glucoside
Mass : 627.52480
Formula : C27H31O17
55455
delphinidin 3,3',5-tri-O-glucoside
Mass : 789.66540
Formula : C33H41O22
55456
malvidin
Mass : 331.29680
Formula : C17H15O7
6674
delphinidin 3-O-beta-D-glucoside
Mass : 465.38420
Formula : C21H21O12
31463
delphinidin 3-O-(6''-O-malonyl)-beta-D-glucoside
Mass : 551.43040
Formula : C24H23O15
55334
ternatin C5
Mass : 875.71160
Formula : C36H43O25
55335
delphinidin is a Structural Derivative of
flavylium
Mass : 207.24724
Formula : C15H11O
36121
1-benzopyran phenylpropanoid
Definition : Any organic aromatic compound with a structure based on a phenylpropane skeleton. The class includes naturally occurring phenylpropanoid esters, flavonoids, anthocyanins, coumarins and many small phenolic molecules as well as their semi-synthetic and synthetic analogues. Phenylpropanoids are also precursors of lignin.
delphinidin is a Conjugate Acid of
delphinidin(1-)
Mass : 301.231
Formula : C15H9O7
144775
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Relationship Types
is a
has part
is conjugate base of
is conjugate acid of
is tautomer of
is enantiomer of
has functional parent
has parent hydride
is substituent group from
has role
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