CHEBI:6674 - malvidin

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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
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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.
Related Structures
malvidin is a Functional Parent of
malvidin 3-O-{6-O-[(E)-caffeoyl]-beta-D-glucoside}
Mass : 655.581
Formula : C32H31O15
131453
malvin
Mass : 655.57800
Formula : C29H35O17
75030
malvidin 3-O-(6-O-acetyl-beta-D-glucoside)
Mass : 535.47410
Formula : C25H27O13
75689
malvidin 3-O-(6-O-(Z)-4-coumaroyl-beta-D-glucoside)
Mass : 639.58010
Formula : C32H31O14
75691
malvidin 3-O-(6-O-(E)-4-coumaroyl-beta-D-glucoside)
Mass : 639.58010
Formula : C32H31O14
75693
malvidin 3-O-beta-D-glucoside
Mass : 493.43740
Formula : C23H25O12
31799
malvidin 3-O-{6-O-[(Z)-caffeoyl]-beta-D-glucoside}
Mass : 655.581
Formula : C32H31O15
131452
malvidin is a Structural Derivative of
delphinidin
Mass : 303.24360
Formula : C15H11O7
28436 		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.
malvidin is a Conjugate Acid of
malvidin(1-)
Mass : 329.285
Formula : C17H13O7
144781
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