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Caffeoylmalic acid
Names
IUPAC name
2-[(E)-3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxybutanedioic acid
Other names
(+)-(E)-caffeoyl-L-malic acid
Identifiers
3D model (JSmol )
ChemSpider
show InChI=1S/C13H12O8/c14-8-3-1-7(5-9(8)15)2-4-12(18)21-10(13(19)20)6-11(16)17/h1-5,10,14-15H,6H2,(H,16,17)(H,19,20)/b4-2+
Key: PMKQSEYPLQIEAY-DUXPYHPUSA-N
InChI=1/C13H12O8/c14-8-3-1-7(5-9(8)15)2-4-12(18)21-10(13(19)20)6-11(16)17/h1-5,10,14-15H,6H2,(H,16,17)(H,19,20)/b4-2+
Key: PMKQSEYPLQIEAY-DUXPYHPUBQ
show C1=CC(=C(C=C1C=CC(=O)OC(CC(=O)O)C(=O)O)O)O
Properties
C 13 H 12 O 8
Molar mass
−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references
Chemical compound
Caffeoylmalic acid is a hydroxycinnamic acid ester found in the leaves and flowers of Parietaria officinalis [1] Chelidonium majus [2] Urtica dioica [citation needed
References [ ]
^ Budzianowski J (January 1990). "Caffeoylmalic and two pyrrole acids from Parietaria officinalis". Phytochemistry . 29 (10): 3299–301. doi :10.1016/0031-9422(90)80203-S . ^ Hahn R, Nahrstedt A (February 1993). "Hydroxycinnamic Acid Derivatives, Caffeoylmalic and New Caffeoylaldonic Acid Esters, from Chelidonium majus*,1". Planta Medica . 59 (1): 71–5. doi :10.1055/s-2006-959608 . PMID 17230338 .
show Aglycones
Precursor Monohydroxycinnamic acids Dihydroxycinnamic acids Trihydroxycinnamic acids O -methylated formsothers
Esters
glycoside-likes
Esters of
Glycosides
Tartaric acid estersOther esters Caffeoyl phenylethanoid
Echinacoside , , ,
, ,
, , , , , , ,
Verbascoside (, )
Oligomeric forms
Conjugates withcoenzyme A (CoA)
Categories :
Hydroxycinnamic acid esters Vinylogous carboxylic acids Aromatic compound stubs Hidden categories:
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