Caffeoylmalic acid

Caffeoylmalic acid
Names
	IUPAC name 2-[(E)-3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxybutanedioic acid
	Other names (+)-(E)-caffeoyl-L-malic acid
Identifiers
CAS Number	39015-77-5 ;
3D model (JSmol)	Interactive image;
ChemSpider	4816367;
PubChem CID	6124299;
UNII	8EY7S5QS7D ;
CompTox Dashboard (EPA)	DTXSID301031926 ;
	InChI 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;
	SMILES C1=CC(=C(C=C1C=CC(=O)OC(CC(=O)O)C(=O)O)O)O;
Properties
Chemical formula	C13H12O8
Molar mass	296.231 g·mol−1
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references

Caffeoylmalic acid is an ester of caffeic acid and malic acid found in the leaves and flowers of Parietaria officinalis.^[1] It is also found in Chelidonium majus^[2] and Urtica dioica.^[3]

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". Planta Medica. 59 (1): 71–5. doi:10.1055/s-2006-959608. PMID 17230338.
^ Farahpour, MR (January 2015). "Antinociceptive and anti-inflammatory activities of hydroethanolic extract of Urtica dioica" (PDF). Int. J. Biol. Pharm. Allied Sci. 4 (1): 165–167 – via Google Scholar.

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