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CN

Phenolic glycosides from berries of Pimenta dioica.

Journal of natural products (2008-03-05)
Hiroe Kikuzaki, Yoshiko Miyajima, Nobuji Nakatani
ABSTRACT

Four new phenolic glycosides, (2-hydroxy-3-methoxy-5-allyl)phenyl beta- d-(6-O-E-sinapoyl)glucopyranoside (1), (1' R,5' R)-5-(5-carboxymethyl-2-oxocyclopentyl)-3 Z-pentenyl beta-D-(6-O-galloyl)glucopyranoside (2), (S)-alpha-terpinyl [alpha-L-(2-O-galloyl)arabinofuranosyl]-(1-->6)-beta-D-glucopyranoside (3), and (R)-alpha-terpinyl [alpha-L-(2-O-galloyl)arabinofuranosyl]-(1-->6)-beta-D-glucopyranoside (4), were isolated from the berries of Pimenta dioica together with eight known flavonoids. The structures of 1-4 were elucidated on the basis of MS and NMR data and enzymatic hydrolysis. All four glycosides showed radical-scavenging activity against 1,1-diphenyl-2-picrylhydrazyl (DPPH) radicals.

MATERIALS
Product Number
Brand
Product Description

Sigma-Aldrich
Eugenol, ReagentPlus®, 99%
Sigma-Aldrich
Gallic acid monohydrate, ACS reagent, ≥98.0%
Sigma-Aldrich
Sinapic acid, ≥98%, powder
Supelco
Sinapic acid, suitable for matrix substance for MALDI-MS, ≥99.0% (T)
Supelco
Eugenol, PESTANAL®, analytical standard
Sigma-Aldrich
Eugenol, natural, ≥98%, FG
Sigma-Aldrich
Eugenol, ≥98%, FCC, FG
Supelco
Sinapic acid, suitable for matrix substance for MALDI-MS, ≥99.5%, Ultra pure
Sigma-Aldrich
Gallic acid, 97.5-102.5% (titration)