1.
Chem Pharm Bull (Tokyo)
; 49(7): 858-62, 2001 Jul.
Article
in English
| MEDLINE
| ID: mdl-11456092
ABSTRACT
Five new stilbene dimers were isolated from the lianas of Gnetum parvifolium in addition to known stilbenoids. The structures of the compounds were established on the basis of spectroscopic evidence, including long-range coupling and nuclear Overhauser effect experiments, in NMR spectrum. Among the isolates, 2b-hydroxyampelopsin F showed potent inhibitory activity in the Maillard reaction.
Subject(s)
Plants, Medicinal/chemistry , Stilbenes/isolation & purification , Acetylation , Brazil , Magnetic Resonance Spectroscopy , Maillard Reaction , Methylation , Spectrometry, Mass, Fast Atom Bombardment , Spectrophotometry, Ultraviolet
2.
West J Nurs Res
; 12(1): 60-70; discussion 70-4, 1990 Feb.
Article
in English
| MEDLINE
| ID: mdl-2301171