Cytotoxic Compounds from the Roots of Juglans mandshurica
- 1 May 1998
- journal article
- research article
- Published by American Chemical Society (ACS) in Journal of Natural Products
- Vol. 61 (5) , 643-645
- https://doi.org/10.1021/np970413m
Abstract
Three new compounds, a diarylheptanone glucoside (1), 4,5,8-trihydroxy-α-tetralone 5-O-β-d-[6‘-O−(3‘‘,5‘‘-dimethoxy-4‘‘-hydroxybenzoyl)]glucopyranoside (2), and 1,4,8-trihydroxy-3-naphthalenecarboxylic acid 1-O-β-d-glucopyranoside methyl ester (3), were isolated from the roots of Juglans mandshurica, and their structures were elucidated on the basis of spectroscopic studies including 2D-NMR.Keywords
This publication has 9 references indexed in Scilit:
- Comparison of In Vitro Anticancer-Drug-Screening Data Generated With a Tetrazolium Assay Versus a Protein Assay Against a Diverse Panel of Human Tumor Cell LinesJNCI Journal of the National Cancer Institute, 1990
- Iodine Catalysed Alkyloxylation of NaphthoquinonesSynthetic Communications, 1989
- Eight 1,4-naphthoquinones from JuglansPhytochemistry, 1989
- Naphthoquinones from juglandaceaePhytochemistry, 1986
- Nuclear Magnetic ResonancePublished by Springer Nature ,1986
- Distribution of juglone and related compounds in pecan and their effect on Fusicladium effusumJournal of Agricultural and Food Chemistry, 1980
- Studies on the constituents of aceraceae plants. II. Structure of aceroside I, a glucoside of a novel cyclic diarylheptanoid from Acer nikoense Maxim.CHEMICAL & PHARMACEUTICAL BULLETIN, 1978
- A new bisjuglone from Juglans regia root barkPhytochemistry, 1978
- Terpenoid composition of some Canadian LabiataePhytochemistry, 1972