Taxonomic group: plant / Streptophyta
(Phylum: Streptophyta)
Organ / tissue: aerial part
Publication DOI: 10.1002/jccs.200000050Journal NLM ID: 16210600RPublisher: Taipei: Chinese Chemical Society
Institutions: Graduate Institute of Natural Products, Kaohsiung Medical University, Kaohsiung, Taiwan, China, Department of Chemical Engineering, Kao Yuan Institute of Technology, Kaohsiung, Taiwan, China
Twenty-eight compounds including seven alkaloids, (+)-3-chloro-N-formylnornantenine (1), (+)-N-formylnornantenine (2), (+)-boldine (3), (+)-norboldine (4), (-)-norboldine (5), lycicamine (6), and tetrahydroberberine (7); four flavonoids, kaempferol (8), kaempferol-3-O-arabinoside (9), quercetin (10), and quercetin-3-O-rhamnoside (11); one butanolide, akolactone A (12); one p-quinone, 2,6-dimethoxy-p-quinone (13); one cyclohex-2-en-1-one, blumenol A (14); six benzenoids, methylparaben (15), p-hydroxybenzoic acid (16), vanillic acid (17), syringic acid (18), 3,4,5-trimethoxybenzoic acid (19), and 3-(3,4-dihydroxyphenyl) propionic acid (20); one diterpene, phytol (21); one triterpene, squalene (22); six steroids, (3-sitosterol (23), β-sitostenone (24), stigmasta-4,22-dien-3-one (25), 6β-hydroxy-β-sitostenone (26), 6β-hydroxystigmasterone (27), and β-sitosteryl-D-glucoside (28) were isolated from the aerial part of Lindera glauca. These compounds were characterized and identified by physical and spectral method. All compounds were isolated for the first time from this plant. Among them, (+)-3-chloro-N-formylnornantenine (1) is a new one.
Lindera glauca
Structure type: monomer
Location inside paper: p. 374, structure 9
Compound class: glycoside, flavonoid glycoside
Methods: 13C NMR, 1H NMR, EI-MS, IR, UV, extraction, optical rotation measurement, CC, melting point determination, evaporation, PTLC
Related record ID(s): 65048, 65049
NCBI Taxonomy refs (TaxIDs): 332435
Show glycosyltransferases
There is only one chemically distinct structure:
Found 
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