Taxonomic group: plant / Streptophyta
(Phylum: Streptophyta)
Organ / tissue: fruit,
stem
Publication DOI: 10.1002/jccs.200000124Journal NLM ID: 16210600RPublisher: Taipei: Chinese Chemical Society
Institutions: Graduate Institute of Natural Products, Kaohsiung Medical University, Kaohsiung, Taiwan, China
Twenty compounds including a dioxoaporphine, annobraine (1); two oxoaporphines, liriodenine (2) and lysicamine (3); five aporphines, (-)-nornuciferine (4), (-)-anonaine (5), (-)-N-formylanonaine (6), (-)-asimilobine (7) and (+)-nordomesticine (8); one proaporphine, (+)-stepharine (9); two protoberberines, (-)-kikemanine (10) and dehydrocorydalmine (11); one azaanthraquinone, 1-aza-4-methyl-2-oxo-1,2-dihydro-9,10-anthracenedione (12); two amides, N-trans-feruloyltyramine (13) and N-p-coumaroyltyramine (14); one ionone, blumenol A (15); and five steroids, β-sitosterol (16), stigmasterol (17), β-sitosteryl-D-glucoside (18), stigmasteryl-D-glucoside (19) and 6-O-palmitoyl-β-sitosteryl-D-glucoside (20), were isolated from the fruits and stems of Annona glabra. Among them, 1 is a novel dioxoaporphine alkaloid and 12 was obtained for the first time from natural sources. These compounds were characterized and identified by physical and spectral evidence.
Annona glabra
Structure type: monomer
Location inside paper: p. 914, structure 19
Trivial name: stigmasterol 3-O-β-D-glucopyranoside
Compound class: saponin glycoside, glycoside, steroid glycoside, triterpenoid glycoside
Contained glycoepitopes: IEDB_142488,IEDB_146664,IEDB_983931,SB_192
Methods: 13C NMR, 1H NMR, EI-MS, NMR-2D, IR, TLC, UV, extraction, CC, melting point determination, evaporation, HR-EI-MS
Related record ID(s): 65044, 65046
NCBI Taxonomy refs (TaxIDs): 301703
Show glycosyltransferases
There is only one chemically distinct structure: