Taxonomic group: plant / Streptophyta
(Phylum: Streptophyta)
Organ / tissue: leaf
NCBI PubMed ID: 11105566Publication DOI: 10.1055/s-2000-8633Journal NLM ID: 0066751Publisher: George Thieme
Correspondence: hdsun

mail.kib.ac.cn
Institutions: Laboratory of Phytochemistry, Kunming Institute of Botany, Academia Sinica, Kunming, China, Department of Phytochemistry, Henan College of Traditional Chinese Medicine, Zhengzhou, China
Two new gallotannins, pistafolins A (1) and B (2), were isolated from the leaf extract of Pistacia weinmannifolia. Their structures were determined by spectral methods. Four known gallotannins (3 - 6), seven known flavonoid glycosides (7 - 13), along with 1-O-β-D-(6′-O-galloyl)-glucopyranosyl-3-methoxy-5-hydroxybenzene (14), gallic acid (15), methyl gallate (16), (+)-catechin (17), and (+)-gallocatechin (18), were also isolated. Some of these compounds were tested for their cytotoxicity toward K562 cells, and two small molecular phenolic compounds, 15 and 18, showed significant inhibitory effects with IC50 values less than 5 μg/ml.
cytotoxicity, B, polyphenols, Anacardiaceae, Pistacia weinmannifolia, gallotannin, pistafolins A
Structure type: monomer
C
21H
20O
11
Trivial name: quercitrin, baohuoside-II, quercetin 3-rhamnoside, quercetin 3-O-rhamnoside
Compound class: saponin glycoside, glycoside, flavonoid glycoside, flavonol glycoside
Contained glycoepitopes: IEDB_136105,IEDB_225177,IEDB_885823
Methods: 13C NMR, 1H NMR, NMR-2D, IR, FAB-MS, UV, extraction, optical rotation measurement, column chromatography, cytotoxicity assay, evaporation, HR-FAB-MS
Related record ID(s): 65853, 65855, 65856, 65857, 65858, 65859, 65860
NCBI Taxonomy refs (TaxIDs): 371727Reference(s) to other database(s): CCSD:
49971, CBank-STR:599
Show glycosyltransferases
There is only one chemically distinct structure: