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Taxonomic group: plant / Streptophyta (Phylum: Streptophyta)
Organ / tissue: leaf

Publication DOI: 10.1055/s-2006-960785
Journal NLM ID: 0066751
Publisher: George Thieme
Institutions: Departamento de Qulmica, Universidade Federal de Santa Catarina, Florianópois, Brazil, Ncleo de lnvestigaçOes QuImico-Farmacêuticas (NIQFAR)/Curso de Farmácia-CCS, Universidade do Vale do Itajal (UNIVALI), Brazil, Departamento de Ciências Biológicas, Universidade do Oeste de Santa Catarina (UNOESC), Chapecó, Brazil, Centro Chimica dei Recettori, Rome, Italy

glycoside, flavonoid, Aleurites moluccana

Structure type: oligomer
Location inside paper: compound 2, 2''-rhamnosyl swertisin, p. 293 (fig., 2)
Compound class: flavonol glycoside
Contained glycoepitopes: IEDB_136105,IEDB_1394181,IEDB_225177,IEDB_613414,IEDB_885823

Methods: 13C NMR, 1H NMR, IR, FAB-MS, TLC, antinociceptive action assay
Biological activity: Compound 2 inhibits dose-dependently the abdominal constrictions caused by acetic acid, with a calculated ID50 value of 8.4 (6.9-10.2 μmol/kg) and maximal inhibition of 92% ± 4.
3D data: 62344

NCBI Taxonomy refs (TaxIDs): 123498
Show glycosyltransferases

There are 2 chemically distinct structures. Please, select:

COc1cc2oc(-c3ccc(O)cc3)cc(=O)c2c(O)c1[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1OC1O[C@H](C)[C@@H](O)[C@H](O)[C@@H]1O

SVG MW SMILES 3D mol Ionize

glycoside, flavonoid, Aleurites moluccana

Structure type: monomer
Location inside paper: compound 1, swertisin, p. 293 (fig., 1)
Trivial name: swertisin
Compound class: glycoside, flavonoid glycoside, flavonol glycoside
Contained glycoepitopes: IEDB_613414

Methods: 13C NMR, 1H NMR, IR, FAB-MS, TLC, antinociceptive action assay
3D data: 62343

NCBI Taxonomy refs (TaxIDs): 123498
Show glycosyltransferases

There is only one chemically distinct structure:

COc1cc2oc(-c3ccc(O)cc3)cc(=O)c2c(O)c1[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O

SVG MW SMILES 3D mol Ionize