| Literature DB >> 26026223 |
Shin-Ichiro Kurimoto1, Jian-Xin Pu2, Han-Dong Sun2, Yoshihisa Takaishi1, Yoshiki Kashiwada3.
Abstract
Scutefolides A1 and A2, two acylated neo-clerodanes with a 19,18-γ-lactone, scutefolides B1, B2 and C, three 19-nor-neo-clerodanes, together with scutefolides D, E1, E2 and F, four neo-clerodanes, were isolated from the EtOAc-soluble fraction of the aerial parts of Scutellaria coleifolia. Their structures were established on the basis of spectroscopic analysis. The absolute configurations of four of these compounds were elucidated by the CD exciton chirality method. Cytotoxic activities of scutefolides D-F against four cancer cell lines (KB, A549, HeLa, and MCF7) were also evaluated, but they were inactive.Entities:
Keywords: Diterpenoid; Lamiaceae; Neo-clerodane; Scutellaria coleifolia
Mesh:
Substances:
Year: 2015 PMID: 26026223 DOI: 10.1016/j.phytochem.2015.05.012
Source DB: PubMed Journal: Phytochemistry ISSN: 0031-9422 Impact factor: 4.072