| Literature DB >> 28215606 |
Bin Li1, Zulfiqar Ali2, Michael Chan3, Juan Li4, Mei Wang2, Naohito Abe2, Can-Rong Wu4, Ikhlas A Khan5, Wei Wang6, Shun-Xiang Li7.
Abstract
Two 9,10-dihydrophenanthrenes trivially named phocantol and phocantone, two diterpenoid glycosidesnamed phocantoside A and phocantoside B were isolated from the ethanol extract of the air-dried whole plant of Pholidota cantonensis Rolfe, together with seventeen known compounds. The structures of the four compounds were identified as 1-hydroxy-2,7-dimethoxy-9,10-dihydrophenanthro-[4,5-bcd]furan, 5-hydroxy-2,7-dimethoxy-9,10-dihydro-1,4-phenanthrenedione, (8R,13E)-ent-labd-13-ene-3α,8,15-triol 15-O-β-D-gluco-pyranoside and (5S,8R,9S,10R)-cis-cleroda-3,13(E)-diene-15,18-diol 15-O-β-D-glucopyranosyl-18-O-β-D-glucopyranoside by chemical and spectroscopic methods, including 1D and 2D NMR. Twenty compounds were evaluated for their cytotoxic activities against mouse leukemia p388D1 cancer cells, and compound phocantone, phocantoside A, tanshinone IIA and syringate exhibited cytotoxic activity against the mouse leukemia p388D1 cancer cells with IC50 values ranging from 13.37 to 27.5 μM.Entities:
Keywords: 9,10-Dihydrophenanthrene; Cytotoxicity; Diterpenoid glycosides; Orchidaceae; Pholidota cantonensis
Mesh:
Substances:
Year: 2017 PMID: 28215606 DOI: 10.1016/j.phytochem.2017.02.005
Source DB: PubMed Journal: Phytochemistry ISSN: 0031-9422 Impact factor: 4.072