| Literature DB >> 33930986 |
Nguyen Huu Toan Phan1, Nguyen Thi Dieu Thuan1, Nguyen Thi Thu Hien1, Pham Van Huyen1, Nguyen Huu Huong Duyen1, Tran Thi Hong Hanh2, Nguyen Xuan Cuong2, Tran Hong Quang2, Nguyen Hoai Nam2, Chau Van Minh2.
Abstract
Chemical investigation of the roots of Codonopsis javanica resulted in isolation of 12 compounds, including one new polyacetylene, codojavanyol (1), one new phenolic glycoside, codobenzyloside (7), and 10 known compounds, (2E,8E)-9-(tetrahydro-2H-pyran-2-yl)nona-2,8-diene-4,6-diyl-1-ol (2), lobetyol (3), lobetyolin (4), lobetyolinin (5), cordifolioidyne B (6), benzyl-α-L-arabinopyranosyl (1-6)-β-D-glucopyranoside (8), (Z)-8-β-D-glucopyranosyloxycinnamic acid (9), syringin (10), syringaresinol (11), and tryptophan (12). Their structures were elucidated by 1 D and 2 D NMR and MS spectroscopic analyses in comparison with the data reported in the literature. The stereochemistry of the C-2' position of 1 was identified based on time-dependent density functional theory (TDDFT) electronic circular dichroism (ECD) calculation. Among the isolates, compounds 3-5 were shown to have weak cytotoxicity toward three human carcinoma cell lines, including lung (A549), liver (HepG2), and breast (MCF7), with the induction of 41.4 to 55.6% cell death at the concentration of 100 µM.Entities:
Keywords: Campanulaceae; Campanumoea javanica; Codonopsis javanica; cytotoxic; phenolic; polyacetylene
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Year: 2020 PMID: 33930986 DOI: 10.1080/14786419.2020.1833200
Source DB: PubMed Journal: Nat Prod Res ISSN: 1478-6419 Impact factor: 2.861