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Nat Prod Res ; 33(2): 212-218, 2019 Jan.
Article in English | MEDLINE | ID: mdl-29468891

ABSTRACT

Two new prenylisoflavones, 3',4',5-trihydroxy-8-prenyl-dihydrofuran[2″,3″:7,6]isoflavone (1) and 4',5-dihydroxy-8-prenyl-dihydrofuran[2″,3″:7,6]isoflavone (2), along with five known prenylisoflavones (3-7), benzylalcohol-4-O-ß-d-glucoside (8) and two cinnamic acid esters (9, 10) were isolated from the leaves of Maclura cochinchinensis (Cudrania cochinchinensis). Their structures were elucidated by analysis of NMR (1H-, 13C-NMR, HSQC, HMBC), MS spectra and comparison with the published data. Compounds 4-10 were the first time isolated from this species. Prenylisoflavones 1-4 and 6-7 were evaluated for their in vitro cytotoxic activity on KB and HepG2 cancer cell lines. Compound 4 showed cytotoxic activity against both cancer cell lines with IC50 values of 26.99 and 19.95 µM, respectively. The other compounds were considered as inactive.


Subject(s)
Antineoplastic Agents, Phytogenic/pharmacology , Furans/chemistry , Isoflavones/chemistry , Maclura/chemistry , Antineoplastic Agents, Phytogenic/chemistry , Drug Screening Assays, Antitumor/methods , Furans/isolation & purification , Hep G2 Cells , Humans , Inhibitory Concentration 50 , Isoflavones/isolation & purification , KB Cells , Magnetic Resonance Spectroscopy , Mass Spectrometry , Molecular Structure , Plant Extracts/chemistry , Plant Leaves/chemistry , Prenylation , Vietnam
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