Synthesis of chrysin derivatives and screening of antitumor activity.

Abstract:

:A series of aromatic or long-chain chrysin derivatives (1-10) were synthesized by esterification of chrysin and acyl chloride. The chemical structures of these compounds were determined by mass spectrum (MS), 1H NMR, and 13C NMR spectra. Though aromatic chrysin derivatives (1-9) with a rigid structure were hard to dissolve in common organic solvents, the long-chain chrysin derivative (10) with a flexible structure had better solubility, and its anticancer activity (IC50 = 14.79 μmol/L) against liver cancer cell lines was 5.4 times better than chrysin (IC50 = 74.97 μmol/L), which showed superposition of pharmacological activity.

journal_name

J Asian Nat Prod Res

authors

Chen N,Wang R,Lu LJ,Yan LJ,Bai LL,Fu Y,Wang Y,Peng DQ,Chen X,Wang CH,Li J,Zhao K

doi

10.1080/10286020.2019.1586677

subject

Has Abstract

pub_date

2020-05-01 00:00:00

pages

444-451

issue

5

eissn

1028-6020

issn

1477-2213

journal_volume

22

pub_type

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