Synthesis, characterization, anticancer activity, and molecular docking of some new sugar hydrazone and arylidene derivatives

被引:16
|
作者
Alotabi, Saad H. [1 ]
机构
[1] Taif Univ, Turabah Univ Coll, Dept Chem, Box 311, At Taif 21995, Saudi Arabia
关键词
Sugar hydrazones; Arylidene derivatives; Oxadiazolines; Molecular docking; Antimicrobial activity; DRUG DISCOVERY; PREDICTION;
D O I
10.1016/j.arabjc.2019.12.006
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
New sugar hydrazone moieties, their oxadiazoline derivatives, and arylidene analogues were prepared and chemically elucidated using spectroscopic analysis, such as nuclear magnetic resonance, for hydrogen (HNMR)-H-1, carbon (CNMR)-C-13, elemental analysis, and Infrared (IR). The prepared compounds were purified and tested against breast cancer cells (MCF-7). Compounds 4c, 4d, 6b, and 6d exhibited moderate to very high anti-breast cancer activity, with a percentage of inhibition of 96.19%, 93.08%, 74.33%, and 86.05% respectively; the reference 5-fluorouracil had an inhibitory percentage of 96.02%. (C) 2020 The Author. Published by Elsevier B.V. on behalf of King Saud University.
引用
收藏
页码:4771 / 4784
页数:14
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