Synthesis and Cytostatic Activity of Substituted Derivatives of Sodium 1-Amino-2-cyano-1,6-dioxo-4-{[3-(ethoxycarbonyl)thiophen-2-yl]amino}hexa-2,4-dien-3-olates

被引：0
作者：
Gorbunova, I. A. [1 ,2 ]
Mitusova, K. A. [1 ]
Parkhoma, K. Yu. [3 ]
Sharavyova, Yu. O. [3 ]
Makhmudov, R. R. [3 ,4 ]
Ustinova, O. Yu. [4 ]
Denislamova, E. S. [5 ]
Shipilovskikh, D. A. [1 ,5 ]
机构：
[1] Peter Great St Petersburg Polytech Univ, St Petersburg 195251, Russia
[2] ITMO Univ, St Petersburg 197101, Russia
[3] Perm State Univ, Perm 614990, Russia
[4] Fed Sci Ctr Med & Prevent Hlth Risk Management Tec, Perm 614045, Russia
[5] Perm Natl Res Polytech Univ, Perm 614990, Russia
来源：
RUSSIAN JOURNAL OF GENERAL CHEMISTRY | 2024年 / 94卷 / 12期
基金：
俄罗斯科学基金会;
关键词：
Gewald thiophenes; 3-(thiophen-2-yl)iminofuran-2(3H)-ones; antitumor activity; toxicity; drugs; ANALGESIC ACTIVITY; ANTIINFLAMMATORY ACTIVITY; ACUTE TOXICITY; RESISTANCE; DESIGN; STRATEGIES;
D O I：
10.1134/S1070363224120028
中图分类号：
O6 [化学];
学科分类号：
0703 ;
摘要：
AbstractA series of new substituted derivatives of sodium 1-amino-1,6-dioxo-2-cyano-4-{[3-(ethoxycarbonyl)thiophen-2-yl]amino}hexa-2,4-dien-3-olates was synthesized by the furan ring opening reaction of substituted 3-thienylimino-3H-furan-2-ones under the action of amide of cyanoacetic acid in the presence of sodium carbonate as a base. The cytotoxic effect on 4T1 breast cancer cells was studied and the acute toxicity of the obtained compounds was assessed. It was found that the obtained compounds have pronounced anticancer activity and are practically non-toxic drugs (hazard class IV).
引用
收藏
页码：3140 / 3148
页数：9
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