Isatin Derivatives Containing Sterically Hindered Phenolic Fragment and Water-Soluble Acyl Hydrazones on Their Basis: Synthesis and Antimicrobial Activity

被引:23
|
作者
Bogdanov, A. V. [1 ]
Zaripova, I. F. [2 ]
Voloshina, A. D. [1 ]
Strobykina, A. S. [1 ]
Kulik, N. V. [1 ]
Bukharov, S. V. [2 ]
Mironov, V. F. [1 ]
机构
[1] Russian Acad Sci, Kazan Sci Ctr, AE Arbuzov Inst Organ & Phys Chem, Ul Akad Arbuzova 8, Kazan 420088, Tatarstan, Russia
[2] Kazan Natl Res Technol Univ, Kazan, Tatarstan, Russia
基金
俄罗斯科学基金会;
关键词
isatin; phenolic fragment; hydrazides; hydrazones; antimicrobial activity; SELECTIVE NONPEPTIDE INHIBITORS; IN-VITRO; ANTICANCER ACTIVITIES; PRIVILEGED STRUCTURES; CASPASE-3; ACTIVATION; APOPTOSIS; DESIGN; AGENTS; ANALOGS; POTENT;
D O I
10.1134/S1070363218010097
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Condensation reactions of isatin derivatives with 3,5-di(tert-butyl)-4-hydroxybenzyl acetate and the Girard's reagent T has afforded a series of novel water-soluble isatin-3-acyl hydrazones containing a sterically hindered phenolic fragment in position 1 of the heterocycle; antimicrobial activity of the products has been estimated. It has been shown that the isatin derivatives with bromine or methoxy substituent in the benzo fragment as well as the acyl hydrazones containing 5-methyl or 5-ethyl group are the most active against Staphylococcus aureus and Bacillus cereus.
引用
收藏
页码:57 / 67
页数:11
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