Synthesis, Spectroscopic Analysis and Assessment of the Biological Activity of New Hydrazine and Hydrazide Derivatives of 3-Formylchromone

被引:16
|
作者
Slomiak, Krzysztof [1 ]
Lazarenkow, Andrzej [1 ]
Checinska, Lilianna [2 ]
Kusz, Joachim [3 ]
Ochocki, Justyn [1 ]
Nawrot-Modranka, Jolanta [1 ]
机构
[1] Med Univ Lodz, Dept Bioinorgan Chem, Muszynskiego 1, PL-90151 Lodz, Poland
[2] Univ Lodz, Fac Chem, Dept Phys Chem, Pomorska 163-165, PL-90236 Lodz, Poland
[3] Univ Silesia, Inst Phys, Dept Phys Crystals, Uniwersytecka 4, PL-40007 Katowice, Poland
关键词
hydrazine; hydrazide; benzo--pyrones; 3-formylchromone; XTT-assay; anti-proliferative activity; CHROMONE DERIVATIVES; ANTIMICROBIAL ACTIVITY; MEDICINAL CHEMISTRY; SCHIFF-BASES; AGENTS; ANTIOXIDANT; COMPLEXES; FLUORINE; COPPER; ANTIBACTERIAL;
D O I
10.3390/molecules23082067
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The hydrazine and hydrazide derivatives of benzo--pyrones with fluorine substituents remain an unexplored group of chemical compounds. This preliminary study reports the synthesis, structural assessment, initial microbiological screening and biological testing of the synthesized compounds on cell lines using the XTT-assay. A series of 10 novel hydrazine and hydrazide derivatives of 3-formylchromone were synthesized and their structures determined. Structural assessment consisted of elemental analysis, IR, H-1-NMR, C-13-NMR, MS and crystallographic studies. Antimicrobial activity was tested on standard strains representing different groups of microorganisms. The tested compounds were found to inhibit microbial growth. Concentrations of 0.01-1250 mu mol/L were found to influence cell proliferation, demonstrating antiproliferative and stimulation of proliferation against two cell lines: the L929 cell line (mouse fibroblast cell line) and the EA.hy926 cell line (the human umbilical vein, somatic cell hybrid).
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页数:16
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