Synthesis and Antimicrobial Activities of a Series of 2,5-Substituent 1,4-Cyclohexanedione Derivatives

被引:0
作者
Liu, Hui-Lian [1 ]
Wang, Qing-Zhong [1 ]
Guo, Shu-Hua [1 ]
机构
[1] Weifang Univ, Coll Bioengn, Microscale Sci Inst, Weifang 261061, Shandong, Peoples R China
关键词
Cyclohexanedione derivatives; Antimicrobial activities; Structure-activity relationships;
D O I
暂无
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A series of 2,5-substituent 1,4-cyclohexanedione derivatives compounds were designed and synthesized. Their structures were identified 1 by elemental analysis, H-1 NMR, IR spectra, Their assayed antibacterial (Escherichia coli, Bacillus subtilis) and antifungal (Candida albicans) activities were also evaluated by MTT (3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl tetrazolium bromide) method. The results of I. biological test showed 2,5-dibenzylformate 1,4-cyclohexanedione (11) and 2,5-diformanilide 1,4-cyclohexanedione (12) have favorable I antimicrobial activity with MICs of 26.7, 33.6, 24.2 and 32.3 mu g/mL against Escherichia coli and Bacillus subtilis, respectively.
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页码:1349 / 1352
页数:4
相关论文
共 13 条
[1]   Three-dimensional spiral waves in an excitable reaction system:: Initiation and dynamics of scroll rings and scroll ring pairs [J].
Bansagi, Tamas, Jr. ;
Steinbock, Oliver .
CHAOS, 2008, 18 (02)
[2]  
Basavaraja C, 2009, B KOREAN CHEM SOC, V30, P907
[3]   REACTIONS WITH DERIVATIVES OF GAMMA-CHLOROACETOACETIC ACID [J].
BOOSEN, KJ .
HELVETICA CHIMICA ACTA, 1977, 60 (04) :1256-1261
[4]   Synthesis and cytotoxic evaluation of substituted urea derivatives as inhibitors of human-leukemia K562 cells [J].
Cao, Ping ;
Huang, Xian-Feng ;
Ding, Hui ;
Ge, Hui-Ming ;
Li, Huan-Qiu ;
Ruan, Ban-Feng ;
Zhu, Hai-Liang .
CHEMISTRY & BIODIVERSITY, 2007, 4 (05) :881-886
[5]   New directions in antibacterial research [J].
Chu, DTW ;
Plattner, JJ ;
Katz, L .
JOURNAL OF MEDICINAL CHEMISTRY, 1996, 39 (20) :3853-3874
[6]   Syntheses and antibacterial activity of a series of 3-(pyridine-3-yl)-2-oxazolidinone [J].
Cui, YJ ;
Dang, YX ;
Yang, YS ;
Zhang, SH ;
Ji, RY .
EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, 2005, 40 (02) :209-214
[7]  
Fatiad A.J., 1976, SYNTHESIS, V65
[8]   Comparison of NCCLS and 3-(4,5-dimethyl-2-thiazyl)-2,5-diphenyl-2H-tetrazolium bromide (MTT) methods of in vitro susceptibility testing of filamentous fungi and development of a new simplified method [J].
Meletiadis, J ;
Meis, JFGM ;
Mouton, JW ;
Donnelly, JP ;
Verweij, PE .
JOURNAL OF CLINICAL MICROBIOLOGY, 2000, 38 (08) :2949-2954
[9]  
Nielsen A. T., 1965, ORG SYNTH, V45, P25
[10]   Designer antibacterial peptides kill fluoroquinolone-resistant clinical isolates [J].
Otvos, L ;
Wade, JD ;
Lin, F ;
Condie, BA ;
Hanrieder, J ;
Hoffmann, R .
JOURNAL OF MEDICINAL CHEMISTRY, 2005, 48 (16) :5349-5359