Synthesis, Characterization and Antibacterial Activity of Some Schiff Bases Derived from 4-Aminobenzoic Acid

被引:0
|
作者
Dilmaghani, Karim Akbari [1 ]
Jazani, Nima Hosseini [1 ,2 ]
Behrouz, Abbas [1 ]
Fakhraee, Farrin Mir [1 ,3 ]
机构
[1] Urmia Univ, Dept Chem, Fac Sci, Orumiyeh 57159, Iran
[2] Urmia Med Sci Univ, Dept Microbiol, Fac Med, Orumiyeh, Iran
[3] Inst Stand & Ind Res Iran, Orumiyeh, Iran
关键词
Schiff bases; 4-Aminobenzoic acid; Aromatic aldehydes; Antibacterial activity; Parekh method; DERIVATIVES; AGENTS; SALICYLALDEHYDE;
D O I
暂无
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
In the present study, a series of Schiff bases were synthesized from aromatic amines (4-aminobenzoic acid and ethyl-4-aminobenzoate) and aromatic aldehydes (salicylaldehyde, 5-chloro-salicylaldehyde, 5-bromosalicylaldehyde, 3-nitrobenzaldehyde, 2-nitrobenzaldehyde, 4-hydroxybenzaldehyde and 4-methoxybenzaldehyde). The chemical structures of these compounds were confirmed by means of FT-IR, (1)H NMR and (13)C NMR and elemental analysis. The synthesized compounds screened for antibacterial activity against Pseudomonas aeruginosa ATCC 27853, Entrococcus faecalis ATCC 29212, Acinetobacter calcoaceticus ATCC 23055, Klebsiella pneumoniae ATCC 10031, Vibrio cholerae 56913, Escherichia coli ATCC 25922, Staphylococcus aureus PTCC 1112 and Salmonella typhimurium PTCC 1735. The bioassay was carried out in vitro antibacterial property of these synthesized compounds, using dimethylsulfoxide as solvent.
引用
收藏
页码:5947 / 5954
页数:8
相关论文
共 50 条
  • [1] Synthesis and antibacterial activity of some Schiff bases derived from 4-aminobenzoic acid
    Parekh, J
    Inamdhar, P
    Nair, R
    Baluja, S
    Chanda, S
    JOURNAL OF THE SERBIAN CHEMICAL SOCIETY, 2005, 70 (10) : 1155 - 1161
  • [2] Synthesis and antimycobacterial activity of some coupling products from 4-aminobenzoic acid hydrazones
    Küçükgüzel, SG
    Rollas, S
    Küçükgüzel, I
    Kiraz, M
    EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, 1999, 34 (12) : 1093 - 1100
  • [3] Synthesis, structural characterization, in silico ADMET and molecular docking studies of a Schiff base derived from 4-hydroxybenzaldehyde and 4-aminobenzoic acid
    Nowak, Patryk
    Sikorski, Artur
    NEW JOURNAL OF CHEMISTRY, 2025, 49 (14) : 5940 - 5949
  • [4] Synthesis, Characterization and Antibacterial Activity of Some Halo Substituted Schiff Bases
    Junne, S. B.
    Kadam, Archana B.
    Shinde, S. L.
    Waghamare, G. S.
    Vibhute, Y. B.
    E-JOURNAL OF CHEMISTRY, 2010, 7 (03) : 882 - 886
  • [5] Synthesis and study of antibacterial activity of some Schiff bases derived from sulfonamide, 4-amino antipyrene and raceacetophenone
    Nair, R
    Shah, A
    Baluja, S
    Chanda, SV
    MEDICINAL CHEMISTRY RESEARCH, 2002, 11 (08) : 463 - 479
  • [6] Synthesis, characterization and antibacterial activity of some new pyrazole based Schiff bases
    Malladi, Shridhar
    Isloor, Arun M.
    Isloor, Shrikrishna
    Akhila, D. S.
    Fun, Hoong-Kun
    ARABIAN JOURNAL OF CHEMISTRY, 2013, 6 (03) : 335 - 340
  • [7] Synthesis, characterization and structural studies of dibutyltin(IV) complex with Schiff base ligand salicylaldehyde 4-aminobenzoic acid
    Chen, MS
    Kuang, DZ
    Deng, YF
    Zhang, CH
    Feng, YL
    CHINESE JOURNAL OF INORGANIC CHEMISTRY, 2006, 22 (02) : 367 - 370
  • [8] Crystal structure, spectroscopic characterization, and computational study of two new 4-aminobenzoic acid derived Schiff base ligands
    Kia, R.
    Kargar, H.
    SCIENTIA IRANICA, 2015, 22 (06) : 2298 - 2308
  • [9] Synthesis, Characterization, and Antibacterial Activity of Two Zinc(II) Complexes with Schiff Bases Derived from Rimantadine
    Jin, X. D.
    Xu, C.
    Yin, X. Y.
    Wang, H. B.
    Zou, Z. Y.
    Liu, D. L.
    Ge, C. H.
    Chang, X. H.
    Jin, Y. H.
    RUSSIAN JOURNAL OF COORDINATION CHEMISTRY, 2014, 40 (06) : 371 - 378
  • [10] Synthesis, characterization, and antibacterial activity of two zinc(II) complexes with Schiff bases derived from rimantadine
    X. D. Jin
    C. Xu
    X. Y. Yin
    H. B. Wang
    Z. Y. Zou
    D. L. Liu
    C. H. Ge
    X. H. Chang
    Y. H. Jin
    Russian Journal of Coordination Chemistry, 2014, 40 : 371 - 378