Preparation of Some Thiazolyl Hydrazone Derivatives and Evaluation of Their Antibacterial Activities

被引:5
|
作者
Turan-Zitouni, Guelhan [1 ]
Ozdemir, Ahmet [1 ]
Kaplancikli, Zafer Asim [1 ]
Fehrentz, Jean-Alain [2 ,3 ]
Martinez, Jean [2 ,3 ]
Chevallet, Pierre [2 ,3 ]
Dusart, Gislaine [4 ]
机构
[1] Anadolu Univ, Fac Pharm, Dept Pharmaceut Chem, TR-26470 Eskisehir, Turkey
[2] Univ Montpellier I, CNRS, Inst Biomol Max Mousseron, UMR 5247, Montpellier, France
[3] Univ Montpellier 2, Fac Pharm, Montpellier, France
[4] Fac Pharm Montpellier, Bacteriol Lab, F-34060 Montpellier, France
关键词
Amino acid; antibacterial activity; thiazole; BACTERIAL PROTEIN-SYNTHESIS; INHIBITOR; BIOSYNTHESIS; THIOSTREPTON; ANTIBIOTICS; BINDING;
D O I
10.1080/10426500802534176
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The increasing clinical importance of drug-resistant fungal and bacterial pathogens has provided additional urgency to microbiological research and to the development of new antibacterial compounds. For this purpose, new tert-butyl [1-aryl/alkyl-2[(4-aryl-2-thiazolyl)hydrazono]ethyl]carbamate derivatives were synthesized and evaluated for antibacterial activity. The reaction of Boc-L-phenylalaninal, Boc-D-phenylalaninal, Boc-L-leucinal, and Boc-L-tryptophanal with thiosemicarbazide yielded the thiosemicarbazones, which furnished the title compounds on reaction with phenacyl bromides. The new compounds were screened for antibacterial activity. The results from the bioassay tests show that some of the compounds have notable activity against Gram-positive bacteria.
引用
收藏
页码:2613 / 2623
页数:11
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