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Synthesis and Biological Evaluation of Novel 2,4-Thiazolidinedione Derivatives as Antibacterial Agent

机译:新型2,4-噻唑烷二酮类衍生物的合成及生物评价

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摘要

A novel series of 5-[1-substituted-3-(substituted phenyl)allylidine]thiazolidine-2,4-dione was synthesized. The target compounds 3(a-1) were synthesized by azotropic removal of water by condensation of 2,4-thiazolidinedione with substituted benzylideneacetones/substi- tuted cinnamaldehyde in presence of piperidine. The spectral characteristics (FT-IR, ~1H NMR spectroscopy) and physical properties (melting point) of the synthesized compounds were identified. The compounds synthesized were evaluated for their antibacterial activity by using cup plate method and minimum inhibitory concentration by two fold serial dilution method. The screening results of the synthesized compounds indicated that the compound (3a), (3b), (3c), (3e), (3f), (3g), (3h), (3i), (3j), (31) exhibited significant antibacterial activity against gram positive and gram negative bacteria.
机译:合成了一系列新的5- [1-取代-3-(取代苯基)烯丙基]噻唑烷-2,4-二酮。在哌啶存在下,通过2,4-噻唑烷二酮与取代的亚苄基丙酮/取代的肉桂醛的缩合偶合除去水,合成了目标化合物3(a-1)。鉴定了合成化合物的光谱特征(FT-IR,〜1H NMR光谱)和物理性质(熔点)。通过杯板法评估合成的化合物的抗菌活性,并通过两倍连续稀释法评估其最低抑菌浓度。合成化合物的筛选结果表明,化合物(3a),(3b),(3c),(3e),(3f),(3g),(3h),(3i),(3j),(31)对革兰氏阳性和革兰氏阴性细菌显示出显着的抗菌活性。

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