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一些新型2,4-二取代噻唑作为潜在抗菌和抗炎剂的合成。

Synthesis of some new 2,4-disubstituted thiazoles as possible antibacterial and anti-inflammatory agents.

作者信息

Holla B Shivarama, Malini K V, Rao B Sooryanarayana, Sarojini B K, Kumari N Suchetha

机构信息

Department of Post-Graduate Studies and Research in Chemistry, Mangalore University, 574 199, Mangalagangothri, India.

出版信息

Eur J Med Chem. 2003 Mar;38(3):313-8. doi: 10.1016/s0223-5234(02)01447-2.

Abstract

A series of arylthioureas (1), aromatic aldehyde thiosemicarbazones (2) and 5-aryl-2-furfuraldehyde thiosemicarbazones (3) were condensed with 2,4-dichloro-5-fluorophenacyl bromide to yield respective arylaminothiazoles, arylidene/5-aryl-2-furfurylidene hydrazinothiazoles (4). The newly synthesized compounds were characterized by IR, 1H-NMR and mass spectral studies. These compounds were also screened for their antibacterial and anti-inflammatory activities. Two of the newly synthesized compounds showed anti-inflammatory activity comparable with that of Ibuprofen.

摘要

一系列芳基硫脲(1)、芳香醛缩氨基硫脲(2)和5-芳基-2-糠醛缩氨基硫脲(3)与2,4-二氯-5-氟苯甲酰溴缩合,得到相应的芳氨基噻唑、亚芳基/5-芳基-2-糠叉肼基噻唑(4)。通过红外光谱、1H-核磁共振光谱和质谱研究对新合成的化合物进行了表征。还对这些化合物的抗菌和抗炎活性进行了筛选。两种新合成的化合物显示出与布洛芬相当的抗炎活性。

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