Skip to the main content

Original scientific paper

https://doi.org/10.2478/v10007-009-0033-8

Synthesis and biological activities of new substituted thiazoline-quinoline derivatives

MOSTAFA A. HUSSEIN ; Department of Pharmaceutical Organic Chemistry, Faculty of Pharmacy, Assiut University, Assiut-71526, Egypt
ABDEL-HAMID N. KAFAFY ; Department of Pharmaceutical Organic Chemistry, Faculty of Pharmacy, Assiut University, Assiut-71526, Egypt
SAMIA G. ABDEL-MOTY ; Department of Pharmaceutical Organic Chemistry, Faculty of Pharmacy, Assiut University, Assiut-71526, Egypt
OLA MOHAMED F. ABOU-GHADIR ; Department of Pharmaceutical Organic Chemistry, Faculty of Pharmacy, Assiut University, Assiut-71526, Egypt


Full text: english pdf 111 Kb

page 365-382

downloads: 2.078

cite


Abstract

5-Acyl-8-hydroxyquinoline-2-(3'-substituted-4'-aryl-2,3-dihydrothiazol-2'-ylide- ne)hydrazones, 5a-e to 10a-c, were prepared by the reaction of the appropriate 5-acyl-8-hydroxyquinoline-4-substituted thiosemicarbazones 3a-e and phenacyl bromides 4a-e. Structures of the new compounds were verified on the basis of spectral and elemental analyses. Twenty-eight new compounds were tested for their possible antimicrobial activities. Most of the tested compounds showed weak to moderate antibacterial activity against most of the bacterial strains used in comparison with gatifloxacin as a reference drug. The test compounds showed weak to moderate antifungal activity against tested fungi in comparison with ketoconazole as a reference drug. On the other hand, the newly synthesized compounds were tested for their anti-inflammatory effects and most of them showed good to excellent anti-inflammatory activity compared to indomethacin. Moreover, ulcerogenicity and the median lethal dose (LD50) of the most active anti-inflammatory compounds 6b and 9e were determined in mice; they were non-toxic at doses up to 400 mg kg-1 after i.p. administration.

Keywords

quinoline; thiosemicarbazone; thiazoline; phenacyl bromide; antimicrobial; anti-inflammatory

Hrčak ID:

40499

URI

https://hrcak.srce.hr/40499

Publication date:

1.12.2009.

Article data in other languages: croatian

Visits: 3.648 *