دورية أكاديمية

Synthesis, Characterization, and BSA Binding Studies of Some New Benzamides Related to Schiff Base.

التفاصيل البيبلوغرافية
العنوان: Synthesis, Characterization, and BSA Binding Studies of Some New Benzamides Related to Schiff Base.
المؤلفون: Prashanth, M. K., Madaiah, M., Revanasiddappa, H. D., Amruthesh, K. N.
المصدر: ISRN Organic Chemistry; 2013, p1-12, 12p
مصطلحات موضوعية: BINDING agents, BENZAMIDE, SCHIFF bases, AMINES, ALDEHYDES, BENZOFURAN synthesis, SUBSTITUTION reactions
مستخلص: Condensation of amine 1 with aldehyde 2 gives Schiff base, N-(4-((benzofuran-2-ylmethylene) amino)phenyl)acetamide 3. Schiff base on N-acylation with different substituted acid chlorides in the presence of triethylamine gives the corresponding benzamides, N-acetyl-N-(4-((benzofuran-2-ylmethylene)amino)phenyl)substitutedbenzamide (NABP) 5a-j. The structures of newly synthesized compounds were characterized by elemental analysis, ¹HNMR, 13CNMRFT-IR, and mass spectral studies. Compounds 3 and 5a-j have been screened for their antimicrobial activity using the disc diffusion and minimum inhibitory concentration (MIC) method against the selected bacterial and fungal strain. Compounds 5a, 5e, 5g, and 5h were found to be more active against all tested strains. The antioxidant properties were evaluated by 2,2-diphenyl-1-picrylhydrazyl (DPPH) and superoxide radical scavenging methods. Compounds 5i and 5j showed predominant antioxidant activities among the synthesized analogues. The interaction between NABP and bovine serum albumin (BSA) was investigated using fluorescence and ultraviolet spectroscopic techniques at 298K under imitated physiological conditions. The results revealed that NABP caused the fluorescence quenching of BSA through a static quenching procedure. The binding constants and the number of binding sites were calculated. The binding distance between the donor (BSA) and acceptor (NABP) was determined based on Forster's theory. [ABSTRACT FROM AUTHOR]
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قاعدة البيانات: Complementary Index
الوصف
تدمد:20905149
DOI:10.1155/2013/791591