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Research Article

Synthesis and biological evaluation of O-methyl and O-ethyl NSAID hydroxamic acids

, , , , , , & show all
Pages 1179-1187 | Received 26 Sep 2008, Accepted 27 Jan 2009, Published online: 23 Sep 2009

Figures & data

Figure 1. Synthesis of NSAID hydroxamic acids and their O-alkyl derivatives.

Figure 1.  Synthesis of NSAID hydroxamic acids and their O-alkyl derivatives.

Table 1. Reaction conditions and analytical data for compounds 3a–i.

Table 2. Spectroscopic data and atom enumeration for compounds 3a–i.

Table 3. Antimicrobial activity of NSAID hydroxamic acid derivatives 3 and 4 determined by hole-plate diffusion method.

Table 4. Minimal inhibitory (MIC) and minimal microbicidal concentrations (MMcC) of NSAID hydroxamic acid derivatives 3 and 4 determined by microdilution broth methoda.

Figure 2. Dose-dependent inhibition of jack bean urease by NSAID hydroxamic acid derivatives: 3i (▴), 4a (♦), 4c (▪), 4e (*), 4h (•).

Figure 2.  Dose-dependent inhibition of jack bean urease by NSAID hydroxamic acid derivatives: 3i (▴), 4a (♦), 4c (▪), 4e (*), 4h (•).

Table 5. Interaction with DPPH, in vitro inhibition of soybean lipoxygenase (LO), lipid peroxidation (LP), and theoretically calculated Clog P values.

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