| 要約: | In this study,
N-benzylidene-4-fluoroaniline (3a), N-benzylidene-4-nitroaniline (3b) as a
result of condensation of benzaldehyde (1) and 4-fluoroaniline (2a),
4-nitroaniline (2b) using a microwave method was synthesized. The structures of
the synthesized compounds were characterized by Fouirer Transform İnfrared
Spektrofotometre (FTIR spectroscopy), Nuclear Magnetic Resonance (NMR
spectroscopy) and elemental analysis methods. The prepared compounds were
tested for their inhibitory effects on carbonic anhydrase isoenzymes (hCA-I and
hCA-II). The results showed that the synthesized compounds 3a and 3b had a
strong inhibitory effect on hCA-I and hCA-II enzymes activity in vitro. By
testing these compounds in other CA isoenzymes, more effective CA inhibitors
can be formed. Thus, new therapeutic applications can be made for enzyme
activators in the near future.
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