Synthesis of New Schiff Bases and Assessment of Their in vitro Biological Effects on Acetylcholinesterase and Carbonic Anhydrase Isoenzymes Activities

We have performed docking studies of compounds 9a–c within the hCA I and II active sites, using as templates hCA I and II adducts for which the X-ray crystal structures have

Finally, the interactions and binding modes of the synthesized chromenes 3(a- l) and 4(a-c) with the binding site of a -glucosidase and tyrosinase were evaluated using molecular

The electronic absorption spectra of the free ligands (TA, TAAP and TAAH) in buffer solutions of different pH values and spectrophotometric determination of their dissociation

In view of the importance of manganese(III) compounds and our interest in the chemistry of coordination compounds involving chelating Schiff bases, we report here the

(b) For the pyrido[2,3-d]pyrimidine derivatives, (i) the compounds (7e, 7g, and 7h) which have methyl group at the 3-position of uracil ring showed a higher inhibitory effect than