Synthesis and Anti-Oxidant Evaluation of Some Novel Sulfa Drugs
作者:Moustafa A. Gouda、Belal H.M. Hussein
DOI:10.2174/1570180814666170607144811
日期:2017.10.31
scavenger than vitamin E. Moreover, cyanoacetamides were reported to possess, antimicrobial antifungal, insulin releasing, antiinflammatory and antitumor. Thus the present study focuses on the synthesis of somenovel structure hybrids incorporating either curcumin or cyanoacetamide with sulphonamide, aiming to reach a more potent antioxidant agent. Methods: 4-arylazoenol derivatives 12-16 and E-hydrazo
Polymer complexes: XLXII-interplay of coordination π–π stacking and hydrogen bonding in supramolecular assembly of [sulpha drug derivatives-N,S:N,O] complexes
HLn (n = 1–5) is coordinated to the metal ion in a neutral tetradentate manner with NSNO donor sites of NH (hydrazone's), NH (3-phenylamine), carbonyl group and Ph-NH. The title [Ni3(HLn)2(μ-OAc)2(OAc)4]n consists of three Ni(II) atoms linked by interchain π–π interaction are observed between aromatic rings of two ligands (HLn) which are further doubly bridged two adjacent nickel atoms by acetate group