2020
DOI: 10.1016/j.inoche.2020.108271
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Synthesis, structural, pharmacological and molecular docking simulations studies of some transition metal complexes

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Cited by 9 publications
(5 citation statements)
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“…Soundaranayaki et al . [ 51 ] developed a series of transition metal complexes 167 – 171 by reacting metal chlorides with a Schiff base derivative of 4-aminoantipyrine. The ligand was prepared by refluxing benzalidene-4-iminoantipyrine with tyrosine.…”
Section: Transition Metal Complexes Of 4-aminoantipyrine Derivatives ...mentioning
confidence: 99%
“…Soundaranayaki et al . [ 51 ] developed a series of transition metal complexes 167 – 171 by reacting metal chlorides with a Schiff base derivative of 4-aminoantipyrine. The ligand was prepared by refluxing benzalidene-4-iminoantipyrine with tyrosine.…”
Section: Transition Metal Complexes Of 4-aminoantipyrine Derivatives ...mentioning
confidence: 99%
“…Amoxicillin -Histidine ternary system, (e) Eu(III)-Amoxicillin-Histidine ternary system, (f) Tb(III) -Amoxicillin- Distribution curves of all the binary and ternary systems of Cu(II), Co(II), Ni(II), Zn(II), Eu(III), and Tb(III) were drawn by the HYSS computer program and are given in Figures (7)(8)(9)(10)(11). In figure (7): metal ions were 100% at the beginning, as reaction proceeded and pH increased, its concentration decreased and binary complexes started to form and had grown until reached maximum values (50% at pH 5.9),(70%,pH 7.5),(80%,pH 7.5),(70%,pH 7), (70%,pH 6.5) and (30%, pH 6.5) for (Cu(II), Co(II), Ni(II), Zn(II), Eu(III) and Tb(III)-Ala binary systems respec tively, while binary systems of amoxicillin reached maximum values (70%, pH 7.7), (20%,pH 8.2), (20%, pH 8.5), (10%,pH 8), (25%,pH 7.5) and (15%,pH 7.1) for (Cu(II), Co(II), Ni(II), Zn(II), Eu(III) and Tb(III) respectively.…”
Section: Glycine Ternary Systemmentioning
confidence: 99%
“…In recent years, the chemistry of β-lactam antibiotics about their bioactivities has been of considerable interest [9][10][11].…”
Section: Introductionmentioning
confidence: 99%
“…Schiff base ligands have gained tremendous attention due to their simple synthesis, strong metal chelating ability, adaptability, and diverse applications. Schiff bases are termed “special ligands” due to their wide range of biological and pharmacological activities [1] like antifungal, [2,3] antidiabetic, [4,5] anti‐inflammatory, [6,7] antibacterial, [8,9] analgesic, [10] antitubercular, [11,12] anticancer, [13–15] and antiasthmatic [16] . The enhanced pharmacological properties of these compounds are due to the presence of electron availability on imine nitrogen, which makes them favourable for complexation with donor heteroatoms (nitrogen, sulphur, oxygen) in combination with different metal atoms connected to pharmacological active complexes.…”
Section: Introductionmentioning
confidence: 99%