1-1-diphenyl-2-picrylhydrazyl has been researched along with morpholine* in 2 studies
2 other study(ies) available for 1-1-diphenyl-2-picrylhydrazyl and morpholine
| Article | Year |
|---|---|
Synthesis of novel Schiff bases and azol-β-lactam derivatives starting from morpholine and thiomorpholine and investigation of their antitubercular, antiurease activity, acethylcolinesterase inhibition effect and antioxidant capacity.
In this study, new Schiff bases and β-lactam derivatives containing morpholine and thio morpholine nuclei were synthesized. Antimicrobial, antioxidant, antimicrobial and antioxidant properties of all synthesized compounds were investigated and highly effective products were obtained. In this context, new effective structures were introduced to the literature. Topics: Acetylcholinesterase; Antioxidants; Antitubercular Agents; beta-Lactams; Biphenyl Compounds; Dose-Response Relationship, Drug; Enzyme Inhibitors; Microbial Sensitivity Tests; Molecular Structure; Morpholines; Mycobacterium smegmatis; Picrates; Schiff Bases; Structure-Activity Relationship; Urease | 2019 |
Synthesis, structural characterization and antiproliferative and toxic bio-activities of copper(II) and nickel(II) citronellal N4-ethylmorpholine thiosemicarbazonates.
This paper reports the syntheses and characterization of ethylmorpholine substituted citronellal thiosemicarbazone copper(II) and nickel(II) metal complexes. The compounds were characterized through elemental analyses and spectroscopic (IR, UV-Vis, NMR, MS) methods. The X-ray analysis of the two complexes shows that both Ni and Cu derivatives present a square planar coordination, where the coordinating homologous donor atoms bind in trans to each other. The compounds were tested for their biological activity after determination of their octanol-saline partition coefficients, followed by their radical scavenging properties. Eventually the complexes were tested for their proliferation inhibition on human histiocytic lymphoma U937 cell line. The GI(50) values resulted to be 2.3microM for the copper derivative and 12.3microM for the nickel derivative. Topics: Acyclic Monoterpenes; Aldehydes; Antioxidants; Biphenyl Compounds; Cell Proliferation; Cell Survival; Coordination Complexes; Copper; Crystallography, X-Ray; Dose-Response Relationship, Drug; Humans; Magnetic Resonance Spectroscopy; Mass Spectrometry; Models, Chemical; Molecular Structure; Monoterpenes; Morpholines; Nickel; Oxidation-Reduction; Picrates; Spectrophotometry; Thiosemicarbazones; U937 Cells | 2010 |