The current research focuses on the treatment of Cr(III), Fe(III) and Cu(II) metal ions with aryl hydrazone ligand named (E)-4-(((diphenylmethylene)hydrazono)methyl)benzene-1,3-diol (DPHB) to afford four novel solid complexes with high yields. Different characterization approaches, including infrared, UV-visible, and NMR spectroscopies, elemental analyses, and thermal gravimetric analysis (TGA), revealed that all mononuclear crystalline metal chelates with good thermal stability had a six-coordination with octahedral geometry. Density Functional Theory (DFT) computations were used and provided a reasonable explanation for these metal chelates' electrical and structural features. Furthermore, investigations of electronic absorption spectroscopy, hydrodynamics, and electrophoresis demonstrated that these new compounds interact with calf thymus deoxyribonucleic acid (CT-DNA) in a variety of ways. As a result, the K and ∆G values of such interactions were in the following order: DPHBCu > DPHBCr > DPHBFe complex. Additionally, the novel metal chelates have been studied anti-bathogenically and found to be significantly effective compared to the comparable DPHB hydrazone ligand. The anti-proliferative activities of the investigated compounds were also evaluated against different lines of cancer cells and exhibited significant cytotoxic activity. In addition, observations of antioxidant activity suggest that antioxidant activity relative to ordinary ascorbic acid was demonstrated in the molecule.

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.compbiolchem.2022.107643DOI Listing

Publication Analysis

Top Keywords

aryl hydrazone
8
hydrazone ligand
8
metal chelates
8
antioxidant activity
8
synthesis structural
4
structural elucidation
4
elucidation dft
4
dft calculation
4
calculation biological
4
biological studies
4

Similar Publications

A photocatalytic sulfamoylation/5- cyclization of ()-'-arylidene--phenylmethacrylohydrazides with sulfamoyl chlorides was developed. The chemoselective intramolecular addition of the carbon-centered radical intermediate to the CN bond in the hydrazone motif gave the sulfamoylated pyrazolin-5-one. Besides, sulfonyl chlorides are also suitable reaction partners to access sulfonylated pyrazolin-5-ones.

View Article and Find Full Text PDF

In response to the escalating crisis of antimicrobial resistance (AMR), there is an urgent need to research and develop novel antibiotics. This study presents the synthesis and assessment of innovative 4-aminoquinoline-benzohydrazide-based molecular hybrids bearing aryl aldehydes () and substituted isatin warheads (), characterized using multispectroscopic techniques with high purity confirmed by HRMS. The compounds were evaluated against a panel of clinically relevant antibacterial strains including the Gram-positive , , and and a Gram-negative bacterial strain.

View Article and Find Full Text PDF

Multicomponent Diversity-Oriented Access to Boronic-Acid-Derived Pyrrolide Salicyl-Hydrazone Fluorophores with Strong Solid-State Emission.

Inorg Chem

November 2024

Anhui Laboratory of Molecule-Based Materials; The Key Laboratory of Functional Molecular Solids, Ministry of Education, School of Chemistry and Materials Science; Anhui Province Key Laboratory of Optoelectrical Materials Science and Technology, School of Physics and Electronic Information, Anhui Normal University, Wuhu, Anhui 241002, China.

Article Synopsis
  • Fluorescent molecular platforms are valuable for biology and optoelectronics but face solid-state emission quenching challenges, which can be addressed by using bulky substituents or aggregation-induced emission techniques to boost brightness.
  • A new class of fluorophores called BPSHY was developed from pyrrole and salicylaldehyde derivatives, enhanced with boronic acids to improve solubility and optical properties, achieving high quantum yields and strong absorption in the visible region.
  • BPSHY probes can label specific subcellular organelles, like lysosomes and mitochondria, with high efficiency, indicating their potential for real-time monitoring of organelle dynamics in live cells.
View Article and Find Full Text PDF

Background: Non-Nucleoside Reverse Transcriptases Inhibitors (NNRTIs) are among the most extensively studied enzymes for understanding the biology of Human Immunodeficiency Viruses (HIV) and designing inhibitors for managing HIV infections. Indolyl aryl sulfones (IASs), an underexplored class of potent NNRTIs, require further exploration for the development of newer drugs for HIV.

Aims: In this context, we synthesized a series of novels by Indolyl Aryl Sulfones with a hydrazone moiety at the carboxylate site of the indole nucleus.

View Article and Find Full Text PDF

Synthesis, anticancer activity, and mechanistic investigations of aryl-alkyl diorganotin arylformylhydrazone complexes.

J Inorg Biochem

January 2025

Key Laboratory of Green Chemistry, Jiangxi Province, College of Chemistry and Materials, Jiangxi Normal University, Nanchang, Jiangxi 330022, China. Electronic address:

Article Synopsis
  • Diorganotin acylhydrazone complexes show promise as alternatives to platinum-based drugs due to their strong anticancer effects.
  • Twelve such complexes were synthesized using a quick "one-pot" microwave method and thoroughly analyzed using various techniques like FT-IR and NMR.
  • Among the tested complexes, complex 8 was most effective against HepG2 cancer cells, demonstrating its ability to induce cell death through mitochondrial pathways and halt the cell cycle at the G2/M phase.
View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!