Skip to content

Author

Nafeesa Naeem

4 papers indexed here

We haven’t gathered this author’s papers yet. Follow them and we’ll fetch their work.

Not the right person? Other researchers publish under this name.

Open access Sep 2026

DFT, TDDFT, UV-Vis and electrochemical investigation of chalcone sulfonate esters: Structure-property relationships and substituent effects.

Chalcone sulfonate esters constitute an emerging class of hybrid molecules in which the conjugated chalcone framework is combined with an arylsulfonyloxy substituent, providing opportunities to modulate their electronic and electrochemical properties. In this study, three chalcone sulfonate esters were investigated usi...

E. Mughal, A. S. Cheema, Nafeesa Naeem et al. · 0 citations
Open access Aug 2026

Discovery of 4-aminochalcone-based dual α-glucosidase and aldose reductase inhibitors: in vitro, in vivo, and in silico studies

Diabetes mellitus is a chronic metabolic disorder associated with persistent hyperglycemia and the development of numerous secondary complications. In the present study, a series of 4-aminochalcone derivatives (1N–10N) were synthesized and evaluated as potential dual inhibitors of α-glucosidase and aldose reductase usi...

E. Mughal, Nafeesa Naeem, Songül Bayrak et al. · 0 citations
Aug 2026

Synthesis and multimodal characterization of flavonols: electrochemical, spectroscopic, and DFT approaches.

Five flavonols bearing electron-donating and electron-withdrawing substituents were synthesized and characterized by NMR spectroscopy, mass spectrometry, UV-Vis spectroscopy, and cyclic voltammetry. Density functional theory (DFT) and time-dependent DFT (TDDFT) calculations were performed to investigate their molecular...

Nafeesa Naeem, N. G. Mateyise, Charlene Marais et al. · 0 citations
Jul 2026

Exploring chalcone-based azo dyes as potential carbonic anhydrase-I/II inhibitors through experimental and computational studies.

It is demonstrated that azo-chalcone hybrids constitute a promising scaffold for the development of potent carbonic anhydrase inhibitors, with compound 1 identified as a strong candidate for further optimization and preclinical investigation.

E. Mughal, Nafeesa Naeem, Ishtiaq Ahmed et al. · 0 citations

We use cookies to run the site and, with your consent, for analytics and to show ads. See our Cookie Policy.