Antimalarial properties of transition metal complexes of sulfonamides

Abstract The antimalarial properties of various transition metal complexes of benzenesulfonamide were investigated. The sulphonamides were synthesized from the reaction of substituted benzenesulfonyl chloride and amino acids in aqueous basic medium. The dissolution of the sulfonamides in methanol and subsequent reaction with Co(II) and Ni(II) afforded the complexes in 53–94% yields. The compounds were characterized using infrared, nuclear magnetic resonance, and mass spectroscopies. The IC50 of the complexes against Plasmodium falciparum ranged from 2.61 to 2.82 mg/mL. The synthesized compounds had good inhibitory activities against β-hematin of Plasmodium falciparum and could further be developed as therapeutic agents for malaria.

Authors

Publication Details

Journal
Discover Chemistry.
Published
2026-04-30
DOI
https://doi.org/10.1007/s44371-026-00692-8
Primary Topic
Enzyme function and inhibition
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Antimalarial properties of transition metal complexes of sulfonamides

Kingsley O. Omeje, Florence Uchenna Eze, David Izuchukwu Ugwu, Kingsley Uchenna Ugwoke
Discover Chemistry.
Enzyme function and inhibition
article

Antimalarial properties of transition metal complexes of sulfonamides

Kingsley O. Omeje, Florence Uchenna Eze, David Izuchukwu Ugwu, Kingsley Uchenna Ugwoke
article en

Abstract

Abstract The antimalarial properties of various transition metal complexes of benzenesulfonamide were investigated. The sulphonamides were synthesized from the reaction of substituted benzenesulfonyl chloride and amino acids in aqueous basic medium. The dissolution of the sulfonamides in methanol and subsequent reaction with Co(II) and Ni(II) afforded the complexes in 53–94% yields. The compounds were characterized using infrared, nuclear magnetic resonance, and mass spectroscopies. The IC50 of the complexes against Plasmodium falciparum ranged from 2.61 to 2.82 mg/mL. The synthesized compounds had good inhibitory activities against β-hematin of Plasmodium falciparum and could further be developed as therapeutic agents for malaria.

Discover Chemistry.Vol. 3(1)
Openalex Percentile: Top 9%
Enzyme function and inhibition
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.