Unique Bidentate Chelators of Functionalized HeterocyclicFluoroquinolones with Dual Anti-Inflammatory and SelectiveCytotoxic Effects via a C7-C8 Ethylene Diamine Bridge

The mechanism of action of the FQs involved acidic functional groups and a C7-C8 ethylenediamine chelation bridge, with iron chelation being the predominant pathway.

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Publication Details

Journal
Current Medicinal Chemistry
Published
2026-01-28
DOI
https://doi.org/10.2174/0109298673338657251018045851
Citations
2
Primary Topic
Cancer therapeutics and mechanisms
Type
article
Field-Weighted Citation Impact
44.47
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article

Unique Bidentate Chelators of Functionalized HeterocyclicFluoroquinolones with Dual Anti-Inflammatory and SelectiveCytotoxic Effects via a C7-C8 Ethylene Diamine Bridge

Violet Kasabri, Imad I. Hamdan, Qosay Al‐Balas, Yusuf Al‐Hiari et al.
2 citations
Current Medicinal Chemistry
Cancer therapeutics and mechanisms
44.47
article

Unique Bidentate Chelators of Functionalized HeterocyclicFluoroquinolones with Dual Anti-Inflammatory and SelectiveCytotoxic Effects via a C7-C8 Ethylene Diamine Bridge

Violet Kasabri, Imad I. Hamdan, Qosay Al‐Balas, Yusuf Al‐Hiari, Shereen Arabiyat, Dalya Alsaad, Moneera Alzghoul, Ahmad Telfah, Mohammad Bashar AlQazzan
article en
2 citations

Abstract

The mechanism of action of the FQs involved acidic functional groups and a C7-C8 ethylenediamine chelation bridge, with iron chelation being the predominant pathway.

Current Medicinal ChemistryVol. 33
University of Jordan (JO), Al-Zaytoonah University of Jordan (JO), Jordan University of Science and Technology (JO), Dortmund University of Applied Sciences and Arts (DE), American University of Madaba (JO), Alrafidain University College (IQ), Al-Balqa Applied University (JO)
Openalex Percentile: Top 0%
Cancer therapeutics and mechanisms
44.47
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