Iron Chelators of the Dipyridylketone Thiosemicarbazone Class: Precomplexation and Transmetalation Effects on Anticancer Activity-Reference-Cited by-同舟云学术

Iron Chelators of the Dipyridylketone Thiosemicarbazone Class: Precomplexation and Transmetalation Effects on Anticancer Activity

Published:2008-12-17 Issue:2 Volume:52 Page:407-415
ISSN:0022-2623
Container-title:Journal of Medicinal Chemistry
language:en
Short-container-title:J. Med. Chem.

Author:

Bernhardt Paul V.¹,Sharpe Philip C.¹,Islam Mohammad¹,Lovejoy David B.¹,Kalinowski Danuta S.¹,Richardson Des R.¹

Affiliation:

1. Centre for Metals in Biology, School of Chemistry and Molecular Biosciences, University of Queensland, Brisbane, Qld 4072, Australia, and Department of Pathology and Bosch Institute, University of Sydney, Sydney, NSW 2006, Australia

Publisher

American Chemical Society (ACS)

Subject

Drug Discovery,Molecular Medicine

Link

https://pubs.acs.org/doi/pdf/10.1021/jm801012z

Reference52 articles.

1. Cytotoxic iron chelators: characterization of the structure, solution chemistry and redox activity of ligands and iron complexes of the di-2-pyridyl ketone isonicotinoyl hydrazone (HPKIH) analogues

2. Dipyridyl Thiosemicarbazone Chelators with Potent and Selective Antitumor Activity Form Iron Complexes with Redox Activity

3. Design, Synthesis, and Characterization of New Iron Chelators with Anti-Proliferative Activity: Structure−Activity Relationships of Novel Thiohydrazone Analogues

4. Design, Synthesis, and Characterization of Novel Iron Chelators: Structure−Activity Relationships of the 2-Benzoylpyridine Thiosemicarbazone Series and Their 3-Nitrobenzoyl Analogues as Potent Antitumor Agents

5. Iron Chelators in Cancer Chemotherapy

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