Structure–Activity Relationships of Novel Iron Chelators for the Treatment of Iron Overload Disease: The Methyl Pyrazinylketone Isonicotinoyl Hydrazone Series-Reference-Cited by-同舟云学术

Structure–Activity Relationships of Novel Iron Chelators for the Treatment of Iron Overload Disease: The Methyl Pyrazinylketone Isonicotinoyl Hydrazone Series

Published:2007-12-27 Issue:2 Volume:51 Page:331-344
ISSN:0022-2623
Container-title:Journal of Medicinal Chemistry
language:en
Short-container-title:J. Med. Chem.

Author:

Kalinowski Danuta S.¹,Sharpe Philip C.¹,Bernhardt Paul V.¹,Richardson Des R.¹

Affiliation:

1. Iron Metabolism and Chelation Program, Department of Pathology, University of Sydney, Sydney, New South Wales 2006, Australia, and Centre for Metals in Biology, Department of Chemistry, University of Queensland, Brisbane, Queensland 4072, Australia

Publisher

American Chemical Society (ACS)

Subject

Drug Discovery,Molecular Medicine

Link

https://pubs.acs.org/doi/pdf/10.1021/jm7012562

Reference62 articles.

1. Polyamine-Vectored Iron Chelators: The Role of Charge

2. Impact of the 3,6,9-Trioxadecyloxy Group on Desazadesferrithiocin Analogue Iron Clearance and Organ Distribution

3. The Design, Synthesis, and Evaluation of Organ-Specific Iron Chelators

4. Coordination chemistry and biology of chelators for the treatment of iron overload disorders

5. The Evolution of Iron Chelators for the Treatment of Iron Overload Disease and Cancer

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