Structure-Function Investigation of the Interaction of 1- and 2-Substituted 3-Hydroxypyridin-4-ones with 5-Lipoxygenase and Ribonucleotide Reductase-Reference-Cited by-同舟云学术

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Structure-Function Investigation of the Interaction of 1- and 2-Substituted 3-Hydroxypyridin-4-ones with 5-Lipoxygenase and Ribonucleotide Reductase

Published:2001-12 Issue:52 Volume:276 Page:48814-48822
ISSN:0021-9258
Container-title:Journal of Biological Chemistry
language:en
Short-container-title:Journal of Biological Chemistry

Author:

Kayyali Reem,Porter John B.,Liu Zu Dong,Davies Nathan A.,Nugent Jonathan H.,Cooper Chris E.,Hider Robert C.

Publisher

Elsevier BV

Subject

Cell Biology,Molecular Biology,Biochemistry

Reference43 articles.

1. Comparison of the subacute toxicity and efficacy of 3-hydroxypyridin-4- one iron chelators in overloaded and nonoverloaded mice

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1. Recent advances in therapeutical applications of the versatile hydroxypyridinone chelators;Journal of Inclusion Phenomena and Macrocyclic Chemistry;2022-01-16

2. Hydroxypyrone derivatives in drug discovery: from chelation therapy to rational design of metalloenzyme inhibitors;RSC Medicinal Chemistry;2022

3. Iron status influences the response of cord blood megakaryocyte progenitors to eltrombopag in vitro;Blood Advances;2021-12-30

4. Hydroxypyridinone-Based Iron Chelators with Broad-Ranging Biological Activities;Journal of Medicinal Chemistry;2020-10-07

5. HPO iron chelator, CP655, causes the G1/S phase cell cycle block via p21 upregulation;Immunity, Inflammation and Disease;2020-08-31

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