Dual-action inhibitors of HIF prolyl hydroxylases that induce binding of a second iron ion.

Inhibition of the hypoxia-inducible factor (HIF) prolyl hydroxylases (PHD or EGLN enzymes) is of interest for the treatment of anemia and ischemia-related diseases. Most PHD inhibitors work by binding to the single ferrous ion and competing with 2-oxoglutarate (2OG) co-substrate for binding at the P...

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Հիմնական հեղինակներ: Yeoh, K, Chan, M, Thalhammer, A, Demetriades, M, Chowdhury, R, Tian, Y, Stolze, I, McNeill, L, Lee, M, Woon, E, Mackeen, M, Kawamura, A, Ratcliffe, P, Mecinović, J, Schofield, C
Ձևաչափ: Journal article
Լեզու:English
Հրապարակվել է: 2013
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author Yeoh, K
Chan, M
Thalhammer, A
Demetriades, M
Chowdhury, R
Tian, Y
Stolze, I
McNeill, L
Lee, M
Woon, E
Mackeen, M
Kawamura, A
Ratcliffe, P
Mecinović, J
Schofield, C
author_facet Yeoh, K
Chan, M
Thalhammer, A
Demetriades, M
Chowdhury, R
Tian, Y
Stolze, I
McNeill, L
Lee, M
Woon, E
Mackeen, M
Kawamura, A
Ratcliffe, P
Mecinović, J
Schofield, C
author_sort Yeoh, K
collection OXFORD
description Inhibition of the hypoxia-inducible factor (HIF) prolyl hydroxylases (PHD or EGLN enzymes) is of interest for the treatment of anemia and ischemia-related diseases. Most PHD inhibitors work by binding to the single ferrous ion and competing with 2-oxoglutarate (2OG) co-substrate for binding at the PHD active site. Non-specific iron chelators also inhibit the PHDs, both in vitro and in cells. We report the identification of dual action PHD inhibitors, which bind to the active site iron and also induce the binding of a second iron ion at the active site. Following analysis of small-molecule iron complexes and application of non-denaturing protein mass spectrometry to assess PHD2·iron·inhibitor stoichiometry, selected diacylhydrazines were identified as PHD2 inhibitors that induce the binding of a second iron ion. Some compounds were shown to inhibit the HIF hydroxylases in human hepatoma and renal carcinoma cell lines.
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spelling oxford-uuid:744f7f95-15d7-44e9-b358-f2da8c120abf2022-03-26T20:01:56ZDual-action inhibitors of HIF prolyl hydroxylases that induce binding of a second iron ion.Journal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:744f7f95-15d7-44e9-b358-f2da8c120abfEnglishSymplectic Elements at Oxford2013Yeoh, KChan, MThalhammer, ADemetriades, MChowdhury, RTian, YStolze, IMcNeill, LLee, MWoon, EMackeen, MKawamura, ARatcliffe, PMecinović, JSchofield, CInhibition of the hypoxia-inducible factor (HIF) prolyl hydroxylases (PHD or EGLN enzymes) is of interest for the treatment of anemia and ischemia-related diseases. Most PHD inhibitors work by binding to the single ferrous ion and competing with 2-oxoglutarate (2OG) co-substrate for binding at the PHD active site. Non-specific iron chelators also inhibit the PHDs, both in vitro and in cells. We report the identification of dual action PHD inhibitors, which bind to the active site iron and also induce the binding of a second iron ion at the active site. Following analysis of small-molecule iron complexes and application of non-denaturing protein mass spectrometry to assess PHD2·iron·inhibitor stoichiometry, selected diacylhydrazines were identified as PHD2 inhibitors that induce the binding of a second iron ion. Some compounds were shown to inhibit the HIF hydroxylases in human hepatoma and renal carcinoma cell lines.
spellingShingle Yeoh, K
Chan, M
Thalhammer, A
Demetriades, M
Chowdhury, R
Tian, Y
Stolze, I
McNeill, L
Lee, M
Woon, E
Mackeen, M
Kawamura, A
Ratcliffe, P
Mecinović, J
Schofield, C
Dual-action inhibitors of HIF prolyl hydroxylases that induce binding of a second iron ion.
title Dual-action inhibitors of HIF prolyl hydroxylases that induce binding of a second iron ion.
title_full Dual-action inhibitors of HIF prolyl hydroxylases that induce binding of a second iron ion.
title_fullStr Dual-action inhibitors of HIF prolyl hydroxylases that induce binding of a second iron ion.
title_full_unstemmed Dual-action inhibitors of HIF prolyl hydroxylases that induce binding of a second iron ion.
title_short Dual-action inhibitors of HIF prolyl hydroxylases that induce binding of a second iron ion.
title_sort dual action inhibitors of hif prolyl hydroxylases that induce binding of a second iron ion
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