Selective small molecule probes for the hypoxia inducible factor (HIF) Prolyl Hydroxylases

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dc.contributor.authorR Chowdhury-
dc.contributor.authorJ I Candela-Lena-
dc.contributor.authorM C Chan-
dc.contributor.authorD J Greenald-
dc.contributor.authorK K Yeoh-
dc.contributor.authorY M Tian-
dc.contributor.authorM A McDonough-
dc.contributor.authorA Tumber-
dc.contributor.authorN R Rose-
dc.contributor.authorA Conejo-Garcia-
dc.contributor.authorM Demetriades-
dc.contributor.authorS Mathavan-
dc.contributor.authorA Kawamura-
dc.contributor.authorMyung Kyu Lee-
dc.contributor.authorF Eeden-
dc.contributor.authorC W Pugh-
dc.contributor.authorP J Ratcliffe-
dc.contributor.authorC J Schofield-
dc.date.accessioned2017-04-19T09:41:29Z-
dc.date.available2017-04-19T09:41:29Z-
dc.date.issued2013-
dc.identifier.issn1554-8929-
dc.identifier.uri10.1021/cb400088qko
dc.identifier.urihttps://oak.kribb.re.kr/handle/201005/11420-
dc.description.abstractThe hypoxia inducible factor (HIF) system is central to the signaling of low oxygen (hypoxia) in animals. The levels of HIF-α isoforms are regulated in an oxygen-dependent manner by the activity of the HIF prolyl-hydroxylases (PHD or EGLN enzymes), which are Fe(II) and 2-oxoglutarate (2OG) dependent oxygenases. Here, we describe biochemical, crystallographic, cellular profiling, and animal studies on PHD inhibitors including selectivity studies using a representative set of human 2OG oxygenases. We identify suitable probe compounds for use in studies on the functional effects of PHD inhibition in cells and in animals.-
dc.publisherAmer Chem Soc-
dc.titleSelective small molecule probes for the hypoxia inducible factor (HIF) Prolyl Hydroxylases-
dc.title.alternativeSelective small molecule probes for the hypoxia inducible factor (HIF) Prolyl Hydroxylases-
dc.typeArticle-
dc.citation.titleACS Chemical Biology-
dc.citation.number7-
dc.citation.endPage1496-
dc.citation.startPage1488-
dc.citation.volume8-
dc.contributor.affiliatedAuthorMyung Kyu Lee-
dc.contributor.alternativeNameChowdhury-
dc.contributor.alternativeNameCandela-Lena-
dc.contributor.alternativeNameChan-
dc.contributor.alternativeNameGreenald-
dc.contributor.alternativeNameYeoh-
dc.contributor.alternativeNameTian-
dc.contributor.alternativeNameMcDonough-
dc.contributor.alternativeNameTumber-
dc.contributor.alternativeNameRose-
dc.contributor.alternativeNameConejo-Garcia-
dc.contributor.alternativeNameDemetriades-
dc.contributor.alternativeNameMathavan-
dc.contributor.alternativeNameKawamura-
dc.contributor.alternativeName이명규-
dc.contributor.alternativeNameEeden-
dc.contributor.alternativeNamePugh-
dc.contributor.alternativeNameRatcliffe-
dc.contributor.alternativeNameSchofield-
dc.identifier.bibliographicCitationACS Chemical Biology, vol. 8, no. 7, pp. 1488-1496-
dc.identifier.doi10.1021/cb400088q-
dc.description.journalClassY-
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