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Novel Drugs and the Response to Hypoxia: HIF Stabilizers and Prolyl Hydroxylase.

Novel Drugs and the Response to Hypoxia: HIF Stabilizers and Prolyl Hydroxylase. Research Abstract Details 

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  • Novel Drugs and the Response to Hypoxia: HIF Stabilizers and Prolyl Hydroxylase. Abstract Text:

    masaomi nangakuMasaomi Nangaku,ichiro kojimaIchiro Kojima,tetsuhiro tanakaTetsuhiro Tanaka,takamoto ohseTakamoto Ohse,hideki katoHideki Kato,toshiro fujitaToshiro Fujita,masaomi nangakuMasaomi Nangaku,ichiro kojimaIchiro Kojima,tetsuhiro tanakaTetsuhiro Tanaka,takamoto ohseTakamoto Ohse,hideki katoHideki Kato,toshiro fujitaToshiro Fujita,masaomi nangakuMasaomi Nangaku,ichiro kojimaIchiro Kojima,tetsuhiro tanakaTetsuhiro Tanaka,takamoto ohseTakamoto Ohse,hideki katoHideki Kato,toshiro fujitaToshiro Fujita,

    Tissue hypoxia occurs when local metabolism is disturbed by an imbalance between oxygen supply and consumption. This condition can lead to a variety of serious ischemic disorders, including a number of important cardiovascular diseases. In the search for therapeutic approaches, focused modalities which specifically target hypoxia have been particularly sought. These efforts would profit from the ability to utilize the mechanisms by which cells adjust to hypoxic conditions. At the center of the cellular response to hypoxia is hypoxia-inducible factor, HIF. This factor is composed of two subunits, an oxygen-sensitive HIF-alpha subunit and a constitutively expressed HIF-beta subunit. Intracellular accumulation of HIF induces the coordinated expression of a number of adaptive genes against hypoxic insult. Because activation of HIF is a promising therapeutic modality for ischemic cardiovascular disease, recent studies have focused on the development of HIF stimulators. HIF levels are regulated by prolyl hydroxylation and asparaginyl hydroxylation of the HIF-alpha subunit. To date, a single HIF asparaginyl hydroxylase has been identified, factor inhibiting HIF (FIH), whereas the mammalian genome encodes three closely related proteins that have HIF prolyl hydroxylase activity, PHD1, PHD2 and PHD3. Recent patents have disclosed methods for identifying modulators of HIF or PHD as well as novel compounds with properties of HIF modulation or prolyl hydroxylase inhibition. This review highlights the identification of novel HIF stabilizers as specific molecularly targeted therapies against cardiovascular disease.

    Novel Drugs and the Response to Hypoxia: HIF Stabilizers and Prolyl Hydroxylase. Publishing Authors By Initials

    m nangakuM Nangaku,i kojimaI Kojima,t tanakaT Tanaka,t ohseT Ohse,h katoH Kato,t fujitaT Fujita,m nangakuM Nangaku,i kojimaI Kojima,t tanakaT Tanaka,t ohseT Ohse,h katoH Kato,t fujitaT Fujita,m nangakuM Nangaku,i kojimaI Kojima,t tanakaT Tanaka,t ohseT Ohse,h katoH Kato,t fujitaT Fujita,

    For similar abstracts research abstracts see: abstracts research

    PUBMED ID PMID:

    MEDLINE DATE:

    Novel Drugs and the Response to Hypoxia: HIF Stabilizers and Prolyl Hydroxylase. Journal Published:

    PUBLICATION TYPE: Journal Article

    Journal: Recent patents on cardiovascular drug discovery

    VOLUME: 1

    Page Numbers: 126-9

    Journal Abbreviation:

    ISSN: 1574-8901

    DAY: 28

    MONTH: Jun

    YEAR: 2006

    Novel Drugs and the Response to Hypoxia: HIF Stabilizers and Prolyl Hydroxylase. Information

    Number of References:

    LANGUAGE: eng

    NlmUniqueID: 101263805

    Novel Drugs and the Response to Hypoxia: HIF Stabilizers and Prolyl Hydroxylase. Keywords Mesh Terms:

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    Grant and Affiliation Information for Novel Drugs and the Response to Hypoxia: HIF Stabilizers and Prolyl Hydroxylase.

    AFFILIATION: Division of Nephrology and Endocrinology, University of Tokyo School of Medicine, 7-3-1, Hongo, Bunkyo-ku, Tokyo 113-8655, Japan. mnangaku-tky@umin.ac.jp.

    Country: United Arab Emirates

    United Arab Emirates Research PublicationUnited Arab Emirates Research Publication

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    MEDLINETA: Recent Patents Cardiovasc Drug

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