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HIF

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Hypoxia inducible factors (HIFs) are heterodimeric proteins belonging to the basic helix-loop-helix-PAS (bHLH/PAS) family of transcription factors that mediate the primary transcriptional response to stress caused by hypoxia (accessible O2 level < 2%). HIFs are characterized by containing two subunits, including O2-labile α subunit (HIFα) and constitutively expressed β subnit (HIFβ). Mammalian HIFα consists of three isoforms, including HIF1α, HIF2α and HIF3α, which play an essential role in the regulation of HIF activity by O2 availability. Under normal O2 tension, HIFα is hydroxylated at the two conserved proline residues within the O2-dependent degradation (ODD) domain by prolylhydroxylase domain proteins (PHDs) and undergoes proteosomal degradation catalyzed by a complex formed by E3 ubiquitin ligase and the von Hippel-Lindau protein (pVHL); while, under hypoxia, HIFα stabilizes with PHDs being deactivated and hence induce transcription of genes with adaptive functions.

Products Related to HIF(59)

  • GC10046 structure
    GC10046Molidustat (BAY85-3934)
    CAS: 1154028-82-6
    Purity: >99.00%

    Molidustat (BAY85-3934) (BAY 85-3934) is a novel inhibitor of hypoxia-inducible factor prolyl hydroxylase (HIF-PH) with mean IC50 values of 480 nM for PHD1, 280 nM for PHD2, and 450 nM for PHD3.

  • GC11031 structure
    GC11031PX-478 2HCl
    CAS: 685898-44-6
    Purity: >98.00%

    PX-478 is a selective inhibitor that suppresses constitutive and hypoxia-induced HIF-1α levels.

  • GC11767 structure
    GC11767Hydralazine HCl
    CAS: 304-20-1
    Purity: >99.50%

    Hydralazine HCl is a orally active antihypertensive agent, reduces peripheral resistance directly by relaxing the smooth muscle cell layer in arterial vessel.

  • GC12255 structure
    GC12255IOX4
    CAS: 1154097-71-8
    Purity: >99.50%

    PHD2 inhibitor

  • GC12487 structure
    GC12487Adaptaquin
    CAS: 385786-48-1
    Purity: >98%

    HIF-prolyl hydroxylase-2 (PHD2) inhibitor

  • GC12821 structure
    GC12821Oltipraz
    CAS: 64224-21-1
    Purity: >99.50%

    Oltipraz is an HIF-1α inhibitor (IC 50 =10μM) and an Nrf2 activator.

  • GC14282 structure
    GC14282AKBA (3-acetyl-11-keto-β-Boswellic Acid)
    CAS: 67416-61-9
    Purity: >98.00%

    AKBA (3-acetyl-11-keto-β-Boswellic Acid) is a pentacyclic triterpene acid that effectively and non-competitively inhibits 5-lipoxygenase (5-LOX), exhibiting various biological activities including anti-inflammatory, antitumor, and neuroprotective effects.

  • GC15379 structure
    GC15379JNJ-42041935
    CAS: 1193383-09-3
    Purity: >99.50%

    Hypoxia-inducible factor (HIF) prolyl hydroxylase (PHD) inhibitor

  • GC15473 structure
    GC15473Amifostine
    CAS: 20537-88-6
    Purity: >98.00%

    Amifostine, an inorganic thiophosphate, is a selective broad-spectrum cytoprotector of normal tissues.

  • GC16195 structure
    GC161952,4-DPD
    CAS: 41438-38-4
    Purity: >98%

    Diethyl pyridine-2,4-dicarb is a potent prolyl 4-hydroxylase-directed proinhibitor.

  • GC16638 structure
    GC16638FG2216
    CAS: 223387-75-5
    Purity: >99.00%

    HIF-prolyl hydroxylase inhibitor

  • GC16647 structure
    GC16647Daprodustat(GSK1278863)
    CAS: 960539-70-2
    Purity: >98.00%

    Daprodustat(GSK1278863) (GSK1278863) is an orally active hypoxia-inducible factor prolyl hydroxylase (HIF-PH) inhibitor being developed for the treatment of anemia associated with chronic kidney disease.

  • GC16811 structure
    GC16811Vadadustat
    CAS: 1000025-07-9
    Purity: >98.00%

    HIF-PH inhibitor

  • GC17358 structure
    GC17358Octyl-α-ketoglutarate
    CAS: 876150-14-0
    Purity: >95.00%

    prolyl hydroxylases (PHD) activator

  • GC18236 structure
    GC18236Echinomycin
    CAS: 512-64-1
    Purity: >95.00%

    An inhibitor of HIF1mediated gene transcription

  • GC19251 structure
    GC19251MK-8617
    CAS: 1187990-87-9
    Purity: >98.00%

    MK-8617 is an orally active pan-inhibitor of hypoxia-inducible factor prolyl hydroxylase 1-3 (HIF PHD1-3) with an IC50 of 1 nM for PHD2.

  • GC30263 structure
    GC30263Glucosamine (D-Glucosamine)
    CAS: 3416-24-8
    Purity: >98.00%

    Glucosamine (D-Glucosamine) (D-Glucosamine (D-Glucosamine)) is an amino sugar and a prominent precursor in the biochemical synthesis of glycosylated proteins and lipids, is used as a dietary supplement.

  • GC31230 structure
    GC31230Dencichin (Dencichine)
    CAS: 5302-45-4
    Purity: >98.00%

    Dencichin is a non-protein amino acid originally extracted from Panax notoginseng, and can inhibit HIF-prolyl hydroxylase-2 (PHD-2) activity.

  • GC31358 structure
    GC31358HIF-2α-IN-1
    CAS: 1799948-06-3
    Purity: >99.50%

    HIF-2α-IN-1 is a HIF-2α inhibitor has an IC50 of less than 500 nM in HIF-2α scintillation proximity assay.

  • GC31498 structure
    GC31498TP0463518
    CAS: 1558021-37-6
    Purity: >98.00%

    TP0463518 is a potent hypoxia-inducible factor prolyl hydroxylases (PHDs) inhibitor

  • GC32083 structure
    GC32083Acriflavine
    CAS: 8048-52-0
    Purity: >98.00%

    Acriflavine is a fluorescent dye for labeling high molecular weight RNA.

  • GC32228 structure
    GC32228Tilorone dihydrochloride
    CAS: 27591-69-1
    Purity: >99.50%

    An interferon-inducing antiviral agent

  • GC32449 structure
    GC32449Desidustat
    CAS: 1616690-16-4
    Purity: >98.00%

    An inhibitor of HIF-PH

  • GC32680 structure
    GC32680PT-2385
    CAS: 1672665-49-4
    Purity: >99.00%

    PT-2385 is a selective HIF-2α inhibitor with a Ki of less than 50 nM.