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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(118)

  • GC73945 structure
    GC73945DYB-03
    CAS: 2982792-85-6
    Purity: >99.00%

    DYB-03 is an oral active HIF-1α/EZH2 inhibitor.

  • GC74310 structure
    GC74310Cyclo(CKLIIF) TFA
    Purity: >97.00%

    Cyclo CKLIIF is a dual inhibitor for poxia inducible factor (HIF) 1 and 2, with affinity for HIF1-α and HIF2-α PAS-B domains KD of 2.6 and 2.2 μM, respectively.

  • GC78962 structure
    GC78962MS1129
    Purity: >98%

    MS1129 is a DNMT degrader that induces proteasomal degradation of DNMT1, DNMT3A and DNMT3B proteins.

  • GC79574 structure
    GC79574mCPX
    CAS: 1351572-56-9
    Purity: >98%

    mCPX is a prodrug of the antifungal agent Ciclopirox olamine (CPX).

  • GC79669 structure
    GC79669PHD-1-IN-4
    CAS: 2009343-19-3
    Purity: >99.50%

    PHD-1-IN-4 is a brain-penetrant PHD-1 inhibitor with an IC 50 of 0.074 μM [1] .

  • GC79670 structure
    GC79670ZG-2686
    CAS: 1795110-22-3
    Purity: >98%

    ZG-2686 is a potent and selective HIF-2α agonist with an EC 50 of 0.25 µM.

  • GC79671 structure
    GC79671HIF-IN-2
    CAS: 1040535-05-4
    Purity: >95.00%

    HIF-IN-2 is a HIF/HIF prolyl hydroxylase inhibitor.

  • GC79816 structure
    GC79816Cryptolepine
    CAS: 480-26-2
    Purity: >98%

    Cryptolepine is an orally active multi-potent alkaloid with anti-cancer, anti-bacterial, anti-viral, anti-malarial, anti-inflammatory, anti-hyperglycemic, relieve pain and other properties.

  • GC80483 structure
    GC80483IOX2-NH2
    CAS: 931400-77-0
    Purity: >98.00%

    IOX2 -NH2 (example 115) is a derivative of IOX2.

  • GC80928 structure
    GC80928NP1192
    CAS: 2966791-41-1
    Purity: >99.00%

    NP1192 is a potent, selective PROTAC NAT10 degrader.

  • GC81027 structure
    GC81027PROTAC HIF-1α degrader-2
    CAS: 3095636-64-6
    Purity: >98%

    PROTAC HIF-1α degrader-2 is a highly efficient and selective PROTAC degrader targeting HIF-1α. PROTAC HIF-1α degrader-2 promotes HIF-1α degradation via the ubiquitin-proteasome pathway by facilitating the formation of a HIF-1α/VHL ternary complex.

  • GC81031 structure
    GC81031NEO-811
    CAS: 3084635-77-5
    Purity: >98%

    NEO-811 is a selective and orally active ARNT (HIF-1β) molecular glue degrader.

  • GC81447 structure
    GC81447ALDOA-IN-1
    Purity: >98.00%

    ALDOA-IN-1 is an aldolase A (ALDOA) inhibitor.

  • GC81584 structure
    GC815842-Amino-2-deoxy-D-glucopyranose
    CAS: 90-77-7
    Purity: >98.00%

    2-Amino-2-deoxy-D-glucopyranose is an isomeric form of Glucosamine.

  • GC81595 structure
    GC81595BCS12
    CAS: 329719-71-3
    Purity: >99.50%

    BCS12 is a CAIX inhibitor.

  • GC81602 structure
    GC81602Glucosamine sulfate potassium chloride
    CAS: 1296149-08-0
    Purity: >98.00%

    Glucosamine sulfate potassium chloride is an amino sugar and a prominent precursor in the biochemical synthesis of glycosylated proteins and lipids, is used as a dietary supplement.

  • GC81639 structure
    GC81639SH-26
    Purity: >98%

    SH-26 is a PHD1 PROTAC degrader with DC 50 s of 1.06 μM, 4.16 μM and 4.91 μM in MDA-MB-231, HepG2 and HEK-293T cells, respectively.

  • GC91083 structure
    GC91083Tiopronin-Cysteine Disulfide
    CAS: 77591-18-5
    Purity: >95.00%

    A metabolite of tiopronin

  • GN10308 structure
    GN10308Chlorogenic acid
    CAS: 327-97-9
    Purity: >98.00%

    Chlorogenic acid is a potent neuroprotective agent and also has antiviral,antifungal antioxidant and antitumor properties. CGA is also involved in regulating glucose and lipid metabolism and improving insulin sensitivity.

  • GN10452 structure
    GN10452Paeoniflorin
    CAS: 23180-57-6
    Purity: >98.00%

    Paeoniflorin is a pinane monoterpene glycoside extracted from the roots of Paeonia plants of the Ranunculaceae family, possessing multiple biological activities.

  • GN10518 structure
    GN10518Chitosamine hydrochloride
    CAS: 66-84-2
    Purity: >98.00%
  • GN10669 structure
    GN10669Glucosamine sulfate
    CAS: 29031-19-4
    Purity: >98.00%