HIF

HIF(缺氧诱发因素)

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.

HIF 相关产品(101)

  • GC12698 structure
    GC12698BAY 87-2243
    CAS: 1227158-85-1
    纯度: >99.50%

    BAY 87-2243是一种具有高效选择性的缺氧诱导因子-1(HIF-1)抑制剂。

  • GC13018 structure
    GC13018IOX2(Glycine)
    CAS: 931398-72-0
    纯度: >99.50%

    A selective PHD2 inhibitor

  • GC13139 structure
    GC13139FG-4592 (ASP1517)
    CAS: 808118-40-3
    纯度: >99.50%

    FG-4592 作为一种口服生物可利用的缺氧诱导因子 (HIF) 脯氨酰羟化酶抑制剂,可通过 HIF 介导的转录促进协调性红细胞生成。

  • GC13141 structure
    GC13141KC7F2
    CAS: 927822-86-4
    纯度: >99.00% / >98.00%

    KC7F2是转录因子HIF-1(缺氧诱导因子-1)的抑制剂,其IC₅₀分别为20μM ,KC7F2常被用于肿瘤发育和血管形成的研究中

  • GC14319 structure
    GC14319ML 228
    CAS: 1357171-62-0
    纯度: >98.00%

    A HIF pathway activator

  • GC15084 structure
    GC150842-Methoxyestradiol (2-MeOE2)
    CAS: 362-07-2
    纯度: >99.50% / >98.00%

    2-Methoxyestradiol (2-MeOE2/2-Me)是一种HIF-1α抑制剂。

  • GC15594 structure
    GC15594PX 12
    CAS: 141400-58-0
    纯度: >98.00%

    An irreversible inhibitor of thioredoxin-1

  • GC17405 structure
    GC17405Chetomin
    CAS: 1403-36-7
    纯度: >95.00%

    Chetomin是一种来源于 Chaetomium 属真菌的天然生物碱,具有显著的抗癌和抗炎作用。

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

    A pan-HIF-PH inhibitor

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

    PX-478是一种选择性抑制剂,可以抑制常规和低氧诱导的HIF-1α水平。

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

    An antihypertensive agent

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

    A selective, bioavailable inhibitor of HIF-PH2

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

    A Nrf2 and CAR activator

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

    AKBA (3-acetyl-11-keto-β-Boswellic Acid)是一种五环三萜酸,能够有效地非竞争性地抑制5-脂氧合酶(5-lipoxygenase, 5-LOX),具有抗炎、抗肿瘤、神经保护等多种生物活性。

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

    A selective inhibitor of HIF-PH enzymes

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

    An inhibitor of HIF-PH2

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

    A HIF-PH1, -2, and -3 inhibitor

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

    An inhibitor of HIF-PH2 and HIF-PH3

  • GC16973 structure
    GC16973DMOG
    CAS: 89464-63-1
    纯度: >98.50% / >98.00%

    DMOG(二羟基丙氨酸)是 α-酮戊二酸辅助因子的拮抗剂和 HIF-脯氨酸羟化酶的抑制剂,导致 HIF-1α 蛋白在细胞核中的稳定和积累。

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

    An inhibitor of HIF-1-mediated gene transcription

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

    A HIF-PH1, -2, and -3 inhibitor

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

    Glucosamine (2-amino-2-deoxy-D-glucose) is an amino sugar and a prominent precursor in the biochemical synthesis of glycosylated proteins and lipids. It is commonly used as a treatment for osteoarthritis. Glucosamine(GS) treatment selectively downregulates HIF-1α at the protein level in YD-8 cells via interference of production of the citric acid cycle metabolites.

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

    Dencichin是一种最初从三七中提取的非蛋白质氨基酸,可以抑制HIF-脯氨酰羟化酶2(PHD-2)的活性。

  • GC31358 structure
    GC31358HIF-2&alpha;-IN-1
    CAS: 1799948-06-3
    纯度: >99.50%

    HIF-2α-IN-1是一种HIF-2α抑制剂,IC50值小于500nM。