- Signaling Pathways
- Metabolic Enzyme/Protease
- HIF/HIF Prolyl-Hydroxylase
HIF/HIF Prolyl-Hydroxylase
Hypoxia-inducible factors; HIFs; HIF-PH
HIF/HIF Prolyl-Hydroxylase Isoform Specific Products
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HIF/HIF Prolyl-Hydroxylase Inhibitors
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HIF/HIF Prolyl-Hydroxylase Agonists
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HIF/HIF Prolyl-Hydroxylase Antagonists
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HIF/HIF Prolyl-Hydroxylase Related Products (389)
Related Products (389)
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Antibodies (15)
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Related Compound Screening Libraries (1)
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HIF/HIF Prolyl-Hydroxylase Isoform Comparison
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VH-298 (Standard)
0 ImagesCat. No.: HY-100947RCAS No.: 2097381-85-4VH-298 (Standard) is the analytical standard of VH-298 (HY-100947). This product is intended for research and analytical applications. VH-298 is a highly potent inhibitor of the VHL:HIF-α interaction with a Kd value of 80 to 90 nM. VH-298 leads to HIF-α accumulation inside HeLa cells. VH-298 is an E3 ligase Ligand, and can be used for synthesis of PROTACs. -
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Sapanisertib (Standard)
0 ImagesSynonyms: INK-128 (Standard); MLN0128 (Standard); TAK-228 (Standard)Sapanisertib (INK-128; MLN0128; TAK-228) Standard is the analytical standard of Sapanisertib (HY-13328). This product is intended for research and analytical applications. Sapanisertib (INK-128; MLN0128; TAK-228) is an orally active dual mTORC1/mTORC2 inhibitor. Sapanisertib directly and simultaneously inhibits mTORC1/2 activity through competitive binding with ATP, thereby comprehensively blocking downstream processes such as protein and lipid synthesis and cytoskeletal reorganization, consequently suppressing tumor cell proliferation and promoting apoptosis. Sapanisertib is applicable to research on melanoma, ovarian cancer, pulmonary fibrosis, and hematological malignancies. -
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CLB-016
0 ImagesCat. No.: HY-113662CAS No.: 1005636-29-2CLB-016 is a potent Hypoxia-inducible factor (HIF-1) inhibitor with an IC50 of 19.1 μM. CLB-016 significantly suppresses HIF-1-mediated hypoxia response. -
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EZN-2968
0 ImagesCat. No.: HY-158826CAS No.: 1098309-50-2Synonyms: RO 707179EZN-2968 is an antisense oligonucleotide that specifically binds and inhibits the expression of HIF-1α mRNA. EZN-2968, inhibits tumor cell growth. -
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Fibrostatin F
0 ImagesCat. No.: HY-N14340CAS No.: 91776-45-3Fibrostatin F is a proline hydroxylase inhibitor found in Strptomyces catenulae. -
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- ML228 analog
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S 4404
0 ImagesCat. No.: HY-123004CAS No.: 143199-54-6S 4404 is a prolyl-4-hydroxylase inhibitor. S 4404 functions as a non-substrate of hepatobiliary transport systems. S 4404 undergoes metabolic breakdown into fluorescent and red-colored metabolites. S 4404 can be used for the research of liver fibrosis. -
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- MK-8617 (Standard)
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GW405833 hydrochloride (Standard)
0 ImagesCat. No.: HY-110036ARCAS No.: 1202865-22-2Synonyms: L768242 hydrochloride (Standard)GW405833 hydrochloride (Standard) is the analytical standard of GW405833 (hydrochloride) (HY-110036A). This product is intended for research and analytical applications. GW405833 (L768242) hydrochloride is a potent, selective cannabinoid receptor 2 (CB2) agonist. GW405833 has EC50 and Ki values of 0.65 nM and 3.92 nM for CB2, and EC50 and Ki values of 16.1 μM and 4772 nM for CB1. GW405833 hydrochloride also exhibits non-competitive CB1 antagonist, exerting its analgesic effect through a CB1 receptor (rather than CB2) dependent mechanism. GW405833 hydrochloride can significantly inhibit the production of cAMP stimulated by Forskolin (HY-15371). GW405833 hydrochloride inhibits glycolysis by down-regulating HIF-1α, thereby alleviating acute liver failure (ALF). -
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PX-478 (Standard)
0 ImagesCat. No.: HY-10231RCAS No.: 685898-44-6PX-478 (Standard) is the analytical standard of PX-478 (HY-10231). This product is intended for research and analytical applications. PX-478 is a multifunctional HIF-1α inhibitor with properties including radiosensitization, autophagy activation, and lipid accumulation inhibition. PX-478 also blocks hypoxia-induced VEGF production and regulates β-cell phenotypes under hypoxic conditions. PX-478 induces cell cycle arrest and DNA damage, restores autophagic function, reduces foam cell formation, and maintains glucose homeostasis. PX-478 is widely used in research on related diseases such as human tumors (e.g., prostate cancer), type 2 diabetes, and atherosclerosis. -
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MPT0B098
0 ImagesCat. No.: HY-124595CAS No.: 1254363-89-7MPT0B098 is a microtubule inhibitor with a Ki of 0.8 μM and an IC50 of 0.8 μM. MPT0B098 inhibits tubulin polymerization, blocks HuR nuclear-cytoplasmic translocation to decrease HIF-1α mRNA stability, suppresses HIF-1α, TGF-β/Smad, JAK2/STAT3 and FAK/actin cytoskeleton signaling pathways, upregulates SOCS3 to reinforce the inhibition of JAK2/STAT3 cascade, and induces apoptosis. MPT0B098 can be used for research on multiple malignancies including head and neck squamous cell carcinoma and human non-small cell lung cancer. -
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Agnuside (Standard)
0 ImagesSynonyms: Agnoside (Standard)Agnuside (Standard) is the analytical standard of Agnuside. This product is intended for research and analytical applications. Agnuside is used in the study of asthma, inflammation, and angiogenic diseases. Agnuside is an orally active compound that can be extracted from Vitex negundo. -
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Fibrostatin D
0 ImagesCat. No.: HY-N14332CAS No.: 91776-46-4Fibrostatin D is a proline hydroxylase inhibitor found in Strptomyces catenulae. -
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PT2399 (Standard)
0 ImagesCat. No.: HY-108697RCAS No.: 1672662-14-4PT2399 (Standard) is the analytical standard of PT2399 (HY-108697). This product is intended for research and analytical applications. PT2399 is a potent and selective HIF-2α antagonist, which directly binds to HIF-2α PAS B domain with an IC50 of 6 nM. PT2399 displays potent antitumor activity in vivo. -
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Adaptaquin (Standard)
0 ImagesAdaptaquin (Standard) is the analytical standard of Adaptaquin (HY-101449). This product is intended for research and analytical applications. Adaptaquin is a BBB-penetrable HIF-PHDs inhibitor. Adaptaquin has anti-inflammatory and neuroprotective effects. Adaptaquin can effectively inhibit lipid peroxidation, maintain mitochondrial function, and reduce neuronal death. Adaptaquin can be used in the research of nervous system diseases such as Parkinson's disease. -
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ZG-2033
0 ImagesCat. No.: HY-139855CAS No.: 2685739-28-8ZG-2033 (Compound 26) is an orally active HIF-2α agonist that demonstrates nanomolar activity in luciferase reporter gene assays (EC50 = 490 nM). ZG-2033 has the effect of alleviating anemia and exhibits synergistic action with AKB-6548 (HY-101277) in anemia, and can be used in the study of renal anemia. -
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PHD-IN-5
0 ImagesCat. No.: HY-180560CAS No.: 2924181-95-1PHD-IN-5 (ISM4808) is an orally active PHD inhibitor that can be used for studying anemia in chronic kidney disease. -
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M1001 (Standard)
0 ImagesCat. No.: HY-111547RCAS No.: 874590-32-6M1001 (Standard) is the analytical standard of M1001 (HY-111547). This product is intended for research and analytical applications. M1001 is a weak hypoxia-inducible factor-2α (HIF-2α) agonist. M1001 can bind to the HIF-2α PAS-B domain, with a Kd of 667 nM. M1001 can be used in chronic Kidney disease research. -
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Vadadustat-13C6
0 ImagesCat. No.: HY-101277S1Synonyms: PG-1016548-13C6; AKB-6548-13C6Vadadustat-13C6 (PG-1016548-13C6) is 13C labeled Vadadustat. Vadadustat (PG-1016548) is a titratable, oral hypoxia-inducible factor prolyl hydroxylase (HIF-PH) inhibitor. Vadadustat is an erythropoiesis-stimulating agent and has the potential for anemia treatment in chronic kidney disease in vivo. -
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PHD-1-IN-3
0 ImagesCat. No.: HY-153512CAS No.: 2009345-20-2PHD-1-IN-3 is an orally active PHD-1 inhibitor with an IC50 of 0.09 μM. PHD-1-IN-3 acts via monodentate binding interaction with active site Fe2+ ion. -
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Sorry. There is currently no product that acts on isoform Bcl-2, Bcl-W and Bim together.Please
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