- 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 Related Products (384)
Related Products (384)
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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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HIF-2α-IN-12
0 ImagesCat. No.: HY-163599CAS No.: 3034488-33-7HIF-2α-IN-12 (9) is a HIF-2α inhibitor, with an IC50 of 0.9 μM. -
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PHD2-IN-4
0 ImagesCat. No.: HY-170917CAS No.: 2924181-60-0PHD2-IN-4 (compound 1) is a PHD2 inhibitor. PHD2-IN-4 inhibits PHD2 with an IC50 of 4 nM. PHD2-IN-4 is potential for chronic kidney disease research. -
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MO-2097
0 ImagesCat. No.: HY-N13009CAS No.: 2744300-63-6MO-2097 is a RAF-1/HIF-1α inhibitor. MO-2097 induces RAF-1 destabilization, leading to a reduction in EMT-associated transcription factors and mesenchymal markers. MO-2097 inhibits HIF-1a protein expression mediated by hnRNPA2B1 under hypoxic and mimetic hypoxia. MO-2097 induces mitochondrial ROS, which leads to apoptosis in cells. MO-2097 effectively suppresses colorectal cancer metastasis by inhibiting the RAF/MEK/ERK signaling pathway. MO-2097 attenuates tumor growth in a xenograft HCT116 cell mouse model. MO-2097 can be used for the study of colorectal cancer. -
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AJM 290
0 ImagesCat. No.: HY-164259CAS No.: 840474-95-5AJM 290 is a Trx-1 inhibitor. AJM 290 is an inhibitor of the HIF-1α COOH-terminal transactivation domain, and blocks HIF-1 binding to DNA. -
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- HIF-1 inhibitor-5
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DMOG (GMP)
0 ImagesCat. No.: HY-15893GCAS No.: 89464-63-1Synonyms: Dimethyloxallyl Glycine (GMP)DMOG (GMP) is the GMP level of DMOG (HY-15893). GMP small molecules works appropriately as an auxiliary reagent for cell therapy manufacture. DMOG (GMP) is a HIF-1α stabilizer. DMOG (GMP) promotes the osteogenic, angiogenic, and chondrogenic differentiation of stem cells by stabilizing the expression of HIF-1α. DMOG (GMP) can enhance the osteogenic and angiogenic differentiation potential of stem cells, thereby improving bone regeneration in bone defects. DMOG (GMP) can be used in the research of bone defect repair, vascularized bone regeneration, and the treatment of bone-related diseases (such as osteoporosis and femoral head necrosis) . -
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D-01
0 ImagesCat. No.: HY-162601D-01 is a dual-targeting inhibitor of HIF-1α and EZH2 (IC50: 4.86 μM and 0.99 μM respectively). D-01 inhibits the expression of H3K27me3 protein. D-01 inhibits the migration, clone and the invasion of A549 cells, and also inhibits tube formation of HUVECs. D-01 can be used for research of lung cancer. -
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DS79540454
0 ImagesCat. No.: HY-180164CAS No.: 1462947-17-6DS79540454 is a HIF-PHD2 inhibitor with an IC50 0.26 μM. DS79540454 can be used in the research of renal anemia. -
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Amifostine sodium
0 ImagesCat. No.: HY-B0639CCAS No.: 59178-37-9Synonyms: WR2721 sodiumAmifostine sodium (WR2721 sodium) is a phosphorus sulfate with radioprotective activity. Amifostine sodium can cause splenic vasodilation and may block autonomic ganglia. Amifostine sodium is clinically used to prevent cisplatin-induced ototoxicity. -
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HIF-PHD-IN-2
0 ImagesCat. No.: HY-139993CAS No.: 2711720-45-3HIF-PHD-IN-2 (compound 25) is a potent PHD inhibitor with IC50s of <100 nM for PHD1, PHD2 and PHD3, respectively. -
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Threo-Chloramphenicol-d6
0 ImagesCat. No.: HY-B0239S2Threo-Chloramphenicol-d6 is the deuterium labeled Chloramphenicol. Chloramphenicol is an orally active, potent and broad-spectrum antibiotic. Chloramphenicol shows antibacterial activity. Chloramphenicol represses the oxygen-labile transcription factor and hypoxia inducible factor-1 alpha (HIF-1α) in hypoxic A549 and H1299 cells. Chloramphenicol suppresses the mRNA levels of vascular endothelial growth factor (VEGF) and glucose transporter 1, eventually decreasing VEGF release. Chloramphenicol can be used for anaerobic infections and lung cancer research. -
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HIF-2α-IN-10
0 ImagesCat. No.: HY-163597CAS No.: 3034532-74-3HIF-2α-IN-10 (17) is a HIF-2α inhibitor, with an IC50 of 0.05 μM. -
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- Cyclo(CRVIIF)
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- HIF-1α-IN-6
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JPHM-2-167
0 ImagesCat. No.: HY-170914CAS No.: 1258877-17-6JPHM-2-167 (Compound 11) is a selective PHD (prolyl hydroxylase domain enzyme) inhibitor. JPHM-2-167 inhibits PHD2, PHD3 with IC50s of 0.253 μM and 3.95 μM, respectively. JPHM-2-167 can be used for chronic kidney disease . -
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Arylsulfonamide 64B
0 ImagesCat. No.: HY-124875CAS No.: 1342890-83-8Synonyms: HIF inhibitor 64BArylsulfonamide 64B (HIF inhibitor 64B) is an inhibitor of the hypoxia-induced factor (HIF). Arylsulfonamide 64B inhibits hypoxia/HIF-induced expression of c-Met and CXCR4 and reduces primary tumor growth and metastasis of uveal melanoma mouse model. -
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- (Rac)-Dencichine
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Molidustat sodium
0 ImagesCat. No.: HY-W747868CAS No.: 1375799-59-9Molidustat sodium is an orally active inhibitor of hypoxia-inducible factor prolyl hydroxylase (HIF-PH) with IC50 values of 480 nM, 280 nM, and 450 nM for PHD1, PHD2, and PHD3, respectively. Molidustat sodium can elevate the levels of circulating erythropoietin (EPO) to near-normal physiological ranges. Molidustat sodium can be utilized in the research of renal anemia. -
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PHD-1-IN-2
0 ImagesCat. No.: HY-153510CAS No.: 2009344-53-8PHD-1-IN-2 is an orally active inhibitor of hypoxia-inducible factor prolyl hydroxylase domain 1 (PHD-1) with an IC50 of 0.07 μM. PHD-1-IN-2 acts as a substrate of MDR1 in MDR1-MDCK cell monolayer assays. PHD-1-IN-2 can be used in the research of ischemia, inflammatory responses and neurodegenerative diseases, such as inflammatory bowel disease and ischemia-reperfusion injury. -
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Multi-kinase-IN-8
0 ImagesCat. No.: HY-179439Multi-kinase-IN-8 is a muti-kinase inhibitor. Multi-kinase-IN-8 inhibits COX-1 (IC50 of 12.6 μM), COX-2 (IC50 of 0.05 μM) and VEGFR-2 (IC50 of 0.12 nM). Multi-kinase-IN-8 inhibits tumor-associated carbonic anhydrases (CA IX and CA XII with Ki of 31.5 nM and 386.9 nM, respectively). Multi-kinase-IN-8 triggers cell cycle arrest and apoptosis through upregulation of Caspase 9 and Bax along with downregulation of Bcl 2. Multi-kinase-IN-8 suppresses PGE2, p-VEGFR-2, MMP-9 and HIF-1α and exhibits growth-inhibitory activity against breast cancer, lung cancer, and colorectal adenocarcinoma. -
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Sorry. There is currently no product that acts on isoform Bcl-2, Bcl-W and Bim together.Please
try each isoform separately.