46 Results for "

PHD2

" in MedChemExpress (MCE) Product Catalog:
Products (46)

46 Results for "PHD2" in MCE Product Catalog:

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Cat. No.: HY-P5648
Target:  

Bacterial

Research Areas:  

Infection

PhD2 is an antimicrobial peptide derived from monkey white blood cells. PhD2 has activity against bacteria and fungus Candida albicans .
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22
22 Publications Verification
Cat. No.: HY-15468
CAS No.: 931398-72-0
Purity:  98.02%
Research Areas:  

Cancer

IOX2, a chemical probe, is a specific prolyl hydroxylase-2 (PHD2) inhibitor with IC50 of 22 nM. IOX2 regulates platelet function and arterial thrombosis by upregulating HIF-1α expression and inhibiting ROS production. IOX2 can be used in the study of thrombotic diseases [2].
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8
8 Cited Publications
Cat. No.: HY-12654
CAS No.: 1154028-82-6
Purity:  98.58%
Synonyms: BAY 85-3934
Research Areas:  

Cardiovascular Disease

Molidustat (BAY 85-3934) 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 can elevate the levels of circulating erythropoietin (EPO) to near-normal physiological ranges. Molidustat can be utilized in the research of renal anemia [2].
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8
8 Cited Publications
Cat. No.: HY-120110
CAS No.: 1154097-71-8
Purity:  99.83%
IOX4 is a selective HIF prolyl-hydroxylase 2 (PHD2) inhibitor with an IC50 value of 1.6 nM, induces HIFα in cells and in wildtype mice with marked induction in the brain tissue. IOX4 competes with and displaces 2-oxoglutarate (2OG) at the active site of PHD2 .
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6
6 Cited Publications
Cat. No.: HY-15641
CAS No.: 223387-75-5
Purity:  99.46%
Synonyms: IOX3; YM311
Research Areas:  

Metabolic Disease

FG-2216 (IOX3) is a potent and orally active inhibitor of HIF prolyl hydroxylase-2 (PHD2), with an IC50 of 3.9 μM. FG-2216 induces robust erythropoietin and modest fetal hemoglobin in vivo [2] .
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4
4 Cited Publications
Cat. No.: HY-101023
CAS No.: 1187990-87-9
Purity:  99.92%
Research Areas:  

Inflammation/Immunology

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.
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1
1 Cited Publications
Cat. No.: HY-112144
CAS No.: 1558021-37-6
Purity:  99.25%
TP0463518 is an orally active, competitive pan-inhibitor of hypoxia-inducible factor prolyl hydroxylases PHD1/2/3. TP0463518 competitively inhibits human PHD1 (IC50=18 nM), PHD2 (Ki=5.3 nM), and PHD3 (IC50=63 nM), and targets monkey PHD2 with an IC50 of 22 nM. TP0463518 inhibits PHD-catalyzed hydroxylation to stabilize HIFα, thereby upregulating erythropoietin (EPO) expression and enhancing intestinal iron absorption (such as increased DMT-1 and dCYTb expression), improving anemia. TP0463518 is mainly used for the research of renal anemia and inflammatory anemia [2].
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1
1 Cited Publications
Cat. No.: HY-12315
CAS No.: 5262-39-5
Purity:  99.28%
Synonyms: N-Oxaloglycine
Research Areas:  

Cancer

N-Oxalylglycine (N-Oxaloglycine) is a Jumonji C-domain-containing histone lysine demethylase inhibitor. N-Oxalylglycine inhibits JMJD2A, JMJD2C and JMJD2D. N-Oxalylglycine also inhibits HIF prolylhydroxylase domain-1 (PHD-1) and PHD-2, with an IC50 of 2.1 μM and 5.6 μM, respectively [2].
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Cat. No.: HY-N1477
CAS No.: 5302-45-4
Synonyms: Dencichin; ODAP
Category:  

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