23 Results for "

Hepcidin inhibitor

" in MedChemExpress (MCE) Product Catalog:
Products (23)

23 Results for "Hepcidin inhibitor" in MCE Product Catalog:

68
68 Publications Verification
Cat. No.: HY-13426
CAS No.: 808118-40-3
Purity:  99.92%
Synonyms: FG-4592
Research Areas:  

Infection Cancer

Roxadustat is an orally active hypoxia-inducible factor prolyl-hydroxylase (PHD) inhibitor (HIF-PHI) that promotes erythropoiesis through increasing endogenous erythropoietin, improving iron regulation, and reducing hepcidin .
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6
6 Cited Publications
Cat. No.: HY-112220
CAS No.: 2095668-10-1
Target:  

Ferroportin

Research Areas:  

Metabolic Disease

VIT-2763, an oral ferroportin inhibitor, inhibits hepcidin binding to ferroportin and blocks iron efflux. VIT-2763 has the potential in the treatment of β-thalassemia .
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1
1 Cited Publications
Cat. No.: HY-P99590A
Synonyms: RAP-011
Sotatercept (mIgG2a) (RAP-011), the murine homolog of Sotatercept (ACE-011) (HY-P99590), is a soluble activin receptor type IIA (ActRIIA) ligand trap. Sotatercept (mIgG2a) inhibits the binding of activin A and other members of the TGF-β superfamily (such as Activin A/B, GDF11 and BMP9/10) to their receptors by combining and neutralizing them, thereby regulating cell proliferation and differentiation. Sotatercept (mIgG2a) mainly inhibits the SMAD2/3 signaling pathway, and can be used in various diseases such as chronic kidney disease. Sotatercept (mIgG2a) reduces the expression of erythropoietic hepcidin (ERFE), regulates iron metabolism, and promotes red blood cell production. Sotatercept (mIgG2a) has a dual effect of promoting bone formation (anabolic) and inhibiting bone resorption (catabolic) .
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Cat. No.: HY-113066C
CAS No.: 43139-22-6
Purity:  99.88%
Synonyms: GDP sodium, Type I, 96% (HPLC)
Guanosine 5'-diphosphate (GDP) sodium, 96% (HPLC) is a nucleoside diphosphate that activates adenosine 5'-triphosphate-sensitive K + channel. Guanosine 5'-diphosphate sodium, 96% (HPLC) is an iron mobilizer, which forms a complex with hepcidin to inhibit the hepcidin-ferroportin (FPN) interaction and modulates the IL-6/stat-3 pathway. Guanosine 5'-diphosphate sodium, 96% (HPLC) ameliorates the Turpentine-induced anemia of inflammation (AI) in mice when combined with FeSO4. Guanosine 5'-diphosphate sodium, 96% (HPLC) can be used in the research of AI .
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Cat. No.: HY-113066
CAS No.: 146-91-8
Synonyms: GDP
Guanosine 5'-diphosphate (GDP) is a nucleoside diphosphate that activates adenosine 5'-triphosphate-sensitive K + channel. Guanosine 5'-diphosphate is an iron mobilizer, which forms a complex with hepcidin to inhibit the hepcidin-ferroportin (FPN) interaction and modulates the IL-6/stat-3 pathway. Guanosine 5'-diphosphate ameliorates the Turpentine-induced anemia of inflammation (AI) in mice when combined with FeSO4. Guanosine 5'-diphosphate can be used in the research of AI .
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Cat. No.: HY-145608
CAS No.: 2173389-57-4
Purity:  99.77%
Synonyms: INCB-000928; NBU-928
Target:  

TGF-β Receptor

Research Areas:  

Cardiovascular Disease Cancer

Zilurgisertib (INCB-000928; NBU-928) is a selective ALK2 inhibitor with an IC50 value of 15 nM. Zilurgisertib inhibits SMAD1/5 phosphorylation with an IC50 value of 63 nM. Zilurgisertib inhibits hepcidin production and improve anemia. Zilurgisertib can be used in melanoma research .
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Cat. No.: HY-13426S
CAS No.: 2043026-13-5
Purity:  ≥98.0%
Roxadustat-d5 is deuterium labeled Roxadustat. Roxadustat is an oral hypoxia-inducible factor prolyl-hydroxylase inhibitor (HIF-PHI) that promotes erythropoiesis through increasing endogenous erythropoietin, improving iron regulation, and reducing hepcidin .
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Cat. No.: HY-107980
CAS No.: 2146177-09-3
Purity:  98.00%
Target:  

Ferroportin

Research Areas:  

Inflammation/Immunology

DS28120313 (compound 32) is an orally hepcidin production inhibitor with an IC50 of 0.093 μM .
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Cat. No.: HY-P11260
CAS No.: 3051556-89-6
Research Areas:  

Metabolic Disease

MD5 is a selective TMPRSS6 mimetic peptide inhibitor with an IC50 for recombinant human TMPRSS6 protein of 22 nM and a Ki of 3.4 nM. MD5 exhibits the significantly reduced inhibitory effect on Matriptase, with an IC50 of 352 nM and a Ki of 99.2 nM. MD5 exhibits good target specificity and only has a weak inhibitory effect on thrombin (Thrombin), with Ki of 120 nM. MD5 demonstrates good initial drugability and can be used for the study of iron overload diseases (such as hereditary hemochromatosis, β-thalassemia) .
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Cat. No.: HY-125288
CAS No.: 2247168-13-2
Target:  

Ferroportin

Research Areas:  

Metabolic Disease

DS42450411 is an orally active hepcidin production inhibitor with an IC50 of 32 nM. DS42450411 in an acute inflammatory mouse model induced by IL-6, DS42450411 significantly reduces serum hepcidin levels. DS42450411 can be used for studying iron homeostasis .
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Cat. No.: HY-P4370
CAS No.: 342790-23-2
Target:  

Bacterial Fungal

Research Areas:  

Infection

Hepcidin-20 (human) is a histidine-containing, cysteine-rich, β-sheet structured peptide. Hepcidin-20 (human) shows antifungal activity. Hepcidin-20 (human) inhibits biofilm formation and bacterial cell metabolism of polysaccharide intercellular adhesin (PIA)-positive and PIA-negative strains .
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Cat. No.: HY-177641
CAS No.: 1390631-57-8
Synonyms: NOX-H94
Target:  

Hepcidin

Research Areas:  

Others

Lexaptepid Pegol is a pegylated structured L-oligoribonucleotide. It binds and inhibits hepcidin.
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Cat. No.: HY-177641A
Synonyms: NOX-H94 sodium
Target:  

Hepcidin

Research Areas:  

Others

Lexaptepid Pegol sodium is a pegylated structured L-oligoribonucleotide. It binds and inhibits hepcidin.
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Cat. No.: HY-145965
CAS No.: 2443432-65-1
Purity:  99.33%
Target:  

Ferroportin

Research Areas:  

Metabolic Disease

Ferroportin-IN-1 is a ferroportin inhibitor extracted from patent WO2020123850A1 compound 23. Ferroportin-IN-1 can be used for the research of diseases caused by a lack of hepcidin or iron metabolism disorders .
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Cat. No.: HY-13426R
CAS No.: 808118-40-3
Synonyms: FG-4592 (Standard)
Roxadustat (Standard) is the analytical standard of Roxadustat. This product is intended for research and analytical applications. Roxadustat is an orally active hypoxia-inducible factor (HIF) prolyl-hydroxylase (PHD) inhibitor (HIF-PHI) that promotes erythropoiesis through increasing endogenous erythropoietin, improving iron regulation, and reducing hepcidin .
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Cat. No.: HY-W064657
CAS No.: 1380317-28-1
Target:  

JAK

Research Areas:  

Others

Momelotinib (dihydrochloride) is a JAK1/JAK2 inhibitor that also antagonizes ACVR1, leading to downregulation of Hepcidin expression and increased availability of iron for erythropoiesis. Momelotinib (dihydrochloride) can reduce transfusion burden and spleen enlargement caused by myelofibrosis, showing potential value in research and application within the field of myelofibrosis .
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Cat. No.: HY-123878
CAS No.: 2113642-80-9
Target:  

Hepcidin

Research Areas:  

Inflammation/Immunology

DS79182026 is an inhibitor of hepcidin production. DS79182026 exhibits hepcidin lowering ability in IL-6-induced acute inflammatory mouse model .
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Cat. No.: HY-149833
CAS No.: 324022-01-7
Target:  

Estrogen Receptor/ERR

Research Areas:  

Infection Metabolic Disease

ERRγ inverse agonist 2 (compound 19) is a potent and selective ERRγ inverse agonist with a Kd value of 6.5 μM. ERRγ inverse agonist 2 inhibits the expression of hepcidin, fibrinogen and gluconeogenic genes. ERRγ inverse agonist 2 has antimicrobial, anti-coagulant and antidiabetic activities .
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Cat. No.: HY-P991637
CAS No.: 2996101-49-4
Synonyms: REGN7999
Target:  

Ser/Thr Protease

Research Areas:  

Metabolic Disease

REGN7999 is a monoclonal antibody that inhibits TMPRSS6. REGN7999 inhibits TMPRSS6 activity, preventing Hemojuvelin (HJV) lysis, thereby enhancing BMP6-HJV signaling and increasing serum hepcidin. REGN7999 ameliorates iron overload and impaired erythropoiesis in a β-thalassemia mouse model by inhibiting TMPRSS6 activity. REGN7999 is indicated for research in β-thalassemia .
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Cat. No.: HY-107980R
CAS No.: 2146177-09-3
DS28120313 (Standard) is the analytical standard of DS28120313 (HY-107980). This product is intended for research and analytical applications. DS28120313 (compound 32) is an orally hepcidin production inhibitor with an IC50 of 0.093 μM .
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