25 Results for "

Antiprion

" in MedChemExpress (MCE) Product Catalog:
Products (25)

25 Results for "Antiprion" in MCE Product Catalog:

4
4 Cited Publications
Cat. No.: HY-111022
CAS No.: 951441-04-6
Purity:  99.93%
Synonyms: Sephin1; IFB-088
Target:  

Phosphatase

Research Areas:  

Infection Inflammation/Immunology

Icerguastat (Sephin1), a derivative of Guanabenz lacking the α2-adrenergic activity, is a selective inhibitor of the phosphatase regulatory subunit PPP1R15A (R15A). Icerguastat inhibits eIF2α dephosphorylation, thereby prolonging the protective response. Anti-prion effect .
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1
1 Cited Publications
Cat. No.: HY-15728
CAS No.: 926037-48-1
Purity:  98.92%
Synonyms: IY-5511
Radotinib (IY-5511) is an orally active and BBB-permeable selective tyrosine kinase Bcr-Abl1 inhibitor with an IC50 of 34 nM. Radotinib has anti-prion and anti-tumor activities. Radotinib can inhibit the proliferation, induce cell cycle arrest and apoptosis of tumor cells . Radotinib can be used in the research of cancer such as chronic myeloid leukemia and multiple myeloma, as well as neurodegenerative diseases such as prion diseases .
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1
1 Cited Publications
Cat. No.: HY-114621
CAS No.: 1451058-50-6
Purity:  99.50%
Target:  

Flavivirus

Research Areas:  

Infection

DB772 hydrate is a bovine viral diarrhoea virus (BVDV) inhibitor. DB772 also has anti-prion activity .
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1
1 Cited Publications
Cat. No.: HY-114621A
Purity:  99.89%
Target:  

Flavivirus

Research Areas:  

Infection

DB772 hydrate is a bovine viral diarrhoea virus (BVDV) inhibitor. DB772 also has anti-prion activity .
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Cat. No.: HY-150514
CAS No.: 1381459-14-8
Purity:  99.34%
Target:  

Prion Protein

Research Areas:  

Infection

ARN1468 (compound 5) is an orally active and potent SerpinA3n inhibitor. ARN1468 can inhibit serpins activity would set the protease free to further reduce prion accumulation. ARN1468 shows anti-prion effect in ScGT1 RML, ScGT1 22L, ScN2a RML, and ScN2a 22L cell lines, with EC50 values of 8.64, 19.3, 11.2, and 6.27 μM .
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Cat. No.: HY-W081348
CAS No.: 60798-06-3
1-(4-Methoxyphenyl)-3-methyl-1H-pyrazol-5(4H)-one (Compound 2) has antiprion activity in ScN2a and F3 cells with IC50 values of 13 nM and 25 nM, respectively .
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Cat. No.: HY-153756
CAS No.: 749212-56-4
Purity:  ≥95.0%
Target:  

Prion Protein

Research Areas:  

Infection

GFP16 is a low affinity antiprion compound. GFP16 can be used for research of antiprion drug discovery .
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Cat. No.: HY-13735C
CAS No.: 56100-42-6
Purity:  98.35%
Target:  

Bacterial

Research Areas:  

Infection

l-Atabrine dihydrochloride is a less active enantiomer of quinacrine which displays antiprion activity.
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Cat. No.: HY-124375
CAS No.: 1426047-52-0
Target:  

Prion Protein

Research Areas:  

Infection

IND81 is an orally active antiprion with IC50 value of 1.95 μM. IND81 reduces abnormal, misfolded, disease-causing forms of benign prion proteins that are normally present on or within cells .
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Cat. No.: HY-117856
CAS No.: 1426047-44-0
Purity:  99.57%
Target:  

Prion Protein

Research Areas:  

Infection

IND24 is a potent antiprion agent with an EC50 value of 1.27 µM. IND24 decreases abnormal, misfolded, pathogenic forms of benign normally occurring prion protein on the cell surface or inside the cell .
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Cat. No.: HY-138865
CAS No.: 119662-55-4
Purity:  98.35%
Target:  

Prion Protein

Research Areas:  

Infection

BiCAPPA is the first bivalent antiprion ligand. BiCAPPA can decrease infectious conformational form of prion protein (PrP Sc) from scrapie-infected cells, with an EC50 of 0.32 μM .
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Cat. No.: HY-107662
CAS No.: 34320-83-7
Purity:  99.72%
Target:  

Apoptosis

Research Areas:  

Infection Cancer

TCS PrP Inhibitor 13, an antiprion agent, is a cellular prion protein (PrP C) inhibitor. TCS PrP Inhibitor 13, as a protease-resistant form of prion protein (PrP-res) accumulation inhibitor, shows an IC50 value of 3 nM in both ScN2a and F3 cell lines. TCS PrP Inhibitor 13 induces Schwannoma cells apoptosis .
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Cat. No.: HY-147371
CAS No.: 115618-99-0
Target:  

Parasite

Research Areas:  

Infection Neurological Disease

Quinoprazine is a potent inhibitor of Vaccinia virus DNA synthesis with an IC50 value of 10 μM. Quinoprazine has antimalarial activity against Plasmodium berghei and also displays antiprion potency, significantly decreases PrP S c levels - .
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Cat. No.: HY-13735D
CAS No.: 56100-41-5
Purity:  99.64%
Target:  

Bacterial

Research Areas:  

Infection

d-Atabrine dihydrochloride is an active enantiomer of quinacrine which displays antiprion activity.
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Cat. No.: HY-114621B
CAS No.: 433735-90-1
Target:  

Flavivirus

Research Areas:  

Infection

DB772 free base is a bovine viral diarrhoea virus (BVDV) inhibitor. DB772 free base also has anti-prion activity .
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Cat. No.: HY-100857
CAS No.: 1315475-30-9
Target:  

Fluorescent Dye

Research Areas:  

Neurological Disease

PrPSc-IN-1 is a fluorescent probe, binds to the misfolded protein PrP Sc, inhibits its accumulation, with an IC50 of 1.6 μM. Anti-prion activity .
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Cat. No.: HY-110365
CAS No.: 1883549-35-6
Synonyms: Sephin1 Carbonate; IFB-088 Carbonate
Target:  

Phosphatase

Research Areas:  

Infection

Icerguastat (Sephin1) Carbonate, a derivative of Guanabenz lacking the α2-adrenergic activity, is a selective inhibitor of the phosphatase regulatory subunit PPP1R15A (R15A). Icerguastat Carbonate inhibits eIF2α dephosphorylation, thereby prolonging the protective response. Anti-prion effect .
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Cat. No.: HY-147702
CAS No.: 2512200-83-6
Target:  

Prion Protein

Research Areas:  

Infection Neurological Disease

BB 0305179 (compound 59) is a potent anti-prion agent, with an IC50 of 4.7 μM. BB 0305179 inhibits the toxicity of a specific PrP mutant carrying a deletion in the hydrophobic domain . BB 0305179 is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.
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Cat. No.: HY-175136
CAS No.: 2242615-97-8
Synonyms: GAh acetate
Target:  

Adrenergic Receptor

Research Areas:  

Infection Neurological Disease

Chloroguanabenz (acetate) is an antiprion agent and a derivative of the α2-adrenergic receptor agonist guanabenz. Chloroguanabenz (acetate) can inhibit the formation of prion in yeast and mammalian in vitro assays. Chloroguanabenz (acetate) can reduce the levels of truncated Huntingtin derivative Htt48 in HEK293T cells. Chloroguanabenz (acetate) can be studied in research on Huntington’s disease .
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Cat. No.: HY-134561
CAS No.: 651055-83-3
Synonyms: 6A-8tFP
Target:  

Prion Protein

Research Areas:  

Infection

6-Amino-8-trifluoromethylphenanthridine (6A-8tFP) is an antiprion agent and a derivative of 6-aminophenanthridine (HY-135189). It inhibits protein folding activity of the ribosome (PFAR) when used at a concentration of 150 μM.2 6A-8tFP directly competes with protein substrates for the ribosomal active site.
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