23 Results for "

Niclosamide

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

23 Results for "Niclosamide" in MCE Product Catalog:

43
43 Publications Verification
Art. -Nr.: HY-B0497
CAS. Nr.: 50-65-7
Synonyms: BAY2353
Forschungsgebiete:  

Infection Cancer

Niclosamide (BAY2353) is an orally active antihelminthic agent used in parasitic infection research . Niclosamide is a STAT3 inhibitor with an IC50 of 0.25 μM in HeLa cells . Niclosamide has biological activities against cancer, inhibits DNA replication in Vero E6 cells .
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43
43 Publications Verification
Art. -Nr.: HY-B0497C
CAS. Nr.: 1420-04-8
Synonyms: BAY2353 olamine
Forschungsgebiete:  

Infection Cancer

Niclosamide (BAY2353) olamine is an orally active antihelminthic agent used in parasitic infection research . Niclosamide olamin is a STAT3 inhibitor with an IC50 of 0.25 μM in HeLa cells . Niclosamide olamin has biological activities against cancer, and inhibits DNA replication in Vero E6 cells .
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3
3 Cited Publications
Art. -Nr.: HY-W369099
CAS. Nr.: 1420290-88-5
Target:  

STAT Apoptosis

Forschungsgebiete:  

Cancer

HJC0152 (free base) is an orally active and potent inhibitor of STAT3. HJC0152 (free base) inhibits cell cycle progression and induces apoptosis. HJC0152 (free base) significantly suppresses MDA-MB-231 xenograft tumor growth in mice .
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1
1 Cited Publications
Art. -Nr.: HY-P1103
CAS. Nr.: 1030384-98-5
Target:  

CXCR

Forschungsgebiete:  

Cancer

CTCE-9908 is a potent and selective CXCR4 antagonist. CTCE-9908 induces mitotic catastrophe, cytotoxicity and inhibits migration in CXCR4-expressing ovarian cancer cells .
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Art. -Nr.: HY-P4070
CAS. Nr.: 1188379-43-2
Target:  

Insulin Receptor

Forschungsgebiete:  

Metabolic Disease

Insulin icodec is an Insulin (HY-P0035) analog that strongly but reversibly binds to albumin. Insulin icodec has long plasma half-life. Insulin icodec modulates insulin receptor activity, controls blood glucose levels, reduces HbA1c levels, and binds reversibly to human serum albumin. Insulin icodec can be used for the research of type 2 diabetes mellitus .
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Art. -Nr.: HY-B0497R
CAS. Nr.: 50-65-7
Synonyms: BAY2353 (Standard)
Forschungsgebiete:  

Infection Cancer

Niclosamide (Standard) is the analytical standard of Niclosamide. This product is intended for research and analytical applications. Niclosamide (BAY2353) is an orally active antihelminthic agent used in parasitic infection research . Niclosamide is a STAT3 inhibitor with an IC50 of 0.25 μM in HeLa cells . Niclosamide has biological activities against cancer, inhibits DNA replication in Vero E6 cells .
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Art. -Nr.: HY-144772
CAS. Nr.: 1580-42-3
Target:  

SARS-CoV

Forschungsgebiete:  

Infection

SARS-CoV-2-IN-15 (compound 11) is a potent inhibitor of SARS-CoV-2 with an IC50 of 0.49 μM. SARS-CoV-2-IN-15 is a niclosamide analogue. SARS-CoV-2-IN-15 contains higher stability in human plasma and liver S9 enzymes assay than niclosamide, which can improve bioavailability and half-life when administered orally .
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Art. -Nr.: HY-B0497B
CAS. Nr.: 73360-56-2
Synonyms: BAY2353 monohydrate
Target:  

STAT Antibiotic Parasite

Forschungsgebiete:  

Infection Cancer

Niclosamide (BAY2353) monohydrate is an orally active antihelminthic agent used in parasitic infection research . Niclosamide monohydrate is a STAT3 inhibitor with an IC50 of 0.25 μM in HeLa cells . Niclosamide monohydrate has biological activities against cancer, and inhibits DNA replication in Vero E6 cells .
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Art. -Nr.: HY-B0497S1
CAS. Nr.: 1325808-64-7
Synonyms: BAY2353-13C6
Niclosamide- 13C6 is the 13C6 labeled Niclosamide. Niclosamide (BAY2353) is an orally bioavailable chlorinated salicylanilide, with anthelmintic and potential antineoplastic activity. Niclosamide (BAY2353) inhibits STAT3 with IC50 of 0.25 μM in HeLa cells and inhibits DNA replication in a cell-free assay.
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Art. -Nr.: HY-144770
CAS. Nr.: 56961-10-5
Reinheit:  98.90%
Target:  

SARS-CoV

Forschungsgebiete:  

Infection

SARS-CoV-2-IN-13 (compound 5) is a potent inhibitor of SARS-CoV-2 with an IC50 of 0.057 μM. SARS-CoV-2-IN-13 is a niclosamide analogue. SARS-CoV-2-IN-13 contains higher stability in human plasma and liver S9 enzymes assay than niclosamide, which can improve bioavailability and half-life when administered orally .
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Art. -Nr.: HY-B0497A
CAS. Nr.: 40321-86-6
Synonyms: BAY2353 sodium
Target:  

Antibiotic STAT Parasite

Forschungsgebiete:  

Infection Cancer

Niclosamide (BAY2353) sodium is an orally active antihelminthic agent used in parasitic infection research . Niclosamide sodium is a STAT3 inhibitor with an IC50 of 0.25 μM in HeLa cells . Niclosamide sodium has biological activities against cancer, and inhibits DNA replication in Vero E6 cells .
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Art. -Nr.: HY-B0497S2
CAS. Nr.: 2665663-60-3
Synonyms: BAY2353-d3
Niclosamide-d3 (BAY2353-d3) is deuterium labeled Niclosamide. Niclosamide (BAY2353) is an orally active antihelminthic agent used in parasitic infection research . Niclosamide is a STAT3 inhibitor with an IC50 of 0.25 μM in HeLa cells . Niclosamide has biological activities against cancer, inhibits DNA replication in Vero E6 cells .
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Art. -Nr.: HY-B0497G
CAS. Nr.: 50-65-7
Synonyms: BAY2353 (GMP)
Niclosamide (GMP) is Niclosamide (HY-B0497) produced by using GMP guidelines. GMP small molecules work appropriately as an auxiliary reagent for cell therapy manufacture. Niclosamide (BAY2353) is an orally active antihelminthic agent used in parasitic infection research . Niclosamide is a STAT3 inhibitor with an IC50 of 0.25 μM in HeLa cells . Niclosamide has biological activities against cancer, inhibits DNA replication in Vero E6 cells .
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Art. -Nr.: HY-P1103A
Target:  

CXCR

Forschungsgebiete:  

Cancer

CTCE-9908 TFA is a potent and selective CXCR4 antagonist. CTCE-9908 TFA induces mitotic catastrophe, cytotoxicity and inhibits migration in CXCR4-expressing ovarian cancer cells .
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Art. -Nr.: HY-B0497BS
CAS. Nr.: 1325559-12-3
Synonyms: BAY2353-13C6 monohydrate
Niclosamide- 13C6 (monohydrate) is the 13C labeled Niclosamide monohydrate . Niclosamide (BAY2353) monohydrate is an orally active antihelminthic agent used in parasitic infection research . Niclosamide monohydrate is a STAT3 inhibitor with an IC50 of 0.25 μM in HeLa cells . Niclosamide monohydrate has biological activities against cancer, and inhibits DNA replication in Vero E6 cells .
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Art. -Nr.: HY-P11293
CAS. Nr.: 1309855-53-5
Target:  

Melanocortin Receptor

Forschungsgebiete:  

Cancer

DOTA-GGNle-CycMSHhex is a melanocortin-1 receptor (MC1R)-targeting peptide that can be radionuclide-labeled for melanoma imaging .
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Art. -Nr.: HY-P4757
CAS. Nr.: 108081-77-2
Target:  

Parasite

Forschungsgebiete:  

Others

N1-Glutathionyl-spermidine disulfide is a substrate of trypanothione reductase .
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Art. -Nr.: HY-P1321
CAS. Nr.: 158859-98-4
Synonyms: 1229U91; GW1229
Forschungsgebiete:  

Neurological Disease

GR231118, an analogue of the C-terminus of neuropeptide Y, is a potent , competitive and relative seletive antagonist at human neuropeptide Y Y receptor with a pKi of 10.4. GR231118 a potent agonist at the human neuropeptide Y Y4 receptor (pEC50=8.6; pKi=9.6) and a weak agonist at the human and rat neuropeptide YY2 and Y5 receptors. GR231118 also has high affinity for the mouse neuropeptide Y Y6 receptor (pKi= 8.8) .
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Art. -Nr.: HY-144771
CAS. Nr.: 22203-98-1
Reinheit:  99.02%
Target:  

SARS-CoV

Forschungsgebiete:  

Infection

SARS-CoV-2-IN-14 (compound 6) is a potent inhibitor of SARS-CoV-2 with an IC50 of 0.39 μM. SARS-CoV-2-IN-14 is a niclosamide analogue. SARS-CoV-2-IN-14 contains higher stability in human plasma and liver S9 enzymes assay than niclosamide, which can improve bioavailability and half-life when administered orally .
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Art. -Nr.: HY-B0497CR
CAS. Nr.: 1420-04-8
Synonyms: BAY2353 olamine (Standard)
Forschungsgebiete:  

Infection Cancer

Crocin (Standard) is the analytical standard of Crocin. This product is intended for research and analytical applications. Crocin (Crocin I) is an orally active natural product that can be isolated from the stigma of Crocus sativus. Crocin inhibits tumor cell proliferation and promotes apoptosis through JAK pathway. Crocin has anti-inflammatory, antioxidant and antitumor activities .
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