11 Results for "

parainfluenza virus

" in MedChemExpress (MCE) Product Catalog:
Products (11)

11 Results for "parainfluenza virus" in MCE Product Catalog:

1
1 Cited Publications
Cat. No.: HY-107801
CAS No.: 36703-88-5
Purity:  98.11%
Synonyms: Imunovir; Delimmun; Groprinosin
Inosine pranobex is an orally active immunomodulator. Inosine pranobex has broad-spectrum antiviral activity. Inosine pranobex inhibits human immunodeficiency virus (HIV), herpes simplex virus (HSV), vaccinia virus (VACV), human tumor virus (HPV), Cytomegalovirus, influenza virus (INFV), parainfluenza virus (PIV), and Epstein-Barr virus .
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Cat. No.: HY-114784
CAS No.: 219694-63-0
Purity:  99.57%
Synonyms: Ingamine
Target:  

Influenza Virus

Research Areas:  

Infection

Ingavirin (Ingamine) exhibits broad spectrum antiviral activities against human respiratory viruses, such as influenza virus A (IVA), human parainfluenza virus (hPIV) and human adenovirus (AdV). Ingavirin exhibits no toxixcity to mice at the dose of 3000 mg/kg .
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Cat. No.: HY-135319
CAS No.: 517-46-4
Purity:  97.15%
Strictinin is an orally active phenolic compound. Strictinin reduces xanthine oxidase activity, uric acid production, and the activation of ERK1/2, JNK, NF-κB, and NLRP3 inflammasome components in hepatocytes treated with Xanthine (HY-W017389). Strictinin decreases elevated serum uric acid levels and enhanced xanthine oxidase activity in mice treated with potassium oxonate. Strictinin acts as a ROR1 inhibitor and exhibits anticancer activity against highly aggressive non-androgen-dependent prostate cancer. Strictinin induces cancer cell apoptosis (apoptosis), arrests cell cycle, and inhibits cancer cell migration, invasion, and epithelial-mesenchymal transition. Strictinin modulates gut microbiota, inhibits bacterial growth and biofilm formation, accelerates small intestinal transit, and blocks viral entry and replication. Strictinin can be used in research related to hyperuricemia, androgen receptor-negative non-androgen-dependent prostate cancer, triple-negative breast cancer, bacterial infections, constipation, coronavirus infections, dental caries, and infections caused by influenza A, influenza B, and human parainfluenza virus type 1 .
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Cat. No.: HY-107801R
CAS No.: 36703-88-5
Synonyms: Imunovir (Standard); Delimmun (Standard); Groprinosin (Standard); (Standard)
Inosine pranobex (Standard) is the analytical standard of Inosine pranobex. This product is intended for research and analytical applications. Inosine pranobex is an orally active immunomodulator. Inosine pranobex has broad-spectrum antiviral activity. Inosine pranobex inhibits human immunodeficiency virus (HIV), herpes simplex virus (HSV), vaccinia virus (VACV), human tumor virus (HPV), Cytomegalovirus, influenza virus (INFV), parainfluenza virus (PIV), and Epstein-Barr virus .
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Cat. No.: HY-N2982
CAS No.: 204185-91-1
Caesalmin E is a natural cassane furanoditerpene with anti-Para3 (Parainfluenza virus type 3) virus activities .
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Cat. No.: HY-N9220
CAS No.: 178456-58-1
Target:  

Influenza Virus

Research Areas:  

Infection

6-Epi-albassitriol can be isolated from Aspergillus sp. FH-A 6357. 6-Epi-albassitriol inhibits the cholesterol synthesis with an inhibition rate of 40% at a concentration of 10 nM in HepG2. 6-Epi-albassitriol exhibits antiviral activity against influenza A virus and parainfluenza virus with MIC of 44.4-133.3 µg/mL .
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Cat. No.: HY-188062
CAS No.: 138751-31-2
Target:  

VSV CMV VZV

Research Areas:  

Infection

2-Fluoroneplanocin A is an Antiviral agent. 2-Fluoroneplanocin A inhibits rabbit Adenosylhomocysteine hydrolase with an IC50 of 0.20 μg/mL. 2-Fluoroneplanocin A exhibits antiviral activity against vaccinia virus, vesicular stomatitis virus, parainfluenza virus, reovirus, Junín virus, Tacaribe virus, cytomegalovirus, measles virus, mumps virus, and thymidine kinase-deficient varicella-zoster virus; it shows no antiviral activity against herpes simplex virus, coxsackievirus B4, poliovirus type 1, Semliki Forest virus, or HIV at subtoxic concentrations. 2-Fluoroneplanocin A can be used in research related to vaccinia virus infection, vesicular stomatitis virus infection, parainfluenza virus infection, reovirus infection, Junín virus infection, Tacaribe virus infection, human cytomegalovirus infection, measles virus infection, mumps virus infection, and varicella-zoster virus infection .
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Cat. No.: HY-180882
Synonyms: EIDD-3608
Research Areas:  

Infection

GHP-88310 is an orally active broad-spectrum paramyxovirus and orthomyxovirus inhibitor that targets the L protein-RdRP complex, and exhibits activity against respiratory viruses and viruses of the genus Morbillivirus . GHP-88310 binds to the central cavity of the polymerase protein, blocks replicase and transcriptase activities, interferes with the viral life cycle and inhibits viral replication . GHP-88310 can be used in studies of paramyxovirus infections, including morbillivirus-like diseases, human parainfluenza virus type 3 infection and measles .
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Cat. No.: HY-N9574
CAS No.: 30164-95-5
Oleoside dimethylester is a secoiridoid glucoside found in the fruits of Ligustrum lucidum. Oleoside dimethylester exhibits inhibitory activity against type 3 parainfluenza virus (Para 3) and respiratory syncytial virus (RSV), with IC50 values of 20.8 and 83.2 μg/mL. Oleoside dimethylester also shows antioxidant effect .
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Cat. No.: HY-188063
CAS No.: 161128-65-0
Target:  

VSV

Research Areas:  

Cancer

3-Deazahomoneplanocin A is an S-adenosylhomocysteine (AdoHcy) hydrolase inhibitor with an IC50 of 3.76 μM. 3-Deazahomoneplanocin A exhibits antiviral activity against VSV. It also shows anticancer activity against lung cancer, colon cancer, breast cancer, liver cancer and gastric cancer .
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Cat. No.: HY-114562
CAS No.: 10500-82-0
Synonyms: UK 2054 hydrochloride
Target:  

Influenza Virus

Research Areas:  

Infection

Famotine hydrochloride (UK 2054 hydrochloride) is a broad-spectrum antiviral agent as well as an inhibitor of viral and bacterial neuraminidase. Famotine hydrochloride blocks the uptake of Influenza Virus, delays the viral eclipse phase and release, binds reversibly to influenza virus particles, and competes for host cell receptors. Famotine hydrochloride inhibits viral growth and cytopathic effects in vitro, directly inactivates viruses, and interferes with intracellular viral replication steps. Famotine hydrochloride can be used in studies related to viral infections .
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