168 Results for "

virus-1

" in MedChemExpress (MCE) Product Catalog:
Products (168)

168 Results for "virus-1" in MCE Product Catalog:

31
31 Publications Verification
Cat. No.: HY-107433
CAS No.: 3039-71-2
Purity:  99.77%
Research Areas:  

Infection Neurological Disease

U18666A, an intra-cellular cholesterol transport inhibitor, inhibits replication of Ebola virus, dengue virus, and human hepatitis C virus .
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14
14 Cited Publications
Cat. No.: HY-109025
CAS No.: 1985606-14-1
Purity:  99.96%
Synonyms: S-033188; RG 6152
Target:  

Influenza Virus

Research Areas:  

Infection

Baloxavir marboxil (S-033188) is a selective inhibitor of influenza cap-dependent endonuclease. Baloxavir marboxil, a potent antiviral agent, shows activity against influenza A and B virus .
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8
8 Cited Publications
Cat. No.: HY-N6666
CAS No.: 24356-66-9
Vidarabine monohydrate is a Purine nucleoside derivative and Antiviral agent. The triphosphate derivative of Vidarabine monohydrate competitively inhibits DNA polymerase, incorporates into the terminus of elongating DNA molecules, and interferes with the early steps of viral DNA synthesis. Vidarabine monohydrate inhibits the replication of herpes simplex virus, varicella-zoster virus, cytomegalovirus, Epstein-Barr virus and vaccinia virus, reduces viral shedding, and accelerates skin healing. Vidarabine monohydrate is metabolized to arabinosyl hypoxanthine, causes minimal impairment of corneal wound healing in rabbit models, and is associated with recurrence of herpes simplex encephalitis. Vidarabine monohydrate can be used in the research of herpetic keratoconjunctivitis, herpes simplex encephalitis, herpetic uveitis, and chronic active hepatitis associated with hepatitis B virus .
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8
8 Cited Publications
Cat. No.: HY-B0277
CAS No.: 5536-17-4
Synonyms: Ara-A; Adenine Arabinoside; 9-β-D-Arabinofuranosyladenine
Vidarabine (Ara-A) is a Purine nucleoside derivative and Antiviral agent. The triphosphate derivative of Vidarabine competitively inhibits DNA polymerase, incorporates into the terminus of elongating DNA molecules, and interferes with the early steps of viral DNA synthesis. Vidarabine inhibits the replication of herpes simplex virus, varicella-zoster virus, cytomegalovirus, Epstein-Barr virus and vaccinia virus, reduces viral shedding, and accelerates skin healing. Vidarabine is metabolized to arabinosyl hypoxanthine, causes minimal impairment of corneal wound healing in rabbit models, and is associated with recurrence of herpes simplex encephalitis. Vidarabine can be used in the research of herpetic keratoconjunctivitis, herpes simplex encephalitis, herpetic uveitis, and chronic active hepatitis associated with hepatitis B virus .
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7
7 Cited Publications
Cat. No.: HY-146246
CAS No.: 1613589-24-4
Purity:  99.86%
Synonyms: 4'-FlU; 4'-Fluorouridine
Target:  

RSV SARS-CoV HCV

Research Areas:  

Infection

EIDD-2749 (4'-Fluorouridine) is an orally active RdRp inhibitor. EIDD-2749 effectively blocks the replication of RSV and SARS-CoV-2. EIDD-2749 also exhibits activity against HCV and lymphocytic choriomeningitis virus (LCMV). EIDD-2749 is a promising oral therapeutic candidate for COVID-19 and is also suitable for research on other RNA viruses .
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3
3 Cited Publications
Cat. No.: HY-B1414
CAS No.: 88-04-0
Synonyms: p-Chloro-m-xylenol; PCMX
Chloroxylenol is a broad-spectrum antibacterial agent that can be used to control bacteria, algae, fungi and viruses .
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3
3 Cited Publications
Cat. No.: HY-111802
CAS No.: 14919-49-4
Purity:  99.55%
Synonyms: 3,4'-DHF
Target:  

Influenza Virus

Research Areas:  

Infection

3,4'-Dihydroxyflavone (3,4'-DHF) is an oral active flavonoid with antiviral activity against Influenza A virus .
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3
3 Cited Publications
Cat. No.: HY-14805
CAS No.: 869572-92-9
Purity:  99.88%
Synonyms: ST-246
Research Areas:  

Infection

Tecovirimat (ST-246) is an orally bioavailable and selective compound against orthopoxviruses including vaccinia, monkeypox, camelpox, cowpox, ectromelia (mousepox), smallpox and variola viruses. Tecovirimat is evaluated against vaccinia, cowpox virus, ectromelia virus with EC50 values of 0.01 μM, 0.48 μM and 0.05 μM, respectively. Tecovirimat targets the orthopoxvirus protein VP37 which is necessary for membrane envelopment of intracellular mature virus particles to form enveloped virus. Tecovirimat exerts antiviral activity on the target of the cowpox virus V061 gene, which is homologous to vaccinia virus F13L, encoding a major envelope protein (p37) required for production of extracellular virus .
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2
2 Cited Publications
Cat. No.: HY-138941
CAS No.: 3055-98-9
Purity:  ≥98.0%
Synonyms: C12E8
Target:  

Influenza Virus

Research Areas:  

Infection

Octaethylene glycol monododecyl ether (C12E8) is an non-ionic detergent that can be used for membrane protein extraction. Octaethylene glycol monododecyl ether can solubilize the viral membrane of intact influenza virus .
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2
2 Cited Publications
Cat. No.: HY-19961
CAS No.: 1903800-11-2
KIN1408 is an agonist of the RIG-1-like receptor (RLR) pathway and exhibits a broad-spectrum antiviral activity. KIN1408 exhibits activity against HCV, influenza A, dengue virus 2, Ebola, Nipah, and Lassa viruses .
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2
2 Cited Publications
Cat. No.: HY-W019823
CAS No.: 76204-02-9
4-MUNANA is a substrate of influenza virus neuraminidase (NA) with high selectivity and irreversible reaction. In the enzymatic reaction, 4-MUNANA is hydrolyzed by NA to generate fluorescent 4-methylumbelliferone (4-MU). By detecting the fluorescence intensity of 4-MU, quantitative analysis of NA activity can be achieved. 4-MUNANA can be used in influenza-related research, such as screening NA inhibitors, developing new anti-influenza drugs, and studying the infection mechanism of influenza viruses .
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1
1 Cited Publications
Cat. No.: HY-P0281
CAS No.: 191936-91-1
Synonyms: TAT(47-57); HIV-1 TAT protein (47-57)
TAT (YGRKKRRQRRR) is derived from the transactivator of transcription (TAT) of human immunodeficiency virus-1 (HIV-1) and is a cell-penetrating peptide. TAT can increase the yields and the solubility of heterologous proteins [1].
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1
1 Cited Publications
Cat. No.: HY-13269
CAS No.: 729607-74-3
Purity:  99.99%
Target:  

HIV HIV Integrase

Research Areas:  

Infection Inflammation/Immunology

BMS-707035 is a potent orally active HIV-1 integrase strand transfer inhibitor (INSTI). BMS-707035 has enzyme inhibitory with an IC50 value of 3 nM. BMS-707035 also has weak CYP inhibiton and antiviral activity. BMS-707035 can be used for the research of human immunodeficiency virus-1 (HIV-1) [1].
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1
1 Cited Publications
Cat. No.: HY-P0281B
Synonyms: TAT(47-57) acetate; HIV-1 TAT protein (47-57) acetate
Target:  

HIV

Research Areas:  

Infection

TAT (TAT(47-57)) acetate is derived from the transactivator of transcription (TAT) of human immunodeficiency virus-1 (HIV-1) and is a cell-penetrating peptide. TAT acetate can increase the yields and the solubility of heterologous proteins [1].
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1
1 Cited Publications
Cat. No.: HY-N7112
CAS No.: 1392-21-8
Synonyms: Kitasamycin
Leucomycin (Kitasamycin) is an orally active macrolide antibiotic produced by Streptomyces kitasatoensis. Leucomycin has broad-spectrum antibacterial activities against gram-positive and gram-negative bacteria, mycoplasma, leptospira, spirochaetes, rickettsiae and some larger viruses .
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Cat. No.: HY-P99853
CAS No.: 1393659-46-5
Synonyms: CR6261

Target:  

Influenza Virus

Research Areas:  

Infection

Diridavumab is a monoclonal anti-HA stalk antibody. Diridavumab stabilizes the prefusion HA structure and prevents pH-dependent fusion of cellular and viral membranes in endosomes. Diridavumab can be used in research of H2 influenza virus .
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Cat. No.: HY-B1011
CAS No.: 15176-29-1
Synonyms: EUDR
Target:  

Virus Protease

Research Areas:  

Infection

Edoxudine is an antiviral active molecule and thymidine analog. Edoxudine is effective against herpes simplex virus .
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Cat. No.: HY-N10543
CAS No.: 5746-55-4
5-O-(E)-p-Coumaroylquinic acid, a quinic acid derivative, is a potent phytochemical agent against hepatitis B virus .
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Cat. No.: HY-P990643
Target:  

Integrin

Research Areas:  

Neurological Disease Cancer

OS-2966 is a humanized neutralizing monoclonal antibody (huIgG1κ) targeting human CD29 (β1 integrin/ITGB1). OS-2966 blocks integrin β1 signaling, inhibits tumor cell proliferation, invasion, migration and mesenchymal phenotype, and enhances the efficacy of oncolytic herpes simplex virus-1 (oHSV) and anti-angiogenic therapies. OS-2966 can be used in research related to triple-negative breast cancer, high-grade meningioma, glioblastoma and ovarian cancer [1] .
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Cat. No.: HY-124564
CAS No.: 1910-68-5
Purity:  98.26%
Synonyms: Marboran
Target:  

SARS-CoV Orthopoxvirus

Research Areas:  

Infection

Methisazone (Marboran) is an antiviral agent that works by inhibiting mRNA and protein synthesis. Methisazone is also a SARS-CoV-2 (COVID-19) inhibitor. Methisazone is mainly used in pox viruses .
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