GLPBio

Viral Diseases

Research Areas

Products Related to Viral Diseases(300)

  • GC68780 structure
    GC68780BMS-433771 dihydrochloride hydrate
    CAS: 543700-67-0
    Purity: >98.00%

    BMS-433771 dihydrochloride hydrate is an effective inhibitor of respiratory syncytial virus (RSV) with oral activity. It is effective against both group A and B RSV, with an EC50 average of 20 nM. BMS-433771 dihydrochloride hydrate can be used for research on respiratory diseases.

  • GC68881 structure
    GC68881Clemastanin B
    CAS: 112747-98-5
    Purity: >99.00%

    Clemastanin B is a lignin that has strong anti-influenza activity by inhibiting virus proliferation, preventing and blocking virus attachment. Clemastanin B targets the internalization of viruses, uncoating or ribonucleoprotein (RNP) export from the cell nucleus. It also has antioxidant and anti-inflammatory activities.

  • GC68883 structure
    GC68883Clesrovimab
    CAS: 2429913-18-6
    Purity: >99.00%

    Clesrovimab (MK1654) is a fully human monoclonal antibody against respiratory syncytial virus fusion (RSV F) glycoprotein. Clesrovimab has the potential to study respiratory syncytial virus infections.

  • GC68930 structure
    GC68930Cys-TAT(47-57) TFA
    Purity: >97.00%

    Cys-TAT(47-57) (Cys-[HIV-Tat (47-57)]) is a twelve-peptide rich in arginine that can penetrate cells and is a derivative of HIV-1 transactivator protein.

  • GC69045 structure
    GC69045EIDD-2749
    CAS: 1613589-24-4
    Purity: >99.00%

    EIDD-2749 (4'-Fluorouridine) is an orally effective RdRp inhibitor. It can effectively inhibit 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 candidate for COVID-19 research, as well as for other RNA viruses.

  • GC69180 structure
    GC69180Glycolithocholic acid 3-sulfate
    CAS: 15324-64-8
    Purity: >99.00%

    Glycolithocholic acid 3-sulfate (SLCG) is a metabolite of bile acids and glycochenodeoxycholic acid. Glycolithocholic acid 3-sulfate inhibits the replication of HIV-1. It can be used for research on HIV infection and gallbladder disease.

  • GC69230 structure
    GC69230HIV-1 inhibitor-45
    CAS: 2677762-43-3
    Purity: >99.00%

    HIV-1 inhibitor-45 (compound IA-6) is an effective inhibitor of HIV-1 RNase H, with an IC50 of 0.067 μM. HIV-1 inhibitor-45 exhibits antiviral activity.

  • GC69291 structure
    GC69291Isatin-β-thiosemicarbazone
    CAS: 27830-79-1
    Purity: >99.00%

    Isatin-beta-thiosemicarbazone is an effective anti-poxvirus agent (including monkeypox virus, variola virus, cowpox virus, etc.). Isatin-beta-thiosemicarbazone is also an effective inhibitor of herpes simplex virus (HSV). Isatin-beta-thiosemicarbazone has antiviral activity against both HSV-1 and HSV-2.

  • GC69563 structure
    GC69563Nirsevimab
    CAS: 1989556-22-0
    Purity: >95.00%

    Nirsevimab (MEDI8897) is a recombinant human respiratory syncytial virus (RSV) monoclonal antibody with a modified Fc region that extends its half-life. Nirsevimab has an affinity for RSV-B, with a Kd value of 1.5 nM. Nirsevimab can be used in RSV research.

  • GC69974 structure
    GC69974Suptavumab
    CAS: 1629615-23-1
    Purity: >95.00%

    Suptavumab (REGN2222) is a human monoclonal antibody that can bind and block the conserved epitopes on both RSV A and B subtypes. Suptavumab can be used for research on RSV infection.

  • GC70056 structure
    GC70056Trecovirsen
    CAS: 153021-75-1
    Purity: >98.00%

    Trecovirsen (GEM91) is an antisense oligonucleotide that targets the HIV gag gene.

  • GC70227 structure
    GC70227Clathrin-IN-1
    CAS: 1332879-52-3

    Clathrin-IN-1 is a selective clathrin-mediated endocytosis (CME) inhibitor.

  • GC70228 structure
    GC70228SAMT-247
    CAS: 850715-59-2

    SAMT-247 is a microbicide that selectively inactivate the viral nucleocapsid protein NCp7, causing zinc ejection and preventing RNA encapsidation.

  • GC70262 structure
    GC70262Amitivir
    CAS: 111393-84-1

    Amitivir (LY 217896), a thiadiazole derivative, possesses broad antiviral activity against orthomyxo- and paramyxoviruses.

  • GC70316 structure
    GC70316JNJ 2408068
    CAS: 317846-22-3

    JNJ 2408068 is a potent RSV (respiratory syncytial virus) inhibitor.

  • GC70644 structure
    GC70644Influenza A virus-IN-1
    CAS: 2250313-14-3
    Purity: >99.00%

    Influenza A virus-IN-1 is a dihydropyrrolidones derivative and is a potent inhibitor against wide subtypes of influenza A virus (IAV) with IC50 values from 3.11 μM to 7.13 μM.

  • GC70647 structure
    GC70647Emtricitabine triphosphate tetrasodium salt
    CAS: 1188407-46-6
    Purity: >99.00%

    Emtricitabine triphosphate tetrasodium salt is the tetrasodium salt form of Emtricitabine triphosphate .

  • GC70661 structure
    GC70661Dolutegravir-d3
    Purity: >99.00%

    Dolutegravir-d3 is the deuterium labeled Dolutegravir.

  • GC70780 structure
    GC70780Ingenol-3-palmitate
    CAS: 52557-26-3
    Purity: >99.00%

    Ingenol-3-palmitate, an ingenane diterpenoid, is a nature product that could be isolated from the roots of Euphorbia ebracteolata.

  • GC70800 structure
    GC70800EFdA-TP tetrasodium
    CAS: 2883783-00-2

    EFdA-TP tetrasodium is a potent nucleoside reverse transcriptase (RT) inhibitor.

  • GC70929 structure
    GC70929Fipravirimat dihydrochloride
    CAS: 2442512-14-1

    Fipravirimat dihydrochloride is a potent HIV-1 inhibitor.

  • GC70932 structure
    GC70932Onradivir
    CAS: 2200336-20-3
    Purity: >99.50%

    Onradivir is a potent anti-influenza virus agent.

  • GC71094 structure
    GC71094JNJ-8003
    Purity: >99.00%

    JNJ-8003 is a potent inhibitor of RSV Polymerase.

  • GC71227 structure
    GC71227PYR01
    CAS: 2560576-15-8
    Purity: >98.00%

    PYR01 is a potent HIV-1 nonnucleoside reverse transcriptase inhibitor.