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HSV

HSV

HSV inhibitors are compounds that target the Herpes Simplex Virus (HSV), which causes infections such as cold sores and genital herpes. These inhibitors can block viral entry, replication, or the assembly of new viral particles, helping to reduce the severity and duration of HSV infections. Research into HSV inhibitors is essential for developing antiviral therapies that can manage and treat both acute and latent HSV infections. At CymitQuimica, we offer a selection of HSV inhibitors to support your research in virology, antiviral therapy, and infectious disease.

Found 92 products for "HSV".

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  • HSV-1/HSV-2-IN-2
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    HSV-1/HSV-2-IN-2

    CAS:
    HSV-1/HSV-2-IN-2 is a compound that acts as an inhibitor of HSV-1, HSV-2, and VV, demonstrating antiviral activity with EC50 values of 6.8, 8.9, and 8.9 μM,
    Formula:C17H14ClFN4OS
    Color and Shape:Solid
    Molecular weight:376.84

    Ref: TM-T61563

  • B220
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    B220

    CAS:
    B220, an antiviral agent, inhibits the growth of HSV-1, HSV-2, and human cytomegalovirus (CMV).
    Formula:C20H22N4
    Purity:99.61% - 99.9%
    Color and Shape:Yellow Solid
    Molecular weight:318.4155

    Ref: TM-T10445

  • Isatin-β-thiosemicarbazone
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    Isatin-β-thiosemicarbazone

    CAS:
    Isatin-β-thiosemicarbazone is a potent inhibitor of herpes simplex virus (HSV).
    Formula:C9H8N4OS
    Purity:99.51%
    Color and Shape:Yellow Solid
    Molecular weight:220.251

    Ref: TM-T60272

  • Pritelivir mesylate hydrate
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    Pritelivir mesylate hydrate

    CAS:
    Pritelivir mesylate hydrate inhibits herpes simplex 1/2 helicase-primase; IC50: 0.02 μM; effective in vitro and in vivo.
    Formula:C19H24N4O7S3
    Purity:98%
    Color and Shape:Solid
    Molecular weight:516.611

    Ref: TM-T16575

  • Valomaciclovir stearate
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    Valomaciclovir stearate

    CAS:
    S-Allylmercapturic Acid (N-Acetyl-S-allyl-L-cysteine) is a metabolite of S-allyl-L-cysteine present in black garlic, with potential anti-gout effects.
    Formula:C33H58N6O5
    Purity:99.48% - >99.99%
    Color and Shape:Blue Solid
    Molecular weight:618.85

    Ref: TM-T29093

  • 17,17-Ethylendioxyandrost-5-en-3β-ol
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    17,17-Ethylendioxyandrost-5-en-3β-ol

    CAS:
    17,17-Ethylendioxyandrost-5-en-3β-ol, with an EC 50 of 629 μM, acts as an inhibitor of HSV-1. This compound is applicable in research studies focusing on viral infections.
    Formula:C21H32O3
    Color and Shape:Solid
    Molecular weight:332.48

    Ref: TM-T200287

  • Mer-NF5003F
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    Mer-NF5003F

    CAS:
    Mer-NF5003F (Stachybotrydial; F 1839M) is a sesquiterpene isolated from Stachybotrys, effective in inhibiting avian myeloblastosis virus (AMV) protease with an IC50 of 7.8 μM. It also inhibits sialyltransferases ST6N, ST3O, and ST3N with IC50 values of 0.61, 6.7, and 10 μg/mL, respectively, and fucosyltransferase with an IC50 of 11.3 μg/mL. Additionally, Mer-NF5003F exhibits in vitro activity against herpes simplex virus HSV-1 (IC50=4.32 μg/mL) and multi-drug-resistant Plasmodium falciparum K1 strain (IC50=0.85 μg/mL).
    Formula:C23H30O5
    Color and Shape:Solid
    Molecular weight:386.4813

    Ref: TM-T208688

  • Omaciclovir
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    Omaciclovir

    CAS:
    Omaciclovir (ABT-091) is a herpesvirus herpesvirus replication inhibitor with antiviral activity that is used in the study of herpesvirus infections.
    Formula:C10H15N5O3
    Purity:99.46% - 99.46%
    Color and Shape:Solid
    Molecular weight:253.2578

    Ref: TM-T28234

  • LANA-IN-1
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    LANA-IN-1

    CAS:
    LANA-IN-1 (compound 8) is an N-acetyl derivative that acts as a LANA inhibitor with anti-herpesviral activity. In fluorescence assays involving the LANA probe LBS2, LANA-IN-1 at a concentration of 1 mM demonstrated an inhibition rate of 32%. This compound likely inhibits the interaction between LANA and the viral genome.
    Formula:C9H9N3
    Molecular weight:159.1879

    Ref: TM-T206339

  • PNU-183792
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    PNU-183792

    CAS:
    PNU-183792 is a 4-oxo-1,4-dihydroquinoline that acts as an orally active inhibitor of herpesvirus polymerases (HSV polymerases). It exhibits broad-spectrum antiviral activity, with IC50 values of 0.69 μM for human cytomegalovirus (HCM), 0.37 μM for varicella-zoster virus, and 0.58 μM for herpes simplex virus (HSV) polymerase. PNU-183792 shows no activity against human α, γ, and δ polymerases but inhibits simian varicella virus (SVV), murine cytomegalovirus (MCMV), and rat cytomegalovirus (RCMV).
    Formula:C23H24ClN3O3
    Molecular weight:425.91

    Ref: TM-T211119

  • Cyclopropavir
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    Cyclopropavir

    CAS:
    Cyclopropavir (Filociclovir; MBX-400) is a broad-spectrum anti-herpes drug effective against CMV and HHV-6/8 (EC50: 0.7-8 μM).
    Formula:C11H13N5O3
    Purity:98%
    Color and Shape:Solid
    Molecular weight:263.25

    Ref: TM-T15028

  • HSV-TK substrate
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    HSV-TK substrate

    CAS:
    HSV-TK substrate is a substrate for HSV-TK with antitumor activity. It induces multi-log cytotoxicity in HSV-TK-expressing and bystander cells.
    Formula:C11H15N5O4
    Purity:98%
    Color and Shape:Solid
    Molecular weight:281.27

    Ref: TM-T11582