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HSV

HSV

Os inibidores do vírus Herpes Simplex (HSV) são compostos que têm como alvo o vírus Herpes Simplex, que causa infecções como herpes labial e genital. Esses inibidores podem bloquear a entrada viral, a replicação ou a montagem de novas partículas virais, ajudando a reduzir a gravidade e a duração das infecções por HSV. A pesquisa sobre inibidores do HSV é essencial para desenvolver terapias antivirais que possam gerenciar e tratar tanto as infecções agudas quanto as latentes pelo HSV. Na CymitQuimica, oferecemos uma seleção de inibidores do HSV para apoiar sua pesquisa em virologia, terapia antiviral e doenças infecciosas.

Foram encontrados 87 produtos para "HSV".

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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.
    Fórmula:C33H58N6O5
    Pureza:99.18% - >99.99%
    Cor e Forma:Blue Solid
    Peso molecular:618.85

    Ref: TM-T29093

    1mg
    294,00€
    5mg
    883,00€
    10mg
    1.189,00€
  • 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.
    Fórmula:C11H15N5O4
    Pureza:98%
    Cor e Forma:Solid
    Peso molecular:281.27

    Ref: TM-T11582

    25mg
    A consultar
    50mg
    A consultar
    100mg
    A consultar
  • Omaciclovir

    CAS:
    Omaciclovir (ABT-091) is a herpesvirus herpesvirus replication inhibitor with antiviral activity that is used in the study of herpesvirus infections.
    Fórmula:C10H15N5O3
    Pureza:99.46% - 99.46%
    Cor e Forma:Solid
    Peso molecular:253.26

    Ref: TM-T28234

    1mL*10mM (DMSO)
    33,00€
    1mg
    139,00€
  • 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).
    Fórmula:C11H13N5O3
    Pureza:98%
    Cor e Forma:Solid
    Peso molecular:263.25

    Ref: TM-T15028

    25mg
    2.133,00€
    50mg
    2.592,00€
    100mg
    3.150,00€
  • 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).
    Fórmula:C23H24ClN3O3
    Peso molecular:425.91

    Ref: TM-T211119

    10mg
    A consultar
    50mg
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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.
    Fórmula:C21H32O3
    Cor e Forma:Solid
    Peso molecular:332.48

    Ref: TM-T200287

    25mg
    1.369,00€
    50mg
    1.783,00€
    100mg
    2.250,00€
  • 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).
    Fórmula:C23H30O5
    Cor e Forma:Solid
    Peso molecular:386.48

    Ref: TM-T208688

    10mg
    A consultar
    50mg
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