Pritelivir

CAS No. 348086-71-5

Pritelivir( BAY 57-1293 | AIC316 )

Catalog No. M17491 CAS No. 348086-71-5

Pritelivir (BAY 57-1293) is a potent helicase-primase inhibitor with active against HSV-1 and HSV-2 (IC50: 20 nM).

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
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5MG 35 In Stock
10MG 50 In Stock
25MG 79 In Stock
50MG 110 In Stock
100MG 177 In Stock
500MG 440 In Stock
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Biological Information

  • Product Name
    Pritelivir
  • Note
    Research use only, not for human use.
  • Brief Description
    Pritelivir (BAY 57-1293) is a potent helicase-primase inhibitor with active against HSV-1 and HSV-2 (IC50: 20 nM).
  • Description
    Pritelivir (BAY 57-1293) is a potent helicase-primase inhibitor with active against HSV-1 and HSV-2 (IC50: 20 nM).(In Vivo):Pritelivir is the first in a class of antiviral agents that inhibit HSV replication by targeting the viral helicase-primase enzyme complex.Pritelivir (0.03-45 mg/kg) significantly increases survival. Pritelivir (0.3-30 mg/kg) reduces mortality against HSV-1, E-377. Pritelivir has potent and resistance-breaking antiviral efficacy with potential for the treatment of potentially life-threatening HSV type 1 and 2 infections, including herpes simplex encephalitis.Combination therapies of Pritelivir at 0.1 or 0.3 mg/kg/dose with Acyclovir (10 mg/kg/dose) are protective when compared to the vehicle treated group against HSV-2, strain MS.
  • In Vitro
    ——
  • In Vivo
    Pritelivir is the first in a class of antiviral agents that inhibit HSV replication by targeting the viral helicase-primase enzyme complex. Pritelivir (0.03-45 mg/kg) significantly increases survival. Pritelivir (0.3-30 mg/kg) reduces mortality against HSV-1, E-377. Pritelivir has potent and resistance-breaking antiviral efficacy with potential for the treatment of potentially life-threatening HSV type 1 and 2 infections, including herpes simplex encephalitis. Combination therapies of Pritelivir at 0.1 or 0.3 mg/kg/dose with Acyclovir (10 mg/kg/dose) are protective when compared to the vehicle treated group against HSV-2, strain MS. Animal Model:Female BALB/c mice Dosage:0.03 to 45 mg/kg Administration:Administered orally, twice daily at approximately 12 h intervals, for 7 days Result:Survival was significantly increased to 80-100% as compared to the vehicle treatment. Even the lowest dose of 0.3 mg/kg was effective in increasing survival to 53%.
  • Synonyms
    BAY 57-1293 | AIC316
  • Pathway
    Immunology/Inflammation
  • Target
    Antiviral
  • Recptor
    helicase primase
  • Research Area
    Infection
  • Indication
    ——

Chemical Information

  • CAS Number
    348086-71-5
  • Formula Weight
    402.49
  • Molecular Formula
    C18H18N4O3S2
  • Purity
    >98% (HPLC)
  • Solubility
    DMSO : ≥ 33 mg/mL; 81.99 mM
  • SMILES
    Cc1c(sc(n1)N(C)C(=O)Cc1ccc(cc1)c1ccccn1)S(=O)(=O)N
  • Chemical Name
    ——

Shipping & Storage Information

  • Storage
    (-20℃)
  • Shipping
    With Ice Pack
  • Stability
    ≥ 2 years

Reference

1. Kleymann G, et al. Nat Med. 2002, 8(4), 392-398.
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