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
Size Price / USD Stock Quantity
5MG 35 In Stock
10MG 50 In Stock
25MG 79 In Stock
50MG 110 In Stock
100MG 177 In Stock
500MG 440 In Stock
1G Get Quote In Stock

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.
molnova catalog
related products
  • Somantadine

    Somantadine has antiviral activities and can be used for research on preventing and treating coronavirus-related diseases.

  • EIDD-2749

    EIDD-2749 (4'-FlU), a ribonucleoside analog, is an orally available RdRp inhibitor with spectroscopic antiviral activity that interrupts the replication of respiratory syncytial virus and SARS-CoV-2.

  • (R)-JAK2/STAT3-IN-10...

    (R)-JAK2/STAT3-IN-10a is the R-isomer of JAK2/STAT3-IN-1.JAK2/STAT3-IN-1 is a GP130 D1 structural domain inhibitor with antitumor activity that inhibits the phosphorylation of JAK2 and STAT3. The KD value of (R)-JAK2/STAT3-IN-1 on GP130 protein is 3.8 μM.