Maribavir

CAS No. 176161-24-3

Maribavir( Maribavir | 1263W-94 | BW-1263W-94 | GW-1263 )

Catalog No. M17375 CAS No. 176161-24-3

Maribavir is an orally available benzimidazole riboside compound with activity against cytomegalovirus (CMV).

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
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Biological Information

  • Product Name
    Maribavir
  • Note
    Research use only, not for human use.
  • Brief Description
    Maribavir is an orally available benzimidazole riboside compound with activity against cytomegalovirus (CMV).
  • Description
    Maribavir, also known as 1263W-94; BW-1263W-94; GW-1263; GW-257406X; SHP-620; VP-41263; BW-1263W94, is an UL97 kinase inhibitor potentially for the treatment of cytomegalovirus (CMV) infection. The mechanism by which maribavir inhibits HCMV replication is by inhibition of an HCMV encoded protein kinase enzyme called UL97 or pUL97.(In Vitro):Maribavir is a potent inhibitor of the autophosporylation of the wild type and all the major Ganciclovir (GCV) resistant UL97 mutants analysed with a mean IC50 of 35 nM. The M460I mutation results in hypersensitivity to Maribavir with an IC50 of 4.8 nM. A Maribavir resistant mutant of UL97 (L397R) is functionally compromised as both a Ganciclovir kinase and a protein kinase (~ 10% of wild type levels). Enzyme kinetic experiments demonstrate that Maribavir is a competitive inhibitor of ATP with a Ki of 10 nM. Maribavir (1263W94) inhibits viral replication in a dose-dependent manner, with IC50 of 0.12±0.01 μM as measured by a multicycle DNA hybridization assay. The pUL97 protein kinase is strongly inhibited by Maribavir, with 50% inhibition occurring at 3 nM.
  • In Vitro
    Maribavir is a potent inhibitor of the autophosporylation of the wild type and all the major Ganciclovir (GCV) resistant UL97 mutants analysed with a mean IC50 of 35 nM. The M460I mutation results in hypersensitivity to Maribavir with an IC50 of 4.8 nM. A Maribavir resistant mutant of UL97 (L397R) is functionally compromised as both a Ganciclovir kinase and a protein kinase (~ 10% of wild type levels). Enzyme kinetic experiments demonstrate that Maribavir is a competitive inhibitor of ATP with a Ki of 10 nM. Maribavir (1263W94) inhibits viral replication in a dose-dependent manner, with IC50 of 0.12±0.01 μM as measured by a multicycle DNA hybridization assay. The pUL97 protein kinase is strongly inhibited by Maribavir, with 50% inhibition occurring at 3 nM.
  • In Vivo
    ——
  • Synonyms
    Maribavir | 1263W-94 | BW-1263W-94 | GW-1263
  • Pathway
    GPCR/G Protein
  • Target
    S1P Receptor
  • Recptor
    HCMV
  • Research Area
    Infection
  • Indication
    ——

Chemical Information

  • CAS Number
    176161-24-3
  • Formula Weight
    376.24
  • Molecular Formula
    C15H19Cl2N3O4
  • Purity
    >98% (HPLC)
  • Solubility
    DMSO : ≥ 51 mg/mL 135.55 mM
  • SMILES
    Clc1cc2n([C@@H]3O[C@@H]([C@@H](O)[C@H]3O)CO)c(NC(C)C)nc2cc1Cl
  • Chemical Name
    5,6-Dichloro-2-(isopropylamino)-1-beta-L-ribofuranosyl-1H-benzimidazole

Shipping & Storage Information

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

Reference

1. Karen KB, et al. Antimicrob Agents ChemOthers. August 2002 vol. 46 no. 8 2365-2372 2. Whitehurst CB, et al. MJ Virol. 2013 May;87(9):5311-5.
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  • Maribavir

    Maribavir is an orally available benzimidazole riboside compound with activity against cytomegalovirus (CMV).