GSK-2485852

CAS No. 1331942-30-3

GSK-2485852( GSK2485852 | GSK 2485852 | GSK-5852 )

Catalog No. M11322 CAS No. 1331942-30-3

GSK-2485852 (GSK2485852, GSK5852) is a highly potent, selective HCV NS5B polymerase inhibitor with IC50 of 3.0 and 1.6 nM for HCV genotypes 1a and 1b in replicon assay, respectively.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
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Biological Information

  • Product Name
    GSK-2485852
  • Note
    Research use only, not for human use.
  • Brief Description
    GSK-2485852 (GSK2485852, GSK5852) is a highly potent, selective HCV NS5B polymerase inhibitor with IC50 of 3.0 and 1.6 nM for HCV genotypes 1a and 1b in replicon assay, respectively.
  • Description
    GSK-2485852 (GSK2485852, GSK5852) is a highly potent, selective HCV NS5B polymerase inhibitor with IC50 of 3.0 and 1.6 nM for HCV genotypes 1a and 1b in replicon assay, respectively; displays an excellent resistance profile and shows a <5-fold potency loss across the clinically important NS5B resistance mutations P495L, M423T, C316Y, and Y448H; targets NNI palm site 2 of NS5B and inhibits all HCV genotypes.HCV Infection Phase 1 Clinical.
  • In Vitro
    Nonstructural protein 5B (NS5B) RNA-dependent RNA polymerase (RdRp) is a component of HCV, for researching HCV infection-related diseases.GSK5852 (compound 87) inhibits aggregation by two mechanisms: 1) stabilizing β-flap in a closed inactive state to inhibit the initiation step of the RdRp RNA replication cycle; 2) disruption of RNA processing channels through direct spatial contact.GSK5852 is a non-nucleoside NS5B inhibitor and exhibits inhibitory effect on HCV mutant variants with EC50s of 3.2 nM (GT1a C316Y), 1.9 nM (GT1b C316N), respectively.GSK5852 displays an excellent resistance profile and shows a <5-fold potency loss across the clinically important NS5B resistance mutations.GSK5852 shows no cross-resistance against known resistance mutations in NS5B.GSK5852 (compound 3) (0-10 μM) blocks the initiation step of NS5B polymerase cycle.GSK5852 (0.6, 10 μM; 0-75 h) shows slow binding kinetics with isolated GT1b 316N protein, and with a dissociation half-life of >40 hours.GSK5852 (0.6, 10 μM; 15 min) inhibits NS5B?21 1b 316N with an IC50 value of 130 nM.Western Blot Analysis Cell Line:HCV NS5B Concentration:0, 0.016, 0.08, 0.4, 2, 10 μM Incubation Time:Result:Resulted migration of CTP substrate (at 10 μM), decreased pCpG reaction product with increasing concentrations and significantly decreased at a dosage >2 μM.
  • In Vivo
    ——
  • Synonyms
    GSK2485852 | GSK 2485852 | GSK-5852
  • Pathway
    Microbiology/Virology
  • Target
    HCV
  • Recptor
    HCV
  • Research Area
    Infection
  • Indication
    HCV Infection

Chemical Information

  • CAS Number
    1331942-30-3
  • Formula Weight
    554.3718
  • Molecular Formula
    C27H25BF2N2O6S
  • Purity
    >98% (HPLC)
  • Solubility
    ——
  • SMILES
    OB(C1=CC=C(CN(C2=C(C3CC3)C=C4C(C(NC)=O)=C(C5=CC=C(F)C=C5)OC4=C2)S(=O)(C)=O)C=C1F)O
  • Chemical Name
    B-[4-[[[5-Cyclopropyl-2-(4-fluorophenyl)-3-[(methylamino)carbonyl]-6-benzofuranyl](methylsulfonyl)amino]methyl]-2-fluorophenyl]boronic acid

Shipping & Storage Information

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

Reference

1. Voitenleitner C, et al. Antimicrob Agents Chemother. 2013 Nov;57(11):5216-24. 2. Wilfret DA, et al. Clin Pharmacol Drug Dev. 2014 Nov;3(6):439-48. 3,?Chong PY, et al. J Med Chem. 2019 Feb 14. doi: 10.1021/acs.jmedchem.8b01719.
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