GLS4

CAS No. 1092970-12-1

GLS4 ( GLS 4;Morphothiadin )

Catalog No. M10356 CAS No. 1092970-12-1

GLS4 (Morphothiadin) is a potent inhibitor of HBV capsid assembly, inhibits HBV replication (EC50=62.24 nM) and reduces HBV-DNA levels in HepG.2.2.15 cells (IC50=14 nM).

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
5MG 267 Get Quote
10MG 427 Get Quote
25MG 628 Get Quote
50MG 894 Get Quote
100MG 1206 Get Quote
200MG 1611 Get Quote
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Biological Information

  • Product Name
    GLS4
  • Note
    Research use only, not for human use.
  • Brief Description
    GLS4 (Morphothiadin) is a potent inhibitor of HBV capsid assembly, inhibits HBV replication (EC50=62.24 nM) and reduces HBV-DNA levels in HepG.2.2.15 cells (IC50=14 nM).
  • Description
    GLS4 (Morphothiadin) is a potent inhibitor of HBV capsid assembly, inhibits HBV replication (EC50=62.24 nM) and reduces HBV-DNA levels in HepG.2.2.15 cells (IC50=14 nM), shows efficacy against ADV-resistant HBV mutations; strongly inhibits core gene expression (at 100 to 200 nM), suppresses virus accumulation in the supernantant of HepAD38 cells; inhibits HBV replicative forms in the live, shows strong and sustained suppression of virus DNA in treated mice.HBV Infection Phase 3 Clinical
  • Synonyms
    GLS 4;Morphothiadin
  • Pathway
    Microbiology/Virology
  • Target
    HBV
  • Recptor
    HBV
  • Research Area
    Infection
  • Indication
    HBV Infection

Chemical Information

  • CAS Number
    1092970-12-1
  • Formula Weight
    509.39
  • Molecular Formula
    C21H22BrFN4O3S
  • Purity
    >98% (HPLC)
  • Solubility
    DMSO : 100 mg/mL 196.31 mM; H2O : < 0.1 mg/mL
  • SMILES
    CCOC(=O)C1=C(NC(=NC1C2=C(C=C(C=C2)F)Br)C3=NC=CS3)CN4CCOCC4
  • Chemical Name
    ethyl 4-(2-bromo-4-fluorophenyl)-6-(morpholinomethyl)-2-(thiazol-2-yl)-1,4-dihydropyrimidine-5-carboxylate

Shipping & Storage Information

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

Reference

1. Wang XY, et al. Antivir Ther. 2012;17(5):793-803.
2. Wu G, et al. Antimicrob Agents Chemother. 2013 Nov;57(11):5344-54.
3. Ren Q, et al. Bioorg Med Chem. 2017 Feb 1;25(3):1042-1056.
4. Tu T, et al. J Virol. 2018 Feb 7. pii: JVI.02007-17.
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