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
500MG Get Quote 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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