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 |
|
1G | Get Quote | Get Quote |
|
Biological Information
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Product NameGLS4
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NoteResearch use only, not for human use.
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Brief DescriptionGLS4 (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).
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DescriptionGLS4 (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
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SynonymsGLS 4;Morphothiadin
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PathwayMicrobiology/Virology
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TargetHBV
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RecptorHBV
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Research AreaInfection
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IndicationHBV Infection
Chemical Information
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CAS Number1092970-12-1
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Formula Weight509.39
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Molecular FormulaC21H22BrFN4O3S
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Purity>98% (HPLC)
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SolubilityDMSO : 100 mg/mL 196.31 mM; H2O : < 0.1 mg/mL
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SMILESCCOC(=O)C1=C(NC(=NC1C2=C(C=C(C=C2)F)Br)C3=NC=CS3)CN4CCOCC4
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Chemical Nameethyl 4-(2-bromo-4-fluorophenyl)-6-(morpholinomethyl)-2-(thiazol-2-yl)-1,4-dihydropyrimidine-5-carboxylate
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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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.
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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