An antiviral agent
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GLS4

Item No. 35843

Technical Information
Formal Name
4-(2-bromo-4-fluorophenyl)-1,4-dihydro-6-(4-morpholinylmethyl)-2-(2-thiazolyl)-5-pyrimidinecarboxylic acid, ethyl ester
CAS Number
1092970-12-1
Synonyms
  • Morphothiadin
Molecular Formula
C21H22BrFN4O3S
Formula Weight
Purity
≥98%
A solid
DMF: 12 mg/mlDMSO: 1 mg/mlEthanol: Slightly solublePBS (pH 7.2): 0.3 mg/ml
SMILES
O=C(C1=C(CN2CCOCC2)N=C(C3=NC=CS3)NC1C4=CC=C(C=C4Br)F)OCC
InChi Code
InChI=1S/C21H22BrFN4O3S/c1-2-30-21(28)17-16(12-27-6-8-29-9-7-27)25-19(20-24-5-10-31-20)26-18(17)14-4-3-13(23)11-15(14)22/h3-5,10-11,18H,2,6-9,12H2,1H3,(H,25,26)
InChi Key
SQGRDKSRFFUBBU-UHFFFAOYSA-N
Shipping & Storage Information
Storage
-20°C
Shipping
Room temperature in continental US; may vary elsewhere
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    Product Description

    GLS4 is an antiviral agent.1 It inhibits the replication of wild-type hepatitis B virus (HBV) and the drug-resistant HBV strains rtA181T, rtA181V, and rtN236T (IC50s = 146, 145, 161, and 131 nM, respectively). GSL4 (1 and 10 µM) inhibits the formation of viral capsids and decreases viral core protein levels in HBV-infected HepG2 and HepG2.2.15 cells. It inhibits HBV replication and reduces the levels of viral intracellular core antigens in mice inoculated with HepAD38 cells, which carry and replicate HBV, when administered at doses ranging from 7.5 to 60 mg/kg.2

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Description References

    1. Wang, X.-Y., Wei, Z.-M., Wu, G.-Y., et alIn vitro inhibition of HBV replication by a novel compound, GLS4, and its efficacy against adefovir-dipivoxil-resistant HBV mutations. Antivir. Ther. 17(5), 793-803 (2012).

    2. Wu, G., Liu, B., Zhang, Y., et alPreclinical characterization of GLS4, an inhibitor of hepatitis B virus core particle assembly. Antimicrob. Agents Chemother. 57(11), 5344-5354 (2013).