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JNJ-8003

Chemical Structure : JNJ-8003

CAS No.:

JNJ-8003 (JNJ 8003)

Catalog No.: PC-21284Not For Human Use, Lab Use Only.

JNJ-8003 is a highly potent, selective, non-nucleoside inhibitor of respiratory syncytial virus (RSV) polymerase with IC50 of 0.67 nM, shows EC50 of 0.15 nM in RSV subgenomic replicon assays.

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    Biological Activity

    JNJ-8003 is a highly potent, selective, non-nucleoside inhibitor of respiratory syncytial virus (RSV) polymerase with IC50 of 0.67 nM, shows EC50 of 0.15 nM in RSV subgenomic replicon assays.
    JNJ-8003 targets the RSV L + P polymerase complex in both Flashplate and gel-based 4-mer primer extension assays using the recombinant L and P viral proteins.
    JNJ-8003 does not inhibit human DNA polymerases α, β, and γ, human mitochondrial RNA polymerase, and human RNA polymerase II (IC50>100 uM). JNJ-8003 inhibits viral RNA replication and transcription at the initiation and early elongation stage.
    JNJ-8003 binds within the capping domain of RSV L.

    Physicochemical Properties

    M.Wt 576.52
    Formula C28H25F5N4O4
    Appearance Solid
    CAS No.
    Storage
    Solide Powder
    -20°C 12 Months; 4°C 6 Months
    In Solvent
    -80°C 6 Months; -20°C 6 Months
    Shipping
    Solubility

    10 mM in DMSO

    Chemical Name/SMILES

    (S)-8-methoxy-3-methyl-N-(3,3,3-trifluoro-2-(5-fluoro-6-(4-fluorophenyl)-4-(2-hydroxypropan-2-yl)pyridin-2-yl)-2-hydroxypropyl)cinnoline-6-carboxamide

    References

    1. Xiaodi Yu, et al. Commun Biol. 2023 Oct 21;6(1):1074.

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