Chemical Structure : JNJ-9676
Catalog No.: PC-24314Not For Human Use, Lab Use Only.
JNJ-9676 is a potent, specific small-molecule inhibitor of SARS-CoV-2 and SARS-CoV, binds to SARS-CoV-2 M protein, reduces SARS-CoV-2 (B1 variant) production of viral RNA with EC50/EC90 of 94/132 nM respectively.
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JNJ-9676 is a potent, specific small-molecule inhibitor of SARS-CoV-2 and SARS-CoV, binds to SARS-CoV-2 M protein, reduces SARS-CoV-2 (B1 variant) production of viral RNA with EC50/EC90 of 94/132 nM respectively.
JNJ-9676 demonstrates in vitro nanomolar antiviral activity against SARS-CoV-2, SARS-CoV and sarbecovirus strains from bat and pangolin zoonotic origin
JNJ-9676 binding induces substantial conformational changes in the M protein dimer, resulting in a novel conformational state.
JNJ-9676 (25 mg per kg BID) is able to reduce the viral RNA load and infectious virus in the lung with 3.5 log10[RNA copies per mg lung] and 4 log10[TCID50 per mg lung], respectively.
M.Wt | 497.51 | |
Formula | C28H21F2N5O2 | |
Appearance | Solid | |
Storage |
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Solubility |
10 mM in DMSO |
1. Van Damme E, et al. Nature. 2025 Mar 26. doi: 10.1038/s41586-025-08651-6.
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