Chemical Structure : IDX-375
Catalog No.: PC-62828Not For Human Use, Lab Use Only.
IDX-375 is a novel potent, non-nucleoside, allosteric HCV NS5B RdRp inhibitor with IC50 of 15 nM and 5 nM for 1a-H77 HCV NS5B polymerase and 1b-J4 HCV NS5B polymerase, respectively.
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IDX-375 is a novel potent, non-nucleoside, allosteric HCV NS5B RdRp inhibitor with IC50 of 15 nM and 5 nM for 1a-H77 HCV NS5B polymerase and 1b-J4 HCV NS5B polymerase, respectively.
IDX-375 has no activity against human cellular polymerases (>75 uM).
IDX-375 has an EC50 of 3 nM in HCV replicon luciferase assay.
IDX-375 displays excellent antiviral activity on the genotypes 1a and 1b, and a good PK profile in multiple animal models.
M.Wt | 643.78 | |
Formula | C29H50N5O7PS | |
Appearance | Solid | |
Storage |
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Solubility |
10 mM in DMSO |
1. Paparin JL, et al. Bioorg Med Chem Lett. 2017 Jun 1;27(11):2634-2640.
2. de Bruijne J, et al. Antimicrob Agents Chemother. 2012 Aug;56(8):4525-8.
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