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首页-小分子抑制剂&激动剂-Antibiotics and Antivirals-HCV-IDX-375
IDX-375

Chemical Structure : IDX-375

CAS No.: 1256735-81-5

IDX-375 (IDX375)

货号: 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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纯度 & COA & 质检文件 纯度: >98% (HPLC) Select Batch:

    生物&药学活性

    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.

    物理化学性质&存储条件

    分子量 643.78
    分子式 C29H50N5O7PS
    外观性状 Solid
    CAS No.
    储存条件
    固体粉末
    -20 °C 12 个月; 4°C 6 个月
    配置液
    -80 °C 6 个月; -20°C 6 个月
    Shipping
    Solubility

    10 mM in DMSO

    Chemical Name/SMILES

    2-hydroxy-N,N,N-trimethylethan-1-aminium 2-(tert-butyl)-1-(3,3-dimethylbutyl)-4-(1-(2-hydroxyethyl)-7-(methylsulfonamido)-1-oxido-4H-benzo[c][1,5,2]diazaphosphinin-3-yl)-5-oxo-2,5-dihydro-1H-pyrrol-3-olate

    参考文献

    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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