SOLID FORMS OF A FLAVIVIRIDAE VIRUS INHIBITOR COMPOUND AND SALTS THEREOF
    6.
    发明申请
    SOLID FORMS OF A FLAVIVIRIDAE VIRUS INHIBITOR COMPOUND AND SALTS THEREOF 审中-公开
    维生素A病毒抑制剂化合物的固体形式及其盐

    公开(公告)号:US20170066779A1

    公开(公告)日:2017-03-09

    申请号:US15123170

    申请日:2015-03-04

    摘要: Provided herein are crystalline and salt forms of methyl N-{(1R)-2-[(2S)-2-{5-[4-(6-{2-[(2S)-1-{(2S)-2-[(methoxycarbonyl)amino]-3-methylbutanoyl} pyrrolidin-2-yl]-3H-benzimidazol-5-yl}thieno[3,2-b]thiophen-3-yl)phenyl]-1H-imidazol-2-yl}pyrrolidin-1-yl]-2-oxo-1-phenylethyl} carbamate, a Flaviviridae, including hepatitis C, virus inhibitor, pharmaceutical compositions comprising the compound, and processes of preparation thereof. Also provided are methods of its use for the treatment of a Flaviviridae, including HCV, infection in a subject in need thereof.

    摘要翻译: 本文提供的是N - {(1R)-2 - [(2S)-2- {5- [4-(6- {2 - [(2S)-1 - {(2S)-2 - [(甲氧基羰基)氨基] -3-甲基丁酰基}吡咯烷-2-基] -3H-苯并咪唑-5-基}噻吩并[3,2-b]噻吩-3-基)苯基〕-1H-咪唑-2-基) 吡咯烷-1-基] -2-氧代-1-苯基乙基}氨基甲酸酯,黄病毒科,包括丙型肝炎病毒抑制剂,包含该化合物的药物组合物及其制备方法。 还提供了其用于治疗有需要的受试者中的黄病毒科(包括HCV)感染的方法。

    2′,4′-bridged nucleosides for HCV infection

    公开(公告)号:US10723754B2

    公开(公告)日:2020-07-28

    申请号:US14059233

    申请日:2013-10-21

    摘要: Provided herein are compounds, compositions and methods for the treatment of Flaviviridae infections, including HCV infections. In certain embodiments, compounds and compositions of nucleoside derivatives are disclosed, which can be administered either alone or in combination with other anti-viral agents. In certain embodiments, the compounds are 2′,4′-bridged nucleosides which display remarkable efficacy and bioavailability for the treatment of, for example, HCV infection in a human. In certain embodiments, the 2′,4′-bridged nucleosides are of Formula 3001: or a pharmaceutically acceptable salt, solvate, stereoisomeric form, tautomeric form or polymorphic form thereof, where PD, B, W, X, RA, RB, RC and RD are as described herein.