Invention Grant
US09249176B2 4′-azido, 3′-deoxy-3′-fluoro substituted nucleoside derivatives as inhibitors of HCV RNA replication
有权
4'-叠氮基,3'-脱氧-3'-氟取代的核苷衍生物作为HCV RNA复制的抑制剂
- Patent Title: 4′-azido, 3′-deoxy-3′-fluoro substituted nucleoside derivatives as inhibitors of HCV RNA replication
- Patent Title (中): 4'-叠氮基,3'-脱氧-3'-氟取代的核苷衍生物作为HCV RNA复制的抑制剂
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Application No.: US14279188Application Date: 2014-05-15
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Publication No.: US09249176B2Publication Date: 2016-02-02
- Inventor: Mark Smith , Klaus G. Klumpp
- Applicant: Riboscience LLC
- Applicant Address: US CA Palo Alto
- Assignee: Riboscience LLC
- Current Assignee: Riboscience LLC
- Current Assignee Address: US CA Palo Alto
- Agency: GrayRobinson, P.A.
- Agent Jennifer L. Kisko
- Main IPC: C07H19/10
- IPC: C07H19/10 ; C07H19/20 ; A61K31/7068 ; A61K45/06 ; A61K31/7072

Abstract:
The present disclosure relates to the compound of Formula I: Also disclosed are pharmaceutical compositions comprising the compound of Formula I, methods of using the compound of Formula I and/or compositions comprising the compound of Formula I for the treatment of HCV.
Public/Granted literature
- US20140341848A1 4'-AZIDO, 3'-DEOXY-3'-FLUORO SUBSTITUTED NUCLEOSIDE DERIVATIVES AS INHIBITORS OF HCV RNA REPLICATION Public/Granted day:2014-11-20
Information query
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