Substituted aliphanes, cyclophanes, heteraphanes, heterophanes, hetero-heteraphanes and metallocenes useful for treating hcv infections
US-2016115157-A1 · Apr 28, 2016 · US
US9592222B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9592222-B2 |
| Application number | US-201615271066-A |
| Country | US |
| Kind code | B2 |
| Filing date | Sep 20, 2016 |
| Priority date | May 27, 2011 |
| Publication date | Mar 14, 2017 |
| Grant date | Mar 14, 2017 |
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The present disclosure provides substituted aliphanes, cyclophanes, heteraphanes, heterophanes, hetero-heteraphanes and metallocenes, of Formula I D-M-D (Formula I) useful as antiviral agents. In certain embodiments disclosed herein M is a group —P-A-P— where A is Certain substituted aliphanes, cyclophanes, heteraphanes, heterophanes, hetero-heteraphanes and metallocenes disclosed herein are potent and/or selective inhibitors of viral replication, particularly Hepatitis C virus replication. Pharmaceutical compositions/and combinations containing one or more substituted aliphanes, cyclophanes, heteraphanes, heterophanes, hetero-heteraphanes and metallocenes and a pharmaceutically acceptable carrier are also provided by this disclosure. Methods for treating viral infections, including Hepatitis C viral infections are provided by the disclosure.
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What is claimed is: 1. A pharmaceutical composition comprising from about 10 mg to about 1,000 mg of a compound of the structure: or its pharmaceutically acceptable salt, in a pharmaceutically acceptable carrier. 2. The pharmaceutical composition of claim 1 , which is suitable for oral delivery. 3. The pharmaceutical composition of claim 2 , which is a tablet. 4. The pharmaceutical composition of claim 2 , which is a capsule. 5. The pharmaceutical composition of claim 1 , which is suitable for parenteral delivery. 6. The pharmaceutical composition of claim 1 , which is suitable for topical delivery.
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