1028801-01-5Relevant academic research and scientific papers
Structure-activity relationships of 4-hydroxy-4-biaryl-proline acylsulfonamide tripeptides: A series of potent NS3 protease inhibitors for the treatment of hepatitis C virus
Wang, Alan Xiangdong,Chen, Jie,Zhao, Qian,Sun, Li-Qiang,Friborg, Jacques,Yu, Fei,Hernandez, Dennis,Good, Andrew C.,Klei, Herbert E.,Rajamani, Ramkumar,Mosure, Kathy,Knipe, Jay O.,Li, Danshi,Zhu, Jialong,Levesque, Paul C.,McPhee, Fiona,Meanwell, Nicholas A.,Scola, Paul M.
, p. 590 - 596 (2017/01/17)
The design and synthesis of a series of tripeptide acylsulfonamides as potent inhibitors of the HCV NS3/4A serine protease is described. These analogues house a C4 aryl, C4 hydroxy-proline at the S2 position of the tripeptide scaffold. Information relatin
Hepatitis C Virus Inhibitors
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Page/Page column 10, (2010/06/22)
Hepatitis C virus inhibitors having the general formula are disclosed. Compositions comprising the compounds and methods for using the compounds to inhibit HCV are also disclosed.
Hepatitis C Virus Inhibitors
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Page/Page column 12; 14-15, (2009/12/23)
Hepatitis C virus inhibitors having the general formula are disclosed. Compositions comprising the compounds and methods for using the compounds to inhibit HCV are also disclosed.
MACROCYCLIC PEPTIDES AS HEPATITIS C VIRUS INHIBITORS
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Page/Page column 96-97, (2008/12/05)
Macrocyclic peptides having the general formula (I): are disclosed. Compositions comprising the compounds and methods for using the compounds to inhibit HCV are also disclosed.
