J
Jay O. Knipe
Researcher at Bristol-Myers Squibb
Publications - 48
Citations - 3857
Jay O. Knipe is an academic researcher from Bristol-Myers Squibb. The author has contributed to research in topics: Hepatitis C virus & In vivo. The author has an hindex of 26, co-authored 48 publications receiving 3625 citations.
Papers
More filters
Journal ArticleDOI
Chemical genetics strategy identifies an HCV NS5A inhibitor with a potent clinical effect
Min Gao,Richard E. Nettles,Makonen Belema,Lawrence B. Snyder,Van N. Nguyen,Robert A. Fridell,Michael H. Serrano-Wu,David R. Langley,Jin-Hua Sun,Donald R. O'Boyle,Julie A. Lemm,Chunfu Wang,Jay O. Knipe,Caly Chien,Richard J. Colonno,Dennis M. Grasela,Nicholas A. Meanwell,Lawrence G. Hamann +17 more
TL;DR: These results provide the first clinical validation of an inhibitor of HCV NS5A, a protein with no known enzymatic function, as an approach to the suppression of virus replication that offers potential as part of a therapeutic regimen based on combinations ofHCV inhibitors.
Journal ArticleDOI
Cathepsin B-labile dipeptide linkers for lysosomal release of doxorubicin from internalizing immunoconjugates: model studies of enzymatic drug release and antigen-specific in vitro anticancer activity.
Gene M. Dubowchik,Raymond A. Firestone,Linda Padilla,David Willner,Hofstead Sandra J,Kathleen W. Mosure,Jay O. Knipe,Shirley J. Lasch,Pamela A. Trail +8 more
TL;DR: Against tumor cell lines with varying levels of BR96 expression, both conjugates showed potent, antigen-specific cytotoxic activity, suggesting that they will be effective in delivering DOX selectively to antigen-expressing carcinomas.
Journal ArticleDOI
New hydrazone derivatives of Adriamycin and their immunoconjugates - a correlation between acid stability and cytotoxicity
Takushi Kaneko,David Willner,Ivo Monkovic,Jay O. Knipe,Braslawsky Gary R,Greenfield Robert S,Dolatrai M. Vyas +6 more
TL;DR: New N-substituted hydrazine linkers were synthesized and their hydrazone derivatives of adriamycin derivatives were conjugated with a monoclonal antibody and their relationship to the IC50's of the conjugate against 5E9-positive Daudi cells was investigated.
Journal ArticleDOI
Preclinical Profile and Characterization of the Hepatitis C Virus NS3 Protease Inhibitor Asunaprevir (BMS-650032)
Fiona McPhee,Amy K. Sheaffer,Jacques Friborg,Dennis Hernandez,Paul Falk,Guangzhi Zhai,Steven Levine,Susan Chaniewski,Fei Yu,Diana Barry,Chaoqun Chen,Min S. Lee,Kathy Mosure,Li-Qiang Sun,Michael Sinz,Nicholas A. Meanwell,Richard J. Colonno,Jay O. Knipe,Paul Michael Scola +18 more
TL;DR: Asunaprevir (ASV; BMS-650032) is a hepatitis C virus (HCV) NS3 protease inhibitor that has demonstrated efficacy in patients chronically infected with HCV genotype 1 when combined with alfa interferon and/or the NS5A replication complex inhibitor daclatasvir as discussed by the authors.
Journal ArticleDOI
Cathepsin B-sensitive dipeptide prodrugs. 2. Models of anticancer drugs paclitaxel (Taxol®), mitomycin C and doxorubicin
TL;DR: Substrates containing doxorubicin, paclitaxel, and mitomycin C attached to the cathepsin B-sensitive dipeptide Phe-Lys via a self-immolative spacer were prepared as model compounds for internalizing anticancer immunoconjugates.