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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.

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Chemical genetics strategy identifies an HCV NS5A inhibitor with a potent clinical effect

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.
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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.

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.
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New hydrazone derivatives of Adriamycin and their immunoconjugates - a correlation between acid stability and cytotoxicity

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.
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Preclinical Profile and Characterization of the Hepatitis C Virus NS3 Protease Inhibitor Asunaprevir (BMS-650032)

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.
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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.