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Mark E Flanagan

Showing results (11-20 of 26) with videos related to

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SLAS Discovery : Advancing Life Sciences R & D|January 8, 2021
Selecting Approaches for Hit Identification and Increasing Options by Building the Efficient Discovery of Actionable Chemical Matter from DNA-Encoded LibrariesTimothy L Foley, Woodrow Burchett, Qiuxia Chen, et al.
ACS Medicinal Chemistry Letters|November 20, 2024
Cyclic Peptide C5aR1 Antagonist Design Using Solution Conformational Analysis Derived from Residual Dipolar CouplingsKathleen A Farley, Ye Che, Ricardo Lira, et al.
Chemical Science|June 7, 2021
Merging C(sp<sup>3</sup>)-H activation with DNA-encodingZhoulong Fan, Shuai Zhao, Tao Liu, et al.
Blood|December 21, 2007
The specificity of JAK3 kinase inhibitorsPaul S Changelian, Deborah Moshinsky, Cyrille F Kuhn, et al.
Scientific Reports|December 10, 2016
Chiral Sulfoxide-Induced Single Turn Peptide α-HelicityQingzhou Zhang, Fan Jiang, Bingchuan Zhao, et al.
Angewandte Chemie (International Ed. in English)|February 13, 2020
RASS-Enabled S/P-C and S-N Bond Formation for DEL SynthesisDillon T Flood, Xuejing Zhang, Xiang Fu, et al.
Bioorganic & Medicinal Chemistry|May 17, 2021
Toward the assembly and characterization of an encoded library hit confirmation platform: Bead-Assisted Ligand Isolation Mass Spectrometry (BALI-MS)Anokha S Ratnayake, Mark E Flanagan, Timothy L Foley, et al.
Journal of the American Chemical Society|May 29, 2019
Expanding Reactivity in DNA-Encoded Library Synthesis via Reversible Binding of DNA to an Inert Quaternary Ammonium SupportDillon T Flood, Shota Asai, Xuejing Zhang, et al.
Journal of Medicinal Chemistry|November 7, 2014
Chemical and computational methods for the characterization of covalent reactive groups for the prospective design of irreversible inhibitorsMark E Flanagan, Joseph A Abramite, Dennis P Anderson, et al.
Journal of Medicinal Chemistry|November 26, 2010
Discovery of CP-690,550: a potent and selective Janus kinase (JAK) inhibitor for the treatment of autoimmune diseases and organ transplant rejectionMark E Flanagan, Todd A Blumenkopf, William H Brissette, et al.
Pageof 3

Showing results (11-20 of 26) with videos related to

Sort By:
Pageof 3
SLAS Discovery : Advancing Life Sciences R & D|January 8, 2021
Selecting Approaches for Hit Identification and Increasing Options by Building the Efficient Discovery of Actionable Chemical Matter from DNA-Encoded LibrariesTimothy L Foley, Woodrow Burchett, Qiuxia Chen, et al.
ACS Medicinal Chemistry Letters|November 20, 2024
Cyclic Peptide C5aR1 Antagonist Design Using Solution Conformational Analysis Derived from Residual Dipolar CouplingsKathleen A Farley, Ye Che, Ricardo Lira, et al.
Chemical Science|June 7, 2021
Merging C(sp<sup>3</sup>)-H activation with DNA-encodingZhoulong Fan, Shuai Zhao, Tao Liu, et al.
Blood|December 21, 2007
The specificity of JAK3 kinase inhibitorsPaul S Changelian, Deborah Moshinsky, Cyrille F Kuhn, et al.
Scientific Reports|December 10, 2016
Chiral Sulfoxide-Induced Single Turn Peptide α-HelicityQingzhou Zhang, Fan Jiang, Bingchuan Zhao, et al.
Angewandte Chemie (International Ed. in English)|February 13, 2020
RASS-Enabled S/P-C and S-N Bond Formation for DEL SynthesisDillon T Flood, Xuejing Zhang, Xiang Fu, et al.
Bioorganic & Medicinal Chemistry|May 17, 2021
Toward the assembly and characterization of an encoded library hit confirmation platform: Bead-Assisted Ligand Isolation Mass Spectrometry (BALI-MS)Anokha S Ratnayake, Mark E Flanagan, Timothy L Foley, et al.
Journal of the American Chemical Society|May 29, 2019
Expanding Reactivity in DNA-Encoded Library Synthesis via Reversible Binding of DNA to an Inert Quaternary Ammonium SupportDillon T Flood, Shota Asai, Xuejing Zhang, et al.
Journal of Medicinal Chemistry|November 7, 2014
Chemical and computational methods for the characterization of covalent reactive groups for the prospective design of irreversible inhibitorsMark E Flanagan, Joseph A Abramite, Dennis P Anderson, et al.
Journal of Medicinal Chemistry|November 26, 2010
Discovery of CP-690,550: a potent and selective Janus kinase (JAK) inhibitor for the treatment of autoimmune diseases and organ transplant rejectionMark E Flanagan, Todd A Blumenkopf, William H Brissette, et al.
Pageof 3