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Binqing Wei

Showing results (1-10 of 40) with videos related to

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Current Opinion in Chemical Biology|July 23, 2002
Lead discovery using molecular dockingBrian K Shoichet, Susan L McGovern, Binqing Wei, et al.
ACS Medicinal Chemistry Letters|January 17, 2024
Structure-Based Design and Evaluation of Reversible KRAS G13D InhibitorsChristian Nilewski, Sharada Labadie, Binqing Wei, et al.
Drug Metabolism and Disposition: the Biological Fate of Chemicals|March 13, 2019
A Novel Depurination Methodology to Assess DNA Alkylation of Chloro-Bis-Seco-Cyclopropylbenzoindoles Allowed for Comparison of Minor-Groove ReactivityShuai Wang, Buyun Chen, Peter Dragovich, et al.
Structure (London, England : 1993)|December 4, 2018
Hematopoietic Progenitor Kinase-1 Structure in a Domain-Swapped DimerPing Wu, Christopher J Sneeringer, Keith E Pitts, et al.
ACS Medicinal Chemistry Letters|September 27, 2017
Design of Selective Benzoxazepin PI3Kδ Inhibitors Through Control of Dihedral AnglesBrian S Safina, Richard L Elliott, Andrew K Forrest, et al.
Bioorganic & Medicinal Chemistry Letters|December 4, 2014
Identification of 3,6-disubstituted dihydropyrones as inhibitors of human lactate dehydrogenaseBenjamin P Fauber, Peter S Dragovich, Jinhua Chen, et al.
Bioconjugate Chemistry|September 9, 2017
Attachment Site Cysteine Thiol pK<sub>a</sub> Is a Key Driver for Site-Dependent Stability of THIOMAB Antibody-Drug ConjugatesBreanna S Vollmar, Binqing Wei, Rachana Ohri, et al.
Bioorganic & Medicinal Chemistry Letters|July 23, 2013
Identification of GNE-293, a potent and selective PI3Kδ inhibitor: navigating in vitro genotoxicity while improving potency and selectivityBrian S Safina, Zachary K Sweeney, Jun Li, et al.
Bioorganic & Medicinal Chemistry Letters|December 26, 2012
Cis-amide isosteric replacement in thienobenzoxepin inhibitors of PI3-kinaseSteven T Staben, Nicole Blaquiere, Vickie Tsui, et al.
Journal of Medicinal Chemistry|April 4, 2012
Discovery and optimization of a novel spiropyrrolidine inhibitor of β-secretase (BACE1) through fragment-based drug designIvan V Efremov, Felix F Vajdos, Kris A Borzilleri, et al.
Pageof 4

Showing results (1-10 of 40) with videos related to

Sort By:
Pageof 4
Current Opinion in Chemical Biology|July 23, 2002
Lead discovery using molecular dockingBrian K Shoichet, Susan L McGovern, Binqing Wei, et al.
ACS Medicinal Chemistry Letters|January 17, 2024
Structure-Based Design and Evaluation of Reversible KRAS G13D InhibitorsChristian Nilewski, Sharada Labadie, Binqing Wei, et al.
Drug Metabolism and Disposition: the Biological Fate of Chemicals|March 13, 2019
A Novel Depurination Methodology to Assess DNA Alkylation of Chloro-Bis-Seco-Cyclopropylbenzoindoles Allowed for Comparison of Minor-Groove ReactivityShuai Wang, Buyun Chen, Peter Dragovich, et al.
Structure (London, England : 1993)|December 4, 2018
Hematopoietic Progenitor Kinase-1 Structure in a Domain-Swapped DimerPing Wu, Christopher J Sneeringer, Keith E Pitts, et al.
ACS Medicinal Chemistry Letters|September 27, 2017
Design of Selective Benzoxazepin PI3Kδ Inhibitors Through Control of Dihedral AnglesBrian S Safina, Richard L Elliott, Andrew K Forrest, et al.
Bioorganic & Medicinal Chemistry Letters|December 4, 2014
Identification of 3,6-disubstituted dihydropyrones as inhibitors of human lactate dehydrogenaseBenjamin P Fauber, Peter S Dragovich, Jinhua Chen, et al.
Bioconjugate Chemistry|September 9, 2017
Attachment Site Cysteine Thiol pK<sub>a</sub> Is a Key Driver for Site-Dependent Stability of THIOMAB Antibody-Drug ConjugatesBreanna S Vollmar, Binqing Wei, Rachana Ohri, et al.
Bioorganic & Medicinal Chemistry Letters|July 23, 2013
Identification of GNE-293, a potent and selective PI3Kδ inhibitor: navigating in vitro genotoxicity while improving potency and selectivityBrian S Safina, Zachary K Sweeney, Jun Li, et al.
Bioorganic & Medicinal Chemistry Letters|December 26, 2012
Cis-amide isosteric replacement in thienobenzoxepin inhibitors of PI3-kinaseSteven T Staben, Nicole Blaquiere, Vickie Tsui, et al.
Journal of Medicinal Chemistry|April 4, 2012
Discovery and optimization of a novel spiropyrrolidine inhibitor of β-secretase (BACE1) through fragment-based drug designIvan V Efremov, Felix F Vajdos, Kris A Borzilleri, et al.
Pageof 4