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Analytical Biochemistry
|
March 11, 2006
A fluorescence polarization assay for screening inhibitors against the ribonuclease H activity of HIV-1 reverse transcriptase
Grace R Nakayama, Patrick Bingham, Douglas Tan, et al.
Assay and Drug Development Technologies
|
June 13, 2015
Comparison of a High-Throughput Mass Spectrometry Method and Radioactive Filter Binding to Assay the Protein Methyltransferase PRMT5
Karen A Maegley, Cody Krivacic, Patrick Bingham, et al.
Combinatorial Chemistry & High Throughput Screening
|
June 22, 2006
Analysing the output from primary screening
Dawn Nowlin, Patrick Bingham, Andrew Berridge, et al.
Bioorganic & Medicinal Chemistry Letters
|
March 10, 2015
SAH derived potent and selective EZH2 inhibitors
Pei-Pei Kung, Buwen Huang, Luke Zehnder, et al.
The Journal of Biological Chemistry
|
February 5, 2025
Modulation of the substrate preference of a MYST acetyltransferase by a scaffold protein
Raghuvir N Sengupta, Oleg Brodsky, Patrick Bingham, et al.
Nature Communications
|
April 29, 2016
Polycomb repressive complex 2 structure with inhibitor reveals a mechanism of activation and drug resistance
Alexei Brooun, Ketan S Gajiwala, Ya-Li Deng, et al.
Journal of Medicinal Chemistry
|
November 8, 2017
Discovery of a Novel and Selective Indoleamine 2,3-Dioxygenase (IDO-1) Inhibitor 3-(5-Fluoro-1H-indol-3-yl)pyrrolidine-2,5-dione (EOS200271/PF-06840003) and Its Characterization as a Potential Clinical Candidate
Stefano Crosignani, Patrick Bingham, Pauline Bottemanne, et al.
ACS Medicinal Chemistry Letters
|
June 20, 2020
Characterization of Specific <i>N</i>-α-Acetyltransferase 50 (Naa50) Inhibitors Identified Using a DNA Encoded Library
Pei-Pei Kung, Patrick Bingham, Benjamin J Burke, et al.
Journal of Medicinal Chemistry
|
August 12, 2016
Design and Synthesis of Pyridone-Containing 3,4-Dihydroisoquinoline-1(2H)-ones as a Novel Class of Enhancer of Zeste Homolog 2 (EZH2) Inhibitors
Pei-Pei Kung, Eugene Rui, Simon Bergqvist, et al.
Journal of Medicinal Chemistry
|
December 13, 2016
Correction to Design and Synthesis of Pyridone-Containing 3,4-Dihydroisoquinoline-1(2H)-ones as a Novel Class of Enhancer of Zeste Homolog 2 (EZH2) Inhibitors
Pei-Pei Kung, Eugene Rui, Simon Bergqvist, et al.
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Search research articles
Search
Showing results (1-10 of 12) with videos related to
Sort By:
Page
of 2
Analytical Biochemistry
|
March 11, 2006
A fluorescence polarization assay for screening inhibitors against the ribonuclease H activity of HIV-1 reverse transcriptase
Grace R Nakayama, Patrick Bingham, Douglas Tan, et al.
Assay and Drug Development Technologies
|
June 13, 2015
Comparison of a High-Throughput Mass Spectrometry Method and Radioactive Filter Binding to Assay the Protein Methyltransferase PRMT5
Karen A Maegley, Cody Krivacic, Patrick Bingham, et al.
Combinatorial Chemistry & High Throughput Screening
|
June 22, 2006
Analysing the output from primary screening
Dawn Nowlin, Patrick Bingham, Andrew Berridge, et al.
Bioorganic & Medicinal Chemistry Letters
|
March 10, 2015
SAH derived potent and selective EZH2 inhibitors
Pei-Pei Kung, Buwen Huang, Luke Zehnder, et al.
The Journal of Biological Chemistry
|
February 5, 2025
Modulation of the substrate preference of a MYST acetyltransferase by a scaffold protein
Raghuvir N Sengupta, Oleg Brodsky, Patrick Bingham, et al.
Nature Communications
|
April 29, 2016
Polycomb repressive complex 2 structure with inhibitor reveals a mechanism of activation and drug resistance
Alexei Brooun, Ketan S Gajiwala, Ya-Li Deng, et al.
Journal of Medicinal Chemistry
|
November 8, 2017
Discovery of a Novel and Selective Indoleamine 2,3-Dioxygenase (IDO-1) Inhibitor 3-(5-Fluoro-1H-indol-3-yl)pyrrolidine-2,5-dione (EOS200271/PF-06840003) and Its Characterization as a Potential Clinical Candidate
Stefano Crosignani, Patrick Bingham, Pauline Bottemanne, et al.
ACS Medicinal Chemistry Letters
|
June 20, 2020
Characterization of Specific <i>N</i>-α-Acetyltransferase 50 (Naa50) Inhibitors Identified Using a DNA Encoded Library
Pei-Pei Kung, Patrick Bingham, Benjamin J Burke, et al.
Journal of Medicinal Chemistry
|
August 12, 2016
Design and Synthesis of Pyridone-Containing 3,4-Dihydroisoquinoline-1(2H)-ones as a Novel Class of Enhancer of Zeste Homolog 2 (EZH2) Inhibitors
Pei-Pei Kung, Eugene Rui, Simon Bergqvist, et al.
Journal of Medicinal Chemistry
|
December 13, 2016
Correction to Design and Synthesis of Pyridone-Containing 3,4-Dihydroisoquinoline-1(2H)-ones as a Novel Class of Enhancer of Zeste Homolog 2 (EZH2) Inhibitors
Pei-Pei Kung, Eugene Rui, Simon Bergqvist, et al.
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of 2