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RSC Medicinal Chemistry
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February 23, 2024
Correction: A high-throughput effector screen identifies a novel small molecule scaffold for inhibition of ten-eleven translocation dioxygenase 2
Shubhendu Palei, Jörn Weisner, Melina Vogt, et al.
Plos One
|
June 22, 2022
Design and synthesis of Nrf2-derived hydrocarbon stapled peptides for the disruption of protein-DNA-interactions
Bianca Wiedemann, Dominic Kamps, Laura Depta, et al.
Molecules (Basel, Switzerland)
|
March 25, 2017
Optimized 4,5-Diarylimidazoles as Potent/Selective Inhibitors of Protein Kinase CK1δ and Their Structural Relation to p38α MAPK
Jakob Halekotte, Lydia Witt, Chiara Ianes, et al.
ACS Chemical Biology
|
June 16, 2011
Identification of Ustilago maydis Aurora kinase as a novel antifungal target
Sandra Tückmantel, Jörg N Greul, Petra Janning, et al.
Nature Chemical Biology
|
March 6, 2007
Structure-guided development of affinity probes for tyrosine kinases using chemical genetics
Jimmy A Blair, Daniel Rauh, Charles Kung, et al.
Bioorganic & Medicinal Chemistry Letters
|
July 5, 2016
A cascade screening approach for the identification of Bcr-Abl myristate pocket binders active against wild type and T315I mutant
Marco Radi, Ralf Schneider, Anna Lucia Fallacara, et al.
Bioconjugate Chemistry
|
June 22, 2018
Insights into the Kinetics of the Resistance Formation of Bacteria against Ciprofloxacin Poly(2-methyl-2-oxazoline) Conjugates
Martin Schmidt, Alina Romanovska, Youssef Wolf, et al.
Plos Biology
|
April 1, 2005
An unbiased cell morphology-based screen for new, biologically active small molecules
Masahiro Tanaka, Raynard Bateman, Daniel Rauh, et al.
Chembiochem : a European Journal of Chemical Biology
|
November 17, 2010
Characterization of irreversible kinase inhibitors by directly detecting covalent bond formation: a tool for dissecting kinase drug resistance
Sabine Klüter, Jeffrey R Simard, Haridas B Rode, et al.
Scientific Reports
|
January 11, 2019
A novel scaffold for EGFR inhibition: Introducing N-(3-(3-phenylureido)quinoxalin-6-yl) acrylamide derivatives
Daniel Nascimento do Amaral, Jonas Lategahn, Harold Hilarion Fokoue, et al.
Page
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Search research articles
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Showing results (101-110 of 159) with videos related to
Sort By:
Page
of 16
RSC Medicinal Chemistry
|
February 23, 2024
Correction: A high-throughput effector screen identifies a novel small molecule scaffold for inhibition of ten-eleven translocation dioxygenase 2
Shubhendu Palei, Jörn Weisner, Melina Vogt, et al.
Plos One
|
June 22, 2022
Design and synthesis of Nrf2-derived hydrocarbon stapled peptides for the disruption of protein-DNA-interactions
Bianca Wiedemann, Dominic Kamps, Laura Depta, et al.
Molecules (Basel, Switzerland)
|
March 25, 2017
Optimized 4,5-Diarylimidazoles as Potent/Selective Inhibitors of Protein Kinase CK1δ and Their Structural Relation to p38α MAPK
Jakob Halekotte, Lydia Witt, Chiara Ianes, et al.
ACS Chemical Biology
|
June 16, 2011
Identification of Ustilago maydis Aurora kinase as a novel antifungal target
Sandra Tückmantel, Jörg N Greul, Petra Janning, et al.
Nature Chemical Biology
|
March 6, 2007
Structure-guided development of affinity probes for tyrosine kinases using chemical genetics
Jimmy A Blair, Daniel Rauh, Charles Kung, et al.
Bioorganic & Medicinal Chemistry Letters
|
July 5, 2016
A cascade screening approach for the identification of Bcr-Abl myristate pocket binders active against wild type and T315I mutant
Marco Radi, Ralf Schneider, Anna Lucia Fallacara, et al.
Bioconjugate Chemistry
|
June 22, 2018
Insights into the Kinetics of the Resistance Formation of Bacteria against Ciprofloxacin Poly(2-methyl-2-oxazoline) Conjugates
Martin Schmidt, Alina Romanovska, Youssef Wolf, et al.
Plos Biology
|
April 1, 2005
An unbiased cell morphology-based screen for new, biologically active small molecules
Masahiro Tanaka, Raynard Bateman, Daniel Rauh, et al.
Chembiochem : a European Journal of Chemical Biology
|
November 17, 2010
Characterization of irreversible kinase inhibitors by directly detecting covalent bond formation: a tool for dissecting kinase drug resistance
Sabine Klüter, Jeffrey R Simard, Haridas B Rode, et al.
Scientific Reports
|
January 11, 2019
A novel scaffold for EGFR inhibition: Introducing N-(3-(3-phenylureido)quinoxalin-6-yl) acrylamide derivatives
Daniel Nascimento do Amaral, Jonas Lategahn, Harold Hilarion Fokoue, et al.
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of 16