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Molecules (Basel, Switzerland)
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June 2, 2021
The Glitazone Class of Drugs as Carbonic Anhydrase Inhibitors-A Spin-Off Discovery from Fragment Screening
Sarah L Mueller, Panagiotis K Chrysanthopoulos, Maria A Halili, et al.
Acta Crystallographica. Section F, Structural Biology and Crystallization Communications
|
December 9, 2010
A new crystal form of human vascular adhesion protein 1
Karin Ernberg, Aaron P McGrath, Thomas S Peat, et al.
Advances in Microbial Physiology
|
May 16, 2020
Bacterial catabolism of s-triazine herbicides: biochemistry, evolution and application
Lygie Esquirol, Thomas S Peat, Elena Sugrue, et al.
Chembiochem : a European Journal of Chemical Biology
|
August 19, 2011
Crystal structures of novel allosteric peptide inhibitors of HIV integrase identify new interactions at the LEDGF binding site
David I Rhodes, Thomas S Peat, Nick Vandegraaff, et al.
The Journal of Biological Chemistry
|
March 11, 2018
An unexpected vestigial protein complex reveals the evolutionary origins of an <i>s</i>-triazine catabolic enzyme
Lygie Esquirol, Thomas S Peat, Matthew Wilding, et al.
Biochemistry
|
December 10, 1999
Haloalkane dehalogenases: structure of a Rhodococcus enzyme
J Newman, T S Peat, R Richard, et al.
Applied and Environmental Microbiology
|
November 2, 2014
X-ray structure of the amidase domain of AtzF, the allophanate hydrolase from the cyanuric acid-mineralizing multienzyme complex
Sahil Balotra, Janet Newman, Nathan P Cowieson, et al.
Journal of Medicinal Chemistry
|
February 8, 2020
Discovery of Potent Dual-Tailed Benzenesulfonamide Inhibitors of Human Carbonic Anhydrases Implicated in Glaucoma and in Vivo Profiling of Their Intraocular Pressure-Lowering Action
Mohamed Fares, Wagdy M Eldehna, Silvia Bua, et al.
Experimental Hematology & Oncology
|
August 8, 2025
An ureido-substituted benzenesulfonamide carbonic anhydrase inhibitor exerts a potent antitumor effect in vitro and in vivo
Giorgia Gazzaroli, Camilla Tavani, Serena Filiberti, et al.
Journal of Biomolecular Screening
|
November 10, 2012
Parallel screening of low molecular weight fragment libraries: do differences in methodology affect hit identification?
Jerome Wielens, Stephen J Headey, David I Rhodes, et al.
Page
of 13
Search research articles
Search
Showing results (91-100 of 127) with videos related to
Sort By:
Page
of 13
Molecules (Basel, Switzerland)
|
June 2, 2021
The Glitazone Class of Drugs as Carbonic Anhydrase Inhibitors-A Spin-Off Discovery from Fragment Screening
Sarah L Mueller, Panagiotis K Chrysanthopoulos, Maria A Halili, et al.
Acta Crystallographica. Section F, Structural Biology and Crystallization Communications
|
December 9, 2010
A new crystal form of human vascular adhesion protein 1
Karin Ernberg, Aaron P McGrath, Thomas S Peat, et al.
Advances in Microbial Physiology
|
May 16, 2020
Bacterial catabolism of s-triazine herbicides: biochemistry, evolution and application
Lygie Esquirol, Thomas S Peat, Elena Sugrue, et al.
Chembiochem : a European Journal of Chemical Biology
|
August 19, 2011
Crystal structures of novel allosteric peptide inhibitors of HIV integrase identify new interactions at the LEDGF binding site
David I Rhodes, Thomas S Peat, Nick Vandegraaff, et al.
The Journal of Biological Chemistry
|
March 11, 2018
An unexpected vestigial protein complex reveals the evolutionary origins of an <i>s</i>-triazine catabolic enzyme
Lygie Esquirol, Thomas S Peat, Matthew Wilding, et al.
Biochemistry
|
December 10, 1999
Haloalkane dehalogenases: structure of a Rhodococcus enzyme
J Newman, T S Peat, R Richard, et al.
Applied and Environmental Microbiology
|
November 2, 2014
X-ray structure of the amidase domain of AtzF, the allophanate hydrolase from the cyanuric acid-mineralizing multienzyme complex
Sahil Balotra, Janet Newman, Nathan P Cowieson, et al.
Journal of Medicinal Chemistry
|
February 8, 2020
Discovery of Potent Dual-Tailed Benzenesulfonamide Inhibitors of Human Carbonic Anhydrases Implicated in Glaucoma and in Vivo Profiling of Their Intraocular Pressure-Lowering Action
Mohamed Fares, Wagdy M Eldehna, Silvia Bua, et al.
Experimental Hematology & Oncology
|
August 8, 2025
An ureido-substituted benzenesulfonamide carbonic anhydrase inhibitor exerts a potent antitumor effect in vitro and in vivo
Giorgia Gazzaroli, Camilla Tavani, Serena Filiberti, et al.
Journal of Biomolecular Screening
|
November 10, 2012
Parallel screening of low molecular weight fragment libraries: do differences in methodology affect hit identification?
Jerome Wielens, Stephen J Headey, David I Rhodes, et al.
Page
of 13