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Ruth Brenk

Showing results (51-60 of 65) with videos related to

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Organic & Biomolecular Chemistry|June 6, 2008
The small molecule tool (S)-(-)-blebbistatin: novel insights of relevance to myosin inhibitor designCristina Lucas-Lopez, John S Allingham, Tomas Lebl, et al.
Journal of Molecular Biology|November 24, 2012
Structural insights into the mechanism and inhibition of the β-hydroxydecanoyl-acyl carrier protein dehydratase from Pseudomonas aeruginosaLucile Moynié, Stuart M Leckie, Stephen A McMahon, et al.
Chemmedchem|June 19, 2013
From on-target to off-target activity: identification and optimisation of Trypanosoma brucei GSK3 inhibitors and their characterisation as anti-Trypanosoma brucei drug discovery lead moleculesAndrew Woodland, Raffaella Grimaldi, Torsten Luksch, et al.
Journal of Medicinal Chemistry|June 17, 2009
One scaffold, three binding modes: novel and selective pteridine reductase 1 inhibitors derived from fragment hits discovered by virtual screeningChidochangu P Mpamhanga, Daniel Spinks, Lindsay B Tulloch, et al.
Chemmedchem|January 29, 2011
Design, synthesis and biological evaluation of novel inhibitors of Trypanosoma brucei pteridine reductase 1Daniel Spinks, Han B Ong, Chidochangu P Mpamhanga, et al.
Chemmedchem|September 14, 2011
Identification of inhibitors of the Leishmania cdc2-related protein kinase CRK3Laura A T Cleghorn, Andrew Woodland, Iain T Collie, et al.
Journal of Medicinal Chemistry|November 11, 2017
Design and Synthesis of Brain Penetrant Trypanocidal N-Myristoyltransferase InhibitorsTracy Bayliss, David A Robinson, Victoria C Smith, et al.
RSC Medicinal Chemistry|April 26, 2024
Design, quality and validation of the EU-OPENSCREEN fragment library poised to a high-throughput screening collectionXavier Jalencas, Hannes Berg, Ludvik Olai Espeland, et al.
Chemmedchem|August 12, 2011
Optimisation of the anti-Trypanosoma brucei activity of the opioid agonist U50488Victoria C Smith, Laura A T Cleghorn, Andrew Woodland, et al.
ACS Chemical Biology|November 10, 2012
Allosteric competitive inhibitors of the glucose-1-phosphate thymidylyltransferase (RmlA) from Pseudomonas aeruginosaMagnus S Alphey, Lisa Pirrie, Leah S Torrie, et al.
Pageof 7

Showing results (51-60 of 65) with videos related to

Sort By:
Pageof 7
Organic & Biomolecular Chemistry|June 6, 2008
The small molecule tool (S)-(-)-blebbistatin: novel insights of relevance to myosin inhibitor designCristina Lucas-Lopez, John S Allingham, Tomas Lebl, et al.
Journal of Molecular Biology|November 24, 2012
Structural insights into the mechanism and inhibition of the β-hydroxydecanoyl-acyl carrier protein dehydratase from Pseudomonas aeruginosaLucile Moynié, Stuart M Leckie, Stephen A McMahon, et al.
Chemmedchem|June 19, 2013
From on-target to off-target activity: identification and optimisation of Trypanosoma brucei GSK3 inhibitors and their characterisation as anti-Trypanosoma brucei drug discovery lead moleculesAndrew Woodland, Raffaella Grimaldi, Torsten Luksch, et al.
Journal of Medicinal Chemistry|June 17, 2009
One scaffold, three binding modes: novel and selective pteridine reductase 1 inhibitors derived from fragment hits discovered by virtual screeningChidochangu P Mpamhanga, Daniel Spinks, Lindsay B Tulloch, et al.
Chemmedchem|January 29, 2011
Design, synthesis and biological evaluation of novel inhibitors of Trypanosoma brucei pteridine reductase 1Daniel Spinks, Han B Ong, Chidochangu P Mpamhanga, et al.
Chemmedchem|September 14, 2011
Identification of inhibitors of the Leishmania cdc2-related protein kinase CRK3Laura A T Cleghorn, Andrew Woodland, Iain T Collie, et al.
Journal of Medicinal Chemistry|November 11, 2017
Design and Synthesis of Brain Penetrant Trypanocidal N-Myristoyltransferase InhibitorsTracy Bayliss, David A Robinson, Victoria C Smith, et al.
RSC Medicinal Chemistry|April 26, 2024
Design, quality and validation of the EU-OPENSCREEN fragment library poised to a high-throughput screening collectionXavier Jalencas, Hannes Berg, Ludvik Olai Espeland, et al.
Chemmedchem|August 12, 2011
Optimisation of the anti-Trypanosoma brucei activity of the opioid agonist U50488Victoria C Smith, Laura A T Cleghorn, Andrew Woodland, et al.
ACS Chemical Biology|November 10, 2012
Allosteric competitive inhibitors of the glucose-1-phosphate thymidylyltransferase (RmlA) from Pseudomonas aeruginosaMagnus S Alphey, Lisa Pirrie, Leah S Torrie, et al.
Pageof 7