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Michael D Threadgill

Showing results (11-20 of 62) with videos related to

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Phytochemistry|October 22, 2008
Extraction, structural characterisation and evaluation of hydroxycinnamate esters of orchard grass (Dactylis glomerata) as substrates for polyphenol oxidaseIfat Parveen, Ana Winters, Michael D Threadgill, et al.
Organic & Biomolecular Chemistry|August 22, 2003
Synthesis of meso-substituted porphyrins carrying carboranes and oligo(ethylene glycol) units for potential applications in boron neutron capture therapyChristophe Frixa, Mary F Mahon, Andrew S Thompson, et al.
Molecules (Basel, Switzerland)|July 27, 2010
Synthesis of N-(methoxycarbonylthienylmethyl)thioureas and evaluation of their interaction with inducible and neuronal nitric oxide synthaseGhadeer A R Y Suaifan, Claire L M Goodyer, Michael D Threadgill
The FEBS Journal|February 19, 2008
Alpha-methylacyl-CoA racemase--an 'obscure' metabolic enzyme takes centre stageMatthew D Lloyd, Daniel J Darley, Anthony S Wierzbicki, et al.
Journal of Medicinal Chemistry|January 2, 2009
Design, synthesis, and evaluation in vitro of quinoline-8-carboxamides, a new class of poly(adenosine-diphosphate-ribose)polymerase-1 (PARP-1) inhibitorAnna-Marie Lord, Mary F Mahon, Matthew D Lloyd, et al.
Chemical Communications (Cambridge, England)|December 14, 2002
Formation of a remarkably robust 2:1 complex between beta-cyclodextrin and a phenyl-substituted icosahedral carboraneChristophe Frixa, Martin Scobie, Steven J Black, et al.
Future Medicinal Chemistry|July 2, 2024
Thiourea-functionalized aminoglutethimide derivatives as anti-leishmanial agentsMuhammad Sajid, Hina Siddiqui, Humaira Zafar, et al.
ACS Medicinal Chemistry Letters|June 6, 2014
Design and Discovery of 2-Arylquinazolin-4-ones as Potent and Selective Inhibitors of TankyrasesAmit Nathubhai, Pauline J Wood, Matthew D Lloyd, et al.
Chemical Communications (Cambridge, England)|October 4, 2014
The perils of rational design--unexpected irreversible elimination of fluoride from 3-fluoro-2-methylacyl-CoA esters catalysed by α-methylacyl-CoA racemase (AMACR; P504S)Maksims Yevglevskis, Guat L Lee, Michael D Threadgill, et al.
Bioorganic & Medicinal Chemistry|April 25, 2007
Structure-based design, synthesis and preliminary evaluation of selective inhibitors of dihydrofolate reductase from Mycobacterium tuberculosisMervat H R I El-Hamamsy, Anthony W Smith, Andrew S Thompson, et al.
Pageof 7

Showing results (11-20 of 62) with videos related to

Sort By:
Pageof 7
Phytochemistry|October 22, 2008
Extraction, structural characterisation and evaluation of hydroxycinnamate esters of orchard grass (Dactylis glomerata) as substrates for polyphenol oxidaseIfat Parveen, Ana Winters, Michael D Threadgill, et al.
Organic & Biomolecular Chemistry|August 22, 2003
Synthesis of meso-substituted porphyrins carrying carboranes and oligo(ethylene glycol) units for potential applications in boron neutron capture therapyChristophe Frixa, Mary F Mahon, Andrew S Thompson, et al.
Molecules (Basel, Switzerland)|July 27, 2010
Synthesis of N-(methoxycarbonylthienylmethyl)thioureas and evaluation of their interaction with inducible and neuronal nitric oxide synthaseGhadeer A R Y Suaifan, Claire L M Goodyer, Michael D Threadgill
The FEBS Journal|February 19, 2008
Alpha-methylacyl-CoA racemase--an 'obscure' metabolic enzyme takes centre stageMatthew D Lloyd, Daniel J Darley, Anthony S Wierzbicki, et al.
Journal of Medicinal Chemistry|January 2, 2009
Design, synthesis, and evaluation in vitro of quinoline-8-carboxamides, a new class of poly(adenosine-diphosphate-ribose)polymerase-1 (PARP-1) inhibitorAnna-Marie Lord, Mary F Mahon, Matthew D Lloyd, et al.
Chemical Communications (Cambridge, England)|December 14, 2002
Formation of a remarkably robust 2:1 complex between beta-cyclodextrin and a phenyl-substituted icosahedral carboraneChristophe Frixa, Martin Scobie, Steven J Black, et al.
Future Medicinal Chemistry|July 2, 2024
Thiourea-functionalized aminoglutethimide derivatives as anti-leishmanial agentsMuhammad Sajid, Hina Siddiqui, Humaira Zafar, et al.
ACS Medicinal Chemistry Letters|June 6, 2014
Design and Discovery of 2-Arylquinazolin-4-ones as Potent and Selective Inhibitors of TankyrasesAmit Nathubhai, Pauline J Wood, Matthew D Lloyd, et al.
Chemical Communications (Cambridge, England)|October 4, 2014
The perils of rational design--unexpected irreversible elimination of fluoride from 3-fluoro-2-methylacyl-CoA esters catalysed by α-methylacyl-CoA racemase (AMACR; P504S)Maksims Yevglevskis, Guat L Lee, Michael D Threadgill, et al.
Bioorganic & Medicinal Chemistry|April 25, 2007
Structure-based design, synthesis and preliminary evaluation of selective inhibitors of dihydrofolate reductase from Mycobacterium tuberculosisMervat H R I El-Hamamsy, Anthony W Smith, Andrew S Thompson, et al.
Pageof 7