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Bioorganic & Medicinal Chemistry
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July 16, 2013
One-pot tandem Hurtley-retro-Claisen-cyclisation reactions in the synthesis of 3-substituted analogues of 5-aminoisoquinolin-1-one (5-AIQ), a water-soluble inhibitor of PARPs
Esther C Y Woon, Peter T Sunderland, Helen A Paine, et al.
The Journal of Pharmacology and Experimental Therapeutics
|
January 13, 2005
Inhibitors of poly(ADP-ribose) polymerase modulate signal transduction pathways and the development of bleomycin-induced lung injury
Tiziana Genovese, Emanuela Mazzon, Rosanna Di Paola, et al.
Journal of Medicinal Chemistry
|
September 18, 1992
2-Nitroimidazole dual-function bioreductive drugs: studies on the effects of regioisomerism and side-chain structural modifications on differential cytotoxicity and radiosensitization by aziridinyl and oxiranyl derivatives
M A Naylor, M D Threadgill, P Webb, et al.
Journal of Enzyme Inhibition and Medicinal Chemistry
|
November 27, 2007
Characterisation of recombinant human fatty aldehyde dehydrogenase: implications for Sjögren-Larsson syndrome
Matthew D Lloyd, Kieren D E Boardman, Andrew Smith, et al.
Drug Design and Discovery
|
January 1, 1993
Synthesis of the enantiomers of the bioreductively-activated cytotoxin RSU-1069 and its prodrug RB6145 and lack of stereoselectivity in their cytotoxicity and radiosensitization in vitro
M A Naylor, M D Threadgill, H D Showalter, et al.
European Journal of Medicinal Chemistry
|
May 11, 2016
Structure-activity relationships of 2-arylquinazolin-4-ones as highly selective and potent inhibitors of the tankyrases
Amit Nathubhai, Teemu Haikarainen, Penelope C Hayward, et al.
Journal of Medicinal Chemistry
|
September 1, 1990
Synthesis and evaluation of novel electrophilic nitrofuran carboxamides and carboxylates as radiosensitizers and bioreductively activated cytotoxins
M A Naylor, M A Stephens, S Cole, et al.
Chemical Communications (Cambridge, England)
|
March 25, 2017
A novel colorimetric assay for α-methylacyl-CoA racemase 1A (AMACR; P504S) utilizing the elimination of 2,4-dinitrophenolate
Maksims Yevglevskis, Guat L Lee, Amit Nathubhai, et al.
Bioorganic & Medicinal Chemistry
|
June 1, 2015
Structure-based design, synthesis and evaluation in vitro of arylnaphthyridinones, arylpyridopyrimidinones and their tetrahydro derivatives as inhibitors of the tankyrases
Katerina Kumpan, Amit Nathubhai, Chenlu Zhang, et al.
The Journal of Pharmacology and Experimental Therapeutics
|
September 29, 2004
Inhibitors of poly(ADP-ribose) polymerase modulate signal transduction pathways and secondary damage in experimental spinal cord trauma
Tiziana Genovese, Emanuela Mazzon, Carmelo Muià, et al.
Page
of 13
Search research articles
Search
Showing results (81-90 of 122) with videos related to
Sort By:
Page
of 13
Bioorganic & Medicinal Chemistry
|
July 16, 2013
One-pot tandem Hurtley-retro-Claisen-cyclisation reactions in the synthesis of 3-substituted analogues of 5-aminoisoquinolin-1-one (5-AIQ), a water-soluble inhibitor of PARPs
Esther C Y Woon, Peter T Sunderland, Helen A Paine, et al.
The Journal of Pharmacology and Experimental Therapeutics
|
January 13, 2005
Inhibitors of poly(ADP-ribose) polymerase modulate signal transduction pathways and the development of bleomycin-induced lung injury
Tiziana Genovese, Emanuela Mazzon, Rosanna Di Paola, et al.
Journal of Medicinal Chemistry
|
September 18, 1992
2-Nitroimidazole dual-function bioreductive drugs: studies on the effects of regioisomerism and side-chain structural modifications on differential cytotoxicity and radiosensitization by aziridinyl and oxiranyl derivatives
M A Naylor, M D Threadgill, P Webb, et al.
Journal of Enzyme Inhibition and Medicinal Chemistry
|
November 27, 2007
Characterisation of recombinant human fatty aldehyde dehydrogenase: implications for Sjögren-Larsson syndrome
Matthew D Lloyd, Kieren D E Boardman, Andrew Smith, et al.
Drug Design and Discovery
|
January 1, 1993
Synthesis of the enantiomers of the bioreductively-activated cytotoxin RSU-1069 and its prodrug RB6145 and lack of stereoselectivity in their cytotoxicity and radiosensitization in vitro
M A Naylor, M D Threadgill, H D Showalter, et al.
European Journal of Medicinal Chemistry
|
May 11, 2016
Structure-activity relationships of 2-arylquinazolin-4-ones as highly selective and potent inhibitors of the tankyrases
Amit Nathubhai, Teemu Haikarainen, Penelope C Hayward, et al.
Journal of Medicinal Chemistry
|
September 1, 1990
Synthesis and evaluation of novel electrophilic nitrofuran carboxamides and carboxylates as radiosensitizers and bioreductively activated cytotoxins
M A Naylor, M A Stephens, S Cole, et al.
Chemical Communications (Cambridge, England)
|
March 25, 2017
A novel colorimetric assay for α-methylacyl-CoA racemase 1A (AMACR; P504S) utilizing the elimination of 2,4-dinitrophenolate
Maksims Yevglevskis, Guat L Lee, Amit Nathubhai, et al.
Bioorganic & Medicinal Chemistry
|
June 1, 2015
Structure-based design, synthesis and evaluation in vitro of arylnaphthyridinones, arylpyridopyrimidinones and their tetrahydro derivatives as inhibitors of the tankyrases
Katerina Kumpan, Amit Nathubhai, Chenlu Zhang, et al.
The Journal of Pharmacology and Experimental Therapeutics
|
September 29, 2004
Inhibitors of poly(ADP-ribose) polymerase modulate signal transduction pathways and secondary damage in experimental spinal cord trauma
Tiziana Genovese, Emanuela Mazzon, Carmelo Muià, et al.
Page
of 13