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Natural Product Reports
|
September 28, 2007
Coenzyme biosynthesis: enzyme mechanism, structure and inhibition
Duncan E Scott, Alessio Ciulli, Chris Abell
Current Opinion in Chemical Biology
|
March 13, 2010
Drugging challenging targets using fragment-based approaches
Anthony G Coyne, Duncan E Scott, Chris Abell
Nature Reviews. Drug Discovery
|
April 7, 2016
Small molecules, big targets: drug discovery faces the protein-protein interaction challenge
Duncan E Scott, Andrew R Bayly, Chris Abell, et al.
Biochemistry
|
June 16, 2012
Fragment-based approaches in drug discovery and chemical biology
Duncan E Scott, Anthony G Coyne, Sean A Hudson, et al.
Chembiochem : a European Journal of Chemical Biology
|
October 15, 2009
A fragment-based approach to probing adenosine recognition sites by using dynamic combinatorial chemistry
Duncan E Scott, Gwen J Dawes, Michiyo Ando, et al.
FEBS Letters
|
March 20, 2016
Structure-activity relationship of the peptide binding-motif mediating the BRCA2:RAD51 protein-protein interaction
Duncan E Scott, May Marsh, Tom L Blundell, et al.
Nature Reviews. Drug Discovery
|
September 26, 2024
The benefits of translating biomedical research at drug discovery institutes
David J Huggins, Jonathan Baell, Paul E Brennan, et al.
Chemmedchem
|
December 4, 2014
Small-molecule inhibitors that target protein-protein interactions in the RAD51 family of recombinases
Duncan E Scott, Anthony G Coyne, Ashok Venkitaraman, et al.
FEBS Open Bio
|
July 16, 2016
ATP half-sites in RadA and RAD51 recombinases bind nucleotides
May E Marsh, Duncan E Scott, Matthias T Ehebauer, et al.
SLAS Discovery : Advancing Life Sciences R & D
|
July 20, 2025
Overcoming a false-positive mechanism in RapidFire MRM-based high throughput screening
De Lin, Lesley-Anne Pearson, Shamshad Ahmad, et al.
Page
of 2
Search research articles
Search
Showing results (1-10 of 20) with videos related to
Sort By:
Page
of 2
Natural Product Reports
|
September 28, 2007
Coenzyme biosynthesis: enzyme mechanism, structure and inhibition
Duncan E Scott, Alessio Ciulli, Chris Abell
Current Opinion in Chemical Biology
|
March 13, 2010
Drugging challenging targets using fragment-based approaches
Anthony G Coyne, Duncan E Scott, Chris Abell
Nature Reviews. Drug Discovery
|
April 7, 2016
Small molecules, big targets: drug discovery faces the protein-protein interaction challenge
Duncan E Scott, Andrew R Bayly, Chris Abell, et al.
Biochemistry
|
June 16, 2012
Fragment-based approaches in drug discovery and chemical biology
Duncan E Scott, Anthony G Coyne, Sean A Hudson, et al.
Chembiochem : a European Journal of Chemical Biology
|
October 15, 2009
A fragment-based approach to probing adenosine recognition sites by using dynamic combinatorial chemistry
Duncan E Scott, Gwen J Dawes, Michiyo Ando, et al.
FEBS Letters
|
March 20, 2016
Structure-activity relationship of the peptide binding-motif mediating the BRCA2:RAD51 protein-protein interaction
Duncan E Scott, May Marsh, Tom L Blundell, et al.
Nature Reviews. Drug Discovery
|
September 26, 2024
The benefits of translating biomedical research at drug discovery institutes
David J Huggins, Jonathan Baell, Paul E Brennan, et al.
Chemmedchem
|
December 4, 2014
Small-molecule inhibitors that target protein-protein interactions in the RAD51 family of recombinases
Duncan E Scott, Anthony G Coyne, Ashok Venkitaraman, et al.
FEBS Open Bio
|
July 16, 2016
ATP half-sites in RadA and RAD51 recombinases bind nucleotides
May E Marsh, Duncan E Scott, Matthias T Ehebauer, et al.
SLAS Discovery : Advancing Life Sciences R & D
|
July 20, 2025
Overcoming a false-positive mechanism in RapidFire MRM-based high throughput screening
De Lin, Lesley-Anne Pearson, Shamshad Ahmad, et al.
Page
of 2