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Dafydd R Owen
Author PubWeight™ 9.43
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Top papers
Rank
Title
Journal
Year
PubWeight™
‹?›
1
Identification of a chemical probe for bromo and extra C-terminal bromodomain inhibition through optimization of a fragment-derived hit.
J Med Chem
2012
1.55
2
PFI-1, a highly selective protein interaction inhibitor, targeting BET Bromodomains.
Cancer Res
2013
1.53
3
TAFIa inhibitors in the treatment of thrombosis.
Curr Opin Drug Discov Devel
2008
1.14
4
Rapid assessment of a novel series of selective CB(2) agonists using parallel synthesis protocols: A Lipophilic Efficiency (LipE) analysis.
Bioorg Med Chem Lett
2009
1.04
5
Enantioselective catalytic intramolecular cyclopropanation using modified cinchona alkaloid organocatalysts.
Angew Chem Int Ed Engl
2006
1.04
6
Discovery of potent & selective inhibitors of activated thrombin-activatable fibrinolysis inhibitor for the treatment of thrombosis.
J Med Chem
2007
0.90
7
Synthesis and evaluation of heteroarylalanine diacids as potent and selective neutral endopeptidase inhibitors.
Bioorg Med Chem Lett
2011
0.81
8
Corrigendum: The promise and peril of chemical probes.
Nat Chem Biol
2015
0.79
9
Design, synthesis, and biological evaluation of 3-[4-(2-hydroxyethyl)piperazin-1-yl]-7-(6-methoxypyridin-3-yl)-1-(2-propoxyethyl)pyrido[3,4-b]pyrazin-2(1H)-one, a potent, orally active, brain penetrant inhibitor of phosphodiesterase 5 (PDE5).
J Med Chem
2010
0.76
10
Optimisation of a novel series of selective CNS penetrant CB(2) agonists.
Bioorg Med Chem Lett
2011
0.75
11
Investigation of aminopyridiopyrazinones as PDE5 inhibitors: Evaluation of modifications to the central ring system.
Bioorg Med Chem Lett
2009
0.75
12
Optimization of the aminopyridopyrazinones class of PDE5 inhibitors: discovery of 3-[(trans-4-hydroxycyclohexyl)amino]-7-(6-methoxypyridin-3-yl)-1-(2-propoxyethyl)pyrido[3,4-b]pyrazin-2(1H)-one.
Bioorg Med Chem Lett
2009
0.75