about
Optimization of 3,5-Dimethylisoxazole Derivatives as Potent Bromodomain Ligands3,5-dimethylisoxazoles act as acetyl-lysine-mimetic bromodomain ligands.Small molecule inhibitors of bromodomain-acetyl-lysine interactions.Organocatalytic removal of formaldehyde adducts from RNA and DNA basesProgress in the development and application of small molecule inhibitors of bromodomain-acetyl-lysine interactions.The design and synthesis of 5- and 6-isoxazolylbenzimidazoles as selective inhibitors of the BET bromodomains.Isoxazole-Derived Amino Acids are Bromodomain-Binding Acetyl-Lysine Mimics: Incorporation into Histone H4 Peptides and Histone H3.Reactive-site-centric chemoproteomics identifies a distinct class of deubiquitinase enzymes.Ammonium-directed olefinic epoxidation: kinetic and mechanistic insights
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description
researcher, ORCID id # 0000-0001-9451-8959
@en
wetenschapper
@nl
name
David S Hewings
@ast
David S Hewings
@en
David S Hewings
@es
David S Hewings
@nl
type
label
David S Hewings
@ast
David S Hewings
@en
David S Hewings
@es
David S Hewings
@nl
prefLabel
David S Hewings
@ast
David S Hewings
@en
David S Hewings
@es
David S Hewings
@nl
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53979932100
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0000-0001-9451-8959