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ACS Comb Sci ; 19(10): 657-669, 2017 10 09.
Article in English | MEDLINE | ID: mdl-28746804

ABSTRACT

We herein present broadly useful, readily available and nonintegral hydroxylamine linkers for the routine solid-phase synthesis of hydroxamic acids. The developed protocols enable the efficient synthesis and release of a wide range of hydroxamic acids from various resins, relying on high control and flexibility with respect to reagents and synthetic processes. A trityl-based hydroxylamine linker was used to synthesize a library of peptide hydroxamic acids. The inhibitory effects of the compounds were examined for seven HDAC enzyme subtypes using a chemiluminescence-based assay.


Subject(s)
Histone Deacetylase Inhibitors/chemical synthesis , Histone Deacetylases/chemistry , Hydroxamic Acids/chemical synthesis , Peptides/chemical synthesis , Humans , Peptide Library , Solid-Phase Synthesis Techniques , Structure-Activity Relationship
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