13 articles for thisTarget
The following articles (labelled with PubMed ID or TBD) are for your review
PMID
Data
Article Title
Organization
Structure-Activity Relationships and Kinetic Studies of Peptidic Antagonists of CBX Chromodomains.

University of North Carolina at Chapel Hill
Structure-Guided Discovery of Selective Antagonists for the Chromodomain of Polycomb Repressive Protein CBX7.

Icahn School of Medicine At Mount Sinai
Selective Inhibition of CBX6: A Methyllysine Reader Protein in the Polycomb Family.

University of Victoria
Chromodomain antagonists that target the polycomb-group methyllysine reader protein chromobox homolog 7 (CBX7).

University of Victoria
Small-molecule ligands of methyl-lysine binding proteins: optimization of selectivity for L3MBTL3.

University of North Carolina at Chapel Hill
Discovery of a chemical probe for the L3MBTL3 methyllysine reader domain.

University of North Carolina Eshelman School of Pharmacy
Pan-specific and partially selective dye-labeled peptidic inhibitors of the polycomb paralog proteins.

University of Victoria
Discovery of a Potent and Selective Fragment-like Inhibitor of Methyllysine Reader Protein Spindlin 1 (SPIN1).

Icahn School of Medicine At Mount Sinai
Identification and characterization of benzo[d]oxazol-2(3H)-one derivatives as the first potent and selective small-molecule inhibitors of chromodomain protein CDYL.

Peking University
The structure-activity relationships of L3MBTL3 inhibitors: flexibility of the dimer interface.

University of North Carolina
Methyllysine binding domains: Structural insight and small molecule probe development.

University of Connecticut
AAK1 INHIBITOR AND USE THEREOF

Xizang Haisco Pharmaceutical
In vitro and in vivo pharmacological characterization of N6-cyclopentyl-9-methyladenine (N-0840): a selective, orally active A1 adenosine receptor antagonist.

Whitby Research