11 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.![EBI](/images/logo_chembl.png)
![EBI](/images/logo_chembl.png)
University of North Carolina At Chapel Hill
Structure-Guided Discovery of Selective Antagonists for the Chromodomain of Polycomb Repressive Protein CBX7.![EBI](/images/logo_chembl.png)
![EBI](/images/logo_chembl.png)
Icahn School of Medicine At Mount Sinai
Selective Inhibition of CBX6: A Methyllysine Reader Protein in the Polycomb Family.![EBI](/images/logo_chembl.png)
![EBI](/images/logo_chembl.png)
University of Victoria
Chromodomain antagonists that target the polycomb-group methyllysine reader protein chromobox homolog 7 (CBX7).![EBI](/images/logo_chembl.png)
![EBI](/images/logo_chembl.png)
University of Victoria
Small-molecule ligands of methyl-lysine binding proteins: optimization of selectivity for L3MBTL3.![EBI](/images/logo_chembl.png)
![EBI](/images/logo_chembl.png)
University of North Carolina At Chapel Hill
Pan-specific and partially selective dye-labeled peptidic inhibitors of the polycomb paralog proteins.![EBI](/images/logo_chembl.png)
![EBI](/images/logo_chembl.png)
University of Victoria
Discovery of a Potent and Selective Fragment-like Inhibitor of Methyllysine Reader Protein Spindlin 1 (SPIN1).![EBI](/images/logo_chembl.png)
![EBI](/images/logo_chembl.png)
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.![EBI](/images/logo_chembl.png)
![EBI](/images/logo_chembl.png)
Peking University
The structure-activity relationships of L3MBTL3 inhibitors: flexibility of the dimer interface.![EBI](/images/logo_chembl.png)
![EBI](/images/logo_chembl.png)
University of North Carolina