The following articles (labelled with PubMed ID or TBD) are for your review
PMID | Data | Article Title | Organization |
27598236 |
59 |
High-affinity small molecular blockers of mixed lineage leukemia 1 (MLL1)-WDR5 interaction inhibit MLL1 complex H3K4 methyltransferase activity. |
China Pharmaceutical University |
27720555 |
29 |
Structure-based design of ester compounds to inhibit MLL complex catalytic activity by targeting mixed lineage leukemia 1 (MLL1)-WDR5 interaction. |
China Pharmaceutical University |
27116709 |
28 |
Structure-based design and synthesis of small molecular inhibitors disturbing the interaction of MLL1-WDR5. |
China Pharmaceutical University |
26958703 |
19 |
Structure-Based Optimization of a Small Molecule Antagonist of the Interaction Between WD Repeat-Containing Protein 5 (WDR5) and Mixed-Lineage Leukemia 1 (MLL1). |
Ontario Institute For Cancer Research |
24900672 |
41 |
Synthesis, Optimization, and Evaluation of Novel Small Molecules as Antagonists of WDR5-MLL Interaction. |
Entremed |
20575550 |
54 |
Analysis of the binding of mixed lineage leukemia 1 (MLL1) and histone 3 peptides to WD repeat domain 5 (WDR5) for the design of inhibitors of the MLL1-WDR5 interaction. |
University of Michigan |
32223236 |
31 |
Discovery of WD Repeat-Containing Protein 5 (WDR5)-MYC Inhibitors Using Fragment-Based Methods and Structure-Based Design. |
Vanderbilt University |
31724864 |
148 |
Discovery and Optimization of Salicylic Acid-Derived Sulfonamide Inhibitors of the WD Repeat-Containing Protein 5-MYC Protein-Protein Interaction. |
Vanderbilt University |
31858797 |
22 |
Discovery and Structure-Based Optimization of Potent and Selective WD Repeat Domain 5 (WDR5) Inhibitors Containing a Dihydroisoquinolinone Bicyclic Core. |
Frederick National Laboratory For Cancer Research |
30626558 |
28 |
The identification of novel small-molecule inhibitors targeting WDR5-MLL1 interaction through fluorescence polarization based high-throughput screening. |
Zhejiang Sci-Tech University |
29889518 |
68 |
Discovery of Potent 2-Aryl-6,7-dihydro-5 H-pyrrolo[1,2- a]imidazoles as WDR5-WIN-Site Inhibitors Using Fragment-Based Methods and Structure-Based Design. |
TBA |
29254892 |
18 |
Targeting protein-protein interaction between MLL1 and reciprocal proteins for leukemia therapy. |
China Pharmaceutical University |