Title : Macrocyclic derivatives of 6-methyluracil: New ligands of the peripheral anionic site of acetylcholinesterase.

Pub. Date : 2015

PMID : 26639720






6 Functional Relationships(s)
Download
Sentence
Compound Name
Protein Name
Organism
1 In the present study, taking acyclic derivatives of 6-methyluracil as a model AChE inhibitor, we attempted to develop AChE inhibitors that specifically bind to the PAS with weak binding to the active site of AChE. Aminosalicylic Acid acetylcholinesterase (Cartwright blood group) Homo sapiens
2 In the present study, taking acyclic derivatives of 6-methyluracil as a model AChE inhibitor, we attempted to develop AChE inhibitors that specifically bind to the PAS with weak binding to the active site of AChE. Aminosalicylic Acid acetylcholinesterase (Cartwright blood group) Homo sapiens
3 In the present study, taking acyclic derivatives of 6-methyluracil as a model AChE inhibitor, we attempted to develop AChE inhibitors that specifically bind to the PAS with weak binding to the active site of AChE. Aminosalicylic Acid acetylcholinesterase (Cartwright blood group) Homo sapiens
4 We attempted to increase the size of AChE ligands to restrict specific binding to the PAS of AChE. Aminosalicylic Acid acetylcholinesterase (Cartwright blood group) Homo sapiens
5 We attempted to increase the size of AChE ligands to restrict specific binding to the PAS of AChE. Aminosalicylic Acid acetylcholinesterase (Cartwright blood group) Homo sapiens
6 Based on molecular docking simulations, it was suggested that compounds bind AChE to the active center as well as to the PAS or only to the PAS. Aminosalicylic Acid acetylcholinesterase (Cartwright blood group) Homo sapiens