Unique residues in the ATP gated human P2X7 receptor define a novel allosteric binding pocket for the selective antagonist AZ10606120.
about
Probenecid directly impairs activation of the canine P2X7 receptor.The potential of P2X7 receptors as a therapeutic target, including inflammation and tumour progression.The Molecular Determinants of Small-Molecule Ligand Binding at P2X Receptors.Purinergic drug targets for gastrointestinal disorders.The P2X7 Receptor.Mapping the Allosteric Action of Antagonists A740003 and A438079 Reveals a Role for the Left Flipper in Ligand Sensitivity at P2X7 Receptors.
P2860
Unique residues in the ATP gated human P2X7 receptor define a novel allosteric binding pocket for the selective antagonist AZ10606120.
description
2017 nî lūn-bûn
@nan
2017 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
2017 թվականի ապրիլին հրատարակված գիտական հոդված
@hy
2017年の論文
@ja
2017年論文
@yue
2017年論文
@zh-hant
2017年論文
@zh-hk
2017年論文
@zh-mo
2017年論文
@zh-tw
2017年论文
@wuu
name
Unique residues in the ATP gat ...... lective antagonist AZ10606120.
@ast
Unique residues in the ATP gat ...... lective antagonist AZ10606120.
@en
type
label
Unique residues in the ATP gat ...... lective antagonist AZ10606120.
@ast
Unique residues in the ATP gat ...... lective antagonist AZ10606120.
@en
prefLabel
Unique residues in the ATP gat ...... lective antagonist AZ10606120.
@ast
Unique residues in the ATP gat ...... lective antagonist AZ10606120.
@en
P2860
P1433
P1476
Unique residues in the ATP gat ...... lective antagonist AZ10606120.
@en
P2093
Rebecca C Allsopp
Richard J Evans
P2860
P2888
P356
10.1038/S41598-017-00732-5
P407
P577
2017-04-07T00:00:00Z
P6179
1084537856