about
Electrophilic derivatives of purines as irreversible inhibitors of A1 adenosine receptorsHigh affinity acylating antagonists for the A1 adenosine receptor: identification of binding subunitAdenosine and the auditory system.Trifunctional agents as a design strategy for tailoring ligand properties: irreversible inhibitors of A1 adenosine receptors.Adenosine and ischemic preconditioning.Functionalized congener approach to the design of ligands for G protein-coupled receptors (GPCRs).Xanthines as adenosine receptor antagonists.Functionalized congeners of A3 adenosine receptor-selective nucleosides containing a bicyclo[3.1.0]hexane ring system.Agonist derived molecular probes for A2 adenosine receptorsLighting up G protein-coupled purinergic receptors with engineered fluorescent ligands.Probing adenosine receptors using biotinylated purine derivatives.Molecular probes for muscarinic receptors: derivatives of the M1-antagonist telenzepine.8-Substituted xanthines as antagonists at A1- and A2-adenosine receptors.A new high affinity, iodinated adenosine receptor antagonist as a radioligand/photoaffinity crosslinking probe.Fluorescent ligands for adenosine receptors.RADIOLABELING AND EFFICIENT SYNTHESIS OF TRITIATED 2-CHLORO-N(6)-(3-IODOBENZYL)ADENOSINE-5'-N-METHYLURON-AMIDE, A POTENT, SELECTIVE A3 ADENOSINE RECEPTOR AGONIST.[(3)H]XAC (xanthine amine congener) is a radioligand for A(2)-adenosine receptors in rabbit striatum.2-[2-[4-[2-[2-[ 1,3-Dihydro- 1,1-bis (4-hydroxyphenyl)-3-oxo-5-isobenzofuranthioureidyl]ethylaminocarbonyl]ethyl]phenyl] ethylamino]-5'-N-ethylcarboxamidoadenosine (FITC-APEC): A Fluorescent Ligand For A2a-Adenosine Receptors.Quantitative analysis of the formation and diffusion of A1-adenosine receptor-antagonist complexes in single living cells.Functionalized congeners of tyrosine-based P2X(7) receptor antagonists: probing multiple sites for linking and dimerization.Molecular modeling of adenosine receptors. I. The ligand binding site on the A1 receptor.Sole activation of three luminal adenosine receptor subtypes in different parts of coronary vasculature.Synthesis of BODIPY derivatives substituted with various bioconjugatable linker groups: a construction kit for fluorescent labeling of receptor ligands.An Affinity-Based Probe for the Human Adenosine A Receptor
P2860
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P2860
description
1987 nî lūn-bûn
@nan
1987年の論文
@ja
1987年論文
@yue
1987年論文
@zh-hant
1987年論文
@zh-hk
1987年論文
@zh-mo
1987年論文
@zh-tw
1987年论文
@wuu
1987年论文
@zh
1987年论文
@zh-cn
name
Molecular probes for extracellular adenosine receptors.
@ast
Molecular probes for extracellular adenosine receptors.
@en
type
label
Molecular probes for extracellular adenosine receptors.
@ast
Molecular probes for extracellular adenosine receptors.
@en
prefLabel
Molecular probes for extracellular adenosine receptors.
@ast
Molecular probes for extracellular adenosine receptors.
@en
P2093
P2860
P1476
Molecular probes for extracellular adenosine receptors.
@en
P2093
P2860
P304
P356
10.1016/0006-2952(87)90056-6
P407
P577
1987-05-01T00:00:00Z