Enhanced A<sub>3 </sub>adenosine receptor selectivity of multivalent nucleoside-dendrimer conjugates
<p>Abstract</p> <p>Background</p> <p>An approach to use multivalent dendrimer carriers for delivery of nucleoside signaling molecules to their cell surface G protein-coupled receptors (GPCRs) was recently introduced.</p> <p>Results</p> <p>A known...
Main Authors: | Shainberg Asher, Lloyd John, Gao Zhan-Guo, Klutz Athena M, Jacobson Kenneth A |
---|---|
Format: | Article |
Language: | English |
Published: |
BMC
2008-10-01
|
Series: | Journal of Nanobiotechnology |
Online Access: | http://www.jnanobiotechnology.com/content/6/1/12 |
Similar Items
-
Nucleoside conjugates of quantum dots for characterization of G protein-coupled receptors: strategies for immobilizing A<sub>2A </sub>adenosine receptor agonists
by: Gao Zhan-Guo, et al.
Published: (2010-05-01) -
A<sub>3</sub> Adenosine Receptor Antagonists with Nucleoside Structures and Their Anticancer Activity
by: Andrea Spinaci, et al.
Published: (2022-01-01) -
Physiology and effects of nucleosides in mice lacking all four adenosine receptors.
by: Cuiying Xiao, et al.
Published: (2019-03-01) -
Repurposing of a Nucleoside Scaffold from Adenosine Receptor Agonists to Opioid Receptor Antagonists
by: Dilip K. Tosh, et al.
Published: (2018-10-01) -
Allosteric Antagonism of the A<sub>2A</sub> Adenosine Receptor by a Series of Bitopic Ligands
by: Zhan-Guo Gao, et al.
Published: (2020-05-01)