(Q33754704)

English

Polyamidoamine (PAMAM) dendrimer conjugates of "clickable" agonists of the A3 adenosine receptor and coactivation of the P2Y14 receptor by a tethered nucleotide

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scholarly article

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Europe PubMed Central

PubMed publication ID

29 July 2017

Polyamidoamine (PAMAM) dendrimer conjugates of "clickable" agonists of the A3 adenosine receptor and coactivation of the P2Y14 receptor by a tethered nucleotide (English)

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

1

object named as

Dilip K Tosh

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Europe PubMed Central

PubMed publication ID

29 July 2017

author name string

Lena S Yoo

2

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Europe PubMed Central

PubMed publication ID

29 July 2017

Moshe Chinn

3

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29 July 2017

Kunlun Hong

4

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29 July 2017

S Michael Kilbey

5

1 reference

Europe PubMed Central

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29 July 2017

Matthew O Barrett

6

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Europe PubMed Central

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29 July 2017

Ingrid P Fricks

7

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Europe PubMed Central

PubMed publication ID

29 July 2017

T Kendall Harden

8

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

Zhan-Guo Gao

9

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29 July 2017

Kenneth A Jacobson

10

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29 July 2017

publication date

1 February 2010

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29 July 2017

Bioconjugate Chemistry

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29 July 2017

21

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Europe PubMed Central

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29 July 2017

2

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Europe PubMed Central

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29 July 2017

372-384

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Europe PubMed Central

PubMed publication ID

29 July 2017

2-Dialkynyl derivatives of (N)-methanocarba nucleosides: 'Clickable' A(3) adenosine receptor-selective agonists

1 reference

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21 June 2018

UDP-glucose acting at P2Y14 receptors is a mediator of mast cell degranulation

1 reference

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The A3 adenosine receptor attenuates the calcium rise triggered by NMDA receptors in retinal ganglion cells

1 reference

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Adenosine A2A receptor-antagonist/dopamine D2 receptor-agonist bivalent ligands as pharmacological tools to detect A2A-D2 receptor heteromers

1 reference

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Allosteric communication between protomers of dopamine class A GPCR dimers modulates activation.

1 reference

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Synthesis and applications of biomedical and pharmaceutical polymers via click chemistry methodologies.

1 reference

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21 June 2018

Enhanced potency of nucleotide-dendrimer conjugates as agonists of the P2Y14 receptor: multivalent effect in G protein-coupled receptor recognition

1 reference

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21 June 2018

Growing applications of "click chemistry" for bioconjugation in contemporary biomedical research

1 reference

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21 June 2018

Molecular recognition in the P2Y(14) receptor: Probing the structurally permissive terminal sugar moiety of uridine-5'-diphosphoglucose

1 reference

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Functionalized congeners of A3 adenosine receptor-selective nucleosides containing a bicyclo[3.1.0]hexane ring system.

1 reference

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21 June 2018

Functionalized congener approach to the design of ligands for G protein-coupled receptors (GPCRs).

1 reference

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21 June 2018

Enhanced A3 adenosine receptor selectivity of multivalent nucleoside-dendrimer conjugates.

1 reference

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21 June 2018

Molecular modeling of a PAMAM-CGS21680 dendrimer bound to an A2A adenosine receptor homodimer.

1 reference

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21 June 2018

Adenosine induces airway hyperresponsiveness through activation of A3 receptors on mast cells

1 reference

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21 June 2018

Design of (N)-methanocarba adenosine 5'-uronamides as species-independent A3 receptor-selective agonists.

1 reference

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21 June 2018

UDP is a competitive antagonist at the human P2Y14 receptor

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2845915

21 June 2018

Clinical evidence for utilization of the A3 adenosine receptor as a target to treat rheumatoid arthritis: data from a phase II clinical trial

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An efficient, inexpensive, and shelf-stable diazotransfer reagent: imidazole-1-sulfonyl azide hydrochloride

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Dendrimers as multi-purpose nanodevices for oncology drug delivery and diagnostic imaging

1 reference

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21 June 2018

International Union of Pharmacology LVIII: update on the P2Y G protein-coupled nucleotide receptors: from molecular mechanisms and pathophysiology to therapy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2845915

21 June 2018

Adenosine receptors as therapeutic targets

1 reference

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21 June 2018

Designed multiple ligands. An emerging drug discovery paradigm

1 reference

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21 June 2018

The cross-species A3 adenosine-receptor antagonist MRS 1292 inhibits adenosine-triggered human nonpigmented ciliary epithelial cell fluid release and reduces mouse intraocular pressure

1 reference

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21 June 2018

Pharmacological characterization of novel A3 adenosine receptor-selective antagonists

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2845915

21 June 2018

125I-4-aminobenzyl-5'-N-methylcarboxamidoadenosine, a high affinity radioligand for the rat A3 adenosine receptor

1 reference

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21 June 2018

Opioid agonist and antagonist bivalent ligands as receptor probes

1 reference

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21 June 2018

2-Chloro-N6-[3H]cyclopentyladenosine ([3H]CCPA)--a high affinity agonist radioligand for A1 adenosine receptors

1 reference

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21 June 2018

[3H]CGS 21680, a selective A2 adenosine receptor agonist directly labels A2 receptors in rat brain

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A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding

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Versatile conjugation of octreotide to dendrimers by cycloaddition ("click") chemistry to yield high-affinity multivalent cyclic Peptide dendrimers.

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"Click" glycodendrimers containing 27, 81, and 243 modified xylopyranoside termini.

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Protective roles of adenosine A1, A2A, and A3 receptors in skeletal muscle ischemia and reperfusion injury

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Identifiers

10.1021/BC900473V

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

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