Evidence map›Paper›PMID 23792349›Full record

ArticleEuropean journal of medicinal chemistry2013

Ligand/kappa-opioid receptor interactions: insights from the X-ray crystal structure.

Karina Martinez-Mayorga, Kendall G Byler, Austin B Yongye, Marc A Giulianotti, Colette T Dooley, Richard A Houghten

Open access · greenAbstract read
In one paragraph

Article in European journal of medicinal chemistry, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
1.0field-weighted citation impact, top 29% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors at 2 institutions in 2 countries.

Karina Martinez-MayorgaInstituto de Química, UNAM, Av. Universidad 3000, México DF, Mexico. sasu_mx@yahoo.com
Kendall G Byler
Austin B Yongye
Marc A Giulianotti
Colette T Dooley
Richard A Houghten
Torrey Pines Institute For Molecular Studies · USUniversidad Nacional Autónoma de México · MX

Funding

High throughput in vivo screening: translational generation of novel analgesicsR01DA031370 · NIDA · TORREY PINES INST FOR MOLECULAR STUDIES · PI HOUGHTEN, RICHARD ALLEN · 2011 to 2015
$2.2M
NIDA NIH HHS DA031370NIDA NIH HHS R01 DA031370
6 · The paper itself

Abstract

During the past five years, the three-dimensional structures of 14 different G-protein coupled receptors (GPCRs) have been resolved by X-ray crystallography. The most recently published structures, those of the opioid receptors (ORs), are remarkably important in pain modulation, drug addiction, and mood disorders. These structures, confirmed previously proposed key interactions conferring potency and antagonistic properties, including the well-known interaction with Asp138, conserved in all aminergic GPCRs. In addition, crystallization of the opioid receptors highlighted the potential function of the ECL2 and ICL2 loops. We have previously reported a set of potent and selective kappa opioid receptor peptide agonists, of which ff(D-nle)r-NH₂ is among the most potent and selective ones. These peptides were identified from the deconvolution of a 6,250,000 tetrapeptide combinatorial library. A derivative of this set is currently the subject of a phase 2 clinical trial in the United States. In this work, we describe comparative molecular modeling studies of kappa-OR peptide agonists with the co-crystallized antagonist, JDTic, and also report structure-activity relationships of 23 tetrapeptides. The overall binding and contact interactions are sound and interactions known to favor selectivity and potency were observed. Additional modeling studies will reveal conformational changes that the kappa-OR undergoes upon binding to these peptide agonists.

Indexed as

Binding SitesCrystallography, X-RayLigandsModels, MolecularPeptides, CyclicPiperidinesProtein BindingProtein ConformationReceptors, Opioid, kappaStructure-Activity RelationshipTetrahydroisoquinolines7-hydroxy-N-(1-((4-(3-hydroxyphenyl)-3,4-dimethyl-1-piperidinyl)methyl)-2-methylpropyl)-1,2,3,4-tetrahydro-3-isoquinolinecarboxamideLigandsPeptides, CyclicPiperidinesReceptors, Opioid, kappaTetrahydroisoquinolinesCombinatorial chemistryKappa-opioid receptorMolecular modelingTetrapeptide

Identifiers

PMID23792349
PMCPMC3775475
OpenAlexW1979182035

What OpenQuestion holds

Textmetadata
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Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.