Evidence map›Paper›PMID 29273415›Full record

ArticleBioorganic & medicinal chemistry2018

Design, synthesis, and opioid activity of arodyn analogs cyclized by ring-closing metathesis involving Tyr(allyl).

Wei-Jie Fang, Thomas F Murray, Jane V Aldrich

Abstract read
In one paragraph

Article in Bioorganic & medicinal chemistry, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
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

4 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
  4. Article
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

3 authors.

Wei-Jie FangDepartment of Medicinal Chemistry, University of Kansas, Lawrence, KS 66045, USA.
Thomas F MurrayDepartment of Pharmacology, Creighton University, Omaha, NE 68178, USA.
Jane V AldrichDepartment of Medicinal Chemistry, University of Kansas, Lawrence, KS 66045, USA; Department of Medicinal Chemistry, University of Florida, Gainesville, FL 32610, USA. Electronic address: janealdrich@ufl.edu.

Funding

Peptidic Ligands for Kappa Opioid ReceptorsR01DA018832 · NIDA · UNIVERSITY OF KANSAS LAWRENCE · PI ALDRICH, JANE V · 2005 to 2016
$3.1M
NIDA NIH HHS R01 DA018832
6 · The paper itself

Abstract

Kappa (κ) opioid receptor selective antagonists are useful pharmacological tools in studying κ opioid receptors and have potential to be used as therapeutic agents for the treatment of a variety of diseases including mood disorders and drug addiction. Arodyn (Ac[Phe

Indexed as

Drug DesignAmino Acid SequenceAnalgesics, OpioidAnimalsCHO CellsCricetinaeCricetulusCyclizationDynorphinsProtein BindingReceptors, Opioid, kappaStructure-Activity RelationshipTyrosineAnalgesics, OpioidarodynDynorphinsReceptors, Opioid, kappaTyrosineArodynDynorphin A analogsKappa opioid receptor antagonistsPeptide cyclizationRing-closing metathesisTyrosine(allyl)

Identifiers

PMID29273415
PMCPMC6005658

What OpenQuestion holds

Textmetadata
LicenceTDM
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.