Evidence map›Paper›PMID 26568642›Full record

ArticleSynthesis2015

Synthesis of a Series of Novel 3,9-Disubstituted Phenanthrenes as Analogues of Known NMDA Receptor Allosteric Modulators.

Mark W Irvine, Guangyu Fang, Richard Eaves, Maria B Mayo-Martin, Erica S Burnell, Blaise M Costa, Georgia R Culley, Arturas Volianskis, Graham L Collingridge, Daniel T Monaghan and 1 more

Open access · hybridAbstract read
In one paragraph

Article in Synthesis, 2015. 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
1.1field-weighted citation impact, top 19% 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

4 citing papers in PubMed, 13 citations in OpenAlex.

  1. Review
  2. Article
  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

11 authors at 2 institutions in 2 countries.

Mark W Irvine *School of Physiology & Pharmacology, Medical Sciences Building, University Walk, University of Bristol, Bristol, BS8 1TD, UK.
Guangyu Fang *School of Physiology & Pharmacology, Medical Sciences Building, University Walk, University of Bristol, Bristol, BS8 1TD, UK.
Richard EavesSchool of Physiology & Pharmacology, Medical Sciences Building, University Walk, University of Bristol, Bristol, BS8 1TD, UK.
Maria B Mayo-MartinSchool of Physiology & Pharmacology, Medical Sciences Building, University Walk, University of Bristol, Bristol, BS8 1TD, UK.
Erica S BurnellSchool of Physiology & Pharmacology, Medical Sciences Building, University Walk, University of Bristol, Bristol, BS8 1TD, UK.
Blaise M CostaDepartment of Pharmacology and Experimental Neuroscience, University of Nebraska Medical Center, Omaha, Nebraska 68198-6260 U.S.A.
Georgia R CulleySchool of Physiology & Pharmacology, Medical Sciences Building, University Walk, University of Bristol, Bristol, BS8 1TD, UK.
Arturas VolianskisSchool of Physiology & Pharmacology, Medical Sciences Building, University Walk, University of Bristol, Bristol, BS8 1TD, UK.
Graham L CollingridgeSchool of Physiology & Pharmacology, Medical Sciences Building, University Walk, University of Bristol, Bristol, BS8 1TD, UK.
Daniel T Monaghan *Department of Pharmacology and Experimental Neuroscience, University of Nebraska Medical Center, Omaha, Nebraska 68198-6260 U.S.A.
David E Jane *School of Physiology & Pharmacology, Medical Sciences Building, University Walk, University of Bristol, Bristol, BS8 1TD, UK.
University of Bristol · GBUniversity of Nebraska Medical Center · US

Funding

Development and Pharmacology of Positive Allosteric Modulators of NMDA ReceptorsR01MH060252 · NIMH · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI JANE, DAVID EDWARD, MONAGHAN, DANIEL T · 2001 to 2017
$4.0M
Biotechnology and Biological Sciences Research Council BB/L001977/1Medical Research Council G0601812Medical Research Council MR/K023098/1NIMH NIH HHS R01 MH060252
6 · The paper itself

Abstract

9-Substituted phenanthrene-3-carboxylic acids have been reported to have allosteric modulatory activity at the NMDA receptor. This receptor is activated by the excitatory neurotransmitter L-glutamate and has been implicated in a range of neurological disorders such as schizophrenia, epilepsy and chronic pain and neurodegenerative disorders such as Alzheimer's disease. Herein, the convenient synthesis of a wide range of novel 3,9-disubstituted phenanthrene derivatives starting from a few common intermediates is described. These new phenanthrene derivatives will help to clarify the structural requirements for allosteric modulation of the NMDA receptor.

Indexed as

allosteric modulatorsNMDA receptorpalladium couplingPhenanthrenesWittig reaction

Identifiers

PMID26568642
PMCPMC4641328
OpenAlexW2410499412

What OpenQuestion holds

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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.