Evidence map›Paper›PMID 28029775›Full record

ArticleACS combinatorial science2017

Combining a Ru(II) "Building Block" and Rapid Screening Approach to Identify DNA Structure-Selective "Light Switch" Compounds.

Erin Wachter, Diego Moyá, Edith C Glazer

Abstract read
In one paragraph

Article in ACS combinatorial science, 2017. 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
–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

3 citing papers in PubMed.

  1. Article
  2. Review
  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

3 authors.

Erin WachterDepartment of Chemistry, University of Kentucky , 505 Rose Street, Lexingon, Kentucky 40506, United States.
Diego MoyáDepartment of Chemistry, University of Kentucky , 505 Rose Street, Lexingon, Kentucky 40506, United States.
Edith C GlazerDepartment of Chemistry, University of Kentucky , 505 Rose Street, Lexingon, Kentucky 40506, United States.ORCID 0000-0002-0190-7742

Funding

Protein CoreP30GM110787 · NIGMS · UNIVERSITY OF KENTUCKY · PI MENDENHALL, MICHAEL D. · 2014 to 2018
$5.7M
Light-responsive ruthenium compounds for applications in diseaseR01GM107586 · NIGMS · UNIVERSITY OF KENTUCKY · PI GLAZER, EDITH C · 2014 to 2019
$1.7M
NIGMS NIH HHS P30 GM110787NIGMS NIH HHS R01 GM107586
6 · The paper itself

Abstract

A chemically reactive Ru(II) "building block", able to undergo condensation reactions with substituted diamines, was utilized to create a small library of luminescent "light switch" dipyrido-[3,2-a:2',3'-c] phenazine (dppz) complexes. The impact of substituent identity, position, and the number of substituents on the light switch effect was investigated. An unbiased, parallel screening approach was used to evaluate the selectivity of the compounds for a variety of different biomolecules, including protein, nucleosides, single stranded DNA, duplex DNA, triplex DNA, and G-quadruplex DNA. Combining these two approaches allowed for the identification of hit molecules that showed different selectivities for biologically relevant DNA structures, particularly triplex and quadruplex DNA.

Indexed as

Coordination ComplexesDNADNA, Single-StrandedG-QuadruplexesLuminescenceLuminescent AgentsLuminescent MeasurementsNucleic Acid ConformationPhenazinesRutheniumCoordination ComplexesDNADNA, Single-StrandedLuminescent AgentsPhenazinesRutheniumtriplex DNAbiologically relevantDNA structure-selectivelibrary“light switch” compoundsparallel screeningRu(II)

Identifiers

PMID28029775
PMCPMC5549666

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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.