Evidence map›Paper›PMID 30429096›Full record

ArticleBioorganic & medicinal chemistry2018

Modifying aroylhydrazone prochelators for hydrolytic stability and improved cytoprotection against oxidative stress.

Qin Wang, Katherine J Franz

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 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.6field-weighted citation impact, top 32% 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, 6 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

2 authors at 1 institution in 1 country.

Qin WangDuke University, Department of Chemistry, 124 Science Dr., Durham, NC 27708, USA.
Katherine J FranzDuke University, Department of Chemistry, 124 Science Dr., Durham, NC 27708, USA. Electronic address: katherine.franz@duke.edu.
Duke University · US

Funding

Metals, Drugs and Fungal PathogensR01GM084176 · NIGMS · DUKE UNIVERSITY · PI FRANZ, KATHERINE J. · 2008 to 2021
$4.3M
NIGMS NIH HHS R01 GM084176
6 · The paper itself

Abstract

BSIH ((E)-N'-(2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzylidene)isonicotinohydrazide) is a prodrug version of the metal chelator SIH ((E)-N'-(2-hydroxybenzylidene)isonicotinohydrazide) in which a boronate group prevents metal chelation until reaction with hydrogen peroxide releases SIH, which is then available for sequestering iron(III) and inhibiting iron-catalyzed oxidative damage. While BSIH has shown promise for conditionally targeting iron sequestration in cells under oxidative stress, the yield of SIH is limited by the fact that BSIH exists in cell culture media as an equilibrium mixture with its hydrolysis products isoniazid and 2-formylphenyl boronic acid. In the current study, several BSIH analogs were evaluated for their hydrolytic stability, reaction outcomes with H

Indexed as

Cells, CulturedCell SurvivalChelating AgentsCytoprotectionDose-Response Relationship, DrugHumansHydrazonesHydrolysisMolecular StructureOxidative StressStructure-Activity RelationshipChelating AgentsHydrazonesChelating agentCytoprotectionFenton chemistryIronOxidative stress

Identifiers

PMID30429096
PMCPMC6314015
OpenAlexW2900290675

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.