Evidence map›Paper›PMID 25935643›Full record

ArticleBioorganic & medicinal chemistry letters2015

N-Oxide derivatives of 3-(3-pyridyl)-2-phosphonopropanoic acids as potential inhibitors of Rab geranylgeranylation.

Xiang Zhou, Ella J Born, Cheryl Allen, Sarah A Holstein, David F Wiemer

Open access · greenAbstract read
In one paragraph

Article in Bioorganic & medicinal chemistry letters, 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
0.5field-weighted citation impact, top 34% 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, 10 citations in OpenAlex.

  1. Targeting the Isoprenoid Biosynthetic Pathway in Multiple Myeloma.International journal of molecular sciences · 2022
    Review
  2. Review
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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

5 authors at 2 institutions in 1 country.

Xiang ZhouDepartment of Chemistry, University of Iowa, Iowa City, IA 52242-1294, USA.
Ella J BornDepartment of Internal Medicine, University of Iowa, Iowa City, IA 52242-1294, USA.
Cheryl AllenDepartment of Medicine, Roswell Park Cancer Institute, Buffalo, NY 14263, USA.
Sarah A HolsteinDepartment of Medicine, Roswell Park Cancer Institute, Buffalo, NY 14263, USA.
David F WiemerDepartment of Chemistry, University of Iowa, Iowa City, IA 52242-1294, USA. Electronic address: david-wiemer@uiowa.edu.
University of Iowa · USRoswell Park Comprehensive Cancer Center · US

Funding

Rab Geranylgeranylation: a Novel Therapeutic Target in Multiple MyelomaR01CA172070 · NCI · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI HOLSTEIN, SARAH A · 2013 to 2016
$1.3M
NCI NIH HHS R01 CA172070NCI NIH HHS R01CA-172070
6 · The paper itself

Abstract

The N-oxide derivatives of [2-(3-pyridinyl)-1-hydroxyethylidene-1,1-phosphonocarboxylic acid (or PEHPC) and [2-(3-pyridinyl)-1-ethylidene-1,1-phosphonocarboxylic acid (or PEPC) have been prepared and evaluated for their activity against several enzymes which utilize isoprenoids. The parent pyridines are known inhibitors of GGTase II, but the N-oxide derivatives show no improvement in biological activity in assays with the isolated enzyme. However, the PEHPC N-oxide did induce significant accumulation of intracellular light chain in myeloma cells, consistent with inhibition of Rab geranylgeranylation.

Indexed as

Alkyl and Aryl TransferasesCell Line, TumorDrug DiscoveryHumansMolecular StructureMultiple MyelomaPropionatesStructure-Activity RelationshipAlkyl and Aryl TransferasesPropionatesRab geranylgeranyltransferaseApoptosisBioassayGGTase IIMyelomaPyridyl N-oxidesRab GGTase

Identifiers

PMID25935643
PMCPMC4462192
OpenAlexW2001920292

What Socratic 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 Socratic graph.