Evidence map›Paper›PMID 24656801›Full record

ArticleBioorganic & medicinal chemistry2014

Synthesis and structure activity relationships of schweinfurthin indoles.

John G Kodet, John A Beutler, David F Wiemer

Abstract read
In one paragraph

Article in Bioorganic & medicinal chemistry, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.6field-weighted citation impact, top 33% 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

7 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. The Search for Anticancer Agents from Tropical Plants.Progress in the chemistry of organic natural products
    Review
  7. 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 at 2 institutions in 1 country.

John G KodetDepartment of Chemistry, University of Iowa, Iowa City, IA 52242-1294, United States.
John A BeutlerMolecular Targets Laboratory, Center for Cancer Research, NCI-Frederick, Frederick, MD 21702, United States.
David F WiemerDepartment of Chemistry, University of Iowa, Iowa City, IA 52242-1294, United States. Electronic address: david-wiemer@uiowa.edu.
University of Iowa · USTarget (United States) · US

Funding

Development of Natural Product Leads as Anticancer TherapeuticsZIABC011470 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI BEUTLER, JOHN · 2012 to 2025
$7.8M
Intramural NIH HHS ZIA BC011470
6 · The paper itself

Abstract

As part of a program to explore the biological activity of analogues of the natural schweinfurthins, a set of compounds has been prepared where an indole system can be viewed as a substitution for the resorcinol substructure of the schweinfurthin's D-ring. Twelve of these schweinfurthin indoles have been prepared and evaluated in the 60 cell line screen of the National Cancer Institute. While a range of activity has been observed, it is now clear that schweinfurthin indoles can demonstrate the intriguing pattern of activity associated with the natural stilbenes. In the best cases, these indole analogues display both potency and differential activity across the various cell lines comparable to the best resorcinol analogues.

Indexed as

Antineoplastic AgentsCell Line, TumorCell SurvivalDrug Screening Assays, AntitumorHumansIndolesStilbenesStructure-Activity RelationshipAntineoplastic AgentsindoleIndolesStilbenesIndoleSARSchweinfurthinStilbene analogues

Identifiers

PMID24656801
PMCPMC4030441
OpenAlexW2080626073

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.