Evidence map›Paper›PMID 23518276›Full record

ArticleBioorganic & medicinal chemistry letters2013

Tricyclic thiazoles are a new class of angiogenesis inhibitors.

Shridhar Bhat, Joong Sup Shim, Jun O Liu

Abstract read
In one paragraph

Article in Bioorganic & medicinal chemistry letters, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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.

Shridhar BhatDepartment of Pharmacology & Molecular Sciences, 725 North Wolfe Street, Baltimore, MD 21205, USA.
Joong Sup Shim
Jun O Liu

Funding

Structure, Function and Inhibition of Human Methionine AminopeptidasesR01CA078743 · NCI · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI LIU, JUN O. · 1998 to 2012
$4.7M
NCI NIH HHS R01 CA078743
6 · The paper itself

Abstract

Tricyclic thiazoleamine derivatives that were identified as hits in a screen against human umbilical vein endothelial cell proliferation were subjected to a structure-activity relationship study. Two structurally superimposable scaffolds-4H-thiochromeno[4,3-d]thiazol-2-amine and 5,6-dihydro-4H-benzo[6,7]cyclohepta[1,2-d]thiazol-2-amine derivatives-yielded low-micromolar inhibitors, and two among them 37 and 43 also exhibited antiangiogenic activity in an endothelial tube formation assay. Thus, 37 and 43 can serve as leads to develop a novel class of antiangiogenic agents.

Indexed as

Angiogenesis InhibitorsCell ProliferationCyclizationHeLa CellsHumansHuman Umbilical Vein Endothelial CellsJurkat CellsStructure-Activity RelationshipThiazolesAngiogenesis InhibitorsThiazoles

Identifiers

PMID23518276
PMCPMC3670749

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.