Evidence map›Paper›PMID 28653846›Full record

ArticleJournal of medicinal chemistry2017

In Vivo and Mechanistic Studies on Antitumor Lead 7-Methoxy-4-(2-methylquinazolin-4-yl)-3,4-dihydroquinoxalin-2(1H)-one and Its Modification as a Novel Class of Tubulin-Binding Tumor-Vascular Disrupting Agents.

Mu-Tian Cui, Li Jiang, Masuo Goto, Pei-Ling Hsu, Linna Li, Qi Zhang, Lei Wei, Shou-Jun Yuan, Ernest Hamel, Susan L Morris-Natschke and 2 more

Abstract read
In one paragraph

Article in Journal of medicinal chemistry, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
0.9field-weighted citation impact, top 30% 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

11 citing papers in PubMed, 33 citations in OpenAlex.

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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

12 authors at 3 institutions in 3 countries.

Mu-Tian CuiBeijing Institute of Pharmacology and Toxicology , 27 Tai-Ping Road, Beijing 100850, China.
Li JiangBeijing Institute of Pharmacology and Toxicology , 27 Tai-Ping Road, Beijing 100850, China.
Masuo GotoNatural Products Research Laboratories, UNC Eshelman School of Pharmacy, University of North Carolina , Chapel Hill, North Carolina 27599, United States.
Pei-Ling HsuNatural Products Research Laboratories, UNC Eshelman School of Pharmacy, University of North Carolina , Chapel Hill, North Carolina 27599, United States.
Linna LiBeijing Institute of Radiation Medicine , 27 Tai-Ping Road, Beijing 100850, China.
Qi ZhangBeijing Institute of Radiation Medicine , 27 Tai-Ping Road, Beijing 100850, China.
Lei WeiBeijing Institute of Pharmacology and Toxicology , 27 Tai-Ping Road, Beijing 100850, China.
Shou-Jun YuanBeijing Institute of Radiation Medicine , 27 Tai-Ping Road, Beijing 100850, China.
Ernest HamelScreening Technologies Branch, Developmental Therapeutics Program, Division of Cancer Treatment and Diagnosis, National Cancer Institute, Frederick National Laboratory for Cancer Research, National Institutes of Health , Frederick, Maryland 21702, United States.
Susan L Morris-NatschkeNatural Products Research Laboratories, UNC Eshelman School of Pharmacy, University of North Carolina , Chapel Hill, North Carolina 27599, United States.
Kuo-Hsiung LeeNatural Products Research Laboratories, UNC Eshelman School of Pharmacy, University of North Carolina , Chapel Hill, North Carolina 27599, United States.ORCID 0000-0002-6562-0070
Lan XieBeijing Institute of Pharmacology and Toxicology , 27 Tai-Ping Road, Beijing 100850, China.
University of North Carolina at Chapel Hill · USBeijing Radiation Center · CNNational Institutes of Health · US

Funding

Novel Antitumor AgentsR01CA177584 · NCI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI LEE, KUO-HSIUNG · 2013 to 2017
$1.9M
NCI NIH HHS R01 CA177584
6 · The paper itself

Abstract

7-Methoxy-4-(2-methylquinazolin-4-yl)-3,4-dihydroquinoxalin-2(1H)-one (2), a promising anticancer lead previously identified by us, inhibited tumor growth by 62% in mice at 1.0 mg/kg without obvious signs of toxicity. Moreover, compound 2 exhibited extremely high antiproliferative activity in the NIH-NCI 60 human tumor cell line panel, with low to sub-nanomolar GI

Indexed as

Angiogenesis InhibitorsAnimalsAntineoplastic AgentsApoptosisCell Line, TumorCell ProliferationHumansMice, NudeMolecular Docking SimulationNeoplasmsQuinazolinesTubulinTubulin ModulatorsAngiogenesis InhibitorsAntineoplastic AgentsQuinazolinesTubulinTubulin Modulators

Identifiers

PMID28653846
PMCPMC6432920
OpenAlexW2726402529

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.