Evidence map›Paper›PMID 30015487›Full record

ArticleJournal of medicinal chemistry2018

Structure-Based Discovery of CF53 as a Potent and Orally Bioavailable Bromodomain and Extra-Terminal (BET) Bromodomain Inhibitor.

Yujun Zhao, Bing Zhou, Longchuan Bai, Liu Liu, Chao-Yie Yang, Jennifer L Meagher, Jeanne A Stuckey, Donna McEachern, Sally Przybranowski, Mi Wang and 10 more

Open access · greenAbstract read
In one paragraph

Article in Journal of medicinal chemistry, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.6field-weighted citation impact, top 16% 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

13 citing papers in PubMed, 37 citations in OpenAlex.

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  10. Discovery of a Potent Degrader for Fibroblast Growth Factor Receptor 1/2.Angewandte Chemie (International ed. in English) · 2021
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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

20 authors at 1 institution in 1 country.

Yujun Zhao
Longchuan Bai
Liu Liu
Chao-Yie Yang
Jennifer L Meagher
Jeanne A Stuckey
Donna McEachern
Sally Przybranowski
Mi Wang
Xu Ran
Angelo Aguilar
Yang Hu
Jeff W Kampf
Xiaoqin Li
Ting Zhao
Siwei Li
Bo Wen
Duxin Sun
University of Michigan · US

Funding

XenograftP30CA046592 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI THEODORE S LAWRENCE · 1988 to 2026
$178.2M
Tissue/InformaticsP50CA186786 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Robert Timothy Dess · 2014 to 2026
$27.6M
NCI NIH HHS P30 CA046592NCI NIH HHS P50 CA186786
6 · The paper itself

Abstract

We report the structure-based discovery of CF53 (28) as a highly potent and orally active inhibitor of bromodomain and extra-terminal (BET) proteins. By the incorporation of a NH-pyrazole group into the 9H-pyrimido[4,5- b]indole core, we identified a series of compounds that bind to BRD4 BD1 protein with K

Indexed as

Drug DiscoveryAdministration, OralBiological AvailabilityBromodomain Containing ProteinsCell Cycle ProteinsHumansModels, MolecularMolecular StructureNuclear ProteinsProteinsTranscription FactorsBRD4 protein, humanbromodomain and extra-terminal domain protein, humanBromodomain Containing ProteinsCell Cycle ProteinsNuclear ProteinsProteinsTranscription Factors

Identifiers

PMID30015487
PMCPMC6489120
OpenAlexW2883987961

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.