Evidence map›Paper›PMID 32730943›Full record

ArticleBioorganic & medicinal chemistry letters2020

Mechanistic insights into the activation of ester prodrugs of 666-15.

Fuchun Xie, Pedro Martín-Acosta, Bingbing X Li, Xiangshu Xiao

Open access · greenAbstract read
In one paragraph

Article in Bioorganic & medicinal chemistry letters, 2020. 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
0.2field-weighted citation impact, top 50% 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

2 citing papers in PubMed, 2 citations in OpenAlex.

  1. Article
  2. Review
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

4 authors at 1 institution in 1 country.

Fuchun XieProgram in Chemical Biology, Department of Chemical Physiology and Biochemistry, 3181 SW Sam Jackson Park Road, Portland, OR 97239, United States.
Pedro Martín-AcostaProgram in Chemical Biology, Department of Chemical Physiology and Biochemistry, 3181 SW Sam Jackson Park Road, Portland, OR 97239, United States.
Bingbing X LiProgram in Chemical Biology, Department of Chemical Physiology and Biochemistry, 3181 SW Sam Jackson Park Road, Portland, OR 97239, United States.
Xiangshu XiaoProgram in Chemical Biology, Department of Chemical Physiology and Biochemistry, 3181 SW Sam Jackson Park Road, Portland, OR 97239, United States; Knight Cancer Institute, Oregon Health & Science University, 3181 SW Sam Jackson Park Road, Portland, OR 97239, United States. Electronic address: xiaoxi@ohsu.edu.
Oregon Health & Science University · US

Funding

Targeting Hsp60 to Inhibit CREB-mediated Gene TranscriptionR01GM122820 · NIGMS · OREGON HEALTH & SCIENCE UNIVERSITY · PI XIAO, XIANGSHU · 2017 to 2023
$1.9M
NIGMS NIH HHS R01 GM122820
6 · The paper itself

Abstract

cAMP-response element binding protein (CREB) is an oncogenic transcription factor implicated in many different types of cancer. We previously reported the discovery of 666-15 as a potent inhibitor of CREB-mediated gene transcription. In an effort to improve the aqueous solubility of 666-15, amino ester prodrugs 1 and 4 were designed and synthesized. Detailed chemical and biological studies of 1 and 4 revealed that a small portion of the prodrugs were converted into 666-15 through intermediate 3 instead of a long-range O,N-acyl transfer reaction that was initially proposed. These results provide unique insights into the activation of these ester prodrugs.

Indexed as

AnilidesCyclic AMP Response Element-Binding ProteinDrug StabilityEstersHEK293 CellsHumansHydrolysisNaphthalenesProdrugsSolubility666-15 compoundAnilidesCREB1 protein, humanCyclic AMP Response Element-Binding ProteinEstersNaphthalenesProdrugsCancerCREBInhibitorProdrugTranscription

Identifiers

PMID32730943
PMCPMC7530057
OpenAlexW3044098632

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.