Evidence map›Paper›PMID 38938790›Full record

ArticleJACS Au2024

Molecular Aggregation Strategy for Inhibiting DNases.

Kenta Morita, Tomoko Moriwaki, Shunsuke Habe, Mariko Taniguchi-Ikeda, Tadao Hasegawa, Yusuke Minato, Takashi Aoi, Tatsuo Maruyama

Abstract read
In one paragraph

Article in JACS Au, 2024. 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. Review
  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

8 authors.

Kenta MoritaDepartment of Chemical Science and Engineering, Graduate School of Engineering, Kobe University 1-1 Rokkodai, Nada-ku, Kobe 657-8501, Japan.ORCID https://orcid.org/0000-0002-2156-4812
Tomoko MoriwakiDepartment of Chemical Science and Engineering, Graduate School of Engineering, Kobe University 1-1 Rokkodai, Nada-ku, Kobe 657-8501, Japan.
Shunsuke HabeDepartment of Chemical Science and Engineering, Graduate School of Engineering, Kobe University 1-1 Rokkodai, Nada-ku, Kobe 657-8501, Japan.
Mariko Taniguchi-IkedaDepartment of Clinical Genetics, Fujita Health University Hospital 1-98 Dengakugakubo, Kutsukake-chou, Toyoake, Aichi 470-1192, Japan.
Tadao HasegawaDepartment of Bacteriology, Graduate School of Medical Sciences, Nagoya City University, 1 Kawasumi, Mizuho-cho, Mizuho-ku, Nagoya 467-8601, Japan.
Yusuke MinatoDepartment of Microbiology, School of Medicine, Fujita Health University, 1-98 Dengakugakubo, Kutsukake-chou, Toyoake, Aichi 470-1192, Japan.
Takashi AoiDivision of Stem Cell Medicine, Graduate School of Medicine, Kobe University, 7-5-1 Kusunoki-cho, Chuo-ku, Kobe 650-0017, Japan.
Tatsuo MaruyamaDepartment of Chemical Science and Engineering, Graduate School of Engineering, Kobe University 1-1 Rokkodai, Nada-ku, Kobe 657-8501, Japan.ORCID https://orcid.org/0000-0003-2428-1911

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This study highlights the novel potential of molecular aggregates as inhibitors of a disease-related protein. Enzyme inhibitors have been studied and developed as molecularly targeted drugs and have been applied for cancer, autoimmune diseases, and infections. In many cases, enzyme inhibitors that are used for therapeutic applications interact directly with enzymes in a molecule-to-molecule manner. We found that the aggregates of a small compound, Mn007, inhibited bovine pancreatic DNase I. Once Mn007 molecules formed aggregates, they exhibited inhibitory effects specific to DNases that require divalent metal ions. A DNase secreted by

Identifiers

PMID38938790
PMCPMC11200219

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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.