Evidence map›Paper›PMID 38670538›Full record

ArticleJournal of medicinal chemistry2024

Development of Benziodarone Analogues with Enhanced Potency for Selective Binding to Transthyretin in Human Plasma.

Mineyuki Mizuguchi, Yusuke Nakagawa, Takeshi Yokoyama, Takuya Okada, Kanako Fujii, Kanoko Takahashi, Nguyen Ngoc Thanh Luan, Yuko Nabeshima, Kayoko Kanamitsu, Shinsaku Nakagawa and 4 more

Open access · hybridAbstract read
In one paragraph

Article in Journal of medicinal chemistry, 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
1.4field-weighted citation impact, top 20% 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, 6 citations in OpenAlex.

  1. Article
  2. A Snapshot of the Most Recent Transthyretin Stabilizers.International journal of molecular sciences · 2024
    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

14 authors at 5 institutions in 1 country.

Mineyuki MizuguchiFaculty of Pharmaceutical Sciences, University of Toyama, Toyama 930-0194, Japan.ORCID 0000-0003-0450-0339
Yusuke NakagawaGraduate School of Innovative Life Science, University of Toyama, Toyama 930-8555, Japan.
Takeshi YokoyamaFaculty of Pharmaceutical Sciences, University of Toyama, Toyama 930-0194, Japan.ORCID 0000-0002-5362-8606
Takuya OkadaGraduate School of Innovative Life Science, University of Toyama, Toyama 930-8555, Japan.ORCID 0000-0003-2228-7711
Kanako FujiiGraduate School of Medicine and Pharmaceutical Sciences, University of Toyama, Toyama 930-0194, Japan.
Kanoko TakahashiGraduate School of Pharma-Medical Sciences, University of Toyama, Toyama 930-8555, Japan.
Nguyen Ngoc Thanh LuanGraduate School of Innovative Life Science, University of Toyama, Toyama 930-8555, Japan.
Yuko NabeshimaFaculty of Pharmaceutical Sciences, University of Toyama, Toyama 930-0194, Japan.
Kayoko KanamitsuGraduate School of Pharmaceutical Sciences, the University of Tokyo, Tokyo 113-0033, Japan.
Shinsaku NakagawaGraduate School of Pharmaceutical Sciences, Osaka University, Osaka 565-0871, Japan.
Shiori YamakawaDepartment of Neurology, Graduate School of Medical Sciences, Kumamoto University, Kumamoto 860-8556, Japan.
Mitsuharu UedaDepartment of Neurology, Graduate School of Medical Sciences, Kumamoto University, Kumamoto 860-8556, Japan.
Yukio AndoFaculty of Pharmaceutical Sciences, Nagasaki International University, Sasebo 859-3298, Japan.
Naoki ToyookaGraduate School of Innovative Life Science, University of Toyama, Toyama 930-8555, Japan.ORCID 0000-0002-9568-1528
University of Toyama · JPKumamoto University · JPNagasaki International University · JPOsaka University of Pharmaceutical Sciences · JPThe University of Tokyo · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Transthyretin amyloidosis is a fatal disorder caused by transthyretin amyloid aggregation. Stabilizing the native structure of transthyretin is an effective approach to inhibit amyloid aggregation. To develop kinetic stabilizers of transthyretin, it is crucial to explore compounds that selectively bind to transthyretin in plasma. Our recent findings demonstrated that the uricosuric agent benziodarone selectively binds to transthyretin in plasma. Here, we report the development of benziodarone analogues with enhanced potency for selective binding to transthyretin in plasma compared to benziodarone. These analogues featured substituents of chlorine, bromine, iodine, a methyl group, or a trifluoromethyl group, at the 4-position of the benzofuran ring. X-ray crystal structure analysis revealed that CH···O hydrogen bonds and a halogen bond are important for the binding of the compounds to the thyroxine-binding sites. The bioavailability of benziodarone analogues with 4-Br, 4-Cl, or 4-CH

Identifiers

PMID38670538
PMCPMC11089511
OpenAlexW4395659463

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.