Evidence map›Paper›PMID 37627746›Full record

ArticleAntibiotics (Basel, Switzerland)2023

Enhancing Chemical Stability through Structural Modification of Antimicrobial Peptides with Non-Proteinogenic Amino Acids.

Takahito Ito, Natsumi Matsunaga, Megumi Kurashima, Yosuke Demizu, Takashi Misawa

Open access · goldAbstract read
In one paragraph

Article in Antibiotics (Basel, Switzerland), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
2.2field-weighted citation impact, top 12% 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

7 citing papers in PubMed, 12 citations in OpenAlex.

  1. Novel Peptide-Triazole Conjugates: Strategic Synthesis, Antimicrobial Properties, and Molecular Docking Study.Journal of peptide science : an official publication of the European Peptide Society · 2026
    Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Total synthesis of [β-HIle]RSC advances · 2024
    Article
  7. 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

5 authors at 1 institution in 1 country.

Takahito ItoNational Institute of Health Sciences, 3-25-26, Tonomachi, Kawasaki-shi 210-9501, Japan.ORCID 0009-0006-0170-436X
Natsumi MatsunagaNational Institute of Health Sciences, 3-25-26, Tonomachi, Kawasaki-shi 210-9501, Japan.
Megumi KurashimaNational Institute of Health Sciences, 3-25-26, Tonomachi, Kawasaki-shi 210-9501, Japan.
Yosuke DemizuNational Institute of Health Sciences, 3-25-26, Tonomachi, Kawasaki-shi 210-9501, Japan.ORCID 0000-0001-7521-4861
Takashi MisawaNational Institute of Health Sciences, 3-25-26, Tonomachi, Kawasaki-shi 210-9501, Japan.
National Institute of Health Sciences · JP

Funding

Japan Agency for Medical Research and Development 21fk08622j0001Japan Agency for Medical Research and Development 22ak0101185j0301Japan Agency for Medical Research and Development 22fk0108622j0002Japan Agency for Medical Research and Development 22fk0210110j0401Japan Agency for Medical Research and Development 22fk0310506j0701Japan Agency for Medical Research and Development 22mk0101197j0002Japan Society for the Promotion of Science 20K06958Japan Society for the Promotion of Science 21K05320Japan Society for the Promotion of Science JP18H05502
6 · The paper itself

Abstract

Multidrug-resistant bacteria (MDRB) remain a significant threat to humanity, resulting in over 1.2 million deaths per year. To combat this problem effectively, the development of therapeutic agents with diverse mechanisms of action is crucial. Antimicrobial peptides (AMPs) have emerged as promising next-generation therapeutics to combat infectious diseases, particularly MDRB. By targeting microbial membranes and inducing lysis, AMPs can effectively inhibit microbial growth, making them less susceptible to the development of resistance. Numerous structural advancements have been made to optimize the efficacy of AMPs. Previously, we developed 17KKV-Aib, a derivative of the Magainin 2 (Mag2) peptide, by incorporating a,a-disubstituted amino acids (dAAs) to modulate its secondary structure. 17KKV-Aib demonstrated potent antimicrobial activity against Gram-positive and Gram-negative bacteria, including multidrug-resistant

Indexed as

antimicrobial peptidescationic α,α-disubstituted amino acidsdigestion tolerancesecondary structure

Identifiers

PMID37627746
PMCPMC10451648
OpenAlexW4385948824

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.