Evidence map›Paper›PMID 31391913›Full record

ArticleChemical science2019

Isolated α-turn and incipient γ-helix.

Fatemeh M Mir, Marco Crisma, Claudio Toniolo, William D Lubell

Abstract read
In one paragraph

Article in Chemical science, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Turn-Induction in Peptides Incorporating Novel Cyrene-Derived α,α-Disubstituted Amino Acid.Journal of peptide science : an official publication of the European Peptide Society · 2026
    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

4 authors.

Fatemeh M MirDépartement de Chimie , Université de Montréal , C. P. 6128, Succursale Centre-Ville , Montréal , Québec , Canada H3C 3J7 . Email: william.lubell@umontreal.ca.ORCID 0000-0002-0653-9010
Marco CrismaDepartment of Chemistry , University of Padova and Institute of Biomolecular Chemistry , Padova Unit , CNR , 35131 Padova , Italy.ORCID 0000-0003-3552-4106
Claudio TonioloDepartment of Chemistry , University of Padova and Institute of Biomolecular Chemistry , Padova Unit , CNR , 35131 Padova , Italy.ORCID 0000-0002-2327-1423
William D LubellDépartement de Chimie , Université de Montréal , C. P. 6128, Succursale Centre-Ville , Montréal , Québec , Canada H3C 3J7 . Email: william.lubell@umontreal.ca.ORCID 0000-0002-3080-2712

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The unique abilities of homo-oligo-adamantyl peptides to adopt α- and γ-turn conformations are demonstrated by X-ray diffraction, and NMR and FT-IR absorption spectroscopies. Assembled by an Ugi multiple component reaction strategy,

Identifiers

PMID31391913
PMCPMC6640192

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.