Evidence map›Paper›PMID 27046675›Full record

ArticleChemical communications (Cambridge, England)2016

An optimal hydrogen-bond surrogate for α-helices.

Stephen T Joy, Paramjit S Arora

Abstract read
In one paragraph

Article in Chemical communications (Cambridge, England), 2016. 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
–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

7 citing papers in PubMed.

  1. Reengineering of a Proteomimetic Pan-Ras Inhibitor into a Ras Degrader.Angewandte Chemie (International ed. in English) · 2025
    Article
  2. Review
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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

2 authors.

Stephen T JoyDepartment of Chemistry, New York University, New York, NY 10003, USA. arora@nyu.edu.
Paramjit S AroraDepartment of Chemistry, New York University, New York, NY 10003, USA. arora@nyu.edu.

Funding

Biomolecular Recognition with Artificial Alpha-HelicesR01GM073943 · NIGMS · NEW YORK UNIVERSITY · PI ARORA, PARAMJIT S · 2005 to 2018
$4.4M
NIGMS NIH HHS R01 GM073943NIGMS NIH HHS R01GM073943
6 · The paper itself

Abstract

Substitution of a main chain i → i + 4 hydrogen bond with a covalent bond can nucleate and stabilize the α-helical conformation in peptides. Herein we describe the potential of different alkene isosteres to mimic intramolecular hydrogen bonds and stabilize α-helices in diverse peptide sequences.

Indexed as

Hydrogen BondingPeptidesProtein ConformationPeptides

Identifiers

PMID27046675
PMCPMC4836946

What OpenQuestion holds

Textmetadata
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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.