Evidence map›Paper›PMID 25958855›Full record

ArticleOrganic & biomolecular chemistry2015

HIV-1 drug discovery: targeting folded RNA structures with branched peptides.

Jessica E Wynn, Webster L Santos

Open access · hybridAbstract read
In one paragraph

Article in Organic & biomolecular chemistry, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.4field-weighted citation impact, top 19% 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

4 citing papers in PubMed, 17 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. 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

2 authors at 1 institution in 1 country.

Jessica E WynnDepartment of Chemistry and Virginia Tech Center for Drug Discovery, Virginia Tech, Blacksburg, Virginia 24061, USA. santosw@vt.edu.
Webster L Santos
Virginia Tech · US

Funding

RNA As A Therapeutic TargetR01GM093834 · NIGMS · VIRGINIA POLYTECHNIC INST AND ST UNIV · PI SANTOS, WEBSTER L · 2010 to 2014
$1.6M
NIGMS NIH HHS GM093834NIGMS NIH HHS R01 GM093834
6 · The paper itself

Abstract

Human immunodeficiency virus type 1 (HIV-1) is an RNA virus that is prone to high rates of mutation. While the disease is managed with current antiretroviral therapies, drugs with a new mode of action are needed. A strategy towards this goal is aimed at targeting the native three-dimensional fold of conserved RNA structures. This perspective highlights medium-sized peptides and peptidomimetics used to target two conserved RNA structures of HIV-1. In particular, branched peptides have the capacity to bind in a multivalent fashion, utilizing a large surface area to achieve the necessary affinity and selectivity toward the target RNA.

Indexed as

Amino Acid SequenceAnti-HIV AgentsBase SequenceDrug DiscoveryHIV-1HIV InfectionsHumansModels, MolecularMolecular Sequence DataMolecular Targeted TherapyNucleic Acid ConformationPeptide LibraryPeptidesRNA, ViralAnti-HIV AgentsPeptide LibraryPeptidesRNA, Viral

Identifiers

PMID25958855
PMCPMC4511164
OpenAlexW2124618116

What OpenQuestion holds

Textmetadata
LicenceTDM
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.