Evidence map›Paper›PMID 31391890›Full record

ArticleMedChemComm2019

Importance of lipophilicity for potent anti-herpes simplex virus-1 activity of α-hydroxytropolones.

Alex J Berkowitz, Abaigeal D Franson, Andreu Gazquez Cassals, Katherine A Donald, Alice J Yu, Aswin K Garimallaprabhakaran, Lynda A Morrison, Ryan P Murelli

Open access · bronzeAbstract read
In one paragraph

Article in MedChemComm, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.8field-weighted citation impact, top 27% 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

8 citing papers in PubMed, 8 citations in OpenAlex.

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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

8 authors at 3 institutions in 2 countries.

Alex J BerkowitzDepartment of Chemistry , Brooklyn College , The City University of New York , Brooklyn , NY , USA . Email: RPMurelli@brooklyn.cuny.edu.
Abaigeal D FransonDepartment of Molecular Microbiology and Immunology , Saint Louis University School of Medicine , St. Louis , MO , USA . Email: lynda.morrison@health.slu.edu.
Andreu Gazquez CassalsDepartment of Molecular Microbiology and Immunology , Saint Louis University School of Medicine , St. Louis , MO , USA . Email: lynda.morrison@health.slu.edu.
Katherine A DonaldDepartment of Molecular Microbiology and Immunology , Saint Louis University School of Medicine , St. Louis , MO , USA . Email: lynda.morrison@health.slu.edu.
Alice J YuDepartment of Molecular Microbiology and Immunology , Saint Louis University School of Medicine , St. Louis , MO , USA . Email: lynda.morrison@health.slu.edu.
Aswin K GarimallaprabhakaranDepartment of Chemistry , Brooklyn College , The City University of New York , Brooklyn , NY , USA . Email: RPMurelli@brooklyn.cuny.edu.
Lynda A MorrisonDepartment of Molecular Microbiology and Immunology , Saint Louis University School of Medicine , St. Louis , MO , USA . Email: lynda.morrison@health.slu.edu.
Ryan P MurelliDepartment of Chemistry , Brooklyn College , The City University of New York , Brooklyn , NY , USA . Email: RPMurelli@brooklyn.cuny.edu.ORCID 0000-0002-4247-3936
UCLouvain Saint-Louis Brussels · BEThe Graduate Center, CUNY · USCity University of New York · US

Funding

Development and Exploitation of New Synthetic Strategies for TropolonesSC1GM111158 · NIGMS · BROOKLYN COLLEGE · PI MURELLI, RYAN · 2015 to 2023
$3.1M
NIGMS NIH HHS SC1 GM111158
6 · The paper itself

Abstract

We previously reported that troponoid compounds profoundly inhibit replication of herpes simplex virus (HSV)-1 and HSV-2 in cell culture, including acyclovir-resistant mutants. Synthesis of 26 alpha-hydroxylated tropolones (αHTs) led to a preliminary structure-activity relationship highlighting the potency of bi-phenyl side chains. Here, we explore the structure-activity relationship in more detail, with a focus on various biaryl and other lipophilic molecules. Along with our prior structure-function analysis, we present a refined structure-activity relationship that reveals the importance of the lipophilicity and nature of the side chain for potent anti-HSV-1 activity in cells. We expect this new information will help guide future optimization of αHTs as HSV antivirals.

Identifiers

PMID31391890
PMCPMC6640544
OpenAlexW2947815615

What OpenQuestion holds

Textmetadata
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.