Evidence map›Paper›PMID 38646883›Full record

ArticleACS chemical biology2024

GS-441524-Diphosphate-Ribose Derivatives as Nanomolar Binders and Fluorescence Polarization Tracers for SARS-CoV-2 and Other Viral Macrodomains.

Kewen Peng, Shamar D Wallace, Saket R Bagde, Jialin Shang, Ananya Anmangandla, Sadhan Jana, J Christopher Fromme, Hening Lin

Open access · hybridAbstract read
In one paragraph

Article in ACS chemical biology, 2024. 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
0.4field-weighted citation impact, top 41% 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, 1 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 2 institutions in 1 country.

Kewen PengDepartment of Chemistry and Chemical Biology, Cornell University, Ithaca, New York 14853, United States.
Shamar D WallaceDepartment of Molecular Biology and Genetics, Weill Institute for Cell and Molecular Biology, Cornell University, Ithaca, New York 14853, United States.
Saket R BagdeDepartment of Molecular Biology and Genetics, Weill Institute for Cell and Molecular Biology, Cornell University, Ithaca, New York 14853, United States.ORCID 0000-0001-9800-9326
Jialin ShangDepartment of Chemistry and Chemical Biology, Cornell University, Ithaca, New York 14853, United States.
Ananya AnmangandlaDepartment of Chemistry and Chemical Biology, Cornell University, Ithaca, New York 14853, United States.ORCID 0000-0002-2999-4067
Sadhan JanaDepartment of Chemistry and Chemical Biology, Cornell University, Ithaca, New York 14853, United States.
J Christopher FrommeDepartment of Molecular Biology and Genetics, Weill Institute for Cell and Molecular Biology, Cornell University, Ithaca, New York 14853, United States.
Hening LinHoward Hughes Medical Institute, Department of Chemistry and Chemical Biology, Department of Molecular Biology and Genetics, Cornell University, Ithaca, New York 14853, United States.ORCID 0000-0002-0255-2701
Cornell University · USHoward Hughes Medical Institute · US

Funding

Training and OutreachP30GM124166 · NIGMS · CORNELL UNIVERSITY · PI RICHARD A. CERIONE · 2019 to 2026
$28.3M
GTPase Regulation of the Golgi Complex (Diversity Supplement 2023)R35GM136258 · NIGMS · CORNELL UNIVERSITY · PI J Christopher Fromme · 2020 to 2026
$4.0M
Histone lactylation pathway in hair cycle: deacylases and their protein targetsR01AR078555 · NIAMS · UNIVERSITY OF CHICAGO · PI LIN, HENING, ZHAO, YINGMING · 2021 to 2025
$3.3M
Training future leaders at the chemistry-biology interfaceT32GM138826 · NIGMS · CORNELL UNIVERSITY · PI Jeremy Baskin · 2021 to 2026
$2.6M
High-throughput label-free detection system for biomolecular interaction analysisS10OD032273 · OD · CORNELL UNIVERSITY · PI DELISA, MATTHEW P · 2022 to 2022
$350k
NIAMS NIH HHS R01 AR078555NIGMS NIH HHS P30 GM124166NIGMS NIH HHS R35 GM136258NIGMS NIH HHS T32 GM138826NIH HHS S10 OD032273
6 · The paper itself

Abstract

Viral macrodomains that can bind to or hydrolyze protein adenosine diphosphate ribosylation (ADP-ribosylation) have emerged as promising targets for antiviral drug development. Many inhibitor development efforts have been directed against the severe acute respiratory syndrome coronavirus 2 macrodomain 1 (SARS-CoV-2 Mac1). However, potent inhibitors for viral macrodomains are still lacking, with the best inhibitors still in the micromolar range. Based on

Indexed as

Antiviral AgentsFluorescence PolarizationSARS-CoV-2Adenosine Diphosphate RiboseAdenosine MonophosphateChikungunya virusCOVID-19COVID-19 Drug TreatmentEncephalitis Virus, Venezuelan EquineHumansMiddle East Respiratory Syndrome CoronavirusProtein BindingProtein DomainsAdenosine Diphosphate RiboseAdenosine MonophosphateAntiviral AgentsGS-441524 monophosphate

Identifiers

PMID38646883
PMCPMC11106745
OpenAlexW4395003177

What Socratic 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 Socratic graph.