Pilot corpus: NIH-funded biomedical datasets. Any DOI can be scored on demand — network effects sharpen as coverage grows.

Design and synthesis of a library of C2-substituted sulfamidoadenosines to probe bacterial permeability

Bioorganic & Medicinal Chemistry Letters(2023)10.1016/j.bmcl.2023.129486Source: DataRank Database

Design and synthesis of a library of C2-substituted sulfamidoadenosines to probe bacterial permeability is a research paper published in Bioorganic & Medicinal Chemistry Letters (2023). On theSindex it has a DataRank of 0. It has been cited 2 times.

N/A

0DataRank · unranked

Scored on demand from live citation data

Open Access2 citations

Download PDF

Cite:

DataRank reads this dataset's downstream impact straight off the citation graph — no black box, no proprietary weighting. How is this computed?

›Methodology & internals

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Pipeline:MetadataData-paper checkEnrichmentCitation networkScoring

Enrichment:Funding (3 grants)Impact (FWCI 0.23)OA: greenTopics (38)IDs (PubMed, PMC, OpenAlex)SDGs (1)

FAIR Checklist

Context only (not used in score)

Findable (1/2)

Has DOI

Accessible (1/2)

Open Access

Interoperable (0/2)

Reusable (0/3)

FAIR checklist signals are shown for context only and do not affect DataRank scoring.

Run a calibrated FAIR evaluation for this paper →

We only score data papers we can read in full — never from an abstract alone.

Authors (8)

Julian P. Maceren ORCID,Mia Chung ORCID,Samantha Stone ORCID,Raphael Geißen ORCID,Melissa L. Boby ORCID

Live enrichment

PubMed:37734424 PMC:PMC10842738 OpenAlex:https://openalex.org/W4386852050

National Institutes of Health

Grant: P30 CA008748

National Institutes of Health

Grant: R01 AI136795

NIGMS NIH HHS

Grant: T32 GM073546

FWCI

0.23

Citation Percentile

0.4%

Citation Trend

2024

2025

greenLicense: https://doi.org/10.15223/policy-004

repositoryhttps://pmc.ncbi.nlm.nih.gov/articles/PMC10842738/pdf/nihms-1946982.pdf

publisherhttps://api.elsevier.com/content/article/PII:S0960894X23003645?httpAccept=text/xml

publisherhttps://api.elsevier.com/content/article/PII:S0960894X23003645?httpAccept=text/plain

repositoryhttps://www.ncbi.nlm.nih.gov/pmc/articles/10842738

Fields of Study

Synthesis and Catalytic ReactionsPhenothiazines and Benzothiazines Synthesis and ActivitiesClick Chemistry and ApplicationsAnti-Bacterial AgentsDrug DiscoveryEscherichia coliGram-Negative BacteriaPermeabilityAdenosine

MeSH Terms

AdenosineAnti-Bacterial AgentsEscherichia coliGram-Negative BacteriaPermeabilityDrug Discovery

Keywords

ChemistryChemical libraryCombinatorial chemistryEffluxBacteriaCell envelopeEscherichia coliGram-negative bacteriaChemical synthesisReagentSonogashira couplingStereochemistryBiophysicsBiochemistryIn vitroSmall moleculeOrganic chemistryCatalysisBiologyAntibiotic Resistancenucleoside analoguedrug discoveryDiversity-oriented Synthesis

Sustainable Development Goals

SDG 0: Good health and well-being