Evidence map›Paper›PMID 29604582›Full record

ArticleEuropean journal of medicinal chemistry2018

Syntheses and in vitro evaluation of new S1PR1 compounds and initial evaluation of a lead F-18 radiotracer in rodents.

Zonghua Luo, Adam J Rosenberg, Hui Liu, Junbin Han, Zhude Tu

Open access · greenAbstract read
In one paragraph

Article in European journal of medicinal chemistry, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.2field-weighted citation impact, top 21% 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

17 citing papers in PubMed, 26 citations in OpenAlex.

  1. Automated production of radiotracer [Applied radiation and isotopes : including data, instrumentation and methods for use in agriculture, industry and medicine · 2025
    Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Drug Delivery Strategies to Overcome the Blood-Brain Barrier (BBB).Handbook of experimental pharmacology · 2022
    Article
  10. Review
  11. ACS chemical neuroscience · 2021
    Article
  12. Article
  13. A Novel RadioimmuneFrontiers in immunology · 2021
    Article
  14. Review
  15. Review
  16. Review
  17. 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

5 authors at 1 institution in 1 country.

Zonghua LuoDepartment of Radiology, Washington University School of Medicine, St. Louis, MO 63110, USA.
Adam J RosenbergDepartment of Radiology, Washington University School of Medicine, St. Louis, MO 63110, USA.
Hui LiuDepartment of Radiology, Washington University School of Medicine, St. Louis, MO 63110, USA.
Junbin HanDepartment of Radiology, Washington University School of Medicine, St. Louis, MO 63110, USA.
Zhude TuDepartment of Radiology, Washington University School of Medicine, St. Louis, MO 63110, USA. Electronic address: zhudetu@wustl.edu.
Washington University in St. Louis · US

Funding

TrainingP41GM103422 · NIGMS · WASHINGTON UNIVERSITY · PI YARASHESKI, KEVIN E · 2012 to 2019
$12.0M
PET SPHINGOSINE-1-PHOSPHATE RECEPTOR 1 (S1PR1) RADIOTRACERS FOR MULTIPLE SCLEROSISR01NS103988 · NINDS · WASHINGTON UNIVERSITY · PI Tammie Lee Smith Benzinger, Zhude Tu · 2017 to 2026
$5.3M
PET PROBES FOR IMAGING THE VESICULAR ACETYLCHOLINE TRANSPORTERR01NS075527 · NINDS · WASHINGTON UNIVERSITY · PI TU, ZHUDE · 2011 to 2021
$4.9M
Neuroimaging of PDE10AR01NS103957 · NINDS · WASHINGTON UNIVERSITY · PI PERLMUTTER, JOEL SYNES, TU, ZHUDE · 2017 to 2021
$3.1M
A Biomedical Mass Spectrometry Resource: Ongoing Driving Biomedical ProjectsR24GM136766 · NIGMS · WASHINGTON UNIVERSITY · PI GROSS, MICHAEL L · 2020 to 2022
$2.3M
DEVELOPING PET AGENTS FOR IMAGING PHOSPHODIESTERASE 10A (PDE10A)R33MH092797 · NIMH · WASHINGTON UNIVERSITY · PI TU, ZHUDE · 2013 to 2015
$1.5M
DEVELOPING PET AGENTS FOR IMAGING PHOSPHODIESTERASE 10A (PDE10A)R21MH092797 · NIMH · WASHINGTON UNIVERSITY · PI TU, ZHUDE · 2011 to 2012
$530k
NIGMS NIH HHS P41 GM103422NIGMS NIH HHS R24 GM136766NIMH NIH HHS R21 MH092797NIMH NIH HHS R33 MH092797NINDS NIH HHS R01 NS075527NINDS NIH HHS R01 NS103957NINDS NIH HHS R01 NS103988
6 · The paper itself

Abstract

Thirteen new sphingosine-1-phosphate receptor 1 (S1PR1) ligands were designed and synthesized by replacing azetidine-3-carboxylic acid moiety of compound 4 with new polar groups. The in vitro binding potency of these new analogs toward S1PR1 was determined. Out of 13 new compounds, four compounds 9a, 10c, 12b, and 16b displayed high S1PR1 binding potency with IC

Indexed as

AnimalsAnti-Inflammatory Agents, Non-SteroidalAzetidinecarboxylic AcidDose-Response Relationship, DrugFluorine RadioisotopesInflammationLigandsLipopolysaccharidesMiceMolecular StructurePositron-Emission TomographyRadiopharmaceuticalsReceptors, LysosphingolipidSphingosine-1-Phosphate ReceptorsStructure-Activity RelationshipTissue DistributionAnti-Inflammatory Agents, Non-SteroidalAzetidinecarboxylic AcidFluorine RadioisotopesLigandsLipopolysaccharidesRadiopharmaceuticalsReceptors, LysosphingolipidS1pr1 protein, mouseSphingosine-1-Phosphate ReceptorsAutoradiographyBiodistributionF-18 radiotracerMultiple sclerosisPETSphingosine-1-phosphate receptor 1

Identifiers

PMID29604582
PMCPMC5908474
OpenAlexW2793470573

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.