Evidence map›Paper›PMID 30987302›Full record

ArticleMolecules (Basel, Switzerland)2019

MCR Scaffolds Get Hotter with

Tryfon Zarganes-Tzitzikas, Gonçalo S Clemente, Philip H Elsinga, Alexander Dömling

Abstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
–field-weighted citation impact
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

12 citing papers in PubMed.

  1. A simplified, robust protocol for [Scientific reports · 2025
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  2. Improved Radiosynthesis of [ACS infectious diseases · 2025
    Article
  3. Simple and Efficient Synthesis ofPharmaceuticals (Basel, Switzerland) · 2024
    Article
  4. Automation of Copper-MediatedMolecules (Basel, Switzerland) · 2024
    Article
  5. One-Pot Radiosynthesis of [Molecules (Basel, Switzerland) · 2023
    Article
  6. Detrimental impact of aqueous mobile phases on 18F-labelled radiopharmaceutical analysisAnalytical methods : advancing methods and applications · 2023
    Article
  7. Automated synthesis ofEJNMMI radiopharmacy and chemistry · 2020
    Article
  8. Nucleophilic Synthesis of 6-l-[Molecules (Basel, Switzerland) · 2020
    Review
  9. Article
  10. Review
  11. Article
  12. Multicomponent Reactions.Molecules (Basel, Switzerland) · 2019
    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

4 authors.

Tryfon Zarganes-TzitzikasDepartment of Drug Design, Groningen Research Institute of Pharmacy, University of Groningen, 9713 AV Groningen, The Netherlands. ttzitzikas@yahoo.com.
Gonçalo S ClementeDepartment of Nuclear Medicine and Molecular Imaging, University Medical Center Groningen, University of Groningen, 9713 GZ Groningen, The Netherlands. g.dos.santos.clemente@umcg.nl.ORCID 0000-0002-0386-9559
Philip H ElsingaDepartment of Nuclear Medicine and Molecular Imaging, University Medical Center Groningen, University of Groningen, 9713 GZ Groningen, The Netherlands. p.h.elsinga@umcg.nl.
Alexander DömlingDepartment of Drug Design, Groningen Research Institute of Pharmacy, University of Groningen, 9713 AV Groningen, The Netherlands. a.s.s.domling@rug.nl.

Funding

Real-time discovery of inhibitors among billion compounds for preview and downloadR01GM097082 · NIGMS · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI CAMACHO, CARLOS J. · 2011 to 2020
$2.5M
Foundation for the National Institutes of Health 2R01GM097082-05Horizon 2020 Framework Programme AEGIS, grant agreement No 675555Horizon 2020 Framework Programme COFUND ALERT (grant agreement No 665250)KWF Kankerbestrijding grant agreement No 10504NIGMS NIH HHS R01 GM097082Qatar National Research Foundation NPRP6-065-3-012Stichting voor de Technische Wetenschappen project nº 13547
6 · The paper itself

Abstract

Imaging techniques, such as positron emission tomography (PET), represent great progress in the clinical development of drugs and diagnostics. However, the efficient and timely synthesis of appropriately labeled compounds is a largely unsolved problem. Numerous small drug-like molecules with high structural diversity can be synthesized via convergent multicomponent reactions (MCRs). The combination of PET labeling with MCR synthesis of biologically active compounds can greatly simplify radioanalytical and imaging-based analysis. In a proof-of-concept study, we optimized robust on-site radiolabeling conditions that were subsequently applied to several structurally different drug-like MCR scaffolds (e.g., arenes, β-lactam, tetrazole, and oxazole). These labeled scaffolds were synthesized via pinacol-derived aryl boronic esters (arylBPin) by copper-mediated oxidative

Indexed as

Positron-Emission TomographyStaining and LabelingChromatography, Thin LayerFluorine RadioisotopesRadiochemistryTetrazoles1H-tetrazoleFluorine RadioisotopesTetrazolesboronic pinacol estersfluor-18multicomponent reactionspositron emission tomographyradiochemistry

Identifiers

PMID30987302
PMCPMC6480256

What OpenQuestion holds

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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.