Evidence map›Paper›PMID 42415161›Full record

ArticleChemMedChem2026

Fluorinated Aminopiperidones as Non-Glutarimide Thalidomide Analogs: Stereodivergent Synthesis and Validation.

Boštjan Adamlje, Tihomir Tomašič, Christian Steinebach, Sebastian Ebeling, Alexander Herrmann, Marcus D Hartmann, Jessica L Horner, Kinjal Bhadresha, Cindy H Chau, William D Figg and 2 more

Abstract read
In one paragraph

Article in ChemMedChem, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

12 authors.

Boštjan AdamljeFaculty of Pharmacy, University of Ljubljana, Ljubljana, Slovenia.
Tihomir TomašičFaculty of Pharmacy, University of Ljubljana, Ljubljana, Slovenia.
Christian SteinebachInstitute of Pharmacy, Pharmaceutical/Medicinal Chemistry, University of Greifswald, Greifswald, Germany.
Sebastian EbelingMax Planck Institute for Biology Tübingen, Tübingen, Germany.
Alexander HerrmannMax Planck Institute for Biology Tübingen, Tübingen, Germany.
Marcus D HartmannMax Planck Institute for Biology Tübingen, Tübingen, Germany.ORCID https://orcid.org/0000-0001-6937-5677
Jessica L HornerMolecular Pharmacology Section, Genitourinary Malignancies Branch, Center for Cancer Research, National Cancer Institute, NIH, Bethesda, Maryland, USA.
Kinjal BhadreshaMolecular Pharmacology Section, Genitourinary Malignancies Branch, Center for Cancer Research, National Cancer Institute, NIH, Bethesda, Maryland, USA.
Cindy H ChauMolecular Pharmacology Section, Genitourinary Malignancies Branch, Center for Cancer Research, National Cancer Institute, NIH, Bethesda, Maryland, USA.ORCID https://orcid.org/0000-0002-6928-3833
William D FiggMolecular Pharmacology Section, Genitourinary Malignancies Branch, Center for Cancer Research, National Cancer Institute, NIH, Bethesda, Maryland, USA.
Izidor SosičFaculty of Pharmacy, University of Ljubljana, Ljubljana, Slovenia.
Andrej Emanuel CotmanFaculty of Pharmacy, University of Ljubljana, Ljubljana, Slovenia.ORCID https://orcid.org/0000-0003-2528-396X

Funding

Development of Anticancer AgentsZIASC006538 · NCI · DIVISION OF CLINICAL SCIENCES - NCI · PI FIGG, WILLIAM DOUGLAS · 2009 to 2025
$8.6M
Deutsche Forschungsgemeinschaft 530691087Deutsche Forschungsgemeinschaft 552374678Javna Agencija za Raziskovalno Dejavnost RS J1-50023Javna Agencija za Raziskovalno Dejavnost RS J1-50037Javna Agencija za Raziskovalno Dejavnost RS P1-0208Javna Agencija za Raziskovalno Dejavnost RS SN-ZRD/22-27/510NIH HHS ZIA SC 006538
6 · The paper itself

Abstract

The glutarimide fragment is a key pharmacophore in cereblon-binding immunomodulatory drugs and proteolysis-targeting chimeras, yet exploration of non-glutarimide scaffolds remains limited. Here, we report the design, synthesis, and evaluation of fluorinated aminopiperidones as three-dimensional, non-glutarimide thalidomide analogs. By replacing a single glutarimide carbonyl with a stereogenic C*-CF

Indexed as

PiperidonesThalidomideHalogenationHumansMolecular StructureStereoisomerismStructure-Activity RelationshipglutarimidePiperidonesThalidomidebioisosterismdiastereoselectivitydrug designfluorinePROTAC

Identifiers

PMID42415161
PMCPMC13342437

What OpenQuestion holds

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Registered trials

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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.