Evidence map›Paper›PMID 41885300›Full record

ReviewBioconjugate chemistry2026

Linker Chemistry in Radiopharmaceutical Design.

Ava Stoddard, Kiarra Furey, Gina Dehlavi, Mayuresh M Mane, Joni Sebastiano, Brian M Zeglis

Abstract readReview
In one paragraph

Review in Bioconjugate chemistry, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

6 authors.

Ava StoddardDepartment of Chemistry, Hunter College, City University of New York, New York, New York 10065, United States.
Kiarra FureyDepartment of Chemistry, Hunter College, City University of New York, New York, New York 10065, United States.ORCID 0009-0004-0175-8670
Gina DehlaviDepartment of Chemistry, Hunter College, City University of New York, New York, New York 10065, United States.
Mayuresh M ManeDepartment of Chemistry, Hunter College, City University of New York, New York, New York 10065, United States.
Joni SebastianoDepartment of Chemistry, Hunter College, City University of New York, New York, New York 10065, United States.
Brian M ZeglisDepartment of Chemistry, Hunter College, City University of New York, New York, New York 10065, United States.ORCID 0000-0002-9091-744X

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Nicholas D Socci · 1985 to 2026
$347.4M
Novel Transgenic Mouse Models Addressing Outstanding Translational Barriers in Antibody-Based TherapeuticsR01CA244327 · NCI · ROCKEFELLER UNIVERSITY · PI BOURNAZOS, STYLIANOS · 2020 to 2024
$3.0M
Autoantibodies to tumor-derived neoepitopes as biomarkers and immunoPET agents for the early detection of small cell lung cancerR01CA281801 · NCI · FRED HUTCHINSON CANCER CENTER · PI Delphine L Chen, PAUL D. LAMPE · 2023 to 2026
$2.4M
ImmunoPET Probes for the Imaging of Lyme DiseaseR01AI175417 · NIAID · HUNTER COLLEGE · PI Maria Gomes-Solecki, WEIGANG QIU · 2023 to 2026
$2.2M
Novel Reagents for Rapid and Stable Thiol-Based BioconjugationsR01CA240963 · NCI · HUNTER COLLEGE · PI ZEGLIS, BRIAN MATTHEW · 2019 to 2023
$1.6M
Targeting DNA Mismatches for Auger Electron RadiotherapyR21CA280595 · NCI · HUNTER COLLEGE · PI HUMM, JOHN L, ZEGLIS, BRIAN MATTHEW · 2023 to 2023
$458k
The Development of Radiotherapeutic Paradigms for Desmoplastic Small Round Cell TumorR21CA309945 · NCI · HUNTER COLLEGE · PI Filemon S Dela Cruz, Brian Matthew Zeglis · 2026 to 2026
$431k
NCI NIH HHS P30 CA008748NCI NIH HHS R01 CA240963NCI NIH HHS R01 CA244327NCI NIH HHS R01 CA281801NCI NIH HHS R21 CA280595NCI NIH HHS R21 CA309945NIAID NIH HHS R01 AI175417
6 · The paper itself

Abstract

Over the last half century, molecularly targeted bioconjugates have revolutionized nuclear medicine. An array of vectors, ranging from small molecule peptidomimetics to macromolecular immunoglobulins, has been radiolabeled with radionuclides to create probes that have been deployed in both the laboratory and the clinic for positron emission tomography (PET), single photon emission computed tomography (SPECT), and radiopharmaceutical therapy. Generally speaking, these compounds have four constituent parts: (i) a targeting vector; (ii) a radionuclide; (iii) a labeling moiety, such as a chelator for radiometals or a prosthetic group for radiohalogens; and (iv) a linker that connects the vector and the labeling moiety. Each of these parts is critical to the performance of the radiopharmaceutical, but the importance of the former─the linker─can be lost in the shadow of its flashier teammates. Strictly speaking, the linker's job is simple: stably connect the vector and the radiolabeling moiety so that they do not become detached

Indexed as

Drug DesignRadiopharmaceuticalsAnimalsHumansRadiopharmaceuticals

Identifiers

PMID41885300
PMCPMC13088039

What OpenQuestion holds

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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 OpenQuestion graph.